Literature DB >> 34415963

Sex differences in total cholesterol of Vietnamese adults.

Nga Thi Thu Tran1, Christopher Leigh Blizzard1, Khue Ngoc Luong2, Ngoc Le Van Ngoc Truong2, Bao Quoc Tran2, Petr Otahal1, Mark R Nelson1, Costan G Magnussen1,3, Tan Van Bui1, Velandai Srikanth4, Thuy Bich Au1, Son Thai Ha2, Hai Ngoc Phung1, Mai Hoang Tran1, Michele Callisaya1,4, Seana Gall1.   

Abstract

BACKGROUND: The mid-life emergence of higher levels of total cholesterol (TC) for women than for men has been observed in different Western and Asian populations. The aim of this study was to investigate whether there is evidence of this in Vietnam and, if so, whether it can be explained by ageing, by body size and fatness, or by socio-demographic characteristics and behavioural factors.
METHODS: Participants (n = 14706, 50.9% females) aged 25-64 years were selected by multi-stage stratified cluster sampling from eight provinces each representing one of the eight geographical regions of Vietnam. Measurements were made using the World Health Organization STEPS protocols. Linear regression was used to assess the independent contributions of potential explanatory factors to mean levels of TC. Data were analysed using complex survey methods.
RESULTS: Men and women had similar mean levels of body mass index (BMI), and men had modestly higher mean levels of waist circumference (WC), in each 5-year age category. The mean TC of women increased more or less continuously across the age range but with a step-up at age 50 years to reach higher concentrations on average than those of their male counterparts. The estimated step-up was not eliminated by adjustment for anthropometric indices including BMI or WC, or by adjustment for socio-demographic characteristics or behavioural factors. The estimated step-up was least for women with the greatest weight.
CONCLUSION: There is a marked step-up in TC at age 50 years for Vietnamese women that cannot be explained by their age, or by their body fatness or its distribution, or by their socio-demographic characteristics or behavioural factors, and which results in greater mean levels of TC for middle-aged women than for their male counterparts in Vietnam.

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Year:  2021        PMID: 34415963      PMCID: PMC8378708          DOI: 10.1371/journal.pone.0256589

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Background

Raised total cholesterol is an important risk factor for ischemic heart disease and stroke, and has been estimated to be responsible for 13% of stroke deaths and 48% of ischaemic heart disease deaths [1] that together account for around 2.6 million deaths every year worldwide [2]. The global prevalence of high cholesterol, defined as total cholesterol (TC) equal to or greater than 5.0 mmol/l, was estimated to be 39% among adults aged 25 years or over in 2008 [1]. Reducing cholesterol has preventive and therapeutic benefits. It has been estimated that a 0.6 mmol/l (10%) reduction in serum cholesterol would lower the risk of ischaemic heart disease by 50% for men aged 40 years and by somewhat less for older men, with the reduction falling to 20% for men aged 70 years [3]. The American Heart Association reported the most up-to-date statistics related to heart disease that long-term exposure to even modestly elevated cholesterol levels can lead to coronary heart disease (CHD) later in life [4]. The study from 6 United States cohorts found that CHD rates were significantly elevated among young adults (18–39 years of age) who had to low-density lipoprotein (LDL) cholesterol over 100 (versus under 100) mg/dL, independently of later adults (≥40 years of age) exposures (adjusted HR, 1.64) [4]. In a 20-year follow-up study, early initiation of statin treatment among 214 children with familial hypercholesterolemia was associated with a decrease in LDL cholesterol by 32%, slowed progression of subclinical atherosclerosis, and lower cumulative incidence by 39 years of age of cardiovascular events compared with affected parents (0% versus 7% and 1% versus 26% of fatal and nonfatal cardiovascular events, respectively) [4]. Comparing men and women, mean levels of TC and LDL cholesterol tend to be higher for men than for women in early adulthood but with women catching up in mid-life and typically with the difference reversed after age 50. This pattern has been observed in different Western [5-8] and Asian populations [9-11]. Consistent with this pattern, the incidence of cardiovascular disease (CVD) among women typically lags 10 years behind that of men until the sixth or seventh decade of life when there is a marked increase in female rates [12]. Follow-up studies have suggested that LDL cholesterol rises during the transition to menopause [13-15]. This accords with cross-sectional data showing a step-up in mean levels of TC for women in their late 40s or early 50s [5, 7, 16]. Longitudinal observations of women during the menopausal transition show that changes in TC and LDL cholesterol occurred mainly during the later phases of menopause and were greatest for women who were lightest at baseline [13]. Whilst weight gain is a common occurrence for women during the menopausal years [17], weight gain appears not to be a consequence of menopause per se [18]. The results of some studies suggest that the rise in TC at these ages is independent of any changes in body size and fatness occurring at or around the same time [19, 20]. We had the opportunity to investigate sex differences in TC in a population (that of Vietnam) in which men and women are similar in weight relative to height, and predominately of the same ethnic background. Given the research evidence that the mid-life increase in TC is more pronounced for women of smaller body weight, the rise in TC may be more clearly discernible in a population of women generally smaller than their Western counterparts. Additionally, to the extent that treatment with hormone replacement therapy (HRT) by post-menopaused women can mask sex differences in TC, the lack of widespread use of exogeneous hormones in Vietnam was a benefit for this study. Furthermore, any contribution of tobacco smoking and alcohol consumption would be specific to males in this population because few of the women smoke or consume alcohol. Using data from a national survey of risk factors for non-communicable diseases (NCDs) in Vietnam, the aim of this study was to investigate whether there is evidence of higher female-than-male mean levels of TC in Vietnam and, if so, whether it can be explained by ageing, by body size and fatness, or by socio-demographic characteristics and behavioural factors.

Methods

Study participants and sampling

The data are from a population-based survey of risk factors for non-communicable disease in Vietnam during 2009–2010 that was designed in accordance with the STEPS survey methodology of the World Health Organization (WHO) [21]. The survey participants (n = 14,706, response proportion 64.1%) were selected by multi-stage stratified cluster sampling from eight provinces each representative of one of the eight geographical regions of Vietnam. The study was approved by the Ethics Committee of the Ministry of Health of Vietnam and the Tasmanian Health and Medical Human Research Ethics Committee. Written informed consent was obtained from participants. The details of this survey have been reported elsewhere [22].

Measurements

The STEPS questionnaire was used to collect information on socio-demographic information and measurements of four behavioural factors (tobacco smoking, alcohol, fruit/vegetable consumption, and physical activity) [21]. The questionnaire was translated into Vietnamese and back-translated to check the accuracy of wording of each item. Our previous studies confirmed that the measurements made with the instrument—in aggregate [23], and in respect of tobacco smoking [22], physical activity [24], alcohol intake [25], and fruit and vegetable intake [26]–have validity. Face-to-face interviews were conducted with participants by trained staff of each provincial health authority. Self-reported highest education levels were categorized as less than primary (<5 years), primary (5–8 years), junior secondary (9–11 years), senior secondary (12 years), and college/undergraduate or postgraduate (>12 years). Monthly income was answered in Vitenam Dong and transferred to USD for analysis. Smoking status were categorised as never smokers, former daily smokers, current and former non-daily smokers, and current daily smokers. For alcohol intake status, those who reported consuming at least one alcoholic beverage during the previous year were asked about their frequency of consumption (response categories <1 day/month, 1–3 days/month, 1–4 days/week, 5–6 days/week, and daily). Show cards illustrating the volume of spirits (30 ml of 40% alc/vol), wine (120 ml of 11% alc/vol) and beer (285 ml of 4.5% alc/vol) equivalent to 10 g of ethanol (a standard drink) were used to prompt reporting of the number of standard drinks usually consumed on each drinking occasion. Reported number of standard drinks were categorized as <2, 2–3, 3.1–6 and >6 standard drinks. Alcohol intake status were categorised as low (< 4 standard drinks for men or <2 standard drinks for women), hazardous (4–6 standard drinks for men or 2–4 standard drinks for women), harmful (consuming at least 6 standard drinks for men or 4 standard drinks for women). The participants were asked about the number of days they usually ate fruit, and the number of days they usually ate vegetables (excluding root plants), in a typical week and how many ‘standard serving’ sizes they usually ate of each on those days. A ‘standard serving’ size of vegetables was defined as a cup of raw vegetables, a half cup of cooked or chopped raw vegetables or half cup of vegetable juice. A ‘standard serving’ size of fruit was defined as a piece of whole of fruit, a half cup of cooked, chopped or processed fruit or half cup of fruit juice and assumed to correspond to 80 gram. Visual aids (show-cards) depicting a ‘standard serving’ size of fruit and vegetables were used to facilitate interviewing. Activity levels were calculated as total time spent on work, transport and leisure time activities of each intensity, weighted by The Global Physical Activity Questionnaire-assigned Metabolic Equivalent Task (MET) energy expenditure ratios per kilogram per hour of 4 for moderate and 8 for vigorous intensity activities. Subjects were categorised as having low (<600MET/week), moderate (>600MET/week), or high (>3000MET/week) activity levels. Measurements of behavioural factors were made and categorised according to recommendations of the WHO [21]. Physical measurements included weight (in bare feet without heavy clothing measured using NuWeigh B8271 digital scales with the precision of 0.1 kg), height (in bare feet without headwear measured using a Seca 214 stadiometer with the precision of 0.1 cm), waist circumference (WC, at the narrowest point between the lower costal border and the iliac crest measured horizontally using a constant tension tape while standing), and hip circumference (at the greatest posterior protuberance of the buttocks measured using a constant tension tape) with the participants standing. Body mass index (BMI) was calculated as weight (kg) ÷ height2 (m). Waist-hip-ratio (WHR) was calculated as WC (cm) ÷ hip (cm). Waist-to-height-ratio (WHtR) was calculated as WC (cm) ÷ height (cm). After overnight fasting, TC was measured according to the standardised STEPS procedure [21] from capillary whole blood using Roche Diagnostics Accutrend Plus glucometers. Raised TC was defined as TC ≥ 5.0 mmol/L.

Data analysis

Sampling weights were defined as the inverse probability of selection in the sample, and calculated as the product of the probability that each cluster was chosen and the probability that each person from each selected cluster was chosen. Appropriately weighted and stratified estimates of means and proportions, and of regression coefficients, were made using complex survey estimation methods provided by Stata version 15.0. The effects of fat distribution, sociodemographic, and behavioural factors on the sex differences in TC were examined by linear regression with TC as dependent variables and body fatness including BMI, WC, WHR, WHtR, socio-demographic and behavioural factors as independent variables. TC was transformed to reduce skewness. Change-point analysis was used to identify whether a mean-shift and/or change in slope had occurred in the regression of TC on age. The change-point analyses reported in this study were designed to allow the slope of the relationships of TC with age to change if necessary from any age onwards, and/or for the relationships to shift upwards (“step-up”) or downwards (“step-down”) if necessary at any age. Candidate change-points were identified by trial-and-error and confirmed by Bayesian change-point analysis. The final models included a quadratic (increasing before decreasing) fit in age to the TC data for men, without any discrete change in slope or location, and a step-up at age 50 years in the otherwise consistently increasing linear-in-age relationship for women. For Table 3, a linear regression model with age and a binary (0/1) term as covariates was fitted to the TC data for women. The binary term took the value 0 for women aged less than 50 years or 1 for women aged 50 years or greater. The coefficient of the binary term represents the estimated vertical displacement of the relationship and being positive, is referred to as the “step-up”. The estimated mean value of TC not including (without) and including (with) the step-up is reported, together with the step-up expressed as a percentage increase. To examine whether the step-up in cholesterol at age 50 years remained after adjustment for other factors including indices of body size and fatness, socio-demographic characteristics and behavioural attributes, a covariate for each of these factors was added in turn and the adjusted value of the step-up was used to recalculate these quantities (mean TC without step-up, mean TC with step-up, percentage increase).

Results

Table 1 presents selected characteristics of study subjects, stratified by sex. The sample consisted of 14706 (50.9% female) participants aged 25–64 years, with generally higher participation proportions among older people. Approximately 70% of the sample lived in rural areas and most participants were of Kinh ethnicity. Men had higher average of years of schooling and were more active than women. The proportion of subjects who smoked tobacco and the proportion who consumed alcohol were much higher among men than women. There was a modest difference in mean WC between men and women but mean BMI, WHR and WHtR were similar.
Table 1

Characteristics* of survey participants.

MenWomen
<50 years(n = 3989)≥50years(n = 2815)<50 years(n = 4770)≥50years(n = 3132)
Ethnicity
 Kinh93.7%(3234/3981)95.7%(2392/2806)93.9%(3942/4766)95.5%(2664/3123)
 Non-Kinh6.3%(747/3981)4.3%(414/2806)6.1%(824/4766)4.5%(459/3123)
Residential areas
 Urban29.3%(1311/3989)31.7%(1059/2815)31.1%(1635/4770)31.2%(1188/3132)
 Rural70.7%(2678/3989)68.3%(1756/2815)68.9%(3135/4770)68.8%(1944/3132)
Years of schooling8.8(4.0)8.2(4.1)8.1(4.1)5.9(3.9)
Monthly income80.0(107.9)65.7(83.1)76.1(82.8)57.9(69.3)
Smoking status
 Never smoker31.9%(1268/3979)26.8%(778/2803)98.7%(4683/4764)95.5%(2911/3122)
 Ex-smoker12.4%(562/3979)21.3%(628/2803)0.2%(11/4764)1.2%(59/3122)
 Daily smoker55.7%(2149/3979)51.9%(1397/2803)0.1%(70/4764)3.3%(152/3122)
Alcohol intake
 Low56.3%(2181/3989)68.7%(1967/2815)97.2%(4605/4770)98.3%(3038/3132)
 Hazardous17.5%(717/3989)14.2%(387/2815)1.9%(120/4770)1.2%(69/3132)
 Harmful26.2%(1091/3989)17.1%(461/2815)0.9%(45/4770)0.4%(25/3132)
Standard drinks/day4.7(3.6)4.0(3.5)1.7(0.0)1.5(0.0)
Fruit/veg intake3.2(2.1)3.1(2.0)3.2(2.0)3(1.9)
Physical activity (min)1395.7(1524.2)1071(0)1026.4(1359.6)935(1149.7)
Weight (kgs)57.0(9.2)55.9(9.3)49.8(7.4)50.4(8.5)
BMI (kg/m2)21.5(3.1)21.4(3.1)21.3(2.9)22.0(3.4)
WC (cms)74.5(8.8)76.2(9.2)71.1(8.1)74.7(9.6)
WHR0.8(0.1)0.9(0.1)0.8(0.1)0.9(0.1)
WHtR0.5(0.1)0.5(0.1)0.5(0.1)0.5(0.1)
Cholesterol (mmol/L)4.7(0.7)4.8(0.8)4.7(0.7)5.2(0.8)
Raised cholesterol §26.0%(906/3794)34.3%(875/2700)25.4%(1112/4565)53.2%(1508/2996)

* The data reported are mean (standard deviation) or percentage (relative frequency).

† Waist-to-hip ratio.

‡ Waist-to-height ratio.

§ Total cholesterol > 5 mmol/L.

* The data reported are mean (standard deviation) or percentage (relative frequency). † Waist-to-hip ratio. ‡ Waist-to-height ratio. § Total cholesterol > 5 mmol/L. Table 2 presents rank correlation coefficients to summarise the associations of TC with measures of body size and fatness, socio-demographic characteristics and behavioural factors for men and women. The anthropometric indices most strongly associated with TC were WC or measures based on girths for men, and weight or measures based on weight (particularly BMI) for women. Other factors associated with TC were age and physical activity (both men and women).
Table 2

Rank correlations of TC with measures of body size and fatness, socio-demographic characteristics, and behavioural factors by age group and sex.

MenWomen
<50 years(n = 3989)≥50years(n = 2815)<50 years(n = 4770)≥50years(n = 3132)
Years of schooling0.030.08 * –0.030.03
Monthly income0.06 * 0.10 ** 0.05 * 0.04
Smoking status0.08 ** 0.010.010.08
Alcohol intake status0.050.020.05–0.03
Fruit/vegetable intake–0.010.02–0.01–0.03
Physical activity–0.20 *** -0.16 *** –0.12 *** –0.17 ***
Weight0.21 *** 0.23 *** 0.21 *** 0.23 ***
BMI0.26 *** 0.24 *** 0.25 *** 0.26 ***
WC0.28 *** 0.27 *** 0.21 *** 0.24 ***
WHR0.24 *** 0.22 *** 0.15 *** 0.19 ***
WHtR0.29 *** 0.26 *** 0.21 *** 0.24 ***

* denotes p<0.05,

** denotes p<0.01,

*** denotes p<0.001.

† Waist-to-hip ratio.

‡ Waist-to-height ratio.

* denotes p<0.05, ** denotes p<0.01, *** denotes p<0.001. † Waist-to-hip ratio. ‡ Waist-to-height ratio. The sex-specific means of TC stratified by 5-year age group are depicted in Fig 1. The mean TC of men increased with age group until reaching a plateau commencing with the 45–49 years of age group. The mean TC of women increased throughout the entire age range rising from concentrations similar to those of men in young adulthood to higher values from age group 50–54 years onwards, and with a noticeable step-up occurring for the 50–54 years of age group. Commencing with that age group, the mean values of TC of middle-aged women exceeded markedly those of their male counterparts, whereas in younger age groups the mean TC levels for women were comparable to men.
Fig 1

Mean of total cholesterol by age group and sex.

The sex-specific means of two measures of body size and fatness—BMI and WC—stratified by 5-year age group are depicted in Fig 2A and 2B. The relationships with age group are mildly curvilinear in each case, with the mean values initially increasing before decreasing with advancing age group, and without visual evidence of a mean shift in the grouped data such as that in mean TC for women.
Fig 2

Means of body mass index (A) and waist circumference (B) by age group and sex.

In analyses of single year of age data, a quadratic (increasing before decreasing) fit in age to the TC data was statistically significant (p = 0.002) for men. The maximum fitted mean value of TC was reached at age 56 years. For women, there was a step-up (p<0.001) of 3.5% (95% CI 1.9%, 5.1%) at age 50 years in the otherwise consistently increasing linear-in-age relationship. In respect of the relationships of age with BMI or WC in single year of age data, quadratic (increasing before decreasing) fits in age were statistically significant for men (BMI p = 0.002, WC p<0.001) and women (BMI p<0.001, WC p<0.001). The maximum fitted mean values for men were 44 years for BMI, and 52 years for WC. The maximum fitted mean values for women were 47 years for BMI, and 57 years for WC. There were not material mean shifts for either men or women: the largest found for women were 0.7% (95% CI –1.2%, 2.6%) at age 47 years in BMI, and 0.9% (95% CI –0.5%, 2.3%) at age 48 years in WC. In consequence, adjusting for BMI, WC or other anthropometric indices did not eliminate the estimated step-up in TC for women at age 50. Instead, Table 3 shows that the estimate was increased by adjustment for weight or BMI. That increase on adjustment requires the step-up to be greatest, on average, for women of lesser weight or BMI. Adjusting instead or adjusting additionally for indices based on girth produced only minor reductions in the estimated step-up. Adjustment for socio-demographic characteristics and behavioural factors for women that were associated with TC levels had limited impact also (see Table 3).
Table 3

Estimates of the step-up in the mean value of TC occurring at around 50 years of age for women in Vietnam.

Estimate of age at step-upTC without step-upTC with step-upPercentage increase
Mean(95% CI)Mean(95% CI)Step-up(95% CI)
Unadjusted504.73(4.68, 4.77)4.89(4.85, 4.93)3.5%(1.9%, 5.1%)
Adjusted for
 Weight504.70(4.65, 4.75)4.90(4.86, 4.94)4.2%(2.6%, 5.8%)
 BMI504.70(4.65, 4.75)4.88(4.84, 4.93)4.0%(2.4%, 5.6%)
 WC504.72(4.67, 4.77)4.88(4.84, 4.93)3.5%(1.9%, 5.1%)
 WHR504.73(4.68, 4.78)4.88(4.84, 4.93)3.3%(1.6%, 4.9%)
 WtHR504.72(4.67, 4.77)4.87(4.83, 4.92)3.3%(1.7%, 4.9%)
 BMI and WC504.70(4.65, 4.75)4.88(4.84, 4.92)3.9%(2.3%, 5.5%)
 BMI and WHR504.70(4.65, 4.75)4.88(4.84, 4.92)3.8%(2.2%, 5.4%)
 BMI and WtHR504.70(4.65, 4.75)4.88(4.84, 4.92)3.8%(2.2%, 5.4%)
 BMI and years of schooling504.70(4.65, 4.75)4.87(4.83, 4.92)3.7%(2.1%, 5.4%)
 BMI and monthly income504.70(4.65, 4.75)4.88(4.83, 4.93)3.9%(2.1%, 5.7%)
 BMI and smoking504.69(4.48, 4.89)5.00(4.79, 5.21)6.7%(-1%, 14.4%)
 BMI and alcohol504.62(4.50, 4.73)4.85(4.74, 4.97)5.1%(1.2%, 9.0%)
 BMI and fruit/vegetable intake504.70(4.65, 4.74)4.88(4.83, 4.92)3.9%(2.2%, 5.5%)
 BMI and physical activity504.76(4.71, 4.82)4.94(4.89, 4.99)3.7%(2.0%, 5.4%)
Stratified by weight category*
 Lowest third of weight for age484.53(4.44, 4.61)4.70(4.62, 4.78)3.9%(0.6%, 7.1%)
 Middle third of weight for age504.62(4.54, 4.71)4.93(4.86, 5.01)6.7%(3.8%, 9.7%)
 Highest third of weight for age504.91(4.82, 5)5.05(4.98, 5.12)2.9%(0.1%, 5.6%)

* For women of age 50 years, the weight tertiles were 46.7, 53.6 and 70.7 kgs, and the thirds were 34.0–46.7 kgs, 46.8–53.6 kgs and 53.7–70.7 kgs.

† Weight-to-(height)2 ratio.

‡ Waist-to-hip ratio.

§ Waist-to-height ratio.

* For women of age 50 years, the weight tertiles were 46.7, 53.6 and 70.7 kgs, and the thirds were 34.0–46.7 kgs, 46.8–53.6 kgs and 53.7–70.7 kgs. † Weight-to-(height)2 ratio. ‡ Waist-to-hip ratio. § Waist-to-height ratio. Also shown in Table 3 are estimates of the step-up within strata of weight for age. In this sample, the greatest step-up was that estimated for women in the middle third of weight for age. The estimated step-up was least for women in the highest third, and intermediate for women in the lowest third. At age 50 years, the range of weights for women in this sample were 34.0–46.7 kgs (lowest third), 46.8–53.6 kgs (middle third) and 53.7–70.7 kgs (highest third). The results (not shown) for stratifications by BMI or girths resembled very closely those for stratification by weight.

Discussion

The key finding of this cross-sectional study was that the mean TC of women increased more of less continuously across the age range but with a step-up at age 50 years to reach higher concentrations than those of their male counterparts in a reversal of the male-female difference at lesser adult ages. The estimated step-up was not eliminated by adjustment for anthropometric indices including BMI or WC, or for socio-demographic characteristics or behavioural factors. The estimated step-up was least for women with greatest weight or greatest weight relative to height or WC. Higher concentrations of TC among young adult men than among young adult women, and the reversal of the sex difference at mid-life that we observed, have been described previously in published reports of studies conducted in Netherlands [7] and England [14]. The reversal can be identified in summary data from cross-sectional surveys conducted in Australia [5]. In Asian populations, the same has been observed in Korea [16, 27] China [9], and India [11]. There is general consensus that the increases in TC across the young to middle-aged adult lifespan are related to increasing body size and fatness. The distribution of body fat may be an important determinant of sex differences in lipids, but possibly more so for triglycerides and HDL cholesterol than for TC [20, 28]. In our cross-sectional data, the women reached higher peak values of BMI and similar peak values of WC in their mid-50s, around 3 to 5 years of age later than the men. For this reason, it might be expected that the higher male-than-female mean values of TC found among younger subjects would be reversed among those subjects who had reached mid-life. On the other hand, our cross-sectional data on body size and fat distribution provided no reason to expect the step-up in TC for women that was found at age 50 years. In consequence, adjusting for anthropometric indices of body size and fatness attenuate the estimate of the step-up suggesting it was not due to increases in that factor. Ageing, menopause, and increased risk of CVD for women occur concurrently [15]. Lipid profiles change around the time of menopause, in part related to chronologic aging and in part related to the menopausal transition itself [15]. Changes in TC during the menopausal transition for middle-aged women have been observed in both cross-sectional and longitudinal studies. A cross-sectional analysis of 3,312 UK midlife women free from hormonal treatment demonstrated women who were post-menopausal, compared with those who were pre-menopausal, had higher concentrations of multiple lipoprotein lipids, particularly LDL-cholesterol, and increased concentrations of fatty acids and several non-lipid measures [14]. The menopausal transition has been linked with an accelerated increase in TC of women in longitudinal studies conducted in the United States [13, 29], Australia [30], and China [10]. The estimated step-up in this study occurred at an age by which many or most women would have completed or nearly completed the menopausal transition. The average age of menopause in Vietnam has been reported to be 48 or 49 years [31], and this coincides remarkably closely with the pronounced increases in mean levels of TC at age 50 years we observed. Biologically, estrogens are a group of sex hormones that promote the development and maintenance of female characteristics in the human body [32]. Estrogen can reduce triglycerides synthesis, increase liver uptake of LDL-cholesterol and secretion of cholic acid, accelerate cholesterol removal in vivo, and thereby reduce the serum triglycerides, TC and LDL-cholesterol levels [33, 34]. Reduced estrogen levels at menopause dampen the metabolic activity of macrophages, and thereby contribute to lipid accumulation. A consideration in this study was whether weight modifies the relationship between TC and estrogen levels during the menopausal transition. In the Study of Women’s Health Across the Nation (SWAN), a large prospective study conducted in 7 sites in the USA, the heaviest women had the smallest increases in TC while the lightest women experienced the greatest increases in TC during the menopausal transition [13]. In this population sample also, the estimated step-up in TC was markedly lower for women of greatest weight or greatest weight relative to height, or greatest WC. The lightest Vietnamese women did not have the greatest step-up, however. Those women were much lighter in weight than any in the SWAN, and it may be that the SWAN finding does not extend to the lower end of the range of body weights that exists for women in the Vietnamese population. Sociodemographic characteristics and lifestyle factors may have an effect on lipid profiles [35, 36], and associations of these factors with TC have been observed in some studies [37, 38]. Nevertheless, these factors did not explain the step-up in TC among middle-age Vietnamese women. This is consistent with the findings of longitudinal studies of mainly Western women in the United States [13] and Melbourne [30]. This study has several strengths. The data were collected from a nationally-representative survey of the Vietnamese population. The large sample was stratified by sex and rural/urban location, and the availability of data on range of lifestyle risk factors for non-communicable disease made it possible to take account of potential confounding factors. All measurements were made by trained staff in accordance with standardised protocols designed by the WHO. All participants fasted in preparation for the test of TC. That the Vietnamese population is relatively slim in comparison to Western populations, and naïve in respect of HRT, arguably provided greater opportunity to observe increases in the TC concentrations of the middle-aged women in this study. That few of the women smoked or drank alcohol might have been an advantage also. However, this study has some limitations that need to be taken into account. First, whilst the response proportion was high given the demands of participation in the study, the possibility of non-participation bias cannot be discounted. Second, some environmental factors such as years of smoking, alcohol consumption, fruit/vegetable serves, and physical activity were self-reported. Nevertheless, we used the STEPS standardised questionnaires administered in accordance with WHO protocols in an attempt to ensure consistency in measurement, and in our hands, the self-reported data had some evidence of construct validity [23-26]. Third, study participants contributed a single blood sample for cholesterol assessment, and hence intraindividual variation in cholesterol level could not be assessed or taken into account. Moreover, participants were excluded if they reported taking medication to lower TC. Fourth, information was not collected on the menopausal status of our female participants. Those aged 50 years would have been in a mixture of stages of menopause, and this is likely to have obscured partially the true step-up that occurred. In addition, we did not have information on use of HRT, though it is thought to be limited in Vietnam and confined to women of higher wealth. Fifth, we did not have detailed measurements of some important risk factors for NCD including diet. Failing to adjust for such factors may have influenced the findings. Sixth, this paper does not assess the influence of comorbidities related to blood lipid concentrations, because there was no need to. Elsewhere we have described the inter-dependence of raised blood pressure and elevated blood glucose [39] that should prevent hypertension and hyperglycaemia being modelled in isolation of each other. Seventh, general adiposity and central adiposity that BMI and waist circumference are surrogate markers at best of whatever it is about body size and fatness that confers risk of hypercholesteremia. Finally, we cannot discount cohort effects in this study given that these are cross-sectional data. In conclusion, there is a marked step-up in TC at age 50 years for Vietnamese women that cannot be explained by their age, or by their body fatness or its distribution, or by their socio-demographic characteristics or behavioural factors, and which results in greater mean levels of TC for middle-aged women than for their male counterparts in Vietnam. Cholesterol reduction is effective in reducing morbidity and mortality from CVD, and there may be a case for the Government of the Socialist Republic of Vietnam to invest in HRT. Standard clinic guidelines on HRT in Vietnam have not been developed or issued. The gender and age differences in TC levels found in this study suggest that middle-aged Vietnamese women should be the prioritized target for better control of dyslipidaemia and early prevention of cardiovascular disease.

Study sampling method.

(DOCX) Click here for additional data file.

Stages of sampling (PPS = probability proportional to size of population).

(DOCX) Click here for additional data file. 12 May 2021 PONE-D-20-37824 Factors that influence sex differences in total cholesterol of Vietnamese adults PLOS ONE Dear Dr. Blizzard, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Please submit your revised manuscript by Jun 24 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. 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You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: This paper tried to utilize the existing cohort data in 2009-2010 to demonstrate whether any differences in lipid profiles pattern between sexes. However, several pitfalls and some improvements should be acknowledged and maybe more suitable in other journals as followings ... 1. The title did not congruent with the content of the study. 2. Review literature in both background and discussions should be more updated with latest publications. Also, mechanistic studies should be more explained in the discussions. 3. Total cholesterol from capillary method might not be reflected for LDL which involves in the process of atherosclerosis. 4. Figures should be thoroughly demonstrated in the upper range of age group. 5. Table should be compared between age group of under/over 50 years in each sex. 6. Weight circumference should be acknowledged for the pitfall as a surrogate marker of visceral fat. Reviewer #2: Dear authors: I congratulate you on your work. Studies with such a significant sample size and multi-center are not always found. The introduction provides a useful review of the research field and the significance of lipid disorders (TC) as a public health concern. The objectives of the manuscript are clearly enumerated. There is strong concordance between the objectives and the methods used. The ethical issues were considered. The data set is complete, and the results are presented in detail. The discussion correlates well with the presented data and takes the published literature into account Although I consider that the work has the potential to be published, there are some issues that should deserve your attention: Introduction Your choice was to reference many studies that has more than 10 years. In my opinion there is no need of use 'old' studies, because there are several recent studies that allows to reformulate the introduction and the discussion and keep the oldest references associated with the data collection instruments. Methods Line 123-125: please clarify how to select participants, include and exclude criteria. Line 130 - 132: more information should be provided such as provide the categories of educational level (year of schooling); monthly income (Vietnam Dong or USD?); smoking status, alcohol intake status, fruit/vegetable intake (how to measure?). How to evaluate physical activity? Line 132-133: “The questionnaire was translated into Vietnamese and back-translated to check the accuracy of wording of each item”. The manuscript must be revised to provide a hint at the validity of the so-constructed research tool. Discussion: One of the limitations is that the author does not discuss comorbidities related to blood lipid concentrations (hypertension, diabetes, dyslipidemia…). Another limitation is related to not including blood lipid-lowering medicine. Conclusions You also need to state the implications of the study findings for future research studies, clinical leadership, and policy in the conclusion section References The references included are relevant for the subject under study, but only show 8/47(17%) references from the last 5 years. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: Yes: Vu Thi Thanh Huyen, Hanoi Medical University [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 13 Jul 2021 Editor 1) Please explain why only total cholesterol was examined. After overnight fasting, TC was measured from capillary whole blood using Roche Diagnostics Accutrend Plus glucometers. This method is appropriate for large-scale field work (n = 14,706 in the case of our survey), and was done in accordance with the standardised STEPS protocols [21]. 2) Additional analyses on LDL cholesterol and/or non-HDL cholesterol will be helpful. The Introduction section also discussed about the implications of LDL cholesterol. We do not have the data on LDL and non-HDL cholesterol. We acknowledged this as one of limitations of the study. In the absence of measurements of LDL cholesterol, the implications of LDL cholesterol were not mentioned in the Introduction. 3) Include the sampling method as an Appendix. We have added the sampling method as Appendix 1 of the study. The added text is: Appendix 1: Study sampling method The survey participants were 25 to 64-year-old Vietnamese residents (n=14,706, response proportion 64.1% of the 22,940 eligible subjects) selected by multi-stage stratified cluster sampling from eight provinces (Thai Nguyen, Hoa Binh, Ha Noi, Hue, Binh Dinh, Dak Lak, Ho Chi Minh City and Can Tho) each representative of one of the eight geographical regions of Vietnam. Sampling procedures and measurements were made in accordance with the STEPS methodology [21] The two-stage sampling procedure involved selecting 20 clusters (communes, towns, and city wards) from each of the eight geographically representative provinces with probabilities proportional to population size from four strata defined by urban-rural location and rich-poor classification. For each selected cluster, the provincial health authority prepared a comprehensive listing of 25-64-year-old residents. From those lists, adequate numbers of persons per cluster were selected by age- and sex-stratified random sampling to provide 25 persons in each age group (25−34 years, 35−44 years, 45−54 years, 55−64 years) and with approximately equal members of men and women. Clinics were conducted in the local health station of each participant’s area of residence. Interviewers were local medical personnel who were trained in the implementation of the WHO STEPS methodology. Training of field staff was conducted pre-survey at training centres in Ha Noi, Hue and Ho Chi Minh City, and on-site at regular intervals by local, national and international supervisors. The eligible persons were invited to attend a clinic on a specific date, each clinic commencing in the early morning because overnight fasting was required, and questionnaire data were obtained by face-to-face interview at the survey clinics. Measurements were made, and questionnaires were administered, by trained staff of each provincial health authority. They underwent intensive training and supervision provided by the Menzies Institute for Medical Research, Australia. A pilot study was conducted to test survey instruments and procedures before actual data collection. All measurements were performed in accordance with the STEPS protocols. 4) Include a study flow diagram about patient selection. We have added the flow diagram about patient selection as Appendix 2 of the study. The added diagram is: Appendix 2: Stages of sampling (PPS = Probability Proportional to Size of population) Reviewer #1 1. The title did not congruent with the content of the study. We have changed the title to “Sex differences in total cholesterol of Vietnamese adults”. 2. Review literature in both background and discussions should be more updated with latest publications. Also, mechanistic studies should be more explained in the discussions. Literature has been revised and updated with latest publications. 3. Total cholesterol from capillary method might not be reflected for LDL which involves in the process of atherosclerosis. Yes, we acknowledged this as one of limitations of this study. 4. Figures should be thoroughly demonstrated in the upper range of age group. The figures have been drawn to improve their clarity. Figure 1. Mean of total cholesterol by age group and sex (A) (B) Figure 2. Mean of body mass index (A) and waist circumference (B) by age group and sex 5. Table should be compared between age group of under/over 50 years in each sex. Table 1: Characteristics* of survey participants Men Women <50 years (n=3989) >50years (n=2815) <50 years (n=4770) >50years (n=3132) Ethnicity Kinh 93.7% (3234/3981) 95.7% (2392/2806) 93.9% (3942/4766) 95.5% (2664/3123) Non-Kinh 6.3% (747/3981) 4.3% (414/2806) 6.1% (824/4766) 4.5% (459/3123) Residential areas Urban 29.3% (1311/3989) 31.7% (1059/2815) 31.1% (1635/4770) 31.2% (1188/3132) Rural 70.7% (2678/3989) 68.3% (1756/2815) 68.9% (3135/4770) 68.8% (1944/3132) Years of schooling 8.8 (4.0) 8.2 (4.1) 8.1 (4.1) 5.9 (3.9) Monthly income 80.0 (107.9) 65.7 (83.1) 76.1 (82.8) 57.9 (69.3) Smoking status Never smoker 31.9% (1268/3979) 26.8% (778/2803) 98.7% (4683/4764) 95.5% (2911/3122) Ex-smoker 12.4% (562/3979) 21.3% (628/2803) 0.2% (11/4764) 1.2% (59/3122) Daily smoker 55.7% (2149/3979) 51.9% (1397/2803) 0.1% (70/4764) 3.3% (152/3122) Alcohol intake Low 56.3% (2181/3989) 68.7% (1967/2815) 97.2% (4605/4770) 98.3% (3038/3132) Hazardous 17.5% (717/3989) 14.2% (387/2815) 1.9% (120/4770) 1.2% (69/3132) Harmful 26.2% (1091/3989) 17.1% (461/2815) 0.9% (45/4770) 0.4% (25/3132) Standard drinks/day 4.7 (3.6) 4.0 (3.5) 1.7 (0.0) 1.5 (0.0) Fruit/veg intake 3.2 (2.1) 3.1 (2.0) 3.2 (2.0) 3 (1.9) Physical activity (min) 1395.7 (1524.2) 1071 (0) 1026.4 (1359.6) 935 (1149.7) Weight (kgs) 57.0 (9.2) 55.9 (9.3) 49.8 (7.4) 50.4 (8.5) BMI (kg/m²) 21.5 (3.1) 21.4 (3.1) 21.3 (2.9) 22.0 (3.4) WC (cms) 74.5 (8.8) 76.2 (9.2) 71.1 (8.1) 74.7 (9.6) WHR† 0.8 (0.1) 0.9 (0.1) 0.8 (0.1) 0.9 (0.1) WHtR‡ 0.5 (0.1) 0.5 (0.1) 0.5 (0.1) 0.5 (0.1) Cholesterol (mmol/L) 4.7 (0.7) 4.8 (0.8) 4.7 (0.7) 5.2 (0.8) Raised cholesterol § 26.0% (906/3794) 34.3% (875/2700) 25.4% (1112/4565) 53.2% (1508/2996) * The data reported are mean (standard deviation) or percentage (relative frequency). † Waist-to-hip ratio ‡ Waist-to-height ratio § Total cholesterol > 5 mmol/L. Table 2: Rank correlations of TC with measures of body size and fatness, socio-demographic characteristics, and behavioural factors by age group and sex Men Women <50 years (n=3989) >50years (n=2815) <50 years (n=4770) >50years (n=3132) Years of schooling 0.03 0.08 * –0.03 0.03 Monthly income 0.06 * 0.10 ** 0.05 * 0.04 Smoking status 0.08 ** 0.01 0.01 0.08 Alcohol intake status 0.05 0.02 0.05 –0.03 Fruit/vegetable intake –0.01 0.02 –0.01 –0.03 Physical activity –0.20 *** -0.16 *** –0.12 *** –0.17 *** Weight 0.21 *** 0.23 *** 0.21 *** 0.23 *** BMI 0.26 *** 0.24 *** 0.25 *** 0.26 *** WC 0.28 *** 0.27 *** 0.21 *** 0.24 *** WHR† 0.24 *** 0.22 *** 0.15 *** 0.19 *** WHtR‡ 0.29 *** 0.26 *** 0.21 *** 0.24 *** * denotes p<0.05, ** denotes p<0.01, *** denotes p<0.001 † Waist-to-hip ratio ‡ Waist-to-height ratio. 6. Weight circumference should be acknowledged for the pitfall as a surrogate marker of visceral fat. We have added a note to this effect as a limitation. The added text is: General adiposity and central adiposity that BMI and waist circumference are surrogate markers at best of whatever it is about body size and fatness that confers risk of hypercholesteremia. Reviewer #2: 1. Introduction Your choice was to reference many studies that has more than 10 years. In my opinion there is no need of use 'old' studies, because there are several recent studies that allows to reformulate the introduction and the discussion and keep the oldest references associated with the data collection instruments. The literature review component of the Introduction has been updated. 2. Methods Line 123-125: please clarify how to select participants, include and exclude criteria. To clarify, we have added a description of the sampling method as Appendix 1 of the study Line 130 - 132: more information should be provided such as provide the categories of educational level (year of schooling); monthly income (Vietnam Dong or USD?); smoking status, alcohol intake status, fruit/vegetable intake (how to measure?). How to evaluate physical activity? We have revised the text of the Measurements section. The amended text (lines 135-163) is: Self-reported highest education levels were categorized as less than primary (<5 years), primary (5–8 years), junior secondary (9–11 years), senior secondary (12 years), and college/undergraduate or postgraduate (>12 years). Monthly income was answered in Vitenam Dong and transferred to USD for analysis. Smoking status were categorised as never smokers, former daily smokers, current and former non-daily smokers, and current daily smokers. For alcohol intake status, those who reported consuming at least one alcoholic beverage during the previous year were asked about their frequency of consumption (response categories <1 day/month, 1–3 days/month, 1–4 days/week, 5–6 days/week, and daily. Show cards illustrating the volume of spirits (30 ml of 40% alc/vol), wine (120 ml of 11% alc/vol) and beer (285 ml of 4.5% alc/vol) equivalent to 10 g of ethanol (a standard drink) were used to prompt reporting of the number of standard drinks usually consumed on each drinking occasion. Reported number of standard drinks were categorized as <2, 2–3, 3.1–6 and >6 standard drinks. Alcohol intake status were categorised as low (< 4 standard drinks for men or <2 standard drinks for women), hazardous (4–6 standard drinks for men or 2–4 standard drinks for women), harmful (consuming at least 6 standard drinks for men or 4 standard drinks for women). The participants were asked about the number of days they usually ate fruit, and the number of days they usually ate vegetables (excluding root plants), in a typical week and how many ‘standard serving’ sizes they usually ate of each on those days. A ‘standard serving’ size of vegetables was defined as a cup of raw vegetables, a half cup of cooked or chopped raw vegetables or half cup of vegetable juice. A ‘standard serving’ size of fruit was defined as a piece of whole of fruit, a half cup of cooked, chopped or processed fruit or half cup of fruit juice and assumed to correspond to 80 gram. Visual aids (show-cards) depicting a ‘standard serving’ size of fruit and vegetables were used to facilitate interviewing. Activity levels were calculated as total time spent on work, transport and leisure time activities of each intensity, weighted by The Global Physical Activity Questionnaire-assigned Metabolic Equivalent Task (MET) energy expenditure ratios per kilogram per hour of 4 for moderate and 8 for vigorous intensity activities. Subjects were categorised as having low (<600MET/week), moderate (>600MET/week), or high (>3000MET/week) activity levels. Measurements of behavioural factors were made and categorised according to recommendations of the WHO [21] Line 132-133: “The questionnaire was translated into Vietnamese and back-translated to check the accuracy of wording of each item”. The manuscript must be revised to provide a hint at the validity of the so-constructed research tool. Our previous publications have focused heavily on the validity of measurements made with the questionnaire. In acknowledgement of this, we have added the following text: Our previous studies confirmed that the measurements made with the instrument – in aggregate [23], and in respect of tobacco smoking [22], physical activity [24], alcohol intake [25] and fruit and vegetable intake [26] – have validity. 3. Discussion: One of the limitations is that the author does not discuss comorbidities related to blood lipid concentrations (hypertension, diabetes, dyslipidemia…). The comorbidities related to blood lipid concentrations such as high blood pressure and high blood glucose were examined in another of our studies. (Ref: Nga TTT, Blizzard CL, Khue LN, Le Van Ngoc T, Bao TQ, Otahal P, et al. The Interdependence of Blood Pressure and Glucose in Vietnam. High Blood Press Cardiovasc Prev. 2021 Mar;28(2):141-150). We checked for interdependence of total cholesterol and hypertension or hyperglycaemia, and found no evidence of it. We have added the following text to the Discussion and, at the direction of the reviewer, presented it as a limitation: This paper does not assess the influence of comorbidities related to blood lipid concentrations, because there was no need to. Elsewhere we have described the inter-dependence of raised blood pressure and elevated blood glucose [39] that should prevent hypertension and hyperglycaemia being modelled in isolation of each other. Another limitation is related to not including blood lipid-lowering medicine. To clarify, we have added a sentence to the text of the limitations (line 350). The added text is: Moreover, participants were excluded if they reported taking medication to lower TC. 4. Conclusions You also need to state the implications of the study findings for future research studies, clinical leadership, and policy in the conclusion section To clarify, we have added the text of the conclusion (line 361-367). The added text is: Cholesterol reduction is effective in reducing morbidity and mortality from CVD, and there may be a case for the Government of the Socialist Republic of Vietnam to invest in HRT. Standard clinic guidelines on HRT in Vietnam have not been developed or issued. The gender and age differences in TC levels found in this study suggest that middle-aged Vietnamese women should be the prioritized target for better control of dyslipidaemia and early prevention of cardiovascular disease. 5. References The references included are relevant for the subject under study, but only show 8/47(17%) references from the last 5 years. Literature has been revised and updated with the latest publications. The updated references are: 1. World Health Organization. The global status report on non-communicable diseases. World Health Organization, Geneva; 2010; p.25. 2. Erqou S, Kaptoge S, Perry PL, Di Angelantonio E, Thompson A, White IR, et al. Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA. 2009;302(4):412-23. 3. Hajar R. Risk Factors for Coronary Artery Disease: Historical Perspectives. Heart Views. 2017. 18(3): p. 109-114. 4. Virani SS, Alonso A, Aparicio HJ, Benjamin EJ, Bittencourt MS, Callaway CW, et al. Heart Disease and Stroke Statistics-2021 Update: A Report From the American Heart Association. Circulation. 2021. 143(8): p. e254-e743. 5. Carrington MJ and Stewart S. Australia’s cholesterol crossroads: an analysis of 199,331 GP patient records. Baker IDI Heart and Diabetes Institute, Melbourne, Australia; 2011. 6. Woolf K, Reese CE, Mason MP, Beaird LC, Tudor-Locke C, Vaughan LA. Physical activity is associated with risk factors for chronic disease across adult women's life cycle. J Am Diet Assoc, 2008. 108(6): p. 948-59. 7. Balder JW, de Vries JK, Nolte IM, Lansberg, PJ, Kuivenhoven, JA, Kamphuisen, PW. Lipid and lipoprotein reference values from 133,450 Dutch Lifelines participants: Age- and gender-specific baseline lipid values and percentiles. J Clin Lipidol, 2017. 11(4): p. 1055-1064.e6. 8. Ambrož M, de Vries ST, Vart, P, Dullaart, RPF, Roeters van Lennep J, Denig, P, et al. Sex Differences in Lipid Profile across the Life Span in Patients with Type 2 Diabetes: A Primary Care-Based Study. J Clin Med, 2021. 10(8). 9. Gu T, Zhou W, Sun J, Wang J, Zhu D, Bi Y. Gender and age differences in lipid profile among Chinese adults in Nanjing: a retrospective study of over 230,000 individuals from 2009 to 2015. Exp Clin Endocrinol Diabetes. 2018;126(7):429-36. 10. Zhou JL, Lin SQ, Shen Y, Chen Y, Zhang Y, Chen FL. Serum lipid profile changes during the menopausal transition in Chinese women: a community-based cohort study. Menopause. 2010;17(5):997-1003. 11. Gupta R, Sharma M, Goyal NK, Bansal P, Lodha S, Sharma KK. Gender differences in 7 years trends in cholesterol lipoproteins and lipids in India: Insights from a hospital database. Indian J Endocrinol Metab. 2016. 20(2): p. 211-218. 12. Roger VL, Go AS, Lloyd-Jones DM, Adams RJ, Berry JD, Brown TM, et al. Heart disease and stroke statistics-2011 update: a report from the American Heart Association. Circulation. 2011;123(4):e18-e209. 13. Derby CA, Crawford SL, Pasternak RC, Sowers M, Sternfeld B, Matthews KA. Lipid changes during the menopause transition in relation to age and weight: the Study of Women's Health Across the Nation. Am J Epidemiol. 2009;169(11):1352-61. 14. Wang Q, Ferreira DLS, Nelson SM, Sattar N, Ala-Korpela M, Lawlor DA. Lipid changes during the menopause transition in relation to age and weight: the Study of Women's Health Across the Nation. Am J Epidemiol, 2009. 169(11): p. 1352-61. 15. Chae CU, Derby CA. The menopausal transition and cardiovascular risk. Obstet Gynecol Clin North Am. 2011;38(3):477-88. 16. Lee Yh, Lee SG, Lee MH, Kim JH, Lee BW, Kang ES, et al. Serum cholesterol concentration and prevalence, awareness, treatment, and control of high low‐density lipoprotein cholesterol in the Korea National Health and Nutrition Examination Surveys 2008–2010: beyond the tip of the iceberg. J Am Heart Assoc. 2014;3(1):e000650. 17. Kapoor E, Collazo-Clavell ML, Faubion SS. Weight Gain in Women at Midlife: A Concise Review of the Pathophysiology and Strategies for Management. Mayo Clin Proc, 2017. 92(10): p. 1552-1558. 18. Davis SR, Castelo-Branco C, Chedraui P, Lumsden MA, Nappi RE, Shah D, et al. Understanding weight gain at menopause. Climacteric. 2012;15(5):419-29. 19. Ko SH, Kim HS. Menopause-Associated Lipid Metabolic Disorders and Foods Beneficial for Postmenopausal Women. Nutrients, 2020. 12(1). 20. Park JK, Lim YH, Kim KS, Kim SG, Kim JH, Lim HG, et al. Changes in body fat distribution through menopause increase blood pressure independently of total body fat in middle-aged women: the Korean National Health and Nutrition Examination Survey 2007-2010. Hypertens Res, 2013. 36(5): p. 444-9. 21. World Health Organization. WHO STEPS surveillance manual: The WHO STEPwise approach to chronic disease risk factor surveillance. World Health Organization, Geneva 2008 [cited 2018 September 20]. Available from: http://www.who.int/chp/steps/manual/en/. 22. Bui TV, Blizzard L, Luong KN, Truong Nle V, Tran BQ, Ha ST, et al. Declining prevalence of tobacco smoking in Vietnam. Nicotine Tob Res. 2015;17(7):831-8. 23. Bui TV, Blizzard CL, Luong KN, Truong Nle V, Tran BQ, Otahal P, et al. National survey of risk factors for non-communicable disease in Vietnam: prevalence estimates and an assessment of their validity. BMC Public Health. 2016. 16: p. 498. 24. Bui TV, Blizzard CL, Luong KN, Truong Nle V, Tran BQ, Otahal P, et al. Physical activity in Vietnam: estimates and measurement issues. PloS One. 2015;10(10):e0140941 25. Bui TV, Blizzard CL, Luong KN, Van Truong NL, Tran BQ, Otahal P, et al. Alcohol consumption in Vietnam, and the use of 'standard drinks' to measure alcohol intake. Alcohol Alcohol. 2016;51(2):186-95. 26. Bui TV, Blizzard CL, Luong KN, Truong Nle V, Tran BQ, Otahal P, et al. Fruit and vegetable consumption in Vietnam, and the use of a 'standard serving' size to measure intake. Br J Nutr. 2016;116(1):149-57. 27. Choi JS, Song YM, Sung J. Serum total cholesterol and mortality in middle-aged Korean women. Atherosclerosis. 2007;192(2):445-7. 28. Schorr M, Dichtel LE, Gerweck AV, Valera RD, Torriani M, Miller KK, et al. Sex differences in body composition and association with cardiometabolic risk. Biol Sex Differ. 2018. 9(1): p. 28. 29. Schubert CM, Rogers NL, Remsberg KE, Sun SS, Chumlea WC, Demerath EW, et al. Lipids, lipoproteins, lifestyle, adiposity and fat-free mass during middle age: the Fels Longitudinal Study. Int J Obes. 2006;30(2):251-60. 30. Do KA, Green A, Guthrie JR, Dudley EC, Burger HG, Dennerstein L. Longitudinal study of risk factors for coronary heart disease across the menopausal transition. Am J Epidemiol. 2000;151(6):584-93. 31. Cuong DT. Risks and benefits of hormone replacement therapy. Ha Noi: Institute for the Protection of the Mother and Newborn. 2017; [cited 2019 June 3]. Available from: https://www.gfmer.ch/Books/bookmp/143.htm 32. Sohrabji F, Okoreeh A, Panta A. Sex hormones and stroke: beyond estrogens. Horm Behav. 2019;111:87-95. 33. Mauvais-Jarvis F, Clegg DJ, Hevener AL. The role of estrogens in control of energy balance and glucose homeostasis. Endocr Rev. 2013;34(3):309-38. 34. Sai AJ, Gallagher JC, Fang X. Effect of hormone therapy and calcitriol on serum lipid profile in postmenopausal older women: association with estrogen receptor-alpha genotypes. Menopause. 2011;18(10):1101-12. 35. Muga MA, Owili PO, Hsu CY, Chao JC. Association of lifestyle factors with blood lipids and inflammation in adults aged 40 years and above: a population-based cross-sectional study in Taiwan. BMC Public Health. 2019. 19(1): p. 1346. 36. Suliga E, Kozieł D, Cieśla E, Rębak D, Głuszek S. Factors Associated with Adiposity, Lipid Profile Disorders and the Metabolic Syndrome Occurrence in Premenopausal and Postmenopausal Women. PLoS One. 2016. 11(4): p. e0154511. 37. Kelley GA, Kelley KS, Tran ZV. Exercise, lipids, and lipoproteins in older adults: a meta-analysis. Prev Cardiol. 2005;8(4):206-14. 38. Aadahl M, von Huth Smith L, Pisinger C, Toft UN, Glumer C, Borch-Johnsen K, et al. Five-year change in physical activity is associated with changes in cardiovascular disease risk factors: the Inter99 study. Prev Med. 2009;48(4):326-31. 39. Nga TTT, Blizzard CL, Khue LN, Le Van Ngoc T, Bao TQ, Otahal P, et al. The Interdependence of Blood Pressure and Glucose in Vietnam. High Blood Press Cardiovasc Prev. 2021 Mar;28(2):141-150. Submitted filename: Response to Reviewers.docx Click here for additional data file. 11 Aug 2021 Sex differences in total cholesterol of Vietnamese adults PONE-D-20-37824R1 Dear Dr. Blizzard, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Lee-Ling Lim Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #1: All comments have been addressed Reviewer #2: (No Response) ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: (No Response) ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: (No Response) Reviewer #2: (No Response) ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: No 13 Aug 2021 PONE-D-20-37824R1 Sex differences in total cholesterol of Vietnamese adults Dear Dr. Blizzard: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Lee-Ling Lim Academic Editor PLOS ONE
  34 in total

Review 1.  The menopausal transition and cardiovascular risk.

Authors:  Claudia U Chae; Carol A Derby
Journal:  Obstet Gynecol Clin North Am       Date:  2011-09       Impact factor: 2.844

2.  Exercise, lipids, and lipoproteins in older adults: a meta-analysis.

Authors:  George A Kelley; Kristi S Kelley; Zung V Tran
Journal:  Prev Cardiol       Date:  2005

3.  Serum total cholesterol and mortality in middle-aged Korean women.

Authors:  Ji-Sook Choi; Yun-Mi Song; Joohon Sung
Journal:  Atherosclerosis       Date:  2007-04-27       Impact factor: 5.162

4.  Fruit and vegetable consumption in Vietnam, and the use of a 'standard serving' size to measure intake.

Authors:  Tan Van Bui; Christopher L Blizzard; Khue Ngoc Luong; Ngoc Le Van Truong; Bao Quoc Tran; Petr Otahal; Velandai Srikanth; Mark R Nelson; Thuy Bich Au; Son Thai Ha; Hai Ngoc Phung; Mai Hoang Tran; Michele Callisaya; Kylie Smith; Seana Gall
Journal:  Br J Nutr       Date:  2016-05-12       Impact factor: 3.718

5.  Serum lipid profile changes during the menopausal transition in Chinese women: a community-based cohort study.

Authors:  Jin-Ling Zhou; Shou-Qing Lin; Ying Shen; Ying Chen; Ying Zhang; Feng-Ling Chen
Journal:  Menopause       Date:  2010 Sep-Oct       Impact factor: 2.953

6.  Physical activity is associated with risk factors for chronic disease across adult women's life cycle.

Authors:  Kathleen Woolf; Christine E Reese; Maureen P Mason; Leah C Beaird; Catrine Tudor-Locke; Linda A Vaughan
Journal:  J Am Diet Assoc       Date:  2008-06

7.  Gender and Age Differences in Lipid Profile Among Chinese Adults in Nanjing: a Retrospective Study of Over 230,000 Individuals from 2009 to 2015.

Authors:  Tianwei Gu; Weihong Zhou; Jie Sun; Jing Wang; Dalong Zhu; Yan Bi
Journal:  Exp Clin Endocrinol Diabetes       Date:  2017-09-11       Impact factor: 2.949

Review 8.  Weight Gain in Women at Midlife: A Concise Review of the Pathophysiology and Strategies for Management.

Authors:  Ekta Kapoor; Maria L Collazo-Clavell; Stephanie S Faubion
Journal:  Mayo Clin Proc       Date:  2017-10       Impact factor: 7.616

9.  Sex differences in body composition and association with cardiometabolic risk.

Authors:  Melanie Schorr; Laura E Dichtel; Anu V Gerweck; Ruben D Valera; Martin Torriani; Karen K Miller; Miriam A Bredella
Journal:  Biol Sex Differ       Date:  2018-06-27       Impact factor: 5.027

10.  Serum cholesterol concentration and prevalence, awareness, treatment, and control of high low-density lipoprotein cholesterol in the Korea National Health and Nutrition Examination Surveys 2008-2010: Beyond the Tip of the Iceberg.

Authors:  Yong-Ho Lee; Sang-Guk Lee; Myung Ha Lee; Jeong-Ho Kim; Byung-Wan Lee; Eun Seok Kang; Hyun Chul Lee; Bong Soo Cha
Journal:  J Am Heart Assoc       Date:  2014-02-26       Impact factor: 5.501

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