Literature DB >> 32801969

The Association of Subscapular Skinfold with All-Cause, Cardiovascular and Cerebrovascular Mortality.

Xiao-Cong Liu1, Lin Liu1, Yu-Ling Yu1, Jia-Yi Huang1, Chao-Lei Chen1, Kenneth Lo2, Yu-Qing Huang1, Ying-Qing Feng1.   

Abstract

PURPOSE: Previous studies suggested inconsistent relationship between subscapular skinfold and all-cause, cardiovascular, and cerebrovascular mortality. Therefore, the present study aimed to investigate the associations between subscapular skinfold with all-cause, cardiovascular, and cerebrovascular mortality. PATIENTS AND METHODS: Data were collected from the National Health and Nutrition Examination Survey (NHANES, 1999-2006) with follow-up data through 31 December 2015. Participants were categorized by subscapular skinfold quartiles. The hazard ratios (HRs) and 95% confidence intervals (CIs) were evaluated using the multivariate Cox regression model and subgroup analysis. Kaplan-Meier curves were used to present cause-specific mortalities and used Cox cubic regression splines to examine the association of subscapular skinfold with cause-specific mortalities.
RESULTS: A total of 16,402 subjects (49.61% male) were involved in our study. After a mean follow-up of 141.73 months, there were 3078 (18.77%), 392 (2.39%), and 128 (0.78%) cases of all-cause, cardiovascular, and cerebrovascular mortality, respectively. Participants in the highest quartile of subscapular skinfold (≥24.80mm) versus the lowest (<13.20mm) had lower risk for all-cause mortality (HR, 0.71; 95% CI, 0.57-0.89; P for trend = 0.007) and cardiovascular mortality (HR, 0.44; 95% CI, 0.23-0.83; P for trend = 0.023) in the fully adjusted model. In the age-stratified analysis, subscapular skinfold was only inversely associated with all-cause and cardiovascular disease mortality in people ≥65 years of age (all P-interaction <0.001). No significant difference was found between subscapular skinfold and cerebrovascular mortality (all P > 0.05).
CONCLUSION: Subscapular skinfold showed an inverse association with all-cause and cardiovascular disease mortality in people aged ≥65 years.
© 2020 Liu et al.

Entities:  

Keywords:  NHANES; all-cause mortality; cardiovascular disease; cerebrovascular disease; subscapular skinfold

Year:  2020        PMID: 32801969      PMCID: PMC7407759          DOI: 10.2147/RMHP.S262300

Source DB:  PubMed          Journal:  Risk Manag Healthc Policy        ISSN: 1179-1594


Introduction

According to the Global Burden of Disease study data, the prevalence of obesity has doubled in more than 70 countries and has continuously increased worldwide since 1980, approximately 107.7 million children and 603.7 million adults with obesity all over the world in 2015.1 Overweight and obesity are established risk factors for multiple chronic diseases, including cardiovascular diseases,2–4 cerebrovascular diseases,5 type 2 diabetes,6 cancer,7 and other disease conditions,8,9 as well as all-cause mortality.10 Body mass index (BMI) is the most common indicator for adiposity in epidemiological research. However, “obesity paradox” has been consistently reported.11–13 One of the essential explanations is that BMI fails to describe body fat distribution as an index of adiposity,14,15 when studies have emphasized that the accumulation of visceral and ectopic fat is an independent risk marker of cardiovascular and metabolic morbidity and mortality.2,3 Moreover, visceral and ectopic fat is usually measured by magnetic resonance imaging (MRI) and computerized tomography (CT) imaging. However, the measurement of visceral and ectopic fat is limited in clinical practice and research studies due to the high operation cost. Therefore, alternative indicators were explored, such as skinfold thickness. Skinfold thickness is a simple-to-use index to examine trunk and overall obesity.16 Some reports suggested that skinfold thickness could be used to measure obesity with the advantage of indicating fat distribution.17,18 An increase in subscapular skinfold was associated with cardiovascular mortality in previous studies,19,20 but few studies have examined its link with all-cause and cerebrovascular mortality. Therefore, the aim of the present study was sought to examine the association of subscapular skinfold thickness with all-cause, cardiovascular, and cerebrovascular disease mortalities in US adults from the National Health and Nutrition Examination Survey (NHANES) 1999–2006.

Patients and Methods

Study Design and Study Population

The NHANES is designed to assess the health and nutritional status of adults and children in the United States. Data for analyses were included from the NHANES 1999–2006 with follow-up data through 31 December 2015. Details of recruitment, procedures, population characteristics, and study design for NHANES are available for online access at . Our study included 16,402 participants who were ≥18 years of age with data of subscapular skinfold thickness, and we excluded subjects who missed mortality data (Figure 1).
Figure 1

The research flow chart.

The research flow chart.

Subscapular Skinfold Measurement

Subscapular skinfold was measured in millimeters using the Holtain skinfold caliper by trained personnel at the inferior angle of the right scapula according to NHANES protocols. The protocol stipulates that each skinfold should consist of a double thickness of skin and underlying adipose tissue. The Holtain calipers are designed to provide accurate measurements up to a maximum of 45.0 mm.

Covariates

Weight, height, and blood pressure were measured by trained personnel in a Mobile Examination Center (MEC). BMI was calculated as weight divided by height (kg/m2). Information on age, gender, race (dichotomized into white or non-white), marital status (dichotomized into married or others), education level (dichotomized into less than high school or high school or above), alcohol consumption, smoking (dichotomized into yes or no), and history of cardiovascular diseases (CVD) were self-reported through questionnaire interviews. Prescription medication use was assessed by self-report and verified by interviewers through the examination of medication containers. The biochemistry profile, including total cholesterol (TC, mg/dl), high-density lipoprotein cholesterol (HDL-C, mg/dl), and C-reactive protein (CRP, mg/dl), was collected from laboratory measurements. Estimated glomerular filtration rate (mL/min/1.73 m2) (eGFR) was calculated based on the Modification of Diet in Renal Disease formula (MDRD).21 Hypertension was defined as systolic blood pressures (SBP) ≥140mmHg and/or diastolic blood pressure (DBP) ≥90mmHg, taking antihypertensive medications, or self-reported history of hypertension.22 Diabetes was defined as FBG ≥ 126mg/dl, hemoglobin A1c (HbA1C) ≥6.5%, self-report, or using hypoglycemic agents.23 Full detailed procedures on questionnaires and test methods can be found on the website ().

Mortality Data

National Center for Health Statistics has linked mortality data from NHANES to death certificate data in the National Death Index. Mortality data were extracted from the data of the survey participants, based on a probabilistic match between NHANES and the National Death Index records through 31 December 2015. All-cause mortality included deaths from all causes. Cardiovascular (I00-I09, I11, I13, I20-I51) and cerebrovascular (I60-I69) mortality as defined by International Classification of Diseases, 10th Edition, Clinical Modification System codes derived from death-certificate data. Detailed mortality variables can be referred to on the website ().

Statistical Methods

Subjects were categorized by subscapular skinfold thickness in quartiles (Q1:<13.20mm, Q2:13.20–18.70mm, Q3:18.71–24.79mm, Q4≥24.80mm). Baseline characteristics for the groups of participants were described using frequencies with percentages for categorical variables, and means with standard deviations (SD) for continuous variables. Subgroup difference was examined using chi-square tests, one-way ANOVA, Fisher test, or Kruskal–Wallis H-test whenever appropriate. The Kaplan–Meier curves were used to present the rate of all-cause, cardiovascular, and cerebrovascular mortality. Survival rates by subscapular skinfold thickness were compared using the Log rank test. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated using Cox proportional hazards regression models. Several regression models were built. Model I only included subscapular skinfold thickness, Model II was adjusted for age, gender, and BMI. Model III was additionally adjusted for race, education level, married, smoking, alcohol consumption, SBP, eGFR, HDL-C, TC, CRP, comorbidities (hypertension, diabetes, and cardiovascular disease), and medication use (antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs). A test of the trend across the quartiles of subscapular skinfold thickness was also performed. Cox cubic spline regression models, adjusted for the same covariates in Model III, were used to examine the potential associations of subscapular skinfold thickness with cause-specific mortalities. Subgroup analyses were conducted by stratifying age (<65 or ≥65 years), gender (male or female), race (white or non-white), and BMI (<25 or ≥25 kg/m2) to investigate potential sources of heterogeneity. Statistical significance was detected by P < 0.05. All analyses were performed with R version 3.6.3 (R Foundation for Statistical Computing, Vienna, Austria).

Results

Baseline Characteristics

A total of 16,402 participants were involved in the study and 8137 (49.61%) were males. The average age was 45.80 (SD=20.78) years. Table 1 shows the baseline characteristics of all participants. In general, the mean values of subscapular skinfold thickness from the lowest to highest quartiles were 10.05 (SD, 1.95), 15.95 (SD, 1.59), 21.58 (SD, 1.74), and 30.03 (SD, 3.96). There were 3078 (18.77%) participants died during the mean follow-up period of 141.73 (SD, 42.14) months, 392 (2.39%) from cardiovascular diseases, and 128 (0.78%) from cerebrovascular diseases. Significant differences were detected in most variables (all P < 0.01), except for education level, the prevalence of cardiovascular diseases, the use of antiplatelet drug, and cerebrovascular mortality.
Table 1

Baseline Demographic and Clinical Parameters Among Participants by Subscapular Skinfold Quartiles

TotalSubscapular Skinfold Thickness, mmP-value
Q1: <13.20Q2: 13.20–18.70Q3: 18.71–24.79Q4: ≥24.80
Number16,4024063412041034116
Age, years45.80 ± 20.7841.51 ± 22.9346.55 ± 21.3448.57 ± 19.7146.52 ± 18.23<0.001
Age ≥ 65 years, n (%)3894 (23.74)919 (22.62)1070 (25.97)1087 (26.49)818 (19.87)<0.001
Subscapular skinfold, mm19.43 ± 7.7810.05 ± 1.9515.95 ± 1.5921.58 ± 1.7430.03 ± 3.96<0.001
Body mass index, kg/m226.48 ± 4.9621.94 ± 2.8025.27 ± 3.1827.59 ± 3.5631.04 ± 4.87<0.001
Systolic blood pressure, mmHg117.42 ± 14.79115.00 ± 14.20117.06 ± 14.54118.63 ± 14.90119.07 ± 15.18<0.001
Diastolic blood pressure, mmHg68.34 ± 12.9266.20 ± 12.9767.70 ± 12.7669.12 ± 12.9970.43 ± 12.56<0.001
Total cholesterol, mg/dL198.52 ± 43.90184.82 ± 43.33199.18 ± 42.73205.50 ± 43.98204.18 ± 42.50<0.001
HDL cholesterol, mg/dL53.60 ± 15.9058.22 ± 16.8154.08 ± 15.7951.61 ± 15.4150.50 ± 14.36<0.001
C-reactive protein, mg/L0.65 ± 1.500.59 ± 1.720.63 ± 1.490.67 ± 1.460.71 ± 1.300.003
Alcohol consumption, gm9.45 ± 29.4811.84 ± 38.2310.87 ± 29.238.46 ± 23.546.71 ± 24.63<0.001
eGFR, mg/min/1.73m293.83 ± 34.5995.81 ± 34.3892.64 ± 32.5292.28 ± 34.0594.65 ± 37.12<0.001
Gender-Male, n (%)8137 (49.61)2289 (56.34)2215 (53.76)2071 (50.48)1562 (37.95)<0.001
Smoking, n (%)7093 (48.99)1703 (53.57)1840 (50.34)1854 (48.51)1696 (44.39)<0.001
Race-white, n (%)8151 (49.70)2189 (53.88)2130 (51.70)2032 (49.52)1800 (43.73)<0.001
Education level- High school or above, n (%)11,098 (67.77)2762 (68.15)2775 (67.50)2748 (67.07)2813 (68.36)0.580
Marital status-Married, n (%)7898 (49.39)1438 (36.11)2056 (51.40)2258 (56.24)2146 (53.73)<0.001
Comorbidities, n (%)
 Cardiovascular disease605 (4.20)114 (3.60)153 (4.21)186 (4.87)152 (4.00)0.058
 Diabetes1537 (9.37)157 (3.86)310 (7.52)511 (12.45)559 (13.58)<0.001
 Hypertension5034 (30.69)853 (20.99)1174 (28.50)1435 (34.97)1572 (38.19)<0.001
Treatment, n (%)
 Antihypertensive drugs2952 (18.00)508 (12.50)687 (16.67)858 (20.91)899 (21.84)<0.001
 Lipid-lowering drugs1328 (8.10)171 (4.21)321 (7.79)417 (10.16)419 (10.18)<0.001
 Hypoglycemic agents761 (4.64)66 (1.62)136 (3.30)270 (6.58)289 (7.02)<0.001
 Antiplatelet drugs195 (1.19)38 (0.94)43 (1.04)58 (1.41)56 (1.36)0.124
Outcomes, n (%)
 All-cause mortality3078 (18.77)876 (21.56)827 (20.07)794 (19.35)581 (14.12)<0.001
 Cardiovascular disease mortality392 (2.39)119 (2.93)115 (2.79)88 (2.14)70 (1.70)<0.001
 Cerebrovascular disease mortality128 (0.78)34 (0.84)35 (0.85)38 (0.93)21 (0.51)0.143

Note: Values are mean ± standardized differences or n (%).

Abbreviations: Q, quartile; HDL, high-density lipoprotein; eGFR, estimated glomerular filtration rate.

Baseline Demographic and Clinical Parameters Among Participants by Subscapular Skinfold Quartiles Note: Values are mean ± standardized differences or n (%). Abbreviations: Q, quartile; HDL, high-density lipoprotein; eGFR, estimated glomerular filtration rate.

The Relationship Between Subscapular Skinfold and All-Cause, Cardiovascular, and Cerebrovascular Diseases Mortality

Multivariable-adjusted Cox Cubic spline regression models showed an inverse association between subscapular skinfold and all-cause and cardiovascular mortality (Figure 2). The association between subscapular skinfold and cerebrovascular mortality showed no statistical significance. As shown in Table 2, when treating subscapular skinfold as a categorical variable, people in the upper (Q4) versus the lowest quartile (Q1) had a reduced risk of all-cause (HR, 0.71; 95% CI, 0.57–0.89; P = 0.002) and cardiovascular mortality (HR, 0.44; 95% CI, 0.23–0.83; P = 0.011) after adjusted for multivariate in Model III. When treating subscapular skinfold as a continuous variable, subscapular skinfold was inversely associated with all-cause (HR, 0.98; 95% CI, 0.97–0.98; P < 0.001) and cardiovascular mortality (HR, 0.97; 95% CI, 0.96–0.98; P < 0.001) in univariate analysis. However, after being adjusted for confounders (Model III), subscapular skinfold inversely associated with all-cause mortality (HR, 0.98; 95% CI, 0.97–0.99; P < 0.001) but showed no significant association with cardiovascular mortality (HR, 0.97; 95% CI, 0.94–1.00; P = 0.083). Kaplan–Meier survival curves, as shown in Figure 3, also demonstrate the significant differences in all-cause mortality and cardiovascular mortality (all P < 0.001). No analyses showed significant associations between subscapular skinfold and cerebrovascular mortality.
Figure 2

Association of subscapular skinfold thickness with all-cause (A), cardiovascular (B), and cerebrovascular (C) mortality using Cox cubic spline regression models. Adjusted for age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, hypertension, diabetes, cardiovascular disease, antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs.

Table 2

Multivariate Cox Regression Analysis of Subscapular Skinfold with Cause-Specific Mortality

Model IHR (95% CI), P-valueModel IIHR (95% CI), P-valueModel IIIHR (95% CI), P-value
All-cause mortality
Subscapular Skinfold (per mm increment)0.98 (0.97, 0.98) <0.0010.97 (0.97, 0.98) <0.0010.98 (0.97, 0.99) <0.001
Subscapular skinfold group
 Q11.01.01.0
 Q20.92 (0.84, 1.01) 0.0790.71 (0.64, 0.78) <0.0010.74 (0.63, 0.88) <0.001
 Q30.88 (0.80, 0.97) 0.0090.68 (0.61, 0.76) <0.0010.75 (0.63, 0.90) 0.002
 Q40.62 (0.56, 0.69) <0.0010.60 (0.53, 0.69) <0.0010.71 (0.57, 0.89) 0.002
P for trend<0.001<0.0010.007
Cardiovascular mortality
Subscapular Skinfold (per mm increment)0.97 (0.96, 0.98) <0.0010.98 (0.96, 1.00) 0.0170.97 (0.94, 1.00) 0.083
Subscapular skinfold group
 Q11.01.01.0
 Q20.94 (0.73, 1.21) 0.6190.77 (0.58, 1.02) 0.0640.41 (0.24, 0.69) <0.001
 Q30.72 (0.54, 0.94) 0.0170.65 (0.47, 0.89) 0.0070.49 (0.29, 0.82) 0.008
 Q40.55 (0.41, 0.74) <0.0010.66 (0.45, 0.97) 0.0330.44 (0.23, 0.83) 0.011
P for trend<0.0010.0150.023
Cerebrovascular mortality
Subscapular Skinfold (per mm increment)0.98 (0.96, 1.00) 0.0861.00 (0.97, 1.03) 0.9370.99 (0.94, 1.05) 0.838
Subscapular skinfold group
 Q11.01.01.0
 Q21.00 (0.62, 1.60) 0.9950.88 (0.52, 1.47) 0.6220.80 (0.31, 2.05) 0.641
 Q31.08 (0.68, 1.72) 0.7401.02 (0.59, 1.77) 0.9310.74 (0.27, 2.01) 0.553
 Q40.58 (0.34, 1.00) 0.0510.76 (0.38, 1.54) 0.4450.66 (0.20, 2.15) 0.491
P for trend0.1000.6530.501

Notes: Model I adjust for none; Model II adjust for age, gender, and body mass index; Model III adjust for age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, comorbidities (hypertension, diabetes, and cardiovascular disease), and medication use (antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs).

Abbreviations: HR, hazard ratios; CI, confidence intervals; Q, quartile.

Figure 3

Kaplan–Meier survival curves of all-cause (A), cardiovascular (B), and cerebrovascular (C) mortality based on subscapular skinfold quartiles.

Multivariate Cox Regression Analysis of Subscapular Skinfold with Cause-Specific Mortality Notes: Model I adjust for none; Model II adjust for age, gender, and body mass index; Model III adjust for age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, comorbidities (hypertension, diabetes, and cardiovascular disease), and medication use (antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs). Abbreviations: HR, hazard ratios; CI, confidence intervals; Q, quartile. Association of subscapular skinfold thickness with all-cause (A), cardiovascular (B), and cerebrovascular (C) mortality using Cox cubic spline regression models. Adjusted for age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, hypertension, diabetes, cardiovascular disease, antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs. Kaplan–Meier survival curves of all-cause (A), cardiovascular (B), and cerebrovascular (C) mortality based on subscapular skinfold quartiles.

Subgroup Analysis of Subscapular Skinfold with All-Cause, Cardiovascular and Cerebrovascular Mortality

Table 3 shows the subgroup analysis for the association of subscapular skinfold with all-cause and cardiovascular mortality, when being treated as a continuous variable. We found that subscapular skinfold was only associated with all-cause (HR, 0.97; 95% CI, 0.96–0.98, P < 0.001) and cardiovascular mortality (HR, 0.96; 95% CI, 0.92–0.99, P = 0.028) in people ≥65 years (all P-interaction <0.001). No significant difference was found in other subgroup analyses.
Table 3

Subgroup Analysis of Subscapular Skinfold with All-Cause and Cardiovascular Mortality

All-Cause MortalityCardiovascular Mortality
HR (95% CI), P-valueP-interactionHR (95% CI), P-valueP-interaction
Age, years<0.001<0.001
 <650.99 (0.97, 1.01) 0.1880.97 (0.91, 1.03) 0.301
 ≥650.97 (0.96, 0.98) <0.0010.96 (0.92, 0.99) 0.028
Gender0.7970.236
 Male0.99 (0.97, 1.00) 0.0440.99 (0.95, 1.04) 0.796
 Female0.97 (0.96, 0.99) 0.0020.92 (0.87, 0.98) 0.007
Race0.7490.403
 Non-white0.98 (0.96, 1.00) 0.0140.94 (0.89, 1.00) 0.041
 White0.98 (0.97, 1.00) 0.0130.99 (0.94, 1.03) 0.509
BMI, kg/m20.2030.800
 <250.94 (0.92, 0.97) <0.0010.92 (0.87, 0.99) 0.017
 ≥250.99 (0.98, 1.00) 0.0440.99 (0.95, 1.03) 0.534

Note: When analyzing a subgroup variable, age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, comorbidities (hypertension, diabetes, and cardiovascular disease), and medication use (antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs) except the variable itself.

Abbreviations: HR, hazard ratios; CI, confidence intervals.

Subgroup Analysis of Subscapular Skinfold with All-Cause and Cardiovascular Mortality Note: When analyzing a subgroup variable, age, gender, race, education level, married, smoking, alcohol consumption, body mass index, systolic blood pressure, estimated glomerular filtration rate, high-density lipoprotein cholesterol, total cholesterol, C-reactive protein, comorbidities (hypertension, diabetes, and cardiovascular disease), and medication use (antihypertensive drugs, hypoglycemic agents, antiplatelet drugs, and lipid-lowering drugs) except the variable itself. Abbreviations: HR, hazard ratios; CI, confidence intervals.

Discussion

In the present study, subscapular skinfold was inversely associated with all-cause and cardiovascular mortality in people ≥65 years. No significant relationship had been found between subscapular skinfold and cerebrovascular mortality. “Obesity paradox” has been widely reported in previous studies when using BMI as an index of adiposity,13 suggesting that people with higher than normal weight have lower all-cause mortality. Epidemiological data suggest that the relationship between obesity and all-cause mortality in the general population follows a U-shaped pattern, and the nadir of the curve was observed at the overweight population.24 Similar findings were reported in studies that used CHD, heart failure, atrial fibrillation, diabetes mellitus, and other disease conditions as outcomes.6,7,11,14,25 This is likely because BMI being an inaccurate indicator of body fatness.15 Skinfold thickness may serve as an alternative but its role in clinical practice and research investigation has not been confirmed. The results from previous studies concerning the effects of subscapular skinfold are inconsistent. Studies conducted before the 1990s have mostly demonstrated a positive association of subscapular skinfold with all-cause and cardiovascular mortality.16,19,20,26 However, the more recent studies tended to have different findings. Kalmijn’s study in older Japanese-American men showed that higher subscapular skinfold was associated with lower mortality risk and Loh’s study in UK white males revealed no association.27,28 Our study found that subscapular skinfold shows an inverse association with all-cause and cardiovascular mortality, which was independent from BMI. The vast changes in people’s lifestyle and diet structure, as well as the widespread use of statins in recent years, might lead to a transition of the impact of obesity on public health, as the use of established lipid-modifying drugs has indisputably reduced the risk of having an ASCVD event.29 Subscapular skinfold may also reflect the level of subcutaneous fat.30 Therefore, subscapular skinfold may indicate subcutaneous fat storage. Inadequate subcutaneous adipose tissue expansion in face of excess dietary fat leads to visceral and ectopic fat deposition, inflammatory/adipokine dysregulation and insulin resistance.3,4 In contrary, certain subcutaneous fat regions appear to be metabolically, immunologically, and mechanically protective, and acting as a sink to sequester potentially lipotoxic fatty acids.31 Nevertheless, the precise role of subscapular skinfold in body-fat distribution remains to be investigated. In addition, it is worth noting that subscapular skinfold was only associated with all-cause and cardiovascular mortality in people ≥65 years, which was in accordance with reports from other studies. Chinese Atrial fibrillation registry study found that the “obesity paradox” between high BMI and reduced mortality rate in patients with AF was confined to those with age ≥65 years.25 The Shizuoka Elderly Cohort Study and The Honolulu Heart Program also found that overweight/obesity was inversely associated with mortality in older people, whether defined by BMI or skinfold thickness.27,32 Previous epidemiological studies in the general population have indicated that the relative risk of mortality associated with excess adiposity is lower among older persons.33 It appears that adiposity may have less severe threats on health for older adults than that for young people. Instead, overweight/obesity was associated with lower risk of all-cause mortality in older persons.34 One probable explanation is that people with obesity may have a higher metabolic reserve than lean or normal weight individuals. Obesity might protect against cachexia and energy wasting, with a much more notable effect in older patients with frailty when comorbidities and poor homeostatic reserve are obvious.34 However, obesity and aging are both associated with a higher prevalence of hypertension and other chronic diseases, which may lead to a higher chance of early diagnosis and treatment for severe illnesses. Meanwhile, weight loss will almost certainly have preceded the diagnosis of cancer or be associated with other wasting chronic diseases from which participants may have died, and this would tend to confuse any real association.19 Further studies are needed to establish the precise role of advanced aging in obesity paradox and all-cause mortality. However, our study has several limitations that should be noted. First, the study population was relatively young, which limited the power to reveal the true association. Second, there were no direct measurements of body fat distribution like MRI or CT that could help us to establish the relationship between subscapular skinfold thickness and adiposity. Third, our study is an observational study; no clear conclusions can be drawn when causality has not been involved. Fourth, we were not able to exclude pregnant and lactating ladies. Fifth, the sample of the general population in the United States may limit the applicability in other regions and ethnic populations.

Conclusions

Subscapular skinfold was inversely associated with all-cause and cardiovascular mortality, and the inverse association only occurred in people ≥65 years. Subscapular skinfold was not significantly associated with cerebrovascular mortality. The association of subscapular skinfold with all-cause and specific mortality is needed more researches to clarify.
  34 in total

1.  Skinfold thickness measurements and mortality in white males during 27.7 years of follow-up.

Authors:  Wann Jia Loh; Desmond G Johnston; Nick Oliver; Ian F Godsland
Journal:  Int J Obes (Lond)       Date:  2018-02-20       Impact factor: 5.095

2.  Estimating glomerular filtration rate from serum creatinine and cystatin C.

Authors:  Lesley A Inker; Christopher H Schmid; Hocine Tighiouart; John H Eckfeldt; Harold I Feldman; Tom Greene; John W Kusek; Jane Manzi; Frederick Van Lente; Yaping Lucy Zhang; Josef Coresh; Andrew S Levey
Journal:  N Engl J Med       Date:  2012-07-05       Impact factor: 91.245

3.  Central obesity: predictive value of skinfold measurements for subsequent ischaemic heart disease at 14 years follow-up in the Caerphilly Study.

Authors:  J W Yarnell; C C Patterson; H F Thomas; P M Sweetnam
Journal:  Int J Obes Relat Metab Disord       Date:  2001-10

4.  The magnitude of association between overweight and obesity and the risk of diabetes: a meta-analysis of prospective cohort studies.

Authors:  Asnawi Abdullah; Anna Peeters; Maximilian de Courten; Johannes Stoelwinder
Journal:  Diabetes Res Clin Pract       Date:  2010-05-20       Impact factor: 5.602

5.  The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report.

Authors:  Aram V Chobanian; George L Bakris; Henry R Black; William C Cushman; Lee A Green; Joseph L Izzo; Daniel W Jones; Barry J Materson; Suzanne Oparil; Jackson T Wright; Edward J Roccella
Journal:  JAMA       Date:  2003-05-14       Impact factor: 56.272

Review 6.  Cardiovascular and Metabolic Heterogeneity of Obesity: Clinical Challenges and Implications for Management.

Authors:  Ian J Neeland; Paul Poirier; Jean-Pierre Després
Journal:  Circulation       Date:  2018-03-27       Impact factor: 29.690

Review 7.  Overview of Epidemiology and Contribution of Obesity and Body Fat Distribution to Cardiovascular Disease: An Update.

Authors:  Marie-Eve Piché; Paul Poirier; Isabelle Lemieux; Jean-Pierre Després
Journal:  Prog Cardiovasc Dis       Date:  2018-06-28       Impact factor: 8.194

8.  The timing of the rise in U.S. obesity varies with measure of fatness.

Authors:  Richard V Burkhauser; John Cawley; Maximilian D Schmeiser
Journal:  Econ Hum Biol       Date:  2009-08-05       Impact factor: 2.184

9.  Health Effects of Overweight and Obesity in 195 Countries over 25 Years.

Authors:  Ashkan Afshin; Mohammad H Forouzanfar; Marissa B Reitsma; Patrick Sur; Kara Estep; Alex Lee; Laurie Marczak; Ali H Mokdad; Maziar Moradi-Lakeh; Mohsen Naghavi; Joseph S Salama; Theo Vos; Kalkidan H Abate; Cristiana Abbafati; Muktar B Ahmed; Ziyad Al-Aly; Ala’a Alkerwi; Rajaa Al-Raddadi; Azmeraw T Amare; Alemayehu Amberbir; Adeladza K Amegah; Erfan Amini; Stephen M Amrock; Ranjit M Anjana; Johan Ärnlöv; Hamid Asayesh; Amitava Banerjee; Aleksandra Barac; Estifanos Baye; Derrick A Bennett; Addisu S Beyene; Sibhatu Biadgilign; Stan Biryukov; Espen Bjertness; Dube J Boneya; Ismael Campos-Nonato; Juan J Carrero; Pedro Cecilio; Kelly Cercy; Liliana G Ciobanu; Leslie Cornaby; Solomon A Damtew; Lalit Dandona; Rakhi Dandona; Samath D Dharmaratne; Bruce B Duncan; Babak Eshrati; Alireza Esteghamati; Valery L Feigin; João C Fernandes; Thomas Fürst; Tsegaye T Gebrehiwot; Audra Gold; Philimon N Gona; Atsushi Goto; Tesfa D Habtewold; Kokeb T Hadush; Nima Hafezi-Nejad; Simon I Hay; Masako Horino; Farhad Islami; Ritul Kamal; Amir Kasaeian; Srinivasa V Katikireddi; Andre P Kengne; Chandrasekharan N Kesavachandran; Yousef S Khader; Young-Ho Khang; Jagdish Khubchandani; Daniel Kim; Yun J Kim; Yohannes Kinfu; Soewarta Kosen; Tiffany Ku; Barthelemy Kuate Defo; G Anil Kumar; Heidi J Larson; Mall Leinsalu; Xiaofeng Liang; Stephen S Lim; Patrick Liu; Alan D Lopez; Rafael Lozano; Azeem Majeed; Reza Malekzadeh; Deborah C Malta; Mohsen Mazidi; Colm McAlinden; Stephen T McGarvey; Desalegn T Mengistu; George A Mensah; Gert B M Mensink; Haftay B Mezgebe; Erkin M Mirrakhimov; Ulrich O Mueller; Jean J Noubiap; Carla M Obermeyer; Felix A Ogbo; Mayowa O Owolabi; George C Patton; Farshad Pourmalek; Mostafa Qorbani; Anwar Rafay; Rajesh K Rai; Chhabi L Ranabhat; Nikolas Reinig; Saeid Safiri; Joshua A Salomon; Juan R Sanabria; Itamar S Santos; Benn Sartorius; Monika Sawhney; Josef Schmidhuber; Aletta E Schutte; Maria I Schmidt; Sadaf G Sepanlou; Moretza Shamsizadeh; Sara Sheikhbahaei; Min-Jeong Shin; Rahman Shiri; Ivy Shiue; Hirbo S Roba; Diego A S Silva; Jonathan I Silverberg; Jasvinder A Singh; Saverio Stranges; Soumya Swaminathan; Rafael Tabarés-Seisdedos; Fentaw Tadese; Bemnet A Tedla; Balewgizie S Tegegne; Abdullah S Terkawi; J S Thakur; Marcello Tonelli; Roman Topor-Madry; Stefanos Tyrovolas; Kingsley N Ukwaja; Olalekan A Uthman; Masoud Vaezghasemi; Tommi Vasankari; Vasiliy V Vlassov; Stein E Vollset; Elisabete Weiderpass; Andrea Werdecker; Joshua Wesana; Ronny Westerman; Yuichiro Yano; Naohiro Yonemoto; Gerald Yonga; Zoubida Zaidi; Zerihun M Zenebe; Ben Zipkin; Christopher J L Murray
Journal:  N Engl J Med       Date:  2017-06-12       Impact factor: 91.245

10.  Hospital admissions in relation to body mass index in UK women: a prospective cohort study.

Authors:  Gillian K Reeves; Angela Balkwill; Benjamin J Cairns; Jane Green; Valerie Beral
Journal:  BMC Med       Date:  2014-03-15       Impact factor: 8.775

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  2 in total

1.  Associations Between Adult Triceps Skinfold Thickness and All-Cause, Cardiovascular and Cerebrovascular Mortality in NHANES 1999-2010: A Retrospective National Study.

Authors:  Weiya Li; Han Yin; Yilin Chen; Quanjun Liu; Yu Wang; Di Qiu; Huan Ma; Qingshan Geng
Journal:  Front Cardiovasc Med       Date:  2022-05-10

2.  Quotient of Waist Circumference and Body Mass Index: A Valuable Indicator for the High-Risk Phenotype of Obesity.

Authors:  Xiao-Cong Liu; Yu Huang; Kenneth Lo; Yu-Qing Huang; Ji-Yan Chen; Ying-Qing Feng
Journal:  Front Endocrinol (Lausanne)       Date:  2021-05-31       Impact factor: 5.555

  2 in total

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