Literature DB >> 21160131

Low cholesterol is associated with mortality from stroke, heart disease, and cancer: the Jichi Medical School Cohort Study.

Naoki Nago1, Shizukiyo Ishikawa, Tadao Goto, Kazunori Kayaba.   

Abstract

BACKGROUND: We investigated the relationship between low cholesterol and mortality and examined whether that relationship differs with respect to cause of death.
METHODS: A community-based prospective cohort study was conducted in 12 rural areas in Japan. The study subjects were 12,334 healthy adults aged 40 to 69 years who underwent a mass screening examination. Serum total cholesterol was measured by an enzymatic method. The outcome was total mortality, by sex and cause of death. Information regarding cause of death was obtained from death certificates, and the average follow-up period was 11.9 years.
RESULTS: As compared with a moderate cholesterol level (4.14-5.17 mmol/L), the age-adjusted hazard ratio (HR) of low cholesterol (<4.14 mmol/L) for mortality was 1.49 (95% confidence interval [CI]: 1.23-1.79) in men and 1.50 (1.10-2.04) in women. High cholesterol (≥6.21 mmol/L) was not a risk factor. This association was unchanged in analyses that excluded deaths due to liver disease, which yielded age-adjusted HRs of 1.38 (95% CI, 1.13-1.67) in men and 1.49 (1.09-2.04) in women. The multivariate-adjusted HRs and 95% CIs of the lowest cholesterol group for hemorrhagic stroke, heart failure (excluding myocardial infarction), and cancer mortality significantly higher than those of the moderate cholesterol group, for each cause of death.
CONCLUSIONS: Low cholesterol was related to high mortality even after excluding deaths due to liver disease from the analysis. High cholesterol was not a risk factor for mortality.

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Year:  2010        PMID: 21160131      PMCID: PMC3899519          DOI: 10.2188/jea.je20100065

Source DB:  PubMed          Journal:  J Epidemiol        ISSN: 0917-5040            Impact factor:   3.211


INTRODUCTION

Both medical professionals and patients are well aware of the dangers of high cholesterol, but most know little about the risks of low cholesterol, despite the many studies that have examined the issue.[1]–[3] The first report to show a relationship between low cholesterol and cerebral hemorrhage was a Japanese cohort study,[4] and many subsequent observational studies have shown that low cholesterol is associated with cerebral hemorrhage,[5] cancer, suicide, injury, and non-coronary mortality.[6]–[8] However, there is no explicit evidence that these relationships are causal. A meta-analysis of interventional trials showed that cholesterol-lowering therapy was associated with high mortality in a population with low cardiovascular risk.[9] Although this meta-analysis focused on interventions other than statins, studies of statins have also shown that statin administration is associated with increases in cancer incidence among elderly adults,[10] breast cancer incidence during the secondary prevention phase,[11] and total cancer incidence.[12] Japanese researchers reported that the relationship between low cholesterol and mortality disappeared when deaths due to liver disease were excluded.[13] To clarify this issue, we investigated the relationship between cholesterol and mortality with respect to cause of death (deaths due to stroke, heart disease, and cancer). In addition, the relationship between cholesterol and mortality was examined after excluding deaths due to liver disease.

METHODS

Participants

This study was conducted as part of the Jichi Medical School (JMS) Cohort Study[13]; 12 490 men and women aged 40 to 69 years participated. The JMS Cohort Study is a prospective cohort study that began in 1992 with the aim of investigating risk factors for stroke and cardiovascular diseases. We collected baseline data from April 1992 through July 1995 in 12 rural areas of Japan and completed a follow-up in December 2005, in which 65% of the subjects from mass screening examinations participated. Of these, 96% of participants completed follow-up; incomplete data were obtained for 409 participants who were not followed until the last day of our study because they had left the study area. There were no follow-up data for 97 participants. However, data from the abovementioned 409 subjects were included in the analyses, and the day they left the area was defined as the endpoint. Informed consent for follow-up was not obtained from 95 participants and from 2 additional participants who had already left the area at the beginning of follow-up. These 97 individuals were excluded from the analyses. Furthermore, we were unable to obtain total cholesterol data for 156 participants, including 4 who did not provide informed consent. In total, we analyzed data from 12 241 participants, ie, 98% of the total number of participants. The average follow-up period was 11.9 years. We observed participants for a total of 145 312 person-years. Details regarding the JMS Cohort Study are available elsewhere.[14]

Exposure

Total cholesterol was measured by an enzymatic method (Wako, Osaka, Japan; interassay coefficient of variation: 1.5%). All samples were measured at the same laboratory (SRL, Tokyo, Japan).

Confounding factors

We obtained information on confounding factors (smoking and drinking habits, blood pressure, height, weight, and high-density lipoprotein [HDL] cholesterol) from the baseline data of the JMS Cohort Study.

Outcome

Information regarding cause of death was collected using data from death certificates and national vital statistics with the permission of the Agency of General Affairs. We classified cause of death according to the International Classification of Diseases, 10th Revision (hemorrhagic stroke: I60, I61, I69.0, I69.1; ischemic stroke: I63, I69.3; myocardial infarction: I21, I22; heart failure: I50). Written informed consent was obtained from all participants. The Institutional Review Board of JMS was responsible for ethical review of this research and approved the study.

Statistical analysis

Because the relationship between cholesterol and mortality is not linear, subjects were divided into 4 groups according to total cholesterol level (<4.14 mmol/L, 4.14 mmol/L to <5.17 mmol/L, 5.17 mmol/L to <6.21 mmol/L, and ≥6.21 mmol/L). The second lowest group (4.14 mmol/L to <5.17 mmol/L) was used as the reference group. However, in the analyses of ischemic stroke in men and myocardial infarction in women, the highest group was defined as ≥5.70 mmol/L because there was no ischemic stroke or myocardial infarction in subjects with a total cholesterol level ≥6.21 mmol/L. The cutoff value used for the lowest group was selected on the basis of past research,[1] and the cutoff value for the highest group was based on criteria from the mass screening examination. A Cox proportional hazards model was used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs) for mortality. Both age-adjusted HRs and multivariate-adjusted HRs were calculated. The multivariate-adjusted model adjusted for age, smoking status (current/former/never), drinking status (current/former/never), systolic blood pressure, HDL cholesterol, and body mass index (BMI:<18, 18 to <22, 22 to <26, ≥26). Age, blood pressure, and HDL cholesterol were analyzed as continuous variables. All analyses were performed separately for each sex using STATA/SE for Windows (STATACORP, release 10, TX, USA). A P value of less than 0.05 was considered to indicate statistical significance.

RESULTS

All subjects were included in the age-adjusted analysis. Because of missing values, multivariate-adjusted analyses included data from only 11 869 subjects. Tables 1 and 2 show the baseline characteristics of subjects grouped by sex and cholesterol category. The background characteristics of subjects included and excluded from the multivariate-adjusted analysis did not differ.
Table 1.

Baseline characteristics of participants

VariableMenWomen


nMeanSDnMeanSD
Age483955.212749555.311.3
Height (cm)4649162.56.97250150.36.2
Body weight (kg)465160.99.4725252.48.0
Systolic BP (mm Hg)4664131.520.57297128.321.0
Diastolic BP (mm Hg)466479.212.3729776.312.1
Total cholesterol (mmol/L)48394.80.974955.10.9
HDL cholesterol (mmol/L)48391.30.474951.40.3
Body mass index (kg/m2)464923.02.9725023.23.2
 
Smokingn% n% 


 Current228050.5 3845.5 
 Former127428.2 1952.8 
 Never95721.2 636291.7 
Drinking      
 Current329375.0 169225.0 
 Former1613.7 1031.5 
 Never93521.3 498373.5 

Abbreviations: BP, blood pressure; HDL, high-density lipoprotein.

Table 2.

Baseline characteristics of participants by cholesterol level

Men

VariableTotal cholesterol level (mmol/L)Pa

<4.144.14–5.165.17–6.20≥6.21




nMean (SD)nMean (SD)nMean (SD)nMean (SD)

Age113655.3 (13.2)214255.6 (11.8)127454.9 (11.5)28753.0 (10.7)0.038
Height (cm)1079162.4 (7.2)2068162.3 (6.8)1225162.8 (6.9)277163.4 (6.4)<.0001
Body weight (kg)108158.6 (9.0)206860.5 (9.1)122562.8 (9.6)27764.3 (9.8)<.0001
Systolic BP (mm Hg)1095129.0 (20.9)2069131.3 (20.2)1224133.4 (20.5)276134.5 (20.4)<.0001
Diastolic BP (mm Hg)109577.2 (12.1)206979.1 (12.1)122480.8 (12.4)27681.3 (12.0)<.0001
HDL cholesterol (mmol/L)11361.2 (0.3)21421.3 (0.3)12741.3 (0.4)2871.3 (0.4)<.0001
Body mass index (kg/m2)107922.2 (2.7)206822.9 (2.8)122523.6 (3.0)27724 (2.9)<.0001
 
  n%n%n%n%Pb





SmokingCurrent62759.198649.353245.213549.5<.0001
 Former22721.457929.038933.17928.9 
 Never20719.543521.825621.85921.6 
 
DrinkingCurrent76074.4146175.187175.620174.40.628
 Former474.6663.4413.672.6 
 Never21521.041821.524020.86223.0 
 

Abbreviations: BP, blood pressure; HDL, high-density lipoprotein.

aOne-way analysis of variance.

bChi-square test.

Abbreviations: BP, blood pressure; HDL, high-density lipoprotein. Abbreviations: BP, blood pressure; HDL, high-density lipoprotein. aOne-way analysis of variance. bChi-square test. In total, 635 men and 423 women died during the study period; 34 male deaths and 15 female deaths were due to liver diseases. Table 3a shows the number of deaths according to cause of death, including deaths due to liver disease, and incidence in each cholesterol group by sex. Liver cancer and hepatic failure were the main causes of death due to liver disease.
Table 3a.

Causes of death

Cause of deathMenWomen


n%n%
Stroke6710.66014.4
 SAH71.1174.0
 infarction365.7286.6
 hemorrhage203.1133.0
 other40.620.5
Heart disease7311.56014.2
 infarction314.9276.0
 heart failure203.1133.0
 other223.5204.7
Cancera24037.915436.0
 lung6910.9215.0
 stomach264.1225.0
 colon172.7184.2
 other12820.19322.0
Other25540.114934.7
 pneumonia6710.6255.9
 suicide243.8174.0
 accident304.771.7
 other13320.910023.6
 
Total635100423100

Liver disease    
 cancer1647.1320.0
 liver failure1441.21173.3
 other411.716.7
 
 Total3410015100

Abbreviation: SAH, subarachnoid hemorrhage.

aIncluding liver cancer.

Abbreviation: SAH, subarachnoid hemorrhage. aIncluding liver cancer. aper 1000 person-years. bexcluding myocardial infarction. Table 4a shows HRs and 95% CIs for mortality by cholesterol category. Crude, age-adjusted, and multivariate-adjusted HRs are grouped by sex. Smoking status, drinking status, and BMI were entered into the models as categorical dummy variables. The multivariate-adjusted HR of the lowest cholesterol group (<4.14 mmol/L) was 1.38 (95% CI, 1.13–1.66) for men and 1.42 (1.02–2.00) for women. The HRs of men and women in the highest cholesterol group (≥6.21 mmol/L) were not significant; the HR was less than 1 for women (HR, 0.93; 95% CI, 0.67–1.30).
Table 4a.

Total cholesterol level and mortality

 Total cholesterol level (mmol/L)

 <4.144.14–5.165.17–6.20≥6.21
 Hazard ratio (95% CI)
Men    
Total mortality    
 Crude1.48 (1.23–1.78)10.98 (0.80–1.20)0.85 (0.58–1.23)
 Age-adjusted1.49 (1.23–1.79)11.04 (0.85–1.27)1.12 (0.77–1.64)
 Multivariate-​ adjusteda1.38 (1.13–1.66)11.09 (0.88–1.34)1.21 (0.82–1.78)
 
Excluding deaths due to liver disease
 Crude1.37 (1.13–1.66)10.99 (0.81–1.22)0.87 (0.60–1.28)
 Age-adjusted1.38 (1.13–1.67)11.06 (0.86–1.29)1.16 (0.80–1.71)
 Multivariate-​ adjusteda1.27 (1.03–1.56)11.10 (0.89–1.36)1.25 (0.85–1.85)
 
Women    
Total mortality    
 Crude0.92 (0.67–1.25)11.07 (0.86–1.33)1.06 (0.77–1.45)
 Age-adjusted1.50 (1.10–2.04)10.92 (0.74–1.14)0.97 (0.67–1.26)
 Multivariate-​ adjusteda1.42 (1.02–2.00)10.93 (0.73–1.17)0.93 (0.67–1.30)
 
Excluding deaths due to liver disease
 Crude0.91 (0.66–1.24)11.06 (0.85–1.32)1.04 (0.76–1.44)
 Age-adjusted1.49 (1.09–2.04)10.91 (0.72–1.14)0.91 (0.66–1.26)
 Multivariate-​ adjusteda1.40 (0.99–1.98)10.92 (0.72–1.17)0.93 (0.66–1.31)

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index.

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index. Among women, there was an inverse association between total cholesterol and mortality age-adjusted analysis. The multifactor-adjusted HR in the lowest cholesterol group was 0.50 (95% CI, 0.16–1.55) in premenopausal women and 1.42 (0.98–2.06) in postmenopausal women. Table 4a shows the same results, after excluding deaths due to liver disease. In these analyses, the age-adjusted HRs of the lowest cholesterol group were statistically significant: 1.38 (1.13–1.67) for men and 1.49 (1.09–2.04) for women. There was no difference between these results and those for all causes of mortality. The results of analyses that excluded deaths within the first 5 years of follow-up were similar to those that included all deaths (Table 4b). In addition, the results of analysis that excluded 320 participants with a history of stroke (113), myocardial infarction (65), or cancer (142) were similar (Table 4c).
Table 4b.

Total cholesterol and mortality (excluding deaths within the first 5 years of follow-up)

 Total cholesterol level (mmol/L)

 <4.144.14–5.165.17–6.20≥6.21
 Hazard ratio (95% CI)
Men    
Total mortality    
 Crude1.43 (1.16–1.79)11.01 (0.80–1.27)0.91 (0.60–1.40)
 Age-adjusted1.47 (1.18–1.83)11.07 (0.85–1.35)1.24 (0.81–1.89)
 Multivariate-​ adjusteda1.39 (1.10–1.74)11.07 (0.84–1.37)1.33 (0.87–2.05)
 
Excluding deaths due to liver disease
 Crude1.33 (1.06–1.68)11.03 (0.82–1.30)0.94 (0.62–1.44)
 Age-adjusted1.36 (1.08–1.71)11.09 (0.87–1.38)1.28 (0.84–1.97)
 Multivariate-​ adjusteda1.27 (1.00–1.62)11.11 (0.87–1.41)1.39 (0.90–2.14)
 
Women    
Total mortality    
 Crude0.82 (0.57–1.20)10.99 (0.77–1.29)1.14 (0.80–1.63)
 Age-adjusted1.37 (0.94–2.00)10.86 (0.66–1.11)0.99 (0.70–1.43)
 Multivariate-​ adjusteda1.24 (0.82–1.88)10.92 (0.70–1.22)1.11 (0.76–1.61)
 
Excluding deaths due to liver disease
 Crude0.80 (0.55–1.18)10.99 (0.76–1.30)1.15 (0.80–1.65)
 Age-adjusted1.34 (0.91–1.98)10.86 (0.66–1.12)0.91 (0.66–1.26)
 Multivariate-​ adjusteda1.20 (0.79–1.84)10.92 (0.70–1.23)0.93 (0.66–1.31)

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index.

Table 4c.

Total cholesterol and mortality (excluding participants with a history of cancer, stroke, or myocardial infarction)

 Total cholesterol levels (mmol/L)

 <4.144.14–5.165.17–6.20≥6.21
 Hazard ratio (95% CI)
Men    
Total mortality    
 Crude1.49 (1.21–1.83)10.96 (0.76–1.19)0.87 (0.60–1.27)
 Age-adjusted1.48 (1.21–1.82)11.02 (0.81–1.27)1.06 (0.73–1.55)
 Multivariate-​ adjusteda1.38 (1.12–1.71)11.08 (0.86–1.36)1.25 (0.83–1.87)
 
Excluding deaths due to liver disease
 Crude1.39 (1.12–1.72)10.98 (0.78–1.23)0.91 (0.62–1.33)
 Age-adjusted1.38 (1.13–1.71)11.04 (0.83–1.31)1.11 (0.76–1.62)
 Multivariate-​ adjusteda1.29 (1.03–1.60)11.10 (0.88–1.39)1.30 (0.87–1.94)
 
Women    
Total mortality    
 Crude0.77 (0.53–1.12)11.16 (0.92–1.47)1.09 (0.78–1.53)
 Age-adjusted1.29 (0.89–1.88)10.96 (0.76–1.22)0.90 (0.64–1.26)
 Multivariate-​ adjusteda1.28 (0.88–1.89)10.99 (0.78–1.27)0.90 (0.63–1.30)
 
Excluding deaths due to liver disease
 Crude0.78 (0.53–1.14)11.15 (0.90–1.47)1.08 (0.77–1.53)
 Age-adjusted1.30 (0.89–1.91)10.95 (0.75–1.22)0.89 (0.63–1.26)
 Multivariate-​ adjusteda1.29 (0.88–1.91)10.99 (0.77–1.27)0.90 (0.62–1.30)

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index.

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index. aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index. Table 5 shows HRs and 95% CIs for stroke, heart disease, and cancer mortality according to cholesterol category. The multivariate-adjusted HR of the lowest cholesterol group was higher than 1 for each cause of death and was statistically significant for cancer mortality in men.
Table 5.

Total cholesterol by cause of death

 Total cholesterol level (mmol/L)

 <4.144.14–5.165.17–6.21≥6.21
 Hazard ratio (95% CI)
Men    
Stroke mortality    
  Crude1.23 (0.72–2.27)10.92 (0.50–1.69)0.75 (0.23–2.49)
  Age-adjusted1.28 (0.72–2.28)10.98 (0.53–1.80)1.02 (0.31–3.34)
  Multivariate-adjusteda1.21 (0.66–2.21)10.99 (0.53–1.82)0.98 (0.29–3.23)
 Hemorrhagic stroke    
  Crude1.93 (0.81–4.62)10.65 (0.21–2.01)1.79 (0.50–6.45)
  Age-adjusted1.92 (0.80–4.61)10.69 (0.22–2.19)2.10 (0.58–7.61)
  Multivariate-adjusteda1.96 (0.80–4.79)10.68 (0.21–2.16)1.76 (0.38–8.09)
 Ischemic strokeb    
  Crude0.84 (0.35–2.04)11.56 (0.71–3.40)0.48 (0.14–1.64)
  Age-adjusted0.85 (0.35–2.06)11.59 (0.73–3.47)0.58 (0.17–1.95)
  Multivariate-adjusteda0.79 (0.30–2.04)11.55 (0.70–3.43)0.65 (0.19–2.23)
Heart disease mortality    
  Crude1.74 (1.00–3.01)11.06 (0.58–1.93)1.36 (0.54–3.53)
  Age-adjusted1.75 (1.01–3.04)11.14 (0.62–2.10)1.93 (0.74–5.03)
  Multivariate-adjusteda1.36 (0.76–2.46)11.04 (0.54–2.01)2.14 (0.81–5.65)
 Myocardial infarction    
  Crude1.34 (0.57–3.12)10.76 (0.29–1.99)1.38 (0.40–4.82)
  Age-adjusted1.34 (0.58–3.15)10.84 (0.32–2.19)1.84 (0.53–6.483)
  Multivariate-adjusteda0.99 (0.40–2.46)10.86 (0.30–2.47)2.37 (0.52–10.83)
 Heart failurec    
  Crude1.63 (0.50–5.32)11.64 (0.54–5.01)1.94 (0.40–9.40)
  Age-adjusted1.72 (0.52–5.66)11.90 (0.61–5.89)2.77 (0.56–13.67)
  Multivariate-adjusteda1.32 (0.36–4.79)11.59 (0.48–5.27)3.86 (0.76–19.58)
Cancer mortality    
  Crude1.72 (1.27–2.32)11.08 (0.78–1.49)0.80 (0.42–1.53)
  Age-adjusted1.73 (1.28–2.34)11.13 (0.82–1.57)1.01 (0.53–1.95)
  Multivariate-adjusteda1.66 (1.22–2.27)11.18 (0.85–1.66)1.07 (0.55–2.07)
 
Women    
Stroke mortality    
  Crude0.83 (0.33–2.05)11.37 (0.76–2.46)1.53 (0.70–3.35)
  Age-adjusted1.41 (0.57–3.50)11.19 (0.66–2.15)1.40 (0.64–3.06)
  Multivariate-adjusteda1.84 (0.71–4.76)11.29 (0.68–2.44)1.52 (0.66–3.48)
 Hemorrhagic stroke    
  Crude2.18 (0.70–6.81)12.22 (0.92–5.37)3.28 (1.21–8.87)
  Age-adjusted3.41 (1.07–10.85)11.97 (0.80–4.85)2.92 (1.05–8.07)
  Multivariate-adjusteda3.86 (1.18–12.68)11.94 (0.77–4.89)2.15 (0.68–6.77)
 Ischemic stroke    
  Crude0.23 (0.03–1.81)11.06 (0.48–2.39)1.08 (0.35–3.28)
  Age-adjusted0.44 (0.06–3.39)10.99 (0.44–2.23)1.06 (0.34–3.28)
  Multivariate-adjusteda0.57 (0.07–4.54)10.90 (0.37–2.19)1.17 (0.36–3.85)
Heart disease mortality    
  Crude0.75 (0.33–1.73)10.93 (0.53–1.65)0.66 (0.26–1.73)
  Age-adjusted1.43 (0.62–3.40)10.87 (0.50–1.55)0.69 (0.26–1.80)
  Multivariate-adjusteda1.34 (0.54–3.35)10.78 (0.42–1.42)0.39 (0.11–1.30)
 Myocardial infarctionb    
  Crude0.58 (0.17–2.01)10.51 (0.17–1.53)0.53 (0.20–1.46)
  Age-adjusted1.09 (0.31–3.78)10.50 (0.16–1.49)0.49 (0.18–1.36)
  Multivariate-adjusteda1.07 (0.30–3.79)10.38 (0.11–1.34)0.52 (0.18–1.46)
 Heart failurec    
  Crude3.75 (0.87–16.19)10.71 (0.13–3.99)4.22 (1.00–17.82)
  Age-adjusted6.57 (1.49–28.97)10.66 (0.11–3.77)4.00 (0.92–17.45)
  Multivariate-adjusteda5.79 (1.07–31.27)10.72 (0.12–4.28)2.33 (0.37–14.66)
Cancer mortality    
  Crude1.04 (0.62–1.76)11.26 (0.87–1.84)1.75 (1.09–2.80)
  Age-adjusted1.50 (0.89–2.55)11.09 (0.75–1.58)1.48 (0.92–2.36)
  Multivariate-adjusteda1.44 (0.83–2.49)11.07 (0.72–1.59)1.58 (0.97–2.56)

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index.

bCholesterol levels: <4.13, 4.14–5.16, 5.17–5.69, ≥5.70.

cExcluding myocardial infarction.

aCox proportional hazards model adjusted for age, systolic blood pressure, high-density lipoprotein cholesterol, smoking, drinking, and body mass index. bCholesterol levels: <4.13, 4.14–5.16, 5.17–5.69, ≥5.70. cExcluding myocardial infarction. We separately analyzed participants with and without ischemia for stroke and heart disease. Among subjects with the highest level of total cholesterol, the multivariate-adjusted HRs for ischemic stroke and myocardial infarction were not significant. The corresponding HRs for ischemic stroke in men and myocardial infarction in women were less than 1; however, the HR of the lowest group was 3.86 (95% CI, 1.18–12.68) for hemorrhagic stroke in women and 5.79 (1.07–31.27) for heart failure excluding myocardial infarction in women.

DISCUSSION

We noted a clear relationship between low cholesterol and increased mortality. Okamura et al[13] reported that occult liver diseases are associated with mortality; however, in the present study, the relationship between low cholesterol and increased mortality was unchanged in analyses that excluded deaths due to liver disease. Our results suggest that hemorrhagic stroke and heart failure excluding myocardial infarction, contribute to the relationship between low cholesterol and high mortality. Studies have shown a relationship between low cholesterol and non-cardiovascular mortality; however, in addition to cancer mortality, stroke mortality and heart disease mortality were also related to low cholesterol in our analyses. The relationship between low cholesterol and hemorrhagic stroke was similar to previously reported results.[3],[5] Although the relationship between high cholesterol and ischemic stroke is not constant, it may be that the risk of high cholesterol disappears due to medical interventions for ischemic stroke and that the risk of low cholesterol is thus emphasized because of a lack of such interventions for low cholesterol. It is difficult to interpret the relationship between low cholesterol and heart disease mortality. Although a relationship between cholesterol and heart failure was reported, high cholesterol, too, was a risk factor for non-ischemic heart failure.[16] We found no report of an association between low cholesterol and heart failure. The effects of malnutrition should be considered, as should the possible presence of beriberi heart disease and alcoholism. The relationship between low cholesterol and heart disease mortality was stronger in women than in men, so a disease like hyperthyroidism, which is more common in women, may be the culprit. A meta-analysis found an increase in cardiovascular mortality associated with subclinical hyperthyroidism,[17] but further investigations are necessary to confirm this hypothesis. Because low cholesterol is associated with high cancer mortality, low cholesterol is a key finding in cancer. Previous studies reported an increase in liver cancer[13],[15]; however, in the present study, increased cancer mortality in the lowest cholesterol group was unchanged after excluding cases of liver disease from the analyses. This suggests a need for screening of cancers other than liver cancer in individuals with low cholesterol levels. Our results differ from those of previous studies,[1],[3] in that high cholesterol was not identified as a risk factor for mortality in the present study. The HR was 0.93 (0.67–1.30) for women, which indicates that the focus should be on adults with low cholesterol rather than those with high cholesterol. Our analyses constitute a primary use of existing data. An important advantage of this study was that the follow-up rate was very high because the study was conducted in rural areas, where migration is far less than in urban areas. Cause of death was ascertained using death certificates, so there were potential limitations in accuracy regarding cause of death. The setting was a periodical health examination to screen participants with high cholesterol. Thus, it is also necessary to consider the possibility that risk was underestimated due to medical therapy for high cholesterol. Our results are specific to people living in rural areas of Japan and their lifestyle, and may not be applicable to urban Japanese or other ethnic groups. Because Japanese in rural areas have less coronary disease than people in Western countries, their risks from low cholesterol may be higher. There are many factors that might contribute to the relationship between low cholesterol and high mortality. A correlation between high mortality and low cholesterol clearly exists, especially in populations with a low risk of coronary heart disease.[9] Although the dangers of a high cholesterol level are widely known, they are less important in regions—such as rural Japan—where cardiovascular disease is less common. It may therefore be necessary to highlight the risks of low cholesterol. In Japan, only LDL cholesterol and HDL cholesterol are measured at present; however, total cholesterol remains an important measure in predicting mortality. In conclusion, we observed that low cholesterol was associated with increased risks of cancer, hemorrhagic stroke, and heart failure excluding myocardial infarction.
Table 3b.

Mortality by total cholesterol level

 Total cholesterol level (mmol/L)

<4.144.14–5.165.17–6.20≥6.21




nincidenceanincidencenincidencenincidence
Men
Total mortality19515.0825810.2715210.10308.77
Stroke mortality191.47291.15161.0630.88
 Hemorrhagic stroke100.77100.4040.2720.58
 Ischemic stroke70.54170.68120.8000.00
Heart disease mortality211.62220.88151.0041.17
 Myocardial infarction90.70130.5260.4020.58
 Heart failureb50.3960.2460.4020.58
Cancer mortality806.19913.62593.92102.92
 
Women
Total mortality534.251694.681515.01504.95
Stroke mortality60.48210.58240.8090.89
 Hemorrhagic stroke50.4060.17130.4350.50
 Ischemic stroke10.08120.33110.3740.40
Heart disease mortality70.56260.72170.5650.50
 Myocardial infarction30.24150.4290.3000.00
 Heart failureb40.3230.0820.0730.30
Cancer mortality191.52531.47561.86262.58

aper 1000 person-years.

bexcluding myocardial infarction.

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Authors:  Shizukiyo Ishikawa; Tadao Gotoh; Naoki Nago; Kazunori Kayaba
Journal:  J Epidemiol       Date:  2002-11       Impact factor: 3.211

Review 2.  Serum cholesterol levels and suicide: a meta-analysis.

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Journal:  Lancet       Date:  2002-11-23       Impact factor: 79.321

4.  The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators.

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Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

5.  Multivariate analysis of risk factors for stroke. Eight-year follow-up study of farming villages in Akita, Japan.

Authors:  H Ueshima; M Iida; T Shimamoto; M Konishi; K Tsujioka; M Tanigaki; N Nakanishi; H Ozawa; S Kojima; Y Komachi
Journal:  Prev Med       Date:  1980-11       Impact factor: 4.018

6.  Relations of lipid concentrations to heart failure incidence: the Framingham Heart Study.

Authors:  Raghava S Velagaleti; Joseph Massaro; Ramachandran S Vasan; Sander J Robins; William B Kannel; Daniel Levy
Journal:  Circulation       Date:  2009-11-23       Impact factor: 29.690

Review 7.  Effect of the magnitude of lipid lowering on risk of elevated liver enzymes, rhabdomyolysis, and cancer: insights from large randomized statin trials.

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Journal:  J Am Coll Cardiol       Date:  2007-07-16       Impact factor: 24.094

8.  Meta-analysis: subclinical thyroid dysfunction and the risk for coronary heart disease and mortality.

Authors:  Nicolas Ochs; Reto Auer; Douglas C Bauer; David Nanchen; Jacobijn Gussekloo; Jacques Cornuz; Nicolas Rodondi
Journal:  Ann Intern Med       Date:  2008-05-19       Impact factor: 25.391

9.  Serum total cholesterol and mortality in a Japanese population.

Authors:  H Iso; Y Naito; A Kitamura; S Sato; M Kiyama; Y Takayama; M Iida; T Shimamoto; T Sankai; Y Komachi
Journal:  J Clin Epidemiol       Date:  1994-09       Impact factor: 6.437

10.  Serum cholesterol levels in relation to the incidence of cancer: the JPHC study cohorts.

Authors:  Hiroyasu Iso; Ai Ikeda; Manami Inoue; Shinichi Sato; Shoichiro Tsugane
Journal:  Int J Cancer       Date:  2009-12-01       Impact factor: 7.396

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1.  Metabolic syndrome and total cancer mortality in the Third National Health and Nutrition Examination Survey.

Authors:  Wambui G Gathirua-Mwangi; Patrick O Monahan; Mwangi J Murage; Jianjun Zhang
Journal:  Cancer Causes Control       Date:  2017-01-17       Impact factor: 2.506

2.  The total cholesterol to high-density lipoprotein cholesterol as a predictor of poor outcomes in a Chinese population with acute ischaemic stroke.

Authors:  Lifang Chen; Jianing Xu; Hao Sun; Hao Wu; Jinsong Zhang
Journal:  J Clin Lab Anal       Date:  2017-01-26       Impact factor: 2.352

3.  Survival benefits of metabolic syndrome among older men aged 75 years and over in Taiwan.

Authors:  P-H Chiang; C-L Liu; M-H Lin; L-N Peng; L-K Chen; J-D Chen; S-M Hou
Journal:  J Nutr Health Aging       Date:  2012       Impact factor: 4.075

4.  Lipid biomarkers and long-term risk of cancer in the Women's Health Study.

Authors:  Paulette D Chandler; Yiqing Song; Jennifer Lin; Shumin Zhang; Howard D Sesso; Samia Mora; Edward L Giovannucci; Kathryn E Rexrode; M Vinayaga Moorthy; Chunying Li; Paul M Ridker; I-Min Lee; JoAnn E Manson; Julie E Buring; Lu Wang
Journal:  Am J Clin Nutr       Date:  2016-04-20       Impact factor: 7.045

5.  Prospective associations between serum biomarkers of lipid metabolism and overall, breast and prostate cancer risk.

Authors:  Mathilde His; Laurent Zelek; Mélanie Deschasaux; Camille Pouchieu; Emmanuelle Kesse-Guyot; Serge Hercberg; Pilar Galan; Paule Latino-Martel; Jacques Blacher; Mathilde Touvier
Journal:  Eur J Epidemiol       Date:  2014-02-13       Impact factor: 8.082

6.  Is cholesterol a mediator of cold-induced cancer?

Authors:  Chandi C Mandal; Ankit Sharma; Mahaveer S Panwar; James A Radosevich
Journal:  Tumour Biol       Date:  2016-01-21

7.  Serum lipids and mortality in an American Indian population: A longitudinal study.

Authors:  Stephanie K Tanamas; Pierre-Jean Saulnier; Robert L Hanson; Robert G Nelson; Wen-Chi Hsueh; Maurice L Sievers; Peter H Bennett; William C Knowler
Journal:  J Diabetes Complications       Date:  2017-10-03       Impact factor: 2.852

8.  Lipid levels and the risk of hemorrhagic stroke among women.

Authors:  Pamela M Rist; Julie E Buring; Paul M Ridker; Carlos S Kase; Tobias Kurth; Kathryn M Rexrode
Journal:  Neurology       Date:  2019-04-10       Impact factor: 9.910

9.  Prospective study of cancer in Japanese patients with type 2 diabetes: the Fukuoka Diabetes Registry.

Authors:  Masanori Iwase; Hiroki Fujii; Yasuhiro Idewaki; Udai Nakamura; Toshiaki Ohkuma; Hitoshi Ide; Yuji Komorita; Tamaki Jodai-Kitamura; Masahito Yoshinari; Takanari Kitazono
Journal:  Diabetol Int       Date:  2019-02-20

10.  Association Between Statins and Cancer Incidence in Diabetes: a Cohort Study of Japanese Patients with Type 2 Diabetes.

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