Skip to main content
Scientific Reports logoLink to Scientific Reports
. 2018 Jun 29;8:9863. doi: 10.1038/s41598-018-28316-x

Prevalence of metabolic syndrome risk factors and their relationships with renal function in Chinese centenarians

Shihui Fu 1,2,#, Yao Yao 3,4,#, Fuxin Luan 5,, Yali Zhao 5,
PMCID: PMC6026211  PMID: 29959374

Abstract

As the first time, this study was to investigate the prevalence of metabolic syndrome (MetS) risk factors and explore their relationships with renal function in Chinese centenarians. China Hainan Centenarian Cohort Study was performed in 18 cities and counties of Hainan Province. Home interview, physical examination and blood analysis were performed in 874 centenarians following standard procedures. Prevalence of MetS was 15.6% (136 centenarians). There were 229 centenarians with abdominal obesity (26.2%), 645 centenarians (73.8%) with hypertension, 349 centenarians with dyslipidemia (39.9%) and 92 centenarians with diabetes mellitus (10.5%). In multivariate linear regression, age, smoking, waist circumstance (WC), systolic blood pressure (SBP) and triglyceride levels were inversely and diastolic blood pressure (DBP) levels were positively associated with glomerular filtration rate levels (P < 0.05 for all). This study reported low prevalence of MetS risk factors and demonstrated that age, smoking, abdominal obesity (WC), hypertension (SBP and DBP) and triglyceride levels were independently associated with renal function in Chinese centenarians. This study provided reliable data about Chinese centenarians, analyzed significant relationships between Mets risk factors and renal function, and explained possible reason (low prevalence of MetS and its risk factors) and mechanism (interrelationship of age, Mets risk factors with renal function) of longevity.

Introduction

During the last few decades, metabolic syndrome (MetS) and renal function decline (RFD) continue to grow in prevalence all over the world, and this trend is particularly obvious in developing countries1. MetS refers to a clustering of risk factors: abdominal obesity, hypertension, dyslipidemia and diabetes mellitus (DM), all which contribute to the development of cardiovascular disorders and events24. Meanwhile, RFD plays a significant role in the progression of cardiovascular disorders, and has close association with cardiovascular events5,6. More importantly, both MetS and RFD have obvious effects on mortality, and accelerate the occurrence of adverse outcome7,8. Previous studies have observed the prevalence of MetS and analyzed their relationships with renal function, but drawn controversial conclusions8,9. Meanwhile, most of these studies were performed in the general population of developed countries, and there may be obviously different conclusions in the centenarians in China9. Moreover, different conclusions may also derive from race, and thus it is very essential to perform this study in Chinese10.

The centenarians have been suggested to have a delayed or escaped onset and interaction of age-related illnesses, such as MetS and RFD11. Some centenarians may experience a delayed onset of age-related illnesses (delayers), while others may do not succumb to any age-related illnesses (escapers)12. Thus, the centenarians may represent a prototype of successful aging13. However, it is still under scientific debate14. More importantly, what is this model of successful aging? Studies analyzing this model in the centenarians could provide valuable information for early promoting successful aging and preventing age-related diseases. As a possible part of this model, whether the interaction between MetS and RFD exists in the aging process of centenarians is still unclear and needs further studies.

Prevalence of MetS increases with age, reaching 42.0% in U.S. adults 70 years or older15. However, prevalence of MetS and its risk factors are still unclear in Chinese centenarians16. Moreover, its relationship with renal function still has significant debate in the elderly, not to say the centenarians17. Considering the specificity of centenarians, previous studies in the general population can not accurately represent the centenarians18. Meanwhile, in order to understand the reasons and mechanisms of longevity, it is very valuable to perform the studies in Chinese centenarians. Hainan is a longevity area with the highest population density of centenarians in China, and China Hainan Centenarian Cohort Study (CHCCS) with a considerable sample size provides a significantly population-based sample of Chinese centenarians. As the first time all over the world, this study was designed to investigate the prevalence of MetS risk factors and explore their relationships with renal function in a representative sample of Chinese centenarians.

Results

For all centenarians, median age was 102 (100–115) years, and males account for 18.9%. Prevalence of MetS was 15.6% (136 centenarians). For MetS risk factors, there were 229 centenarians with abdominal obesity (26.2%), 645 centenarians (73.8%) with hypertension, 349 centenarians with dyslipidemia (39.9%) and 92 centenarians with DM (10.5%). There were 371 centenarians with GFR <60 ml/min/1.73 m2 (42.4%). As shown in Table 1, the centenarians with GFR <60 ml/min/1.73 m2 tended to be smoking and have MetS, abdominal obesity and hypertension than those with GFR ≥60 ml/min/1.73 m2 (P < 0.05 for all). There were significantly more participants with higher WC, SBP, TG levels and lower HDL-C levels in the centenarians with GFR <60 ml/min/1.73 m2 than those with GFR ≥60 ml/min/1.73 m2 (P < 0.05 for all). MetS had significant relationship with GFR (r = −0.127, P < 0.001; EXP(β): 1.971, 95% CI: 1.362–2.853, P < 0.001; standard β: −0.112, P = 0.001). The number of MetS risk factors had significant relationship with GFR (r = −0.106, P = 0.002; EXP(β): 1.222, 95% CI: 1.074–1.390, P = 0.002; standard β: −0.094, P = 0.005). In the simple correlation analyses (Table 2), smoking, abdominal obesity, WC, TG and HDL-C levels were significantly related to GFR levels (P < 0.05 for all). SBP (P = 0.070) and DBP (P = 0.054) were moderately but not significantly related to GFR levels. In the multivariate linear regression analysis (Table 3), age, smoking, WC, SBP and TG levels were inversely and DBP levels were positively associated with GFR levels (P < 0.05 for all). In the multivariate logistic regression analysis (Table 4), smoking, abdominal obesity and hypertension were independently associated with GFR <60 ml/min/1.73 m2 (P < 0.05 for all).

Table 1.

Prevalence of metabolic syndrome risk factors and description of other characteristics in centenarians.

Characteristics Total (n = 874) GFR <60 ml/min/1.73 m2 (n = 371) GFR ≥60 ml/min/1.73 m2 (n = 503) P value
Age (year) 102 (101–104) 102 (101–104) 102 (101–104) 0.495
Males (%) 165 (18.9) 75 (20.2) 90 (17.9) 0.386
Smoking (%) 29 (3.3) 21 (5.7) 8 (1.6) 0.001
MetS (%) 136 (15.6) 77 (20.8) 59 (11.7) <0.001
Abdominal obesity (%) 229 (26.2) 115 (31.0) 114 (22.7) 0.006
Hypertension (%) 645 (73.8) 288 (77.6) 357 (71.0) 0.027
Dyslipidemia (%) 349 (39.9) 151 (40.7) 198 (39.4) 0.690
DM (%) 92 (10.5) 37 (10.0) 55 (10.9) 0.647
WC (cm) 75 (70–80) 76 (71–82) 74 (68–80) 0.007
SBP (mmHg) 150 (136–170) 152 (138–172) 148 (133–167) 0.008
DBP (mmHg) 75 (67–83) 74 (67–84) 76 (67–83) 0.549
TC (mmol/L) 4.58 (3.99–5.27) 4.54 (3.96–5.18) 4.62 (4.03–5.31) 0.142
TG (mmol/L) 1.03 (0.80–1.41) 1.11 (0.84–1.47) 0.98 (0.77–1.33) <0.001
HDL-C (mmol/L) 1.40 (1.17–1.67) 1.35 (1.13–1.62) 1.43 (1.20–1.70) 0.014
LDL-C (mmol/L) 2.72 (2.27–3.26) 2.65 (2.26–3.24) 2.75 (2.29–3.27) 0.236
FBG (mmol/L) 4.82 (4.20–5.75) 4.97 (4.22–5.76) 4.75 (4.18–5.72) 0.168
GFR (ml/min/1.73 m2) 63.11 (52.34–73.39) 50.48 (43.82–55.13) 71.70 (65.97–79.94) <0.001

Abbreviations: GFR: glomerular filtration rate; MetS: metabolic syndrome; DM: diabetes mellitus; WC: waist circumstance; SBP: systolic blood pressure; DBP: diastolic blood pressure; TC: total cholesterol; TG: triglyceride; HDL-C: high-density lipoproteincholesterol; LDL-C: low-density lipoprotein cholesterol; FBG: fasting blood glucose.

Table 2.

Relationships between metabolic syndrome risk factors and GFR in simple correlation analyses.

Characteristics r P value
Age (year) −0.043 0.199
Females/males 0.026 0.449
Smoking −0.079 0.020
Abdominal obesity −0.096 0.005
Hypertension −0.045 0.183
Dyslipidemia −0.029 0.389
DM 0.022 0.524
WC (cm) −0.157 <0.001
SBP (mmHg) −0.061 0.070
DBP (mmHg) 0.065 0.054
TC (mmol/L) 0.039 0.247
TG (mmol/L) −0.121 <0.001
HDL-C (mmol/L) 0.067 0.047
LDL-C (mmol/L) 0.036 0.291
FBG (mmol/L) −0.036 0.294

Abbreviations: GFR: glomerular filtration rate; DM: diabetes mellitus; WC: waist circumstance; SBP: systolic blood pressure; DBP: diastolic blood pressure; TC: total cholesterol; TG: triglyceride; HDL-C: high-density lipoproteincholesterol; LDL-C: low-density lipoprotein cholesterol; FBG: fasting blood glucose.

Table 3.

Relationships between metabolic syndrome risk factors and GFR in multivariate linear regression analysis.

Characteristics Standard β t Standard error P value
Age (year) −0.071 −2.129 0.002 0.034
Females/males 0.008 0.215 0.011 0.829
Smoking −0.070 −2.029 0.024 0.043
WC (cm) −0.193 −5.578 <0.001 <0.001
SBP (mmHg) −0.086 −2.102 <0.001 0.036
DBP (mmHg) 0.132 3.205 <0.001 0.001
TC (mmol/L) 0.105 0.803 0.016 0.422
TG (mmol/L) −0.083 −1.985 0.008 0.047
HDL-C (mmol/L) −0.048 −0.855 0.018 0.393
LDL-C (mmol/L) −0.017 −0.150 0.018 0.880
FBG (mmol/L) 0.014 0.411 0.003 0.681

Abbreviations: GFR: glomerular filtration rate; WC: waist circumstance; SBP: systolic blood pressure; DBP: diastolic blood pressure; TC: total cholesterol; TG: triglyceride; HDL-C: high-density lipoproteincholesterol; LDL-C: low-density lipoprotein cholesterol; FBG: fasting blood glucose.

Table 4.

Relationships between metabolic syndrome risk factors and GFR in multivariate logistic regression analysis.

Characteristics EXP(β) 95% confidence interval P value
Age (year) 1.021 0.972–1.073 0.406
Females/males 0.941 0.653–1.358 0.746
Smoking 3.980 1.681–9.424 0.002
Abdominal obesity 1.566 1.143–2.145 0.005
Hypertension 1.396 1.016–1.918 0.040
Dyslipidemia 0.990 0.747–1.314 0.947
DM 0.894 0.571–1.400 0.625

Abbreviations: GFR: glomerular filtration rate; DM: diabetes mellitus.

Discussion

Studies about the centenarians can help us understand the reasons and mechanisms of longevity. In previous studies, Mets has a prevalence more than 20% in the general population and a higher prevalence in the elderly1921. In U.S. adults, prevalence of MetS increases with age, reaching 42.0% in those 70 years or older15. This study reported that there was obviously low prevalence of Mets (15.6%) and its risk factors in Chinese centenarians. Georgia Centenarian Study has concluded that major barriers to reaching centenarians come from several incident chronic age-related disorders, especially cardiovascular disorders20. Meanwhile, Mets and its risk factors play significant roles in the development of cardiovascular and other chronic age-related disorders. Moreover, longevity data from Framingham Study have supported that MetS risk factors, such as blood pressure, glucose and lipids, are significant contributors to morbidity and mortality22. Thus, low prevalence of Mets and its risk factors found in this study was a possible reason of longevity in Chinese centenarians.

Both MetS and RFD have been underlined to be independently associated with cardiovascular incidence, events and mortality28. Previous studies have shown significant relationship between MetS and renal function, but drawn controversial conclusions8,9,17. Meanwhile, most of these studies about the centenarians are performed in the general population of developed countries, with little information available on the centenarians in China9,18. Additionally, the data on ethnic Chinese are limited, and the relationship between MetS and renal function is still unknown in ethnic Chinese9,10. This study realized a possible mechanism of longevity in Chinese centenarians that not only age, but also Mets and its risk factors had significant relationships with renal function. On the one hand, Mets and its risk factors may impair the renal function, aggravate the cardiovascular disorders and reduce the life expectancy. The hypothesized mechanism is that as age increases, the clustering of MetS risk factors may result in oxidative stress and endothelial dysfunction, which consequently cause the atherosclerosis-related RFD23. In turn, RFD may gradually affect the blood pressure, glucose and lipids, and also aggravate the metabolic disturbance and promote the development of MetS24. On the other hand, the relationships between age, Mets and renal function also remind us that Mets and RFD may result from a common cause linked to the aging phenomenon. Either one of MetS and RFD may enforce the effects of other one on cardiovascular disorders and their incidence, and the interrelationship between MetS and RFD may worsen further cardiovascular events and mortality7,8.

Abdominal obesity is a fundamental pathology of MetS, and contributes to the development of other MetS risk factors, such as hypertension, dyslipidemia and DM. Abdominal obesity is significantly associated with high mortality risk, and there is an obviously increased prevalence of abdominal obesity in many developed and developing countries25,26. There have been inconsistent study results on the relationship between abdominal obesity and renal function. Several studies have realized that abdominal obesity is significantly associated with renal function in the general population. But other study has not verified significant association between abdominal obesity and renal function in the elderly16. This study observed that with a prevalence of 26.2%, abdominal obesity was independently associated with renal function in Chinese centenarians.

As prevalence of hypertension is rapidly increasing all over the world, the relationship between blood pressure and renal function has drawn considerable attention. Previous studies have shown that hypertension was significantly associated with renal function27,28. However, other study has also found that blood pressure has no significant association with renal function16. This study showed that with a prevalence of 73.8%, hypertension was inversely associated with renal function. More interestingly, SBP was inversely associated with renal function, but DBP was positively associated with renal function in this study. One the one hand, elevated SBP may induce the glomerulosclerosis and lower GFR, while reduced DBP may cause the renal hypoperfusion and lower GFR. On the other hand, RFD may affect the sodium and water retention, activate the renin-angiotensin-aldosterone system and induce the abnormality of SBP and DBP29.

It is a significant issue to analyze the relationships between different types of dyslipidemia and renal function, especially in the elderly, and there has been a controversial relationship between TG levels and renal function. Previous studies have proved that TG levels were significantly associated with renal function28. Triglyceride-rich apolipoprotein B-containing lipoproteins may promote the progression of RFD30. However, Helsinki Heart Study has provided an evidence that there is no significant association between TG levels and renal function31. This study confirmed that TG levels were significantly associated with renal function in Chinese centenarians, and lowering TG therapy may play a role in preserving renal function in addition to preventing cardiovascular disorders.

Smoking is a significant public health problem all over the world, and has been considered to be harmful to renal function in previous studies32. Meanwhile, there has been a concern for many countries about the relationship between DM and renal function, and previous large-scale survey in the US general population has concluded that DM was not associated with renal function33. Consistent with previous studies, this study demonstrated that with a prevalence of 3.3%, smoking exerted harmful effects on renal function. And with a prevalence of 10.5%, DM had no significant association with renal function in Chinese centenarians.

The current study had one limitation. Smoking was assessed by asking each centenarian whether he or she was a current smoker. Although ex-smoker does not seem to be counted as smoker, it should be considered to be one limitation.

Conclusion

As the first time all over the world, this study reported low prevalence of MetS and its risk factors, and demonstrated that age, smoking, abdominal obesity (or WC), hypertension (or SBP and DBP) and TG levels were independently associated with renal function in Chinese centenarians. Low prevalence of MetS and its risk factors was a possible reason of longevity, and the interrelationship of age, Mets and its risk factors with renal function was a possible mechanism of longevity in Chinese centenarians. Based on CHCCS, this study not only provided reliable data about Chinese centenarians and analyzed significant relationships between Mets risk factors and renal function, but also explained possible reason and mechanism of longevity.

Methods

Study population

CHCCS was performed in population-based individuals aged 100 or above from July 2014 to December 2016 in 18 cities and counties of Hainan Province, China. Its cohort profile has been described previously34. Based on National Civil Registry, a total of 1,002 centenarians were identified by Hainan Civil Affairs Bureau and enrolled in this study. Age was ascertained from national identification cards. The following inclusion criteria were used to recruit study participants: (1) was 100 years or older; (2) volunteered to participate in the study and provided written informed consent; and (3) was conscious and could cooperate to complete the home interview, physical examination and blood analysis. The following were participant exclusion criteria: (1) personal identity information was not complete or identification cards showed an age of less than 100 years; (2) refused to comply with the requirements of the study, including the collection of physical or blood samples. There were 874 centenarians included in the final analysis. This study followed the approval from Ethics Committee of Hainan branch of Chinese People’s Liberation Army General Hospital (Sanya, Hainan; Number: 301hn11201601). Written informed consent was obtained from all centenarians in this study. All methods were performed in accordance with the relevant guidelines and regulations.

Standard procedures

Home interview, physical examination and blood analysis were performed following standard procedures35. The research team included internists, geriatricians, cardiologists, endocrinologists, nephrologists and nurses. Smoking was assessed by asking each centenarian whether he or she was a current smoker36. Waist circumstance (WC) was measured with a soft tape midway between the lowest rib and the iliac crest. Consistent with current recommendations, systolic and diastolic blood pressures (SBP and DBP) were measured with the right arm of centenarians two times consecutively, with at least 1 minute between measurements, and the reported blood pressures were the average of these two measurements. Samples of venous blood were obtained from the centenarians and transported in chilled bio-transport container (4 °C) to our Central Laboratory within 4 hours. Serum concentrations of fasting blood glucose (FBG), total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoproteincholesterol (HDL-C) and creatinine were measured using the enzymatic assays (Roche Products Ltd, Basel, Switzerland) on a fully automatic biochemical autoanalyzer (Cobas c702; Roche Products Ltd, Basel, Switzerland). All assays were performed by qualified technicians without knowledge of clinical data.

Variable definitions

Based on the worldwide consensus on the definition of MetS recommended by International Diabetes Federation, MetS was defined as abdominal obesity plus any two of four additional factors: SBP ≥130 mmHg or DBP ≥85 mmHg (or previously diagnosed hypertension); FBG ≥5.6 mmol/L (or previously diagnosed DM); and TG ≥1.7 mmol/L, HDL-C <1.0 mmol/L in males and <1.3 mmol/L in females (or previously diagnosed dyslipidemia)37. Based on Chinese guidelines on prevention and control of obesity, abdominal obesity was defined as WC ≥85 cm for men and ≥80 cm for women38. Hypertension was defined as SBP ≥140 mmHg, DBP ≥90 mmHg or taking anti-hypertensive drugs39. DM was defined as FBG ≥7.0 mmol/L or taking hypoglycemic drugs/insulin40. Dyslipidemia was defined as TG ≥1.7 mmol/L, LDL-C ≥3.37 mmol/L, HDL-C ≥1.04 mmol/L or taking lipid-regulating drugs41. Estimated glomerular filtration rate (GFR) was calculated using a modified version of Modification of Diet in Renal Disease (MDRD) equation based on the data from Chinese patients as follows: 175 × serum creatinine (mg/dL)−1.234 × age (year)−0.179 × 0.79 (if female)42.

Statistical analyses

Continuous variables were described as the mean and standard deviation for variables with normal distribution and the median and interquartile range for variables with skewed distribution. Categorical variables were described as the number and percentage. Continuous variables were compared with Student’s t-test (normal distribution) and Mann–Whitney U test (skewed distribution). Categorical variables were compared with Chi-square test. Pearson’s (continuous variables with normal distribution) and Spearman’s (continuous variables with skewed distribution and categorical variables) correlations were used to assess the simple relationships between MetS risk factors and renal function. In order to assess the independent relationships between MetS risk factors and renal function, multivariate linear regression analyses were adjusted by age, sex, smoking, WC, SBP, DBP, TC, TG, HDL-C, LDL-C and FBG, and multivariate logistic regression analyses were adjusted by age, sex, smoking, abdominal obesity, hypertension, dyslipidemia and DM. Statistical significance was accepted at the two-sided 0.05 level, and confidence interval (CI) was computed at the 95% level. Statistical analyses were performed with Statistic Package for Social Science (SPSS) version 17 (SPSS Inc., Chicago, IL, U.S.).

Availability of data and materials

In attempt to preserve privacy of patients, clinical data of patients will not be shared; data can be available from authors upon request.

Acknowledgements

We appreciate all the staff of CHCCS for their continued cooperation and contribution in field work. This work was supported by grants from Key Research and Development Program of Hainan (ZDYF2016135 and ZDYF2017095), Sanya Medical and Health Science and Technology Innovation Project (2016YW21), and Clinical Scientific Research Supporting Fund of Chinese People’s Liberation Army General Hospital (2017FC-CXYY-3009). The sponsors had no role in the design, conduct, interpretation, review, approval or control of this article.

Author Contributions

F.S., Y.Y., L.F., Z.Y.: contributed to the study design, performed the data collection and analyses, and drafted the paper.

Competing Interests

The authors declare no competing interests.

Footnotes

Shihui Fua and Yao Yao contributed equally to this work.

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Fuxin Luan, Email: baisui301@163.com.

Yali Zhao, Email: zhaoyl301@163.com.

References

  • 1.Aguilar M, et al. Prevalence of the metabolic syndrome in the United States, 2003–2012. JAMA. 2015, 313(19) (1973). [DOI] [PubMed]
  • 2.Samson SL, Garber AJ. Metabolic syndrome. Endocrinol Metab Clin North Am. 2014;43(1):1e23. doi: 10.1016/j.ecl.2013.09.009. [DOI] [PubMed] [Google Scholar]
  • 3.Sattar N, et al. Can metabolic syndrome usefully predict cardiovascular disease and diabetes? Outcome data from two prospective studies. Lancet. 2008;371(9628):1927–1935. doi: 10.1016/S0140-6736(08)60602-9. [DOI] [PubMed] [Google Scholar]
  • 4.Gami AS, et al. Metabolic syndrome and risk of incident cardiovascular events and death: a systematic review and meta-analysis of longitudinal studies. J Am Coll Cardiol. 2007;49(4):403e14. doi: 10.1016/j.jacc.2006.09.032. [DOI] [PubMed] [Google Scholar]
  • 5.Ronco C, et al. Cardio-renal syndromes: report from the consensus conference of the Acute Dialysis Quality Initiative. Eur Heart J. 2010;31(6):703–711. doi: 10.1093/eurheartj/ehp507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Rifkin DE, et al. Rapid renal function decline and mortality risk in older adults. Arch Intern Med. 2008;168(20):2212–8. doi: 10.1001/archinte.168.20.2212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Gomez P, et al. Prevalence of renal insufficiency in individuals with hypertension and obesity/overweight: the FATH study. J Am Soc Nephrol. 2006;17(12Suppl 3):S194–200. doi: 10.1681/ASN.2006080914. [DOI] [PubMed] [Google Scholar]
  • 8.Chien KL, Hsu HC, Lee YT, Chen MF. Renal function and metabolic syndrome components on cardiovascular and all-cause mortality. Atherosclerosis. 2008;197(2):860–7. doi: 10.1016/j.atherosclerosis.2007.07.037. [DOI] [PubMed] [Google Scholar]
  • 9.Li Y, et al. Metabolic syndrome, but not insulin resistance, is associated with an increased risk of renal function decline. Clin Nutr. 2015;34(2):269–75. doi: 10.1016/j.clnu.2014.04.002. [DOI] [PubMed] [Google Scholar]
  • 10.Peralta CA, et al. Racial and ethnic differences in renal function decline among persons without chronic renal disease. J Am Soc Nephrol. 2011;22(7):1327–34. doi: 10.1681/ASN.2010090960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Evert J, Lawler E, Bogan H, Perls T. Morbidity profiles of centenarians: survivors, delayers, and escapers. J Gerontol A Biol Sci Med Sci. 2003;58(3):232–7. doi: 10.1093/gerona/58.3.M232. [DOI] [PubMed] [Google Scholar]
  • 12.Ismail K, et al. Compression of Morbidity Is Observed Across Cohorts with Exceptional Longevity. J Am Geriatr Soc. 2016;64(8):1583–91. doi: 10.1111/jgs.14222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Motta M, et al. Successful aging in centenarians: myths and reality. Arch Gerontol Geriatr. 2005;40(3):241–51. doi: 10.1016/j.archger.2004.09.002. [DOI] [PubMed] [Google Scholar]
  • 14.Jopp DS, Park MK, Lehrfeld J, Paggi ME. Physical, cognitive, social and mental health in near-centenarians and centenarians living in New York City: findings from the Fordham Centenarian Study. BMC Geriatr. 2016;16:1. doi: 10.1186/s12877-015-0167-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ford ES, Giles WH, Dietz WH. Prevalence of the metabolic syndrome among US adults: findings from the third National Health and Nutrition Examination Survey. JAMA. 2002;287(3):356–359. doi: 10.1001/jama.287.3.356. [DOI] [PubMed] [Google Scholar]
  • 16.Cheng HT, et al. Metabolic syndrome and insulin resistance as risk factors for development of chronic kidney disease and rapid decline in renal function in elderly. J Clin Endocrinol Metab. 2012;97(4):1268–76. doi: 10.1210/jc.2011-2658. [DOI] [PubMed] [Google Scholar]
  • 17.Tanaka H, Shiohira Y, Uezu Y, Higa A, Iseki K. Metabolic syndrome and chronic kidney disease in Okinawa, Japan. Kidney Int. 2006;69(2):369–374. doi: 10.1038/sj.ki.5000050. [DOI] [PubMed] [Google Scholar]
  • 18.O’Hare AM, et al. Age affects outcomes in chronic kidney disease. J Am Soc Nephrol. 2007;18(10):2758–2765. doi: 10.1681/ASN.2007040422. [DOI] [PubMed] [Google Scholar]
  • 19.Mozumdar A, Liguori G. Persistent Increase of Prevalence of Metabolic Syndrome Among USAdults: NHANES III to NHANES 1999–2006. Diabetes Care. 2011;34(1):216. doi: 10.2337/dc10-0879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.van Vliet-Ostaptchouk JV, et al. The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies. BMC Endocr Disord. 2014;14:9. doi: 10.1186/1472-6823-14-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Fu S, Ping P, Luo L, Ye P. Deep analyses of the associations of a series of biomarkers with insulin resistance, metabolic syndrome, and diabetes risk in nondiabetic middle-aged and elderly individuals: results from a Chinese community-based study. Clin Interv Aging. 2016;11:1531–1538. doi: 10.2147/CIA.S109583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Willcox DC, Willcox BJ, Poon LW. Centenarian studies: important contributors to our understanding of the aging process and longevity. Curr Gerontol Geriatr Res. 2010;2010:484529. doi: 10.1155/2010/484529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hostetter TH, Rennke HG, Brenner BM. The case for intrarenal hypertension in the initiation and progression of diabetic and other glomerulopathies. Am J Med. 1982;72(3):375–380. doi: 10.1016/0002-9343(82)90490-9. [DOI] [PubMed] [Google Scholar]
  • 24.Egan BM, Greene EL, Goodfriend TL. Insulin resistance and cardiovascular disease. Am J Hypertens. 2001;14(6 Pt 2):116S–125S. doi: 10.1016/S0895-7061(01)02078-7. [DOI] [PubMed] [Google Scholar]
  • 25.Liu X, Chen Y, Boucher NL, Rothberg AE. Prevalence and change of central obesity among US Asian adults: NHANES 2011–2014. BMC Public Health. 2017;17(1):678. doi: 10.1186/s12889-017-4689-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Sahakyan KR, et al. Normal-Weight Central Obesity: Implications for Total and Cardiovascular Mortality. Ann Intern Med. 2015;163(11):827–35. doi: 10.7326/M14-2525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Wang F, Ye P, Luo L, Xiao W, Wu H. Association of risk factors for cardiovascular disease and glomerular filtration rate: a community-based study of 4925 adults in Beijing. Nephrol Dial Transplant. 2010;25(12):3924–3931. doi: 10.1093/ndt/gfq327. [DOI] [PubMed] [Google Scholar]
  • 28.Kuo HW, Tsai SS, Tiao MM, Yang CY. Epidemiological features of CKD in Taiwan. Am J Kidney Dis. 2007;49(1):46–55. doi: 10.1053/j.ajkd.2006.10.007. [DOI] [PubMed] [Google Scholar]
  • 29.McCullough PA. Why is chronic kidney disease the “spoiler” for cardiovascular outcomes? J Am Coll Cardiol. 2003;41(5):725–8. doi: 10.1016/S0735-1097(02)02955-8. [DOI] [PubMed] [Google Scholar]
  • 30.Samuelsson, et al. Complex apolipoprotein B-containing lipoprotein particles are associated with a higher rate of progression of human chronic renal insufficiency. J Am Soc Nephrol. 1998;9(8):1482–8. doi: 10.1681/ASN.V981482. [DOI] [PubMed] [Google Scholar]
  • 31.Manninen V, et al. Joint effects of serum triglyceride and LDL cholesterol and HDL cholesterol concentrations on coronary heart disease risk in the Helsinki Heart Study. Implications for treatment. Circulation. 1992;85(1):37–45. doi: 10.1161/01.cir.85.1.37. [DOI] [PubMed] [Google Scholar]
  • 32.Khalil MAM, et al. Cigarette Smoking and Its Hazards in Kidney Transplantation. Adv Med. 2017;2017:6213814. doi: 10.1155/2017/6213814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Chen J, et al. The metabolic syndrome and chronic kidney disease in U.S. adults. Ann Intern Med. 2004;140(3):167–74. doi: 10.7326/0003-4819-140-3-200402030-00007. [DOI] [PubMed] [Google Scholar]
  • 34.He Y, et al. Cohort Profile: The China Hainan Centenarian Cohort Study (CHCCS). Int J Epidemiol. 10.1093/ije/dyy017 (2018 Feb 28). [DOI] [PubMed]
  • 35.Yang SH, Dou KF, Song WJ. Prevalence of diabetes among men and women in China. N Engl J Med. 2010;362(25):2425–2426. doi: 10.1056/NEJMc1004671. [DOI] [PubMed] [Google Scholar]
  • 36.Wang F, et al. Lipid-lowering therapy and lipid goal attainment in patients with metabolic syndrome in China:subgroup analysis of the Dyslipidemia International Study-China (DYSIS-China) Atherosclerosis. 2014;237(1):99–105. doi: 10.1016/j.atherosclerosis.2014.08.023. [DOI] [PubMed] [Google Scholar]
  • 37.Alberti, K. G., Zimmet, P. & Shaw, J. IDF Epidemiology Task Force Consensus Group. The metabolic syndrome: a new worldwide definition. Lancet.366(9491), 1059–1062 (2005). [DOI] [PubMed]
  • 38.Chen C, Lu FC. Department of Disease Control Ministry of Health. PR China. The guidelines for prevention and control of overweight and obesity in Chinese adults. Biomed Environ Sci. 2004;17(Suppl):1–36. [PubMed] [Google Scholar]
  • 39.Committee of Cardio-Cerebro-Vascular Diseases of Gerontological Society of China; Chinese College of Cardiovascular Physicians of Chinese Medical Doctor Association. Chinese expert consensus on the diagnosis and treatment of hypertension in the elderly. Zhonghua Nei Ke Za Zhi. 56(11), 885–893 (2017). [DOI] [PubMed]
  • 40.Tong YZ, et al. Consensus on the Prevention of Type 2 Diabetes in Chinese Adults. Chin Med J (Engl). 2017;130(5):600–606. doi: 10.4103/0366-6999.200532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Joint Committee for Developing Chinese guidelines on Prevention and Treatment of Dyslipidemia in Adults. Chinese guidelines on prevention and treatment of dyslipidemia in adults. Zhonghua Xin Xue Guan Bing Za Zhi. 35(5), 390–419 (2007). [PubMed]
  • 42.Ma YC, Zuo L, Chen JH. Modified Glomerular Filtration Rate Estimating Equation for Chinese Patients with Chronic Kidney Disease. J Am Soc Nephrol. 2006;17(10):2937–2944. doi: 10.1681/ASN.2006040368. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

In attempt to preserve privacy of patients, clinical data of patients will not be shared; data can be available from authors upon request.


Articles from Scientific Reports are provided here courtesy of Nature Publishing Group

RESOURCES