Association of high-density lipoprotein cholesterol with all-cause and cause-specific mortality in the general population: insights from NHANES 1999-2018

被引:0
作者
Li, Shan [1 ,3 ]
Fu, Zhiqing [1 ,3 ]
Zhang, Wei [2 ,3 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Gastroenterol, Med Ctr 2, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 2, Dept Outpatient, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Natl Clin Res Ctr Geriatr Dis, Beijing 100853, Peoples R China
关键词
High-density lipoprotein cholesterol; All-cause mortality; Cardiovascular mortality; Non-cardiovascular mortality; Lipid; HDL-CHOLESTEROL; CONSENSUS STATEMENT; CARDIOVASCULAR RISK; HEART-DISEASE; ATHEROSCLEROSIS; INDIVIDUALS; NIACIN; WOMEN;
D O I
10.1186/s12889-025-22251-z
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
BackgroundPrevious studies have shown that extremely high levels of high-density lipoprotein (HDL) cholesterol are paradoxically associated with adverse outcomes in certain clinical settings. We aimed to test the hypothesis that extremely high levels of HDL cholesterol are associated with increased all-cause and cause-specific mortality in the general population.MethodsWe included 51,235 individuals from the National Health and Nutrition Examination Survey (NHANES) 1999 to 2018 with a median follow-up of 9.3 years. Baseline HDL cholesterol levels were measured, and mortality data were ascertained from National Death Index (NDI) records through December 31, 2019. Weighted Cox proportional hazards regression, restricted cubic spline curves, and cumulative incidence analyses were performed.ResultsA U-shaped association was observed between HDL cholesterol levels and all-cause, cardiovascular and non-cardiovascular mortality in the general population. Compared with individuals with HDL cholesterol levels between 50 and 59 mg/dL, the adjusted hazard ratios (95% CIs) for those with extremely high HDL cholesterol levels (>= 80 mg/dL) were 1.24 (1.08-1.43), 1.18 (1.03-1.36) and 1.27 (1.09-1.49) for all-cause, cardiovascular and non-cardiovascular mortality, respectively. Similar U-shaped patterns were replicated in both men and women. Further analyses of cause-specific mortality subcategories showed that extremely high HDL cholesterol levels were also associated with increased mortality from heart disease, respiratory disease, endocrine disease, and cancer.ConclusionExtremely high levels of HDL cholesterol were associated with an increased risk of all-cause, cardiovascular, and non-cardiovascular mortality in the general population. Future studies should investigate the causal factors leading to the association of elevated HDL cholesterol and mortality.
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页数:13
相关论文
共 40 条
[1]   Elevated HDL cholesterol is a risk factor for ischemic heart disease in white women when caused by a common mutation in the cholesteryl ester transfer protein gene [J].
Agerholm-Larsen, B ;
Nordestgaard, BG ;
Steffensen, R ;
Jensen, G ;
Tybjærg-Hansen, A .
CIRCULATION, 2000, 101 (16) :1907-1912
[2]  
Arnett DK, 2019, J AM COLL CARDIOL, V74, pE177, DOI 10.1016/j.jacc.2019.03.010
[3]   Niacin in Patients with Low HDL Cholesterol Levels Receiving Intensive Statin Therapy [J].
Boden, William E. ;
Probstfield, Jeffrey L. ;
Anderson, Todd ;
Chaitman, Bernard R. ;
Desvignes-Nickens, Patrice ;
Koprowicz, Kent ;
McBride, Ruth ;
Teo, Koon ;
Weintraub, William .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (24) :2255-2267
[4]   High Density Lipoprotein Cholesterol and the Risk of All-Cause Mortality among US Veterans [J].
Bowe, Benjamin ;
Xie, Yan ;
Xian, Hong ;
Balasubramanian, Sumitra ;
Zayed, Mohamed A. ;
Al-Aly, Ziyad .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2016, 11 (10) :1784-1793
[5]   Low levels of high-density lipoprotein cholesterol increase the risk of incident kidney disease and its progression [J].
Bowe, Benjamin ;
Xie, Yan ;
Xian, Hong ;
Balasubramanian, Sumitra ;
Al-Aly, Ziyad .
KIDNEY INTERNATIONAL, 2016, 89 (04) :886-896
[6]   Instrumental Variable Analysis with a Nonlinear Exposure-Outcome Relationship [J].
Burgess, Stephen ;
Davies, Neil M. ;
Thompson, Simon G. .
EPIDEMIOLOGY, 2014, 25 (06) :877-885
[7]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[8]  
Di Angelantonio E, 2009, JAMA-J AM MED ASSOC, V302, P1993, DOI 10.1001/jama.2009.1619
[9]   The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical manifestations in a Large Kindred [J].
Fountoulakis, Nikolaos ;
Lioudaki, Eirini ;
Lygerou, Dimitra ;
Dermitzaki, Eleftheria-Kleio ;
Papakitsou, Ioanna ;
Kounali, Vasiliki ;
Holleboom, Adriaan G. ;
Stratigis, Spyros ;
Belogianni, Christina ;
Syngelaki, Paraskevi ;
Stratakis, Stavros ;
Evangeliou, Athanasios ;
Gakiopoulou, Hariklia ;
Kuivenhoven, Jan Albert ;
Wevers, Ron ;
Dafnis, Eugene ;
Stylianou, Kostas .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2019, 74 (04) :510-522
[10]   2013 ACC/AHA Guideline on the Assessment of Cardiovascular Risk A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines [J].
Goff, David C., Jr. ;
Lloyd-Jones, Donald M. ;
Bennett, Glen ;
Coady, Sean ;
D'Agostino, Ralph B., Sr. ;
Gibbons, Raymond ;
Greenland, Philip ;
Lackland, Daniel T. ;
Levy, Daniel ;
O'Donnell, Christopher J. ;
Robinson, Jennifer G. ;
Schwartz, J. Sanford ;
Shero, Susan T. ;
Smith, Sidney C., Jr. ;
Sorlie, Paul ;
Stone, Neil J. ;
Wilson, Peter W. F. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2014, 63 (25) :2935-2959