Lipoprotein insulin resistance score and risk of incident diabetes during extended follow-up of 20 years: The Women's Health Study

被引:40
|
作者
Harada, Paulo H. N. [1 ,2 ,3 ,4 ]
Demler, Olga V. [1 ,2 ]
Dugani, Sagar B. [1 ,2 ,5 ]
Akinkuolie, Akintunde O. [1 ,2 ]
Moorthy, Manickavasagar V. [2 ]
Ridker, Paul M. [2 ,3 ]
Cook, Nancy R. [2 ,6 ]
Pradhan, Aruna D. [2 ,7 ]
Mora, Samia [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Ctr Lipid Metabol, Div Prevent Med, Boston, MA USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA USA
[4] Univ Sao Paulo, Hosp Univ, Ctr Clin & Epidemiol Res, Sao Paulo, SP, Brazil
[5] Univ Toronto, St Michaels Hosp, Div Internal Med, Toronto, ON, Canada
[6] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[7] Vet Affairs Boston Healthcare Syst, Boston, MA USA
关键词
Metabolomics; Lipoprotein; Insulin resistance; Type II diabetes; Risk prediction; Prevention; NUCLEAR-MAGNETIC-RESONANCE; LOW-DOSE ASPIRIN; VLDL-TRIGLYCERIDE; RANDOMIZED-TRIAL; PARTICLE-SIZE; B PRODUCTION; ABNORMALITIES; INDIVIDUALS; PREVENTION; PREDICTION;
D O I
10.1016/j.jacl.2017.06.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Type II diabetes (T2D) is preceded by prolonged insulin resistance and relative insulin deficiency incompletely captured by glucose metabolism parameters, high-density lipoprotein (HDL) cholesterol and triglycerides. OBJECTIVE: Whether lipoprotein insulin resistance (LPIR) score, a metabolomic marker, is associated with incident diabetes and improves risk reclassification over traditional markers on extended follow-up. METHODS: Among 25,925 nondiabetic women aged 45 years or older, LPIR was measured by nuclear magnetic resonance spectroscopy as a weighted score of very low density lipoprotein, low-density lipoprotein, and HDL particle sizes, and their subsets concentrations. We run adjusted cox regression models for LPIR with incident T2D (20.4 years median follow-up). RESULTS: Adjusting for demographics, body mass index, life style factors, blood pressure, and T2D family history, the LPIR hazard ratio for T2D (hazard ratio ERR] per standard deviation, 95% confidence interval) was 1.95 (1.85, 2.06). Further adjusting for HbAlc, C-reactive protein, triglycerides, HDL and low-density lipoprotein cholesterol, LPIR HR was attenuated to 1.41 (1.31, 1.53) and had the strongest association with T2D after HbA1C in mutually adjusted models. The association persisted even in those with optimal clinical profiles, adjusted HR per standard deviation 1.91 (1.17, 3.13). In participants deemed at intermediate T2D risk by the Framingham Offspring T2D score, LPIR led to a net reclassification of 0.145 (0.117, 0.175). CONCLUSION: In middle-aged or older healthy women followed prospectively for over 20 years, LPIR was robustly associated with incident T2D, including among those with an optimal clinical metabolic profile. LPIR improved T2D risk classification and may guide early and targeted prevention strategies. (c) 2017 National Lipid Association. Published by Elsevier Inc.
引用
收藏
页码:1257 / 1267
页数:11
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