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HDL Particle Subspecies and Their Association With Incident Type 2 Diabetes: The PREVEND Study

ContextHigh-density lipoproteins (HDL) may be protective against type 2 diabetes (T2D) development, but HDL particles vary in size and function, which could lead to differential associations with incident T2D. A newly developed nuclear magnetic resonance (NMR)-derived algorithm provides concentratio...

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Published in:The journal of clinical endocrinology and metabolism 2021-06, Vol.106 (6), p.1761-1772
Main Authors: Sokooti, Sara, Flores-Guerrero, Jose L, Kieneker, Lyanne M, Heerspink, Hiddo J L, Connelly, Margery A, Bakker, Stephan J L, Dullaart, Robin P F
Format: Article
Language:English
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Summary:ContextHigh-density lipoproteins (HDL) may be protective against type 2 diabetes (T2D) development, but HDL particles vary in size and function, which could lead to differential associations with incident T2D. A newly developed nuclear magnetic resonance (NMR)-derived algorithm provides concentrations for 7 HDL subspecies. ObjectiveWe aimed to investigate the association of HDL particle subspecies with incident T2D in the general population. MethodsAmong 4828 subjects of the Prevention of Renal and Vascular End-Stage Disease (PREVEND) study without T2D at baseline, HDL subspecies with increasing size from H1P to H7P were measured by NMR (LP4 algorithm of the Vantera NMR platform). ResultsA total of 265 individuals developed T2D (median follow-up of 7.3 years). In Cox regression models, HDL size and H4P (hazard ratio [HR] per 1 SD increase 0.83 [95% CI, 0.69-0.99] and 0.85 [95% CI, 0.75-0.95], respectively) were inversely associated with incident T2D, after adjustment for relevant covariates. In contrast, levels of H2P were positively associated with incident T2D (HR 1.15 [95% CI, 1.01-1.32]). In secondary analyses, associations with large HDL particles and H6P were modified by body mass index (BMI) in such a way that they were particularly associated with a lower risk of incident T2D, in subjects with BMI 
ISSN:0021-972X
1945-7197
DOI:10.1210/clinem/dgab075