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Lipoprotein-associated phospholipase A(2) mass and activity and risk of cardiovascular disease in a population with high prevalences of obesity and diabetes: the Strong Heart Study.

AbstractOBJECTIVE:
To investigate the association of lipoprotein-associated phospholipase A(2) (LpPLA(2)) mass and activity with incident cardiovascular disease (CVD) in a population with high prevalences of insulin resistance and diabetes, conditions for which epidemiological data remain sparse.
RESEARCH DESIGN AND METHODS:
We conducted a nested, case-control study (n = 1,008) within a population-based cohort of American Indians. Case subjects were defined by incidence of first-ever CVD up to 10 years later. Control subjects comprised participants free of CVD events during the follow-up period who were frequency matched to case subjects by age, sex, and diabetes status. LpPLA(2) mass and activity were measured using commercially available assays.
RESULTS:
LpPLA(2) mass and activity were moderately correlated with each other (r = 0.30), but only LpPLA(2) activity exhibited moderate correlations with lipid fractions. After extensive adjustment for covariates, both LpPLA(2) measures were significantly associated with incident CVD, but the relationship was inverse for LpPLA(2) mass (highest versus lowest tertile, relative risk [RR] 0.55 [95% CI 0.39-0.79]) and positive for LpPLA(2) activity (highest versus lowest tertile, 1.65 [1.12-2.42]). These associations were similar when participants with and without diabetes were examined separately.
CONCLUSIONS:
In this population-based cohort enriched with dysmetabolic phenotypes, LpPLA(2) mass and activity showed divergent associations with CVD. The inverse relationship for LpPLA(2) mass is contrary to observations from predominantly nondiabetic populations and will require independent replication. Whether this finding relates to redistribution of LpPLA(2) to lipoprotein classes where it is less atherogenic or reflects incomplete measurement of LpPLA(2) mass associated with altered lipoprotein composition in insulin resistance warrants further investigation.
AuthorsJorge R Kizer, Jason G Umans, Jianhui Zhu, Richard B Devereux, Robert L Wolfert, Elisa T Lee, Barbara V Howard
JournalDiabetes care (Diabetes Care) Vol. 35 Issue 4 Pg. 840-7 (Apr 2012) ISSN: 1935-5548 [Electronic] United States
PMID22338104 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
Topics
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase (blood, chemistry, metabolism, physiology)
  • Aged
  • Cardiovascular Diseases (epidemiology, ethnology, etiology, metabolism)
  • Case-Control Studies
  • Cohort Studies
  • Diabetes Complications (epidemiology, ethnology, metabolism)
  • Enzyme Activation
  • Female
  • Humans
  • Indians, North American (statistics & numerical data)
  • Male
  • Middle Aged
  • Molecular Weight
  • Obesity (complications, epidemiology, ethnology, metabolism)
  • Population
  • Prevalence
  • Risk Factors

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