Lipoprotein-Associated Phospholipase A2 Is Associated with Atherosclerotic Stroke Risk: The Northern Manhattan Study

被引:49
作者
Katan, Mira [1 ,2 ]
Moon, Yeseon P. [1 ]
Paik, Myunghee C. [3 ]
Wolfert, Robert L. [4 ]
Sacco, Ralph L. [5 ,6 ,7 ]
Elkind, Mitchell S. V. [1 ,8 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[2] Univ Zurich Hosp, Dept Neurol, Zurich, Switzerland
[3] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY USA
[4] diaDexus Inc, San Francisco, CA USA
[5] Univ Miami, Miller Sch Med, Dept Neurol, Miami, FL 33136 USA
[6] Univ Miami, Miller Sch Med, Dept Epidemiol, Miami, FL 33136 USA
[7] Univ Miami, Miller Sch Med, Dept Human Genet, Miami, FL 33136 USA
[8] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
基金
美国国家卫生研究院; 瑞士国家科学基金会;
关键词
C-REACTIVE PROTEIN; ISCHEMIC-STROKE; CEREBRAL INFARCTION; RECURRENT STROKE; A(2) ACTIVITY; DISEASE; RACE; COHORT; SEX; ETHNICITY;
D O I
10.1371/journal.pone.0083393
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Lipoprotein-associated phospholipase A2 (LpPLA2) levels are associated with stroke, though whether this extends to all populations and stroke subtypes is unknown. Methods: Serum samples from stroke-free community participants in the Northern Manhattan Study were assayed for LpPLA2 mass and activity. Participants were followed annually for stroke. Cox-proportional-hazard models were fitted to estimate hazard-ratios and 95% confidence intervals (HR, 95% CI) for the association of LpPLA2 levels with ischemic stroke (IS), after adjusting for demographic and medical risk factors. Results: Serum samples were available in 1946 participants, of whom 151 (7.8%) experienced a first IS during median followup 11 years. Mean age was 69 (SD 10), 35.6% were men, 20% non-Hispanic Whites, 22% non-Hispanic Blacks, and 55% Hispanics. LpPLA2 mass and activity levels were not associated with overall IS risk. LpPLA2 mass but not activity levels were associated with strokes due to large artery atherosclerosis (LAA; adjusted HR per SD 1.55, 95% CI 1.17-2.04). There was a dose-response relationship with LAA (compared to first quartile, 2nd quartile HR = 1.43, 95% CI 0.23-8.64; 3rd quartile HR = 4.47, 95% CI 0.93-21.54; 4th quartile HR = 5.07, 95% CI 1.07-24.06). The associations between LpPLA2-mass and LAA-stroke risk differed by race-ethnicity (p = 0.01); LpPLA2-mass was associated with increased risk of LAA among non-Hispanic Whites (adjusted HR per SD 1.44, 95% CI 0.98-2.11), but not other race-ethnic groups. Conclusion: LpPLA2-mass levels were associated with risk of atherosclerotic stroke among non-Hispanic White participants, but not in other race-ethnic groups in the cohort. Further study is needed to confirm these race-ethnic differences and the reasons for them.
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页数:6
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