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LURIC

Publikation · PMID 19480687

Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populations

Karakas M, Hoffmann MM, Vollmert C, Rothenbacher D, Meisinger C, Winkelmann B, Khuseyinova N, Böhm BO et al.

FcgammaRIIa-R/H131 polymorphisms were genotyped in two independent populations – the MONICA-Augsburg survey (527 myocardial infarction cases, 527 controls) and the LURIC cohort (2,227 CHD patients vs. 1,032 individuals with stenosis <50%) – to test for an association with coronary heart disease risk. After multivariable adjustment, FcgammaRIIa genotype was not independently associated with CHD in either population (LURIC OR 0.96, 95% CI 0.81-1.14), indicating that this receptor variant does not meaningfully influence CHD susceptibility.

BMC Medical Genetics, 29. Mai 2009 | PMID 19480687

Zeitschrift
BMC Medical Genetics
DOI
10.1186/1471-2350-10-46
PMID
19480687
Quelle
https://pubmed.ncbi.nlm.nih.gov/19480687/
Zitationen
17 Relative Zitationsrate 0.42 (1,0 = Durchschnitt des Fachgebiets) · NIH iCite, Stand 23.08.2026