Circulating levels of liver enzymes and incidence of atrial fibrillation: the Atherosclerosis Risk in Communities cohort.
Circulating levels of liver enzymes and incidence of atrial fibrillation: the Atherosclerosis Risk in Communities cohort.
复制标题
DOI:
10.1136/heartjnl-2014-305756
复制
发表时间:
2014-10
期刊:
影响因子:
--
通讯作者:
Selvin E
中科院分区:
文献类型:
--
作者:
Alonso A;Misialek JR;Amiin MA;Hoogeveen RC;Chen LY;Agarwal SK;Loehr LR;Soliman EZ;Selvin E
Elevated levels of circulating liver enzymes have been associated with increased risk of cardiovascular disease. Their possible association with atrial fibrillation (AF) has received little attention. We studied 9333 men and women, age 53–75, free of AF participating in the Atherosclerosis Risk in Communities Study followed up from 1996 to 2010. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma glutamyl transpeptidase (GGT) were measured in stored plasma samples. Incident AF was ascertained from hospitalizations and death certificates. Associations between liver enzymes and AF incidence were assessed using multivariable Cox proportional hazards models. During a mean follow-up of 12 years, 1021 incident AF events were identified. Levels of AST, and to a lesser extent of ALT, showed a U-shaped association with AF risk, with higher AF risk among individuals in the two extremes of the distribution in minimally adjusted models. The associations were weakened after adjustment for potential confounders. In contrast, GGT, modeled as log base 2, was linearly associated with AF risk after multivariable adjustment: a doubling of GGT levels was associated with a 20% increased risk of AF (95% confidence interval, 10–30%). Additional adjustment for inflammatory markers did not appreciably affect the results. Associations were not different in men and women, in whites and blacks, among never drinkers of alcohol, and among those without prevalent heart failure. In this community-based prospective study, higher levels of liver enzymes, mainly GGT, were associated with an increased risk of AF. The mechanisms underlying this association deserve further scrutiny.
登录
查看更多内容
影响因子:
37.8
作者:
Huxley RR;Lopez FL;Folsom AR;Agarwal SK;Loehr LR;Soliman EZ;Maclehose R;Konety S;Alonso A
通讯作者:
Alonso A
影响因子:
3.7
作者:
Seymour, Christopher W.;Cooke, Colin R.;Pepe, Margaret S.
通讯作者:
Pepe, Margaret S.
影响因子:
37.8
作者:
Magnani, Jared W.;Rienstra, Michiel;Benjamin, Emelia J.
通讯作者:
Benjamin, Emelia J.
影响因子:
8.3
作者:
Soliman EZ;Prineas RJ;Case LD;Zhang ZM;Goff DC Jr
通讯作者:
Goff DC Jr
影响因子:
5.4
作者:
Alonso A;Krijthe BP;Aspelund T;Stepas KA;Pencina MJ;Moser CB;Sinner MF;Sotoodehnia N;Fontes JD;Janssens AC;Kronmal RA;Magnani JW;Witteman JC;Chamberlain AM;Lubitz SA;Schnabel RB;Agarwal SK;McManus DD;Ellinor PT;Larson MG;Burke GL;Launer LJ;Hofman A;Levy D;Gottdiener JS;Kääb S;Couper D;Harris TB;Soliman EZ;Stricker BH;Gudnason V;Heckbert SR;Benjamin EJ
通讯作者:
Benjamin EJ