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Cystatin C and Sudden Cardiac Death Risk in the Elderly

医学 胱抑素C 内科学 肾功能 置信区间 危险系数 心源性猝死 肌酐 入射(几何) 比例危险模型 心脏病学 多元分析 心力衰竭 光学 物理
作者
Rajat Deo,Nona Sotoodehnia,Ronit Katz,Mark J. Sarnak,Linda F. Fried,Michel Chonchol,Bryan Kestenbaum,Bruce M. Psaty,David S. Siscovick,Michael G. Shlipak
出处
期刊:Circulation-cardiovascular Quality and Outcomes [Ovid Technologies (Wolters Kluwer)]
卷期号:3 (2): 159-164 被引量:81
标识
DOI:10.1161/circoutcomes.109.875369
摘要

Recent studies have demonstrated an association between moderate kidney dysfunction and sudden cardiac death in people with cardiovascular disease.The study was a longitudinal analysis among 4465 participants from the Cardiovascular Health Study without prevalent cardiovascular disease at baseline. Cystatin C and creatinine were measured from baseline sera. Sudden cardiac death (SCD) was defined as a sudden pulseless condition from a cardiac origin in a previously stable individual that occurred out of the hospital or in the emergency room. The association between cystatin C tertiles and SCD was determined with multivariate Cox proportional hazards. A similar analysis compared SCD incidence across creatinine-based estimated glomerular filtration rate (eGFR) tertiles. Over a median follow-up of 11.2 years, 91 adjudicated SCD events occurred. The annual incidence of SCD events increased across cystatin C tertiles: 10 events per 10 000 person years in tertile 1, 25 events per 10 000 person years in tertile 2, and 32 events per 10 000 person-years in the highest cystatin C tertile. These associations persisted after multivariate adjustment: hazards ratio=2.72; 95% confidence interval, 1.44 to 5.16 in tertile 2 and hazards ratio=2.67; 95% confidence interval, 1.33 to 5.35 in tertile 3. After multivariate adjustment, the rate of SCD also increased in a linear distribution across creatinine-based eGFR tertiles: 15 events per 10 000 person-years in tertile 1, 22 events per 10 000 person-years in tertile 2, and 27 events per 10 000 person-years in tertile 3. No significant associations, however, remained between creatinine-based eGFR and SCD after multivariable adjustment.Impaired kidney function, as measured by cystatin C, has an independent association with SCD risk among elderly persons without clinical cardiovascular disease.
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