Chew Kara W, Bhattacharya Debika, McGinnis Kathleen A, Horwich Tamara B, Tseng Chi-Hong, Currier Judith S, Butt Adeel A
1 David Geffen School of Medicine at UCLA , Los Angeles, California.
2 VA Pittsburgh Healthcare System , Pittsburgh, Pennsylvania.
AIDS Res Hum Retroviruses. 2015 Jul;31(7):718-22. doi: 10.1089/AID.2014.0284. Epub 2015 May 11.
We compared the Framingham risk score (FRS) for 10-year coronary heart disease (CHD) risk in age- and race-matched hepatitis C virus (HCV)-infected and HCV-uninfected persons: 114,073 HCV-infected (111,436 HCV-monoinfected and 2,637 HIV/HCV-coinfected) and 122,996 HCV-uninfected (121,380 HIV and HCV-uninfected and 1,616 HIV-monoinfected) males without cardiovascular disease, diabetes, or hepatitis B. In unadjusted analyses, FRS was similar between the HCV-infected and HCV-uninfected groups [median (interquartile range, IQR) risk points 13 (10-14) vs. 13 (10-14), p=0.192]. Cholesterol levels were lower and current smoking more prevalent in the HCV groups (both HCV and HIV/HCV) compared with the uninfected groups (p<0.001 for both). Prevalence of non-FRS CHD risk factors, such as substance abuse and chronic kidney disease, in the cohort was high, and differed by HCV and HIV status. Adjusting for age, race/ethnicity, body mass index, chronic kidney disease, drug and alcohol use, and HIV status, HCV infection was associated with minimally lower FRS (β=-0.095 risk points, p<0.001), suggesting a small but significant difference in 10-year CHD risk estimation in HCV-infected as compared to HCV-uninfected persons when measuring risk by FRS. Given the complex relationship between HCV, HIV, and CHD risk factors, some of which are not captured by the FRS, the FRS may underestimate CHD risk in HCV-monoinfected and HIV/HCV-coinfected persons. HCV- and HIV/HCV-specific risk scores may be needed to optimize CHD risk stratification.
我们比较了年龄和种族匹配的丙型肝炎病毒(HCV)感染和未感染人群中10年冠心病(CHD)风险的弗雷明汉风险评分(FRS):114,073例HCV感染患者(111,436例HCV单感染和2,637例HIV/HCV合并感染)以及122,996例未感染HCV的男性(121,380例未感染HIV和HCV以及1,616例HIV单感染),这些男性均无心血管疾病、糖尿病或乙型肝炎。在未调整分析中,HCV感染组和未感染组的FRS相似[中位数(四分位间距,IQR)风险评分13(10 - 14)对13(10 - 14),p = 0.192]。与未感染组相比,HCV组(包括HCV单感染和HIV/HCV合并感染)的胆固醇水平较低,当前吸烟更为普遍(两者p均<0.001)。队列中非FRS冠心病风险因素(如药物滥用和慢性肾病)的患病率较高,且因HCV和HIV感染状态而异。在调整年龄、种族/民族、体重指数、慢性肾病、药物和酒精使用以及HIV感染状态后,HCV感染与略低的FRS相关(β = -0.095风险评分,p <0.001),这表明在通过FRS测量风险时,与未感染HCV的人相比,感染HCV的人在10年冠心病风险估计上存在微小但显著的差异。鉴于HCV、HIV和冠心病风险因素之间的复杂关系,其中一些未被FRS所涵盖,FRS可能低估了HCV单感染和HIV/HCV合并感染人群的冠心病风险。可能需要特定于HCV和HIV/HCV的风险评分来优化冠心病风险分层。