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Short Communication: Coronary Heart Disease Risk by Framingham Risk Score in Hepatitis C and HIV/Hepatitis C-Coinfected Persons

机译:简短交流:丙型肝炎和艾滋病毒/丙型肝炎合并感染者的弗雷明汉风险评分得出的冠心病风险

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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 (beta = -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.
机译:我们比较了年龄和种族匹配的丙型肝炎病毒(HCV)感染者和未感染HCV的人的10年冠心病(CHD)风险的弗雷明汉风险评分(FRS):114,073 HCV感染(111,436 HCV单感染)和2,637例HIV / HCV感染者和122,996例HCV感染者(121,380例HIV和HCV感染者以及1,616例HIV单感染者),没有心血管疾病,糖尿病或乙型肝炎。未经调整的分析表明,在HCV感染者和未感染者之间,FRS相似HCV未感染组[中位(四分位间距,IQR)危险点分别为13(10-14)和13(10-14),p = 0.192]。与未感染组相比,HCV组(HCV和HIV / HCV)的胆固醇水平较低,当前吸烟更为普遍(两个组的p <0.001)。队列中非FRS CHD危险因素(例如药物滥用和慢性肾脏疾病)的患病率很高,并且HCV和HIV状况有所不同。调整年龄,种族/民族,体重指数,慢性肾脏病,吸毒和酗酒以及艾滋病毒感染状况后,HCV感染与最低的FRS降低相关(β= -0.095风险点,p <0.001),表明该值很小,但在通过FRS测量风险时,与未感染HCV的人群相比,HCV感染者的10年CHD风险估计值有显着差异。考虑到HCV,HIV和CHD危险因素之间的复杂关系,其中一些未被FRS捕获,FRS可能会低估HCV单感染和HIV / HCV合并感染者的CHD风险。可能需要HCV和HIV / HCV特定的风险评分来优化CHD风险分层。

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