Impact of hepatitis C virus clearance by direct-acting antiviral treatment on the incidence of major cardiovascular events: A prospective multicentre study

被引:83
作者
Adinolfi, Luigi Elio [1 ]
Petta, Salvatore [2 ]
Fracanzani, Anna Ludovica [3 ]
Coppola, Carmine [4 ]
Narciso, Vincenzo [5 ]
Nevola, Riccardo [1 ]
Rinaldi, Luca [1 ]
Calvaruso, Vincenza [2 ]
Staiano, Laura [4 ]
Di Marco, Vito [2 ]
Marrone, Aldo [1 ]
Pafundi, Pia Clara [1 ]
Solano, Antonio [5 ]
Lombardi, Rosa [3 ]
Sasso, Ferdinando Carlo [1 ]
Saturnino, Mariarosaria [4 ]
Rini, Francesca [2 ]
Guerrera, Barbara [1 ]
Troina, Graziano [2 ]
Giordano, Mauro [1 ]
Craxi, Antonio [2 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Adv Med & Surg Sci, Piazza Miraglia, I-80100 Naples, Italy
[2] Univ Palermo, Div Gastroenterol & Hepatol, PROMISE, Palermo, Italy
[3] Univ Milan, Fdn Ca Granda IRCCS Osped Maggiore Policlin, Dept Pathophysiol & Transplantat, Milan, Italy
[4] ASL Napoli 3 Sud, Unit Internal Med & Hepatol, Gragnano Hosp, Naples, Italy
[5] Pellegrini Hosp, Unit Hepatol, ASL Napoli 1 Ctr, Naples, Italy
关键词
Ischemic heart disease; Ischemic cerebral stroke; Chronic hepatitis C; Cirrhosis; SUSTAINED VIROLOGICAL RESPONSE; LIVER-RELATED MORTALITY; CORONARY-HEART-DISEASE; CHRONIC HCV INFECTION; ALL-CAUSE; RISK; STATEMENT; THERAPY; STROKE;
D O I
10.1016/j.atherosclerosis.2020.01.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: HCV is associated with an increased risk of cardiovascular events (CV). Whether HCV clearance by direct-acting antivirals (DAA) reduces incident CV disease is poorly understood. We investigate whether HCV eradication reduces CV events. Methods: In a prospective multicentre study, 2204 HCV patients (F0-F2:29.5%, F3-F4: 70.5%) were enrolled. Males were 48%, median age was 68 (59-74) years and BMI 25.9 (23.1-28); 24.7% were smokers, 18% had diabetes, 13.2% had cholesterol levels > 200 mg/dl and 9.1% took statins, 44% had hypertension. During an overall median follow-up of 28 (24-39) months, incident CV events, such as ischemic heart disease (IHD) and ischemic cerebral stroke (ICS), were recorded. An overall of 2204 patients were evaluated as control group and 1668 patients after HCV elimination were followed as a case group. Factors associated with CV events were evaluated by uni- and multi-variate analyses. Results: Incident CV rates per 100 patient years in pre-treatment and untreated controls and treated cases were 1.12, 1.14 and 0.44 (p = 0.0001 vs. controls), respectively, and a decreased of relative risk (RR = 0.379; p = 0.0002) was observed. CV risk was 2.0-3.5 times lower then in controls (HR 3.671; 95%C.I.:1.871-7.201; p < 0.001). The calculated number of patients to be treated to get a benefit in a patient was 55.26. The annual incidence reduction of CV events was 0.68%. HCV clearance was independently associated with CV events reduction (OR, 4.716; 95% C.I.:1.832-12.138; p = 0.001). Conclusions: HCV clearance by DAA reduces CV events (IHD and ICS) with both clinical and socio-economic benefits.
引用
收藏
页码:40 / 47
页数:8
相关论文
共 36 条
[11]   All-Cause, Liver-Related, and Non-Liver-Related Mortality Among HCV-Infected Individuals in the General US Population [J].
El-Kamary, Samer S. ;
Jhaveri, Ravi ;
Shardell, Michelle D. .
CLINICAL INFECTIOUS DISEASES, 2011, 53 (02) :150-157
[12]   EASL Recommendations on Treatment of Hepatitis C 2018 [J].
Pawlotsky J.-M. ;
Negro F. ;
Aghemo A. ;
Berenguer M. ;
Dalgard O. ;
Dusheiko G. ;
Marra F. ;
Puoti M. ;
Wedemeyer H. .
JOURNAL OF HEPATOLOGY, 2018, 69 (02) :461-511
[13]   Beneficial Effects of Vaccination on Cardiovascular Events: Myocardial Infarction, Stroke, Heart Failure [J].
Fountoulaki, Katerina ;
Tsiodras, Sotirios ;
Polyzogopoulou, Eftychia ;
Olympios, Christophoros ;
Parissis, John .
CARDIOLOGY, 2018, 141 (02) :98-106
[14]   Prospective study of guideline-tailored therapy with direct-acting antivirals for hepatitis C virus-associated mixed cryoglobulinemia [J].
Gragnani, Laura ;
Visentini, Marcella ;
Fognani, Elisa ;
Urraro, Teresa ;
De Santis, Adriano ;
Petraccia, Luisa ;
Perez, Marie ;
Ceccotti, Giorgia ;
Colantuono, Stefania ;
Mitrevski, Milica ;
Stasi, Cristina ;
Del Padre, Martina ;
Monti, Monica ;
Gianni, Elena ;
Pulsoni, Alessandro ;
Fiorilli, Massimo ;
Casato, Milvia ;
Zignego, Anna Linda .
HEPATOLOGY, 2016, 64 (05) :1473-1482
[15]   Increased all-cause, liver, and cardiac mortality among hepatitis C virus-seropositive blood donors [J].
Guiltinan, Anne M. ;
Kaidarova, Zhanna ;
Custer, Brian ;
Orland, Jennie ;
Strollo, Angela ;
Cyrus, Sherri ;
Busch, Michael P. ;
Murphy, Edward L. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2008, 167 (06) :743-750
[16]   Interferon-based therapy reduces risk of stroke in chronic hepatitis C patients: a population-based cohort study in Taiwan [J].
Hsu, C-S ;
Kao, J-H ;
Chao, Y-C ;
Lin, H. H. ;
Fan, Y-C ;
Huang, C-J ;
Tsai, P-S .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2013, 38 (04) :415-423
[17]   Antiviral Treatment for Hepatitis C Virus Infection Is Associated With Improved Renal and Cardiovascular Outcomes in Diabetic Patients [J].
Hsu, Yao-Chun ;
Lin, Jaw-Town ;
Ho, Hsiu J. ;
Kao, Yu-Hsi ;
Huang, Yen-Tsung ;
Hsiao, Nai-Wan ;
Wu, Ming-Shiang ;
Liu, Yi-Ya ;
Wu, Chun-Ying .
HEPATOLOGY, 2014, 59 (04) :1293-1302
[18]   Is Hepatitis C Associated with Atherosclerotic Burden? A Systematic Review and Meta-Analysis [J].
Huang, He ;
Kang, Rongyan ;
Zhao, Zhendong .
PLOS ONE, 2014, 9 (09)
[19]   Hepatitis C Virus Infection and Risk of Stroke: A Systematic Review and Meta-Analysis [J].
Huang, He ;
Kang, Rongyan ;
Zhao, Zhendong .
PLOS ONE, 2013, 8 (11)
[20]   Global burden of atherosclerotic cardiovascular disease in people with hepatitis C virus infection: a systematic review, meta-analysis, and modelling study [J].
Lee, Kuan Ken ;
Stelzle, Dominik ;
Bing, Rong ;
Anwar, Mohamed ;
Strachan, Fiona ;
Bashir, Sophia ;
Newby, David E. ;
Shah, Jasmit S. ;
Chung, Michael H. ;
Bloomfield, Gerald S. ;
Longenecker, Chris T. ;
Bagchi, Shashwatee ;
Kottilil, Shyamasundaran ;
Blach, Sarah ;
Razavi, Homie ;
Mills, Peter R. ;
Mills, Nicholas L. ;
McAllister, David A. ;
Shah, Anoop S., V .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2019, 4 (10) :794-804