How does alcohol use impact morbidity and mortality of liver cirrhosis? A systematic review and dose-response meta-analysis

被引:11
|
作者
Llamosas-Falcon, Laura [1 ]
Probst, Charlotte [1 ,2 ,3 ,4 ,5 ]
Buckley, Charlotte [6 ]
Jiang, Huan [1 ,7 ]
Lasserre, Aurelie M. [1 ,8 ]
Puka, Klajdi [1 ,4 ,9 ]
Tran, Alexander [1 ]
Zhu, Yachen [10 ]
Rehm, Jurgen [1 ,4 ,5 ,7 ,11 ,12 ,13 ]
机构
[1] Inst Mental Hlth Policy Res, Ctr Addict & Mental Hlth, 33 Ursula Franklin St, Toronto, ON M5S 2S1, Canada
[2] Heidelberg Inst Global Hlth, Med Fac, Neuenheimer Feld 365, D-69120 Heidelberg, Germany
[3] Univ Hosp, Neuenheimer Feld 365, D-69120 Heidelberg, Germany
[4] Campbell Family Mental Hlth Res Inst, Ctr Addict & Mental Hlth, 33 Ursula Franklin St, Toronto, ON M5T 2S1, Canada
[5] Univ Toronto, Dept Psychiat, 250 Coll St, Toronto, ON M5T 1R8, Canada
[6] Univ Sheffield, Dept Automat Control & Syst Engn, Mappin St, Sheffield S1 3JD, England
[7] Univ Toronto, Dalla Lana Sch Publ Hlth, 155 Coll St, Toronto, ON M5T 1P8, Canada
[8] Lausanne Univ Hosp, Dept Psychiat, Addict Med, Rue Bugnon 23, CH-1011 Lausanne, Switzerland
[9] Western Univ, Dept Epidemiol & Biostat, 1465 Richmond St, London, ON N6G 2M1, Canada
[10] Publ Hlth Inst, Alcohol Res Grp, 6001 Shellmound St 450, Emeryville, CA 94608 USA
[11] Publ Hlth Agcy Catalonia, Program Subst Abuse & WHO CC, 81-95 Roc Boronat St 8005, Barcelona, Spain
[12] Univ Med Ctr Hamburg Eppendorf UKE, Ctr Interdisciplinary Addict Res ZIS, Dept Psychiat & Psychotherapy, Martinistr 52, D-20246 Hamburg, Germany
[13] Univ Toronto, Inst Med Sci, Fac Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
关键词
Liver cirrhosis; Liver disease; Alcohol; Systematic review; Dose-response; Meta-analysis; Epidemiology; Public health; Morbidity; Mortality; RISK; DISEASE;
D O I
10.1007/s12072-023-10584-z
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundAlcohol consumption is the most important risk factor responsible for the disease burden of liver cirrhosis (LC). Estimates of risk relationships available usually neither distinguish between different causes such as alcohol-related LC or hepatitis-related LC, nor differentiate between morbidity and mortality as outcome. We aimed to address this research gap and identify dose-response relationships between alcohol consumption and LC, by cause and outcome.MethodsA systematic review using PubMed/Medline and Embase was conducted, identifying studies that reported an association between level of alcohol use and LC. Meta-regression models were used to estimate the dose-response relationships and control for heterogeneity.ResultsTotally, 44 studies, and 1 secondary data source, with a total of 5,122,534 participants and 15,150 cases were included. Non-linear dose-response relationships were identified, attenuated for higher levels of consumption. For morbidity, drinking 25 g/day was associated with a RR of 1.81 (95% CI 1.68-1.94) compared to lifetime abstention; 50 g/day and 100 g/day corresponded to 3.54 (95% CI 3.29-3.81) and 8.15 (95% CI 7.46-8.91), respectively. For mortality, for 25 g/day, a RR of 2.65 (95% CI 2.22-3.16); for 50 g/day, a RR of 6.83 (95% CI 5.84-7.97); for 100 g/day, a RR of 16.38 (95% CI 13.81-19.42) were identified. A higher risk for alcohol-related and all-cause LC as compared to hepatitis C-related LC was found.ConclusionOur results demonstrated higher acceleration for mortality compared to morbidity. The current findings will inform the way we quantify the burden due to LC attributable to alcohol use.
引用
收藏
页码:216 / 224
页数:9
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