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Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes.
Younossi ZM, et al. · 2016
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⚖️ Lavora su: Peso & grasso viscerale · lente Traiettoria · il corpo nel tempo
tocca anche 🛡️ Protezione d'organo
Meta-analisi di studi osservazionali (certezza bassa-moderata)
La domandaQual e la prevalenza, l'incidenza e la prognosi globale della steatosi epatica non alcolica (NAFLD/NASH)?
Cosa hanno trovatoMeta-analisi a effetti casuali di 86 studi, campione complessivo 8.515.431 da 22 Paesi. Prevalenza globale di NAFLD 25,24% (IC 95% 22,10-28,65), massima in Medio Oriente e Sud America, minima in Africa. Comorbilita metaboliche associate: obesita 51,34% (41,38-61,20), diabete di tipo 2 22,51% (17,92-27,89), iperlipidemia 69,16% (49,91-83,46), ipertensione 39,34% (33,15-45,88), sindrome metabolica 42,54% (30,06-56,05). Nella NASH: progressione della fibrosi 40,76% (34,69-47,13), tasso medio annuo di progressione 0,09 (0,06-0,12). Incidenza di epatocarcinoma tra i pazienti NAFLD 0,44 per 1.000 persone-anno (range 0,29-0,66). Rapporti di rischio di incidenza per mortalita epatica 1,94 (range 1,28-2,92) e per mortalita totale 1,05 (range 0,70-1,56).
Cosa significa per teLa steatosi epatica e frequente nella popolazione generale (circa 1 persona su 4). Tra chi ha la steatosi, le condizioni metaboliche sono molto comuni: circa 1 su 2 e obeso e circa 1 su 4-5 ha il diabete di tipo 2. Utile pensare allo screening del fegato in presenza di diabete/obesita. Sono dati osservazionali di prevalenza: descrivono associazioni, non un rapporto di causa; le stime hanno ampia variabilita tra studi e metodi.
Abstract (in lingua originale)
UNLABELLED: Nonalcoholic fatty liver disease (NAFLD) is a major cause of liver disease worldwide. We estimated the global prevalence, incidence, progression, and outcomes of NAFLD and nonalcoholic steatohepatitis (NASH). PubMed/MEDLINE were searched from 1989 to 2015 for terms involving epidemiology and progression of NAFLD. Exclusions included selected groups (studies that exclusively enrolled morbidly obese or diabetics or pediatric) and no data on alcohol consumption or other liver diseases. Incidence of hepatocellular carcinoma (HCC), cirrhosis, overall mortality, and liver-related mortality were determined. NASH required histological diagnosis. All studies were reviewed by three independent investigators. Analysis was stratified by region, diagnostic technique, biopsy indication, and study population. We used random-effects models to provide point estimates (95% confidence interval [CI]) of prevalence, incidence, mortality and incidence rate ratios, and metaregression with subgroup analysis to account for heterogeneity. Of 729 studies, 86 were included with a sample size of 8,515,431 from 22 countries. Global prevalence of NAFLD is 25.24% (95% CI: 22.10-28.65) with highest prevalence in the Middle East and South America and lowest in Africa. Metabolic comorbidities associated with NAFLD included obesity (51.34%; 95% CI: 41.38-61.20), type 2 diabetes (22.51%; 95% CI: 17.92-27.89), hyperlipidemia (69.16%; 95% CI: 49.91-83.46%), hypertension (39.34%; 95% CI: 33.15-45.88), and metabolic syndrome (42.54%; 95% CI: 30.06-56.05). Fibrosis progression proportion, and mean annual rate of progression in NASH were 40.76% (95% CI: 34.69-47.13) and 0.09 (95% CI: 0.06-0.12). HCC incidence among NAFLD patients was 0.44 per 1,000 person-years (range, 0.29-0.66). Liver-specific mortality and overall mortality among NAFLD and NASH were 0.77 per 1,000 (range, 0.33-1.77) and 11.77 per 1,000 person-years (range, 7.10-19.53) and 15.44 per 1,000 (range, 11.72-20.34) and 25.56 per 1,000 person-years (range, 6.29-103.80). Incidence risk ratios for liver-specific and overall mortality for NAFLD were 1.94 (range, 1.28-2.92) and 1.05 (range, 0.70-1.56). CONCLUSIONS: As the global epidemic of obesity fuels metabolic conditions, the clinical and economic burden of NAFLD will become enormous. (Hepatology 2016;64:73-84).
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