目前在全球范圍內(nèi),糖尿病、肥胖、非酒精性肝炎等代謝疾病的發(fā)病率逐年穩(wěn)步上升。在美國,科學(xué)家認為非酒精性肝炎(NAFLD)是導(dǎo)致機體慢性肝病的禍?zhǔn)住?/P> 咖啡因一直被認為能降低人們患上肝病的風(fēng)險,降低慢性肝病患者纖維化程度。最近,一項發(fā)表在Hepatology雜志上新的研究證實:我們常喝的咖啡中咖啡因可以降低NAFLD患者早期纖維化的程度,多飲用咖啡有可能使非酒精性脂肪肝患者避免出現(xiàn)纖維化癥狀。 來自德克薩斯州布魯克陸軍醫(yī)學(xué)中心的Stephen Harrison博士開展的這項研究所涉及到的病例包括:以往參加過NAFLD相關(guān)研究的參與者以及那些前往該醫(yī)學(xué)中心肝病門診部接受治療的患者,人數(shù)共306人。 研究人員調(diào)查了這306位參與者咖啡使用情況,并通過超聲檢查將這些參與者分為四組:沒有纖維化跡象的患者(對照組)、脂肪病變組、NASH 0-1階段組、NASH 2-4階段組。這四組參與者平均每天攝取總咖啡因的毫克數(shù)分別為307、229、351、252,平均每天攝取咖啡的毫克數(shù)分別為228、160、255、152。結(jié)果發(fā)現(xiàn)NASH 0-1組的參與者咖啡的攝取量明顯要高于NASH 2-4組,并且NASH 0-1組的參與者體內(nèi)58%的咖啡因來自于咖啡的攝取,而這一數(shù)據(jù)在NASH 2-4組僅有36%。 研究中的多元分析表明:咖啡的攝取和肝纖維化風(fēng)險之間呈負相性。研究者稱NASH患者適度攝入咖啡后,其肝臟早期肝纖維化發(fā)生的風(fēng)險會有所降低。(生物谷 Bioon.com) Association of coffee and caffeine consumption with fatty liver disease, nonalcoholic steatohepatitis, and degree of hepatic fibrosis Jeffrey W. Molloy1, Christopher J. Calcagno2, Christopher D. Williams1, Frances J. Jones1, Dawn M. Torres3, Stephen A. Harrison1,§,* Coffee caffeine consumption (CC) is associated with reduced hepatic fibrosis in patients with chronic liver diseases, such as hepatitis C. The association of CC with nonalcoholic fatty liver disease (NAFLD) has not been established. The aim of this study was to correlate CC with the prevalence and severity of NAFLD. Patients involved in a previously published NAFLD prevalence study, as well as additional NASH patients identified in the Brooke Army Medical Center Hepatology clinic, were queried about their caffeine intake. A validated questionnaire for CC was utilized to assess for a relationship between caffeine and four groups: ultrasound negative (controls), bland steatosis/not-NASH, NASH stage 0-1, and NASH stage 2-4. A total of 306 patients responded to the CC questionnaire. Average milligrams of total caffeine/coffee CC per day in controls, bland steatosis/not-NASH, NASH stage 0-1, and NASH stage 2-4 were 307/228, 229/160, 351/255, and 252/152, respectively. When comparing patients with bland steatosis/not-NASH to those with NASH stage 0-1, there was a significant difference in CC between the two groups (P = 0.005). Additionally, when comparing patients with NASH stage 0-1 to those with NASH stage 2-4, there was a significant difference in coffee CC (P = 0.016). Spearman's rank correlation analysis further supported a negative relationship between coffee CC and hepatic fibrosis (r = ?0.215; P = 0.035). Conclusion: Coffee CC is associated with a significant reduction in risk of fibrosis among NASH patients. |
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