Murali Arvind R, Gupta Ashutosh, Brown Kyle
Division of Gastroenterology-Hepatology, Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa.
Iowa City Veterans Administration Medical Center, Iowa City, Iowa.
Hepatol Res. 2018 Feb;48(3):E30-E41. doi: 10.1111/hepr.12921. Epub 2017 Jul 20.
Iron reduction has been proposed as treatment for dysmetabolic iron overload syndrome (DIOS) and non-alcoholic fatty liver disease (NAFLD), but results of published trials are conflicting. We undertook a systematic review and meta-analysis to determine the impact of phlebotomy in DIOS and NAFLD.
We searched multiple databases systematically for studies evaluating the impact of phlebotomy in DIOS and NAFLD. We calculated weighted summary estimates using the inverse variance method. Study quality was assessed using the Cochrane collaboration tool.
We identified nine studies with 820 patients (427 had phlebotomy, 393 lifestyle changes alone). Iron depletion did not improve the Homeostasis Model Assessment (HOMA) index (mean difference [MD] -0.6; confidence interval (CI), -1.7, 0.5; P = 0.3), insulin level (MD -0.8 mU/L; CI, -5.3, 3.7; P = 0.73), or aspartate aminotransferase (AST) (MD -0.7 IU/L; CI, -3.2, 1.8; P = 0.6) in DIOS and/or NAFLD patients as compared to lifestyle changes alone (five studies, 626 patients). There was mild improvement in alanine aminotransferase (ALT) (MD -6.6 IU/L; CI, -11, -2.1); P < 0.01), but the effect size was very small (Cohen's d, 0.15; r statistic, 0.07). Even in the subgroup of patients with NAFLD and hyperferritinemia, phlebotomy did not improve the HOMA index, insulin level, ALT, or AST. Additionally, no study showed significant improvement in liver inflammation or fibrosis with iron reduction.
Phlebotomy does not bring about significant improvement in indices of insulin resistance, liver enzymes, or liver histology in patients with DIOS and/or NAFLD compared to lifestyle changes alone. Current evidence does not support the use of phlebotomy in patients with DIOS or NAFLD.
放血疗法已被提议用于治疗代谢紊乱性铁过载综合征(DIOS)和非酒精性脂肪性肝病(NAFLD),但已发表试验的结果相互矛盾。我们进行了一项系统评价和荟萃分析,以确定放血疗法对DIOS和NAFLD的影响。
我们系统检索了多个数据库,以查找评估放血疗法对DIOS和NAFLD影响的研究。我们使用逆方差法计算加权汇总估计值。使用Cochrane协作工具评估研究质量。
我们确定了9项研究,共820例患者(427例行放血疗法,393例仅改变生活方式)。与仅改变生活方式相比(5项研究,626例患者),在DIOS和/或NAFLD患者中,铁耗竭并未改善稳态模型评估(HOMA)指数(平均差[MD] -0.6;置信区间[CI],-1.7,0.5;P = 0.3)、胰岛素水平(MD -0.8 mU/L;CI,-5.3,3.7;P = 0.73)或天冬氨酸转氨酶(AST)(MD -0.7 IU/L;CI,-3.2,1.8;P = 0.6)。丙氨酸转氨酶(ALT)有轻度改善(MD -6.6 IU/L;CI,-11,-2.1;P < 0.01),但效应量非常小(Cohen's d,0.15;r统计量,0.07)。即使在NAFLD和高铁蛋白血症患者亚组中,放血疗法也未改善HOMA指数、胰岛素水平、ALT或AST。此外,没有研究表明铁减少能使肝脏炎症或纤维化有显著改善。
与仅改变生活方式相比,放血疗法在DIOS和/或NAFLD患者的胰岛素抵抗指标、肝酶或肝脏组织学方面并未带来显著改善。目前的证据不支持对DIOS或NAFLD患者使用放血疗法。