Fukunaga Shuhei, Nakano Dan, Tsutsumi Tsubasa, Kawaguchi Takumi, Eslam Mohammed, Yoshinaga Shinobu, Abe Hirohiko, Nouno Ryuichi, Joh Seiya, Mitsuyama Keiichi, George Jacob, Torimura Takuji
Department of Medicine, Division of Gastroenterology, Kurume University School of Medicine, Kurume, Japan.
Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Sydney, New South Wales, Australia.
Hepatol Res. 2022 Aug;52(8):699-711. doi: 10.1111/hepr.13795. Epub 2022 Jun 7.
Reflux esophagitis is associated with metabolic dysfunction. Recently, fatty liver has been redefined as metabolic dysfunction-associated fatty liver disease (MAFLD). We investigated the impact of MAFLD and its subtypes on the incidence of reflux esophagitis.
This multicenter, observational cohort study enrolled 9100 consecutive health-check examinees who underwent esophagogastroduodenoscopy and ultrasonography. All patients were classified into the MAFLD or non-MAFLD group. Based on the Asian cut-off value for body mass index (BMI), the MAFLD group was further classified into the lean/normal-weight (BMI <23 kg/m ) and overweight/obese (BMI ≥23 kg/m ) subgroups. The impact of MAFLD and its subtypes on the cumulative incidence of reflux esophagitis was evaluated using multivariable Cox proportional hazards regression analysis.
MAFLD was diagnosed in 26.5% (2416/9100) of patients. Multivariable Cox proportional hazards regression analysis indicated that MAFLD (hazard ratio [HR] 1.2183; 95% confidence interval [CI] 1.0954-1.3550; p = 0.0003), hiatal hernia, and aging were independent risk factors for reflux esophagitis. Stratification analysis indicated that cumulative incidence of reflux esophagitis among patients with MAFLD was significantly higher in the lean/normal-weight than in the overweight/obese group (HR 1.3274; 95% CI 1.0043-1.7547; p = 0.0466). Among various metabolic factors, visceral adiposity was the only independent metabolic risk factor for reflux esophagitis (HR 2.8331; 95% CI 1.0201-7.8691; p = 0.0457) in the lean/normal-weight MAFLD group.
MAFLD, in particular lean/normal-weight MAFLD, is independent risk factor for reflux esophagitis. Furthermore, visceral adiposity was identified as the most strong metabolic risk factor for reflux esophagitis in lean/normal-weight patients with MAFLD.
反流性食管炎与代谢功能障碍相关。最近,脂肪肝已被重新定义为代谢功能障碍相关脂肪性肝病(MAFLD)。我们研究了MAFLD及其亚型对反流性食管炎发病率的影响。
这项多中心观察性队列研究纳入了9100名连续接受食管胃十二指肠镜检查和超声检查的健康体检者。所有患者被分为MAFLD组或非MAFLD组。根据亚洲人身体质量指数(BMI)的临界值,MAFLD组进一步分为瘦/正常体重(BMI<23kg/m²)和超重/肥胖(BMI≥23kg/m²)亚组。使用多变量Cox比例风险回归分析评估MAFLD及其亚型对反流性食管炎累积发病率的影响。
26.5%(2416/9100)的患者被诊断为MAFLD。多变量Cox比例风险回归分析表明,MAFLD(风险比[HR]1.2183;95%置信区间[CI]1.0954 - 1.3550;p = 0.0003)、食管裂孔疝和年龄是反流性食管炎的独立危险因素。分层分析表明,MAFLD患者中,瘦/正常体重组反流性食管炎的累积发病率显著高于超重/肥胖组(HR 1.3274;95% CI 1.0043 - 1.7547;p = 0.0466)。在各种代谢因素中,内脏脂肪过多是瘦/正常体重MAFLD组反流性食管炎唯一的独立代谢危险因素(HR 2.8331;95% CI 1.0201 - 7.8691;p = 0.0457)。
MAFLD,尤其是瘦/正常体重的MAFLD,是反流性食管炎的独立危险因素。此外,内脏脂肪过多被确定为瘦/正常体重MAFLD患者反流性食管炎最强的代谢危险因素。