From the Division of Pediatric Gastroenterology, Hepatology, and Nutrition, University of Miami Miller School of Medicine, Miami, FL.
the Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, PA.
J Pediatr Gastroenterol Nutr. 2022 Sep 1;75(3):264-268. doi: 10.1097/MPG.0000000000003534. Epub 2022 Jun 27.
The clinical significance of autoantibody positivity in nonalcoholic fatty liver disease (NAFLD) in the absence of autoimmune hepatitis (AIH) remains uncertain. We aimed to determine the prevalence of autoantibodies in a pediatric cohort with biopsy-proven NAFLD and investigate the association between autoantibodies and NAFLD histologic grade.
Single-center, retrospective study of patients ≤21 years with biopsy-proven NAFLD from 2014 to 2019. Clinical and laboratory data were obtained within 90 days of liver biopsy. Autoantibody positivity was defined as serum titer ≥1:80 or units ≥20. Liver biopsies were evaluated for features of AIH, then scored for steatosis, hepatocyte ballooning, lobular inflammation, and NAFLD activity score (NAS) was calculated. Portal inflammation and fibrosis were scored separately. Multivariable logistic regression was used for continuous and binary outcomes.
Sixty-seven subjects met inclusion criteria. Positive antinuclear antibody (ANA), antismooth muscle antibody (ASMA), antineutrophil cytoplasmic antibody (ANCA), anti-F-actin antibody (F-actin), anti-liver kidney microsomal (LKM) antibody, or any combination was observed in 43%, 39%, 19%, 13%, 0%, and 66% of subjects, respectively. After controlling for confounders, positive ANA and alanine aminotransferase (ALT) >80 had 4.6 greater odds of having an NAS ≥5 ( P = 0.035; 95% confidence interval [CI], 1.12-19.01). Autoantibody positivity resolution occurred in 10%-50% who underwent serial monitoring.
Autoantibodies, except LKM, were frequently encountered in our pediatric NAFLD cohort in the absence of AIH. ANA positivity with ALT may help clinically stratify pediatric patients with suspected NAFLD targeting those at greater risk for nonalcoholic steatohepatitis (NASH).
在不存在自身免疫性肝炎 (AIH) 的情况下,非酒精性脂肪性肝病 (NAFLD) 患者自身抗体阳性的临床意义仍不确定。我们旨在确定经活检证实的 NAFLD 儿科患者队列中自身抗体的患病率,并研究自身抗体与 NAFLD 组织学分级之间的关系。
这是一项 2014 年至 2019 年期间在单中心进行的回顾性研究,纳入了经活检证实的≤21 岁的 NAFLD 患者。在肝活检后 90 天内获得临床和实验室数据。自身抗体阳性定义为血清滴度≥1:80 或单位≥20。对肝活检进行评估以确定 AIH 的特征,然后对脂肪变性、肝细胞气球样变、肝小叶炎症和 NAFLD 活动评分 (NAS) 进行评分。分别对门脉炎症和纤维化进行评分。连续和二分类结果采用多变量逻辑回归分析。
67 名患者符合纳入标准。核抗体 (ANA)、平滑肌抗体 (ASMA)、抗中性粒细胞胞质抗体 (ANCA)、抗肌动蛋白抗体 (F-actin)、抗肝-肾微粒体 (LKM) 抗体或任意组合阳性分别见于 43%、39%、19%、13%、0%和 66%的患者。在校正混杂因素后,ANA 阳性和丙氨酸氨基转移酶 (ALT) >80 与 NAS≥5 的发生几率增加 4.6 倍 ( P = 0.035;95%置信区间 [CI],1.12-19.01)。10%-50%接受连续监测的患者自身抗体阳性得到缓解。
在我们的儿科 NAFLD 队列中,除了 LKM 以外,自身抗体在没有 AIH 的情况下也经常出现。ANA 阳性伴 ALT 可能有助于临床上对疑似 NAFLD 的儿科患者进行分层,以确定那些发生非酒精性脂肪性肝炎 (NASH) 风险较高的患者。