将自身抗体作为代谢功能障碍相关性脂肪性肝病中严重纤维化或肝硬化的预测因子的探索

Mariam Ragheb, M. Grubert Van Iderstine, Gerald Minuk, Nabiha Faisal
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引用次数: 0

摘要

代谢功能障碍相关性脂肪性肝病(MASLD)和代谢功能障碍相关性脂肪性肝炎(MASH)是迅速增长的公共健康问题。确定 MASLD 患者晚期肝病的预测标志物对于早期干预至关重要。本研究调查了不同亚组中自身抗体阳性与严重纤维化或肝硬化风险之间的关联。我们对 1994 年至 2019 年期间确诊为 MASLD 的成年患者进行了一项回顾性研究。通过实验室研究评估了自身抗体状态(抗核抗体和抗平滑肌抗体)。肝纤维化或肝硬化是通过组织学或公认的非侵入性方法确定的。采用逻辑回归分析评估自身抗体阳性与严重肝纤维化或肝硬化之间的关联。同时患有病毒性肝病和酒精性肝病的患者单独进行评估。在2749名MASLD患者中,男性1425人(51.8%),女性1324人(48.2%),平均年龄58.7岁。共有 541 名(19.7%)患者的自身抗体检测呈阳性。自身抗体阳性与MASLD患者发生严重纤维化或肝硬化的风险较高有关(几率比1.28,95% CI [1.0-1.6])。在不同的亚组中,包括同时感染乙型和丙型肝炎病毒的患者,这种相关性依然存在。相比之下,酒精肝患者自身抗体阳性的风险较低。自身抗体阳性是MASLD患者晚期肝病的潜在预测标志物,有助于进行风险分层和有针对性的干预。这项研究强调了自身抗体在MASLD中的临床意义,并强调需要进行前瞻性验证和机理研究,以完善风险评估和管理策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring autoantibodies as predictors of severe fibrosis or cirrhosis in metabolic dysfunction associated steatotic liver disease
Metabolic dysfunction associated steatotic liver disease (MASLD) and metabolic dysfunction associated steatohepatitis (MASH) are rapidly growing public health concerns. Identifying predictive markers for advanced liver disease in MASLD patients is crucial for early intervention. This study investigates the association between autoantibody positivity and risk for severe fibrosis or cirrhosis across various subgroups. We conducted a retrospective study of adult patients diagnosed with MASLD between 1994 and 2019. Autoantibody status (anti-nuclear and anti-smooth muscle antibodies) was assessed using laboratory studies. Hepatic fibrosis or cirrhosis was determined histologically or through accepted non-invasive measures. Logistic regression analyses were employed to evaluate the association between autoantibody positivity and severe fibrosis or cirrhosis. Patients with co-morbid viral and alcohol liver disease were assessed separately. Among 2,749 MASLD patients, 1,425 (51.8%) were males and 1,324 (48.2%) were females, with a mean age of 58.7 years. A total of 541 (19.7%) patients tested positive for autoantibodies. Autoantibody positivity was associated with a higher risk of severe fibrosis or cirrhosis in MASLD patients (odds ratio 1.28, 95% CI [1.0–1.6]). This association persisted across various subgroups, including those with concurrent hepatitis B and C virus infections. In contrast, in alcohol liver disease, autoantibody-positive patients exhibited a lower risk. Autoantibody positivity emerges as a potential predictive marker for advanced liver disease in MASLD patients, facilitating risk stratification and tailored interventions. This study highlights the clinical relevance of autoantibodies in MASLD and underscores the need for prospective validation and mechanistic investigations to refine risk assessment and management strategies.
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