Resolution of metabolic dysfunction improves liver health among Chinese children: evidence from two prospective cohorts.

IF 12 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Lili Yang, Menglong Li, Min Zhao, Yifei Hu, Bo Xi
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Abstract

Background & aims: New metabolic dysfunction-associated steatotic liver disease (MASLD) definition emphasizes the crucial role of metabolic dysfunction in MASLD pathogenesis. This study aimed to examine whether the resolution of metabolic dysfunction can mitigate the risk of hepatic steatosis in Chinese children.

Methods: Data were obtained from two prospective cohort studies in China, including 2,158 children aged 6-11 years at baseline, with a four-year follow-up. Based on metabolic status (normal vs. abnormal) at baseline and follow-up, children were categorized into four distinct groups. Hepatic steatosis was assessed by abdominal ultrasonography and/or serum alanine aminotransferase measurements.

Results: At follow-up, 10.4% (n=225) of children developed hepatic steatosis. Baseline metabolic dysfunction significantly increased the risk of incident hepatic steatosis (odds ratio [OR]: 3.31, 95% confidence interval [CI]: 2.42-4.52). Compared with children who kept metabolically healthy at both baseline and follow-up, those with persistent metabolic dysfunction (OR: 6.01, 95%CI: 3.96-9.12) and those who developed metabolic dysfunction at follow-up (OR: 1.99, 95%CI: 1.19-3.33) had significantly increased risks of hepatic steatosis. Notably, children whose metabolic dysfunction resolved to normal status at follow-up presented no increased risk (OR: 0.64, 95%CI: 0.26-1.57).

Conclusions: Metabolic dysfunction is a strong predictor of incident hepatic steatosis in children, and resolution of this dysfunction attenuates the attendant risk. These findings highlight the importance of primary and secondary interventions targeting metabolic risk factors to improve liver health in children.

代谢功能障碍的解决可改善中国儿童的肝脏健康:来自两个前瞻性队列的证据
背景与目的:代谢功能障碍相关脂肪变性肝病(MASLD)的新定义强调了代谢功能障碍在MASLD发病机制中的关键作用。本研究旨在探讨代谢功能障碍的解决是否可以减轻中国儿童肝脂肪变性的风险。方法:数据来自中国的两项前瞻性队列研究,包括2158名6-11岁的儿童,随访4年。根据基线和随访时的代谢状态(正常与异常),将儿童分为四个不同的组。通过腹部超声检查和/或血清丙氨酸转氨酶测定来评估肝脂肪变性。结果:随访时,10.4% (n=225)的儿童发生肝脂肪变性。基线代谢功能障碍显著增加发生肝脂肪变性的风险(优势比[OR]: 3.31, 95%可信区间[CI]: 2.42-4.52)。与基线和随访时保持代谢健康的儿童相比,持续代谢功能障碍(OR: 6.01, 95%CI: 3.96-9.12)和随访时出现代谢功能障碍(OR: 1.99, 95%CI: 1.19-3.33)的儿童发生肝脂肪变性的风险显著增加。值得注意的是,在随访中代谢功能障碍恢复到正常状态的儿童没有增加风险(OR: 0.64, 95%CI: 0.26-1.57)。结论:代谢功能障碍是儿童发生肝脂肪变性的一个强有力的预测因素,解决这一功能障碍可降低随之而来的风险。这些发现强调了针对代谢危险因素的初级和二级干预措施对改善儿童肝脏健康的重要性。
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来源期刊
CiteScore
16.90
自引率
4.80%
发文量
903
审稿时长
22 days
期刊介绍: Clinical Gastroenterology and Hepatology (CGH) is dedicated to offering readers a comprehensive exploration of themes in clinical gastroenterology and hepatology. Encompassing diagnostic, endoscopic, interventional, and therapeutic advances, the journal covers areas such as cancer, inflammatory diseases, functional gastrointestinal disorders, nutrition, absorption, and secretion. As a peer-reviewed publication, CGH features original articles and scholarly reviews, ensuring immediate relevance to the practice of gastroenterology and hepatology. Beyond peer-reviewed content, the journal includes invited key reviews and articles on endoscopy/practice-based technology, health-care policy, and practice management. Multimedia elements, including images, video abstracts, and podcasts, enhance the reader's experience. CGH remains actively engaged with its audience through updates and commentary shared via platforms such as Facebook and Twitter.
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