Parental obesity and risk of metabolic dysfunction associated steatotic liver disease in adult offspring: UK birth cohort study

医学 后代 肥胖 队列研究 优势比 队列 生命历程法 疾病 可能性 肝病 内科学 儿科 风险因素 脂肪肝 儿童肥胖 年轻人 出生体重 怀孕 内分泌学 非酒精性脂肪肝 风险评估 心理干预 产科 前瞻性队列研究 流行病学 梅德林 横断面研究 生理学 绝对风险降低 代谢综合征 母乳喂养
作者
Stefani Tica,Chongliang Luo,Duo Ren,Xiaoyu Zong,Michael D. Thompson,Janis Stoll,Brian Jesse DeBosch,Tarr Phillip,Yin Cao
出处
期刊:Gut [BMJ]
卷期号:: gutjnl-2025 被引量:3
标识
DOI:10.1136/gutjnl-2025-336165
摘要

Background Metabolic dysfunction associated steatotic liver disease (MASLD), the most common chronic liver disease globally, may originate early in life. While maternal obesity is linked to offspring MASLD, the roles of paternal obesity and mediation by childhood adiposity remain unclear. Objectives This study evaluates prospective associations between pre-pregnancy biparental adiposity and offspring MASLD in adulthood. Design We included 1933 offspring from the UK Avon Longitudinal Study of Parents and Children (ALSPAC) to assess the associations between parental pre-pregnancy body mass index (BMI) and odds of offspring MASLD at age 24 years. MASLD was defined as hepatic steatosis on transient elastography and ≥1 cardiometabolic risk factors. We evaluated causal mediation by childhood adiposity measures. Results At age 24 years, 10.4% of offspring had MASLD. Pre-pregnancy maternal and paternal obesity were independently associated with an increased odds of offspring MASLD. Each 1 kg/m 2 increase in maternal BMI increased the odds of MASLD by 10% (Odds Ratio [OR] 1.10, 95% CI 1.06 to 1.14), while each 1 kg/m 2 increase in paternal BMI raised the odds by 9% (OR 1.09, 95% CI 1.04 to 1.13). Biparental overweight or obesity was associated with 3.73 times the odds of offspring MASLD (OR 3.73, 95% CI 2.43 to 5.73) compared with parents with a normal BMI, with 67% of this association mediated by cumulative excess childhood BMI, a defined area under the curve for BMI Z score >1 for ages 7–17 years. Conclusions Excess parental adiposity pre-pregnancy was associated with a higher odds of offspring MASLD, mediated by cumulative excess childhood BMI, highlighting the potential of life course interventions to reduce the risk of MASLD in future generations.
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