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妊娠期超重肥胖和子代代谢相关脂肪性肝病的Meta分析

吴玉莹 恩卡尔·努尔 王佑新 王明月 杨依凡 杨树涵 孙玲玲 王辉

吴玉莹, 恩卡尔·努尔, 王佑新, 王明月, 杨依凡, 杨树涵, 孙玲玲, 王辉. 妊娠期超重肥胖和子代代谢相关脂肪性肝病的Meta分析[J]. 中国学校卫生, 2025, 46(8): 1079-1083. doi: 10.16835/j.cnki.1000-9817.2025259
引用本文: 吴玉莹, 恩卡尔·努尔, 王佑新, 王明月, 杨依凡, 杨树涵, 孙玲玲, 王辉. 妊娠期超重肥胖和子代代谢相关脂肪性肝病的Meta分析[J]. 中国学校卫生, 2025, 46(8): 1079-1083. doi: 10.16835/j.cnki.1000-9817.2025259
WU Yuying, ENKAER Nuer, WANG Youxin, WANG Mingyue, YANG Yifan, YANG Shuhan, SUN Lingling, WANG Hui. Meta-analysis of maternal overweight/obesity during pregnancy and offspring metabolic dysfunction-associated steatotic liver disease[J]. CHINESE JOURNAL OF SCHOOL HEALTH, 2025, 46(8): 1079-1083. doi: 10.16835/j.cnki.1000-9817.2025259
Citation: WU Yuying, ENKAER Nuer, WANG Youxin, WANG Mingyue, YANG Yifan, YANG Shuhan, SUN Lingling, WANG Hui. Meta-analysis of maternal overweight/obesity during pregnancy and offspring metabolic dysfunction-associated steatotic liver disease[J]. CHINESE JOURNAL OF SCHOOL HEALTH, 2025, 46(8): 1079-1083. doi: 10.16835/j.cnki.1000-9817.2025259

妊娠期超重肥胖和子代代谢相关脂肪性肝病的Meta分析

doi: 10.16835/j.cnki.1000-9817.2025259
基金项目: 

北京大学医学部-潍坊市妇幼健康联合研究中心科研基金项目 PKUWF-Y10

详细信息
    作者简介:

    吴玉莹(2001-),女,河南信阳人,在读硕士,主要研究方向为妇幼健康影响因素及干预措施

    通讯作者:

    孙玲玲,E-mail:sllwf5620@163.com

    王辉,E-mail:huiwang@bjmu.edu.cn

  • 利益冲突声明  所有作者声明无利益冲突。
  • 中图分类号: R179 R723.14 R714.255 Q485

Meta-analysis of maternal overweight/obesity during pregnancy and offspring metabolic dysfunction-associated steatotic liver disease

  • 摘要:   目的  评估妊娠期超重肥胖和子代代谢相关(非酒精性)脂肪性肝病(MASLD)发生风险之间的相关性,为生命早期预防MASLD提供理论依据。  方法  在线检索中国知网、万方数据知识服务平台、中国生物医学文献服务系统SinoMed和PubMed、Embase、Web of Science、Cochrane Library、PROSPERO、PQDT Global、ScienceDirect 10个数据库中有关妊娠期超重肥胖和子代MASLD发生关联的研究文献,检索时间为2014年1月至2024年12月。由2名研究者独立进行筛选文献、资料提取和质量评价,采用R 4.3.3软件进行统计分析。  结果  共纳入10篇文献,涉及10 229名研究对象,包括4篇队列研究和6篇病例对照研究。队列研究合并效应值显示妊娠期超重肥胖会增加子代MASLD发生风险(RR=1.59,95%CI=1.06~2.39,P < 0.05),研究间存在中度异质性(I2=56.9%,P=0.07);病例对照研究合并效应值显示妊娠期超重肥胖与子代MASLD的发生风险呈正相关(OR=2.00,95%CI=1.68~2.39,P < 0.05),异质性较低(I2=48.8%,P=0.08)。  结论  妊娠期超重肥胖与子代MASLD的发生风险呈正相关,孕期体重管理可降低子代MASLD的发生风险。
    1)  利益冲突声明  所有作者声明无利益冲突。
  • 图  1  妊娠期MOO与子代MASLD关联文献检索流程

    Figure  1.  Literature retrieval process for investigating the association between MOO and offspring MASLD

    图  2  队列研究中MOO与子代MASLD发生风险的Meta分析

    Figure  2.  Meta-analysis for cohort studies on the risk of MOO and offspring MASLD

    图  3  病例对照研究中MOO与子代MASLD发生风险的Meta分析

    Figure  3.  Meta-analysis for case control studies on the risk of MOO and offspring MASLD

    表  1  MOO与子代MASLD关系纳入文献的基本信息

    Table  1.   Basic information on the relationship between MOO and offspring MASLD selected in the literature

    第一作者及年份 国家/地区 研究类型 结局指标 样本量 子代年龄/岁 RR/OR值(95%CI) NOS总分
    Zeng(2022)[17] 中国 队列研究 NAFLD(CAP≥214.53 dB/m,肝脏超声) 430 8 1.19(1.09~1.29) 8
    Geurtsen(2021)[28] 荷兰 队列研究 NALFD(MRI) 2 168 10 1.52(0.90~2.58) 9
    Bellatorre(2018)[29] 美国 队列研究 NAFLD(肝脏脂肪分数≥5.56%) 254 16.4±1.5 2.79(0.91~8.54) 6
    Patel(2016)[18] 英国 队列研究 NAFLD(肝脏超声) 1 215 17.8±0.4 2.63(1.20~5.55) 7
    Nairz(2024)[21] 奥地利 病例对照研究 NAFLD(CAP值超过P90,肝脏超声) 595 17 3.59(1.69~7.62) 7
    De Ruyter(2024)[22] 芬兰 病例对照研究 MAFLD(ALT超过2倍正常值上限) 460 2~16 1.16(0.68~1.99) 6
    Abeysekera(2021)[20] 英国 病例对照研究 NAFLD(CAP值≥248 dB/m,肝脏超声) 2 961 24 2.09(1.62~2.68) 9
    Hagström(2021)[19] 瑞典 病例对照研究 NAFLD(活检) 882 < 25 2.24(1.59~3.17) 7
    Cantoral(2020)[30] 墨西哥 病例对照研究 NAFLD(MRI) 97 21.4±0.5 1.79(1.51~2.14) 7
    Ayonrinde(2018)[31] 澳大利亚 病例对照研究 NAFLD(肝脏超声) 1 167 17 2.88(1.64~5.10) 7
    注:既往研究提示,在成人中94.5%的NAFLD患者可归类为MASLD,具有较高的一致性[32];CAP为受控衰减参数(controlled attenuation parameter),MRI为磁共振成像(magnetic resonance imaging),ALT为丙氨酸氨基转移酶(alanine aminotransferase)。
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出版历程
  • 收稿日期:  2025-02-14
  • 修回日期:  2025-04-30
  • 网络出版日期:  2025-08-30
  • 刊出日期:  2025-08-25

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