Libby G Lord, Anthony G B Walters, Caroline A Crowther, Stuart R Dalziel, Carl L Eagleton, Greg D Gamble, Jane E Harding, Christopher J D McKinlay, Barry J Milne, Robyn W May
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In the AST, women (<i>F</i><sub>0</sub>) expected to birth between 24 and 36 weeks' gestation were randomised to betamethasone or placebo. When their children (<i>F</i><sub>1</sub>) were 50 years old, they and their children (<i>F</i><sub>2</sub>) were followed up with a self-report questionnaire and data linkage. The primary outcome for this analysis was body mass index (BMI) z-score in the <i>F</i><sub>2</sub> generation. Secondary outcomes included respiratory, cardiovascular, neurodevelopmental, mental and general health, and social outcomes. Of the 213 <i>F</i><sub>2</sub> participants, 144 had BMI data available. There was no difference in BMI z-score between participants whose parent was exposed to betamethasone versus placebo (mean (<i>SD</i>) 0.63 (1.45), <i>N</i> = 77 vs 0.41 (1.28), <i>N</i> = 67, adjusted mean difference (95% confidence interval) = 0.16 (-0.37, 0.69)). There was no evidence of a difference in rates of overweight, diabetes, respiratory disease, cardiometabolic risk factors, neurodevelopmental difficulties, mental health difficulties and social outcomes between parental betamethasone versus placebo exposure groups, but confidence intervals were wide. These findings are reassuring regarding the intergenerational safety of antenatal corticosteroids.</p>","PeriodicalId":49167,"journal":{"name":"Journal of Developmental Origins of Health and Disease","volume":"16 ","pages":"e25"},"PeriodicalIF":1.5000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Second generation effects of antenatal corticosteroid exposure: 50-year follow-up of the Auckland Steroid Trial.\",\"authors\":\"Libby G Lord, Anthony G B Walters, Caroline A Crowther, Stuart R Dalziel, Carl L Eagleton, Greg D Gamble, Jane E Harding, Christopher J D McKinlay, Barry J Milne, Robyn W May\",\"doi\":\"10.1017/S204017442510007X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Antenatal corticosteroids are given to pregnant people at risk of preterm birth to reduce newborn morbidity, including respiratory distress syndrome. However, there has been concern surrounding potential adverse effects on subsequent generations. Animal studies have demonstrated endocrine and metabolic changes in those exposed to corticosteroids in utero (<i>F</i><sub>1</sub>) and in the second generation (<i>F</i><sub>2</sub>). We aimed to assess the effects of parental antenatal corticosteroid exposure on health of the second generation (<i>F</i><sub>2</sub>) of Auckland Steroid Trial (AST) participants. In the AST, women (<i>F</i><sub>0</sub>) expected to birth between 24 and 36 weeks' gestation were randomised to betamethasone or placebo. When their children (<i>F</i><sub>1</sub>) were 50 years old, they and their children (<i>F</i><sub>2</sub>) were followed up with a self-report questionnaire and data linkage. The primary outcome for this analysis was body mass index (BMI) z-score in the <i>F</i><sub>2</sub> generation. 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These findings are reassuring regarding the intergenerational safety of antenatal corticosteroids.</p>\",\"PeriodicalId\":49167,\"journal\":{\"name\":\"Journal of Developmental Origins of Health and Disease\",\"volume\":\"16 \",\"pages\":\"e25\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Developmental Origins of Health and Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1017/S204017442510007X\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Developmental Origins of Health and Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/S204017442510007X","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0
摘要
对有早产风险的孕妇给予产前皮质类固醇,以减少新生儿发病率,包括呼吸窘迫综合征。然而,人们一直担心对后代的潜在不利影响。动物研究表明,在子宫内(F1)和第二代(F2)暴露于皮质类固醇的人的内分泌和代谢发生了变化。我们的目的是评估父母产前皮质类固醇暴露对奥克兰类固醇试验(AST)第二代(F2)参与者健康的影响。在AST中,预期在妊娠24 - 36周分娩的妇女(0名)被随机分配到倍他米松组或安慰剂组。当他们的孩子(F1) 50岁时,对他们和他们的孩子(F2)进行自我报告问卷和数据链接的随访。本分析的主要结局是F2代的身体质量指数(BMI) z-score。次要结局包括呼吸、心血管、神经发育、心理和一般健康以及社会结局。在213名F2参与者中,144人有BMI数据。父母暴露于倍他米松与安慰剂的参与者之间的BMI z-score没有差异(平均(SD) 0.63 (1.45), N = 77 vs 0.41 (1.28), N = 67,调整平均差异(95%置信区间)= 0.16(-0.37,0.69))。在父母倍他米松和安慰剂暴露组之间,没有证据表明超重、糖尿病、呼吸系统疾病、心脏代谢危险因素、神经发育困难、精神健康困难和社会结果的比率有差异,但置信区间很宽。这些发现让人对产前皮质类固醇的代际安全性感到放心。
Second generation effects of antenatal corticosteroid exposure: 50-year follow-up of the Auckland Steroid Trial.
Antenatal corticosteroids are given to pregnant people at risk of preterm birth to reduce newborn morbidity, including respiratory distress syndrome. However, there has been concern surrounding potential adverse effects on subsequent generations. Animal studies have demonstrated endocrine and metabolic changes in those exposed to corticosteroids in utero (F1) and in the second generation (F2). We aimed to assess the effects of parental antenatal corticosteroid exposure on health of the second generation (F2) of Auckland Steroid Trial (AST) participants. In the AST, women (F0) expected to birth between 24 and 36 weeks' gestation were randomised to betamethasone or placebo. When their children (F1) were 50 years old, they and their children (F2) were followed up with a self-report questionnaire and data linkage. The primary outcome for this analysis was body mass index (BMI) z-score in the F2 generation. Secondary outcomes included respiratory, cardiovascular, neurodevelopmental, mental and general health, and social outcomes. Of the 213 F2 participants, 144 had BMI data available. There was no difference in BMI z-score between participants whose parent was exposed to betamethasone versus placebo (mean (SD) 0.63 (1.45), N = 77 vs 0.41 (1.28), N = 67, adjusted mean difference (95% confidence interval) = 0.16 (-0.37, 0.69)). There was no evidence of a difference in rates of overweight, diabetes, respiratory disease, cardiometabolic risk factors, neurodevelopmental difficulties, mental health difficulties and social outcomes between parental betamethasone versus placebo exposure groups, but confidence intervals were wide. These findings are reassuring regarding the intergenerational safety of antenatal corticosteroids.
期刊介绍:
JDOHaD publishes leading research in the field of Developmental Origins of Health and Disease (DOHaD). The Journal focuses on the environment during early pre-natal and post-natal animal and human development, interactions between environmental and genetic factors, including environmental toxicants, and their influence on health and disease risk throughout the lifespan. JDOHaD publishes work on developmental programming, fetal and neonatal biology and physiology, early life nutrition, especially during the first 1,000 days of life, human ecology and evolution and Gene-Environment Interactions.
JDOHaD also accepts manuscripts that address the social determinants or education of health and disease risk as they relate to the early life period, as well as the economic and health care costs of a poor start to life. Accordingly, JDOHaD is multi-disciplinary, with contributions from basic scientists working in the fields of physiology, biochemistry and nutrition, endocrinology and metabolism, developmental biology, molecular biology/ epigenetics, human biology/ anthropology, and evolutionary developmental biology. Moreover clinicians, nutritionists, epidemiologists, social scientists, economists, public health specialists and policy makers are very welcome to submit manuscripts.
The journal includes original research articles, short communications and reviews, and has regular themed issues, with guest editors; it is also a platform for conference/workshop reports, and for opinion, comment and interaction.