Role of gestational age and intrauterine growth on bone mass in adolescents: findings from a Brazilian Birth Cohort Study.

IF 3.1 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Isabel Oliveira Bierhals, Luciana Tovo-Rodrigues, Alicia Matijasevich, Iná S Santos
{"title":"Role of gestational age and intrauterine growth on bone mass in adolescents: findings from a Brazilian Birth Cohort Study.","authors":"Isabel Oliveira Bierhals, Luciana Tovo-Rodrigues, Alicia Matijasevich, Iná S Santos","doi":"10.1007/s11657-025-01574-9","DOIUrl":null,"url":null,"abstract":"<p><p>Osteoporosis in adulthood often originates in early life, and some forms can be prevented through appropriate attention to bone health during the neonatal period and childhood, particularly in cases involving preterm infants or with intrauterine growth restriction.</p><p><strong>Purpose: </strong>To test the association of gestational age and intrauterine growth with bone mass in adolescents.</p><p><strong>Methods: </strong>With data from the 2004 Pelotas Birth Cohort, the outcomes density (aBMD) and content (BMC) were obtained by dual-energy X-ray absorptiometry, measured at 15 years. The exposures of interest were: prematurity (< 37 weeks of gestation), gestational age (≤ 36, 37-41, and ≥ 42 weeks) and intrauterine growth (small - SGA, appropriate - AGA or large for gestational age - LGA). Linear regression stratified by sex was run. Exclusive breastfeeding at 3 months was tested as an effect modifier.</p><p><strong>Results: </strong>One thousand four hundred ninety-four participants were included. In full adjusted model, including adolescent's height, preterm females had lower aBMD femoral neck than the full-term (β - 0.04 g/cm<sup>2</sup>; 95% CI - 0.07; - 0.01; p = 0.012) and those born with ≥ 42 weeks of gestation (β - 0.07 g/cm<sup>2</sup>; 95% CI - 0.13; - 0.01; p = 0.026). Males born with ≤ 36 and 37-41 weeks of gestation presented less BMC femoral neck than those born with ≥ 42 weeks (β - 0.8 g; 95% CI - 1.4; - 0.2 and β - 0.8 g; 95% CI - 1.4; - 0.2, respectively). LGA females presented approximately 100 g more in the whole-body BMC (β 97.3 g; 95% CI 20.5; 174.1; p = 0.022) than AGA females. SGA females who received exclusive breastfeeding at 3 months presented higher BMD (lumbar spine and femoral neck) and BMC than those who did not receive exclusive breastfeeding.</p><p><strong>Conclusion: </strong>Even the adolescence phase can be impaired due to premature birth and intrauterine growth restriction.</p>","PeriodicalId":8283,"journal":{"name":"Archives of Osteoporosis","volume":"20 1","pages":"89"},"PeriodicalIF":3.1000,"publicationDate":"2025-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Osteoporosis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11657-025-01574-9","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Osteoporosis in adulthood often originates in early life, and some forms can be prevented through appropriate attention to bone health during the neonatal period and childhood, particularly in cases involving preterm infants or with intrauterine growth restriction.

Purpose: To test the association of gestational age and intrauterine growth with bone mass in adolescents.

Methods: With data from the 2004 Pelotas Birth Cohort, the outcomes density (aBMD) and content (BMC) were obtained by dual-energy X-ray absorptiometry, measured at 15 years. The exposures of interest were: prematurity (< 37 weeks of gestation), gestational age (≤ 36, 37-41, and ≥ 42 weeks) and intrauterine growth (small - SGA, appropriate - AGA or large for gestational age - LGA). Linear regression stratified by sex was run. Exclusive breastfeeding at 3 months was tested as an effect modifier.

Results: One thousand four hundred ninety-four participants were included. In full adjusted model, including adolescent's height, preterm females had lower aBMD femoral neck than the full-term (β - 0.04 g/cm2; 95% CI - 0.07; - 0.01; p = 0.012) and those born with ≥ 42 weeks of gestation (β - 0.07 g/cm2; 95% CI - 0.13; - 0.01; p = 0.026). Males born with ≤ 36 and 37-41 weeks of gestation presented less BMC femoral neck than those born with ≥ 42 weeks (β - 0.8 g; 95% CI - 1.4; - 0.2 and β - 0.8 g; 95% CI - 1.4; - 0.2, respectively). LGA females presented approximately 100 g more in the whole-body BMC (β 97.3 g; 95% CI 20.5; 174.1; p = 0.022) than AGA females. SGA females who received exclusive breastfeeding at 3 months presented higher BMD (lumbar spine and femoral neck) and BMC than those who did not receive exclusive breastfeeding.

Conclusion: Even the adolescence phase can be impaired due to premature birth and intrauterine growth restriction.

胎龄和宫内生长对青少年骨量的影响:来自巴西出生队列研究的发现。
成年期骨质疏松症往往起源于生命早期,有些形式可以通过在新生儿期和儿童期适当注意骨骼健康来预防,特别是在早产儿或宫内生长受限的情况下。目的:探讨胎龄、宫内生长与青少年骨量的关系。方法:利用2004年Pelotas出生队列的数据,采用双能x线吸收仪测定15岁时的结果密度(aBMD)和含量(BMC)。感兴趣的暴露是:早产(结果:包括1494名参与者。在全校正模型中,包括青少年身高,早产女性股骨颈aBMD低于足月(β - 0.04 g/cm2;95% ci - 0.07; - 0.01;P = 0.012)和妊娠≥42周出生者(β - 0.07 g/cm2;95% ci - 0.13; - 0.01;p = 0.026)。妊娠≤36周和37-41周出生的男性BMC股骨颈少于妊娠≥42周出生的男性(β - 0.8 g;95% CI - 1.4, - 0.2和β - 0.8 g;95% CI分别为- 1.4和- 0.2)。LGA雌性小鼠全身BMC增加约100 g (β 97.3 g;95% ci 20.5;174.1;p = 0.022)。在3个月时接受纯母乳喂养的SGA女性的BMD(腰椎和股骨颈)和BMC高于未接受纯母乳喂养的女性。结论:早产和宫内发育限制也可影响青春期发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Archives of Osteoporosis
Archives of Osteoporosis ENDOCRINOLOGY & METABOLISMORTHOPEDICS -ORTHOPEDICS
CiteScore
5.50
自引率
10.00%
发文量
133
期刊介绍: Archives of Osteoporosis is an international multidisciplinary journal which is a joint initiative of the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA. The journal will highlight the specificities of different regions around the world concerning epidemiology, reference values for bone density and bone metabolism, as well as clinical aspects of osteoporosis and other bone diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信