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Associations of growth from birth to puberty with glycemic indicators at ~17.5?years: Evidence from Hong Kong's “Children of 1997” birth cohort

机译:生长从出生于血糖指标的生长〜17.5〜17.5?年:来自香港“1997年儿童”出生队列的证据

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摘要

Background From an evolutionary biology perspective, where growth and reproduction trade‐off against longevity, we assessed the associations of growth from birth to puberty by phase with later glycemic indicators and any differences by sex. Methods In the population‐representative Hong Kong Chinese “Children of 1997” birth cohort (n?=?8327), the relation of initial size (weight‐for‐age z score (WAZ) at birth, length/height‐for‐age z score (LAZ) at 3?months or body‐mass‐index‐for‐age z score (BAZ) at 3?months based on the World Health Organization growth standards/references) and growth at different phases (WAZ gains from 0 to 2 and 2 to 8?years, LAZ or BAZ gains from 3?months to 3?years, 3 to 8?years and 8 to 14 years) with fasting plasma glucose (FPG) and glycated hemoglobin (HbA1c) at ~17.5?years, was assessed using adjusted partial least squares regression. Additional analyses further considered growth in late and early infancy. Results This study included 3276 of the cohort participants. Higher WAZ gain from 2 to 8?years, LAZ and BAZ gains from 3 to 8?years were consistently associated with higher FPG, adjusted for maternal and infant characteristics, family history of diabetes and household income. Also, higher BAZ gain from 3 to 8?years was associated with higher HbA1c. These associations did not differ by sex. Conclusions Our findings suggest different mechanisms could underlie the pathogenesis of glucose intolerance. Factors that drive specific growth at different phases need to be evaluated to better inform child growth management for long‐term health outcomes.
机译:背景从进化生物学的角度来看,在生长和繁殖权衡对寿命的影响,我们通过后期血糖指标和性别的任何差异评估了生长到青春期的生长和任何差异。方法在人口代表香港中文“1997年儿童”出生队列(N?=?8327),初始大小的关系(出生时的重量Z分数(WAZ),长度/较高Z基于世界卫生组织增长标准/参考资金的3个月或体重指数Z分数(BAZ)的比分(LAZ),以及不同阶段的增长(WAZ从0到年,Laz或Baz从3个月到3个月,3岁,3至8年和8至14岁),用空腹血糖(FPG)和糖化血红蛋白(HBA1c)在〜17.5?年,使用调整后的部分最小二乘来评估。额外的分析进一步考虑了晚期和早期婴儿期的增长。结果本研究包括3276个群组参与者。从2到8的更高的Waz收益?多年来,Laz和Baz收益从3到8岁到8年始终与更高的FPG相关,适用于孕产妇和婴儿特征,糖尿病和家庭收入的家族史。此外,较高的BAZ收益从3到8岁以下与HBA1C相关联。这些协会的性别没有差异。结论我们的研究结果表明不同的机制可以利于葡萄糖不耐受的发病机制。需要评估推动不同阶段特定增长的因素,以便更好地为长期健康结果提供儿童增长管理。

著录项

  • 来源
    《Pediatric diabetes.》 |2019年第4期|共9页
  • 作者单位

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

    School of Public Health Li Ka Shing Faculty of MedicineThe University of Hong KongHong Kong SAR;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
  • 关键词

    BMI; fasting plasma glucose; HbA1c; length/height; weight;

    机译:BMI;禁食等离子体葡萄糖;HBA1c;长度/高度;重量;

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