Changes in body proportions and body fat content in GH-deficient and non-GH-deficient children during the first year of growth hormone treatment.

IF 0.4 4区 社会学 Q3 ANTHROPOLOGY Anthropologischer Anzeiger Pub Date : 2024-06-24 DOI:10.1127/anthranz/2024/1763
Anna Majcher, Małgorzata Rumińska, Ewelina Witkowska-Sędek, Monika Paluchowska, Maria Krajewska, Dorota Artemniak-Wojtowicz, Beata Pyrżak
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Abstract

Introduction: The growth hormone/insulin-like growth factor-1 axis (GH/IGF-1) is crucial for longitudinal bone growth and exerts several metabolic effects. It is debatable whether and how the recombinant human growth hormone (rhGH) treatment affects the trunk-limb proportions. Aim of the study: We aim to evaluate the changes in body proportions and body fat content in short children with growth hormone deficiency (GHD), children born small for gestational age (SGA), and girls with Turner syndrome (TS) during the first year of rhGH therapy. Material and methods: The data of 70 children with GHD, 40 children born SGA, and 36 girls with TS from 1998 to 2019 were analyzed. The following parameters were measured: height, body weight, sitting height, and two skinfolds on the arm above the triceps brachii and below the scapula at the beginning of rhGH therapy and after the first year of treatment. Sitting height and lower limb length were presented as percentages (%) of body height. Fat mass percentage (%FAT) was calculated using the Slaughter formula. Results: At the beginning of rhGH, TS girls had the greatest height deficit (-2.7 SDS), the highest sitting height (%), and the lowest lower limb length (%) compared to children with GHD and children born SGA. Moreover, TS girls had higher body weight SDS, BMI SDS compared to SGA children (p < 0.001), and higher %FAT compared to both GHD and SGA children (p < 0.001 for both). After the first year of rhGH therapy, a significant increase in lower limb share (%) and a decrease in %FAT were observed in all the study groups. TS girls still had significantly higher sitting height (%), shorter lower limbs (%), and higher %FAT, body weight SDS, and BMI SDS compared to children with GHD and children born SGA (p < 0.05 for all variables). Conclusions: Our results show that rhGH treatment could increase lower limb length in relation to height and reduce fat mass in treated children. Girls with TS had the largest baseline body disproportions and the highest body fat content. Despite a satisfactory reduction in height deficit, after the first year of rhGH therapy, these girls had still higher body weight SDS, BMI SDS, %FAT, the highest sitting height (%), and the lowest lower limb length (%) compared to children with GHD and born SGA.

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生长激素缺乏症和非生长激素缺乏症儿童在接受生长激素治疗第一年期间身体比例和体内脂肪含量的变化。
简介生长激素/胰岛素样生长因子-1轴(GH/IGF-1)对骨骼纵向生长至关重要,并具有多种代谢作用。重组人生长激素(rhGH)治疗是否会影响躯干与四肢的比例,以及如何影响躯干与四肢的比例,目前还存在争议。研究目的我们旨在评估生长激素缺乏症(GHD)矮小儿童、小于胎龄儿(SGA)儿童和特纳综合征(TS)女孩在接受rhGH治疗第一年期间身体比例和体内脂肪含量的变化。材料与方法分析了 1998 年至 2019 年期间 70 名 GHD 儿童、40 名 SGA 出生儿童和 36 名 TS 女孩的数据。在开始接受rhGH治疗时和治疗第一年后,测量了以下参数:身高、体重、坐高以及手臂肱三头肌上方和肩胛骨下方的两个皮褶。坐高和下肢长度以身高的百分比(%)表示。脂肪质量百分比(%FAT)用斯莱特公式计算。结果与GHD儿童和SGA儿童相比,在开始接受rhGH治疗时,TS女孩的身高缺陷最大(-2.7 SDS),坐高(%)最高,下肢长度(%)最低。此外,与SGA儿童相比,TS女孩的体重SDS和BMI SDS更高(p < 0.001),与GHD和SGA儿童相比,TS女孩的脂肪率更高(p < 0.001)。在接受rhGH治疗的第一年后,所有研究组的下肢占地面积(%)都有显著增加,脂肪率则有所下降。与 GHD 儿童和 SGA 出生儿童相比,TS 女孩的坐高(%)、下肢短(%)、脂肪率、体重 SDS 和 BMI SDS 仍明显较高(所有变量的 p < 0.05)。结论我们的研究结果表明,rhGH治疗可增加接受治疗儿童的下肢长度与身高的关系,并减少脂肪量。患有TS的女孩身体比例基线最大,体内脂肪含量最高。尽管身高缺陷有了令人满意的减少,但在接受rhGH治疗的第一年后,这些女孩的体重SDS、BMI SDS、脂肪%、最高坐高(%)和最低下肢长度(%)仍高于GHD和SGA患儿。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
34
期刊介绍: AA is an international journal of human biology. It publishes original research papers on all fields of human biological research, that is, on all aspects, theoretical and practical of studies of human variability, including application of molecular methods and their tangents to cultural and social anthropology. Other than research papers, AA invites the submission of case studies, reviews, technical notes and short reports. AA is available online, papers must be submitted online to ensure rapid review and publication.
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