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21-羟化酶缺乏症患者的肥胖问题。

Obesity in 21-hydroxylase deficient patients.

作者信息

Cornean R E, Hindmarsh P C, Brook C G

机构信息

London Centre for Paediatric Endocrinology, Middlesex Hospital, London.

出版信息

Arch Dis Child. 1998 Mar;78(3):261-3. doi: 10.1136/adc.78.3.261.

DOI:10.1136/adc.78.3.261
PMID:9613359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1717507/
Abstract

OBJECTIVES

To evaluate the natural history and timing of adiposity rebound (nadir of body mass index (BMI)) in children with congenital adrenal hyperplasia 21-hydroxylase deficiency (CYP21).

STUDY DESIGN

A retrospective mixed longitudinal study.

METHODS

Height and changes in body composition (BMI; weight (kg)/height2 (m)), triceps and subscapular skinfolds) were analysed in 22 (14 girls, eight boys) prepubertal patients with CYP21 for whom continuous anthropometric data were available for at least seven years. BMI and height SD scores were compared at 1, 5, and 10 years of age. Skinfold SD scores were compared at 2.5 and 5.5 years. Thirteen children (nine girls, four boys) had records available from birth which allowed the estimation of the age at adiposity "peak" and "rebound".

RESULTS

A significant increase in BMI SD score was found at 5 and 10 years compared with those at 1 year. No significant change in height SD score was observed at these ages. Triceps and skinfold SD score were increased significantly at 5.5 compared with 2.5 years. The "rebound" in BMI SD score took place at 1.74 years (range 0.71-4.57) compared with 5.5 years (range 3.5-7.0) in the normal UK populations.

CONCLUSIONS

Normally growing patients with CYP21 increased their BMI throughout childhood. Adiposity rebound took place on average three years earlier than in the general population. These findings suggest that even when well controlled in terms of their disease process, patients with CYP21 are at risk of obesity, which may have important implications for the evolution of reproductive function (polycystic ovaries), diabetes, hypertension, and cardiovascular disease in these subjects.

摘要

目的

评估先天性肾上腺皮质增生21-羟化酶缺乏症(CYP21)患儿肥胖反弹(体重指数(BMI)最低点)的自然病程及时间。

研究设计

一项回顾性混合纵向研究。

方法

对22例(14例女孩,8例男孩)青春期前CYP21患儿的身高及身体成分变化(BMI;体重(kg)/身高²(m))、肱三头肌和肩胛下皮褶厚度)进行分析,这些患儿至少有连续7年的人体测量数据。比较1岁、5岁和10岁时的BMI和身高标准差分数。比较2.5岁和5.5岁时的皮褶厚度标准差分数。13名儿童(9例女孩,4例男孩)有从出生开始的记录,这使得能够估计肥胖“峰值”和“反弹”的年龄。

结果

与1岁时相比,5岁和10岁时BMI标准差分数显著增加。在这些年龄未观察到身高标准差分数有显著变化。与2.5岁时相比,5.5岁时肱三头肌和皮褶厚度标准差分数显著增加。BMI标准差分数的“反弹”发生在1.74岁(范围0.71 - 4.57),而在英国正常人群中为5.5岁(范围3.5 - 7.0)。

结论

正常生长的CYP21患儿在整个儿童期BMI增加。肥胖反弹平均比一般人群早三年发生。这些发现表明,即使在疾病过程方面得到良好控制,CYP21患儿仍有肥胖风险,这可能对这些受试者生殖功能(多囊卵巢)、糖尿病、高血压和心血管疾病的发展具有重要影响。

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