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体重在特发性性早熟发病和进展中的作用。

Role of Body Weight in the Onset and the Progression of Idiopathic Premature Pubarche.

机构信息

Pediatric Division, Department of Pediatrics, University Hospital of Verona, Verona, Italy,

Pediatric Division, Department of Pediatrics, University Hospital of Verona, Verona, Italy.

出版信息

Horm Res Paediatr. 2020;93(6):351-360. doi: 10.1159/000511873. Epub 2020 Dec 2.

Abstract

BACKGROUND

The term premature pubarche (PP) refers to the appearance of pubic hair before age 8 in girls and before age 9 in boys. Although idiopathic PP (often associated with premature adrenarche) is considered an extreme variation from the norm, it may be an initial sign of persistent hyperandrogenism. Factors contributing to PP onset and progression have not been identified to date.

AIMS

The objectives of this study are to describe a group of Italian children with PP, to identify potential factors for its onset, and to define its clinical and biochemical progression.

METHODS

We retrospectively enrolled all infants born between 2001 and 2014 with PP. Children with advanced bone age (BA) underwent functional tests to determine the cause of PP. Hormonal analysis and BA determination were performed annually during a 4-year follow-up period.

RESULTS

A total of 334 children with PP were identified: idiopathic PP (92.5%, associated with premature adrenarche in some cases); related to precocious puberty (6.6%); late-onset 21-hydroxylase deficiency (0.9%). Low birth weight was associated with premature adrenal activation. Body mass index (BMI) was the only factor that influenced the progression of BA during follow-up.

CONCLUSIONS

Low birth weight is a predisposing factor for premature adrenal activation. The increase in BMI in patients with idiopathic PP during the 4-years of follow-up was responsible for BA acceleration. We recommend prevention of excessive weight gain in children with PP and strict adherence to follow-up in order to prevent serious metabolic consequences.

摘要

背景

早熟性阴毛早现(PP)是指女孩在 8 岁之前、男孩在 9 岁之前出现阴毛。虽然特发性 PP(常与早熟性肾上腺功能初现相关)被认为是一种偏离常态的极端变异,但它可能是持续性高雄激素血症的初始迹象。迄今为止,尚未确定促成 PP 发病和进展的因素。

目的

本研究旨在描述一组患有 PP 的意大利儿童,确定其发病的潜在因素,并定义其临床和生化进展。

方法

我们回顾性纳入了 2001 年至 2014 年间出生的所有患有 PP 的婴儿。骨龄(BA)提前的患儿进行了功能检查以确定 PP 的病因。在 4 年的随访期间,每年进行激素分析和 BA 测定。

结果

共发现 334 例患有 PP 的儿童:特发性 PP(92.5%,在某些情况下与早熟性肾上腺功能初现相关);与性早熟有关(6.6%);迟发性 21-羟化酶缺乏症(0.9%)。低出生体重与过早的肾上腺激活有关。BMI 是随访期间影响 BA 进展的唯一因素。

结论

低出生体重是导致肾上腺过早激活的一个易感因素。特发性 PP 患儿在 4 年随访期间 BMI 的增加是 BA 加速的原因。我们建议预防 PP 患儿体重过度增加,并严格遵循随访,以防止出现严重的代谢后果。

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