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肥胖和家族易感性是导致先天性肾上腺皮质增生症年轻患者代谢异常的重要决定因素。

Obesity and familial predisposition are significant determining factors of an adverse metabolic profile in young patients with congenital adrenal hyperplasia.

机构信息

Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular (LIM/42), Disciplina de Endocrinologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil.

出版信息

Horm Res Paediatr. 2013;80(2):111-8. doi: 10.1159/000353762. Epub 2013 Jul 31.

DOI:10.1159/000353762
PMID:23921174
Abstract

BACKGROUND/AIMS: Glucocorticoid (GC) therapy is known to predispose to an adverse metabolic profile. Therefore, we investigated the prevalence of obesity and metabolic syndrome (MetS) in young patients with congenital adrenal hyperplasia (CAH) and to correlate this prevalence with GC treatment and family history.

METHODS

The study population consisted of 33 young CAH patients who received cortisone acetate during their growth periods; those who were salt wasters also received fludrocortisone. Obesity was defined by a body mass index (BMI) >95th percentile and MetS by the National Cholesterol Education Program Third Adult Treatment Panel modified criteria. Each patient's familial history of MetS components was assessed. The impact of GC therapy on the metabolic profile was analyzed by comparing CAH patients with BMI z-score-matched controls.

RESULTS

MetS and obesity were observed in 12.1 and 30.3% of the CAH patients, respectively, both of which were higher than in the reference population. A positive family history of MetS was found to be more prevalent in the obese patients compared with the nonobese CAH patients, and similar findings were observed for the controls. The metabolic profile did not differ between the CAH patients and matched subjects.

CONCLUSION

CAH patients presented a higher prevalence of obesity and MetS, which were not correlated with the GC treatment. This study suggests that obesity and familial predisposition are significant determining factors for an adverse metabolic profile in CAH patients.

摘要

背景/目的:已知糖皮质激素(GC)治疗会导致不良的代谢特征。因此,我们调查了年轻先天性肾上腺增生症(CAH)患者中肥胖和代谢综合征(MetS)的患病率,并将其与 GC 治疗和家族史相关联。

方法

研究人群包括 33 名在生长期间接受醋酸可的松治疗的年轻 CAH 患者;那些盐耗者还接受氟氢可的松。肥胖定义为体重指数(BMI)>第 95 百分位数,代谢综合征采用国家胆固醇教育计划成人治疗专家组第三次修订标准。评估每位患者代谢综合征成分的家族史。通过比较 CAH 患者与 BMI z 分数匹配的对照组,分析 GC 治疗对代谢特征的影响。

结果

CAH 患者分别有 12.1%和 30.3%患有代谢综合征和肥胖症,均高于参考人群。与非肥胖 CAH 患者相比,肥胖患者的代谢综合征阳性家族史更为普遍,对照组也存在类似的发现。CAH 患者和匹配对象的代谢特征无差异。

结论

CAH 患者表现出更高的肥胖和代谢综合征患病率,与 GC 治疗无关。本研究表明,肥胖和家族易感性是 CAH 患者不良代谢特征的重要决定因素。

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