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细胞色素P450氧化还原酶缺乏症伴安特利-比克斯勒综合征:类固醇生成能力

Cytochrome P450 oxidoreductase deficiency with Antley-Bixler syndrome: steroidogenic capacities.

作者信息

Iijima Shigeo, Ohishi Akira, Ohzeki Takehiko

机构信息

Department of Pediatrics, Hamamatsu University School of Medicine, Japan.

出版信息

J Pediatr Endocrinol Metab. 2009 May;22(5):469-75. doi: 10.1515/jpem.2009.22.5.469.

Abstract

For patients with cytochrome P450 oxidoreductase deficiency (PORD), steroid replacement is recommended at times of stress. However, it is unknown how hormones respond to actual physical stress in these patients. We report a female infant with PORD accompanied by the Antley-Bixler syndrome phenotype. Her urinary steroid profile revealed defective CYP17A1 and CYP21A2 activities, and an adrenocorticotropin (ACTH) stimulation test showed potential adrenal insufficiency. Hormonal responses to actual physical stress were as follows: Vigorous crying during blood sampling rarely affected the serum cortisol level. Acute viral gastroenteritis led to marked increases in blood ACTH and 17alpha-hydroxyprogesterone levels in proportion to the severity of the illness. The serum cortisol level also responded to this stress, but the response might have been blunted. Regarding peri-operative steroid replacement, intravenous hydrocortisone administration even at a dose of 6 mg/kg, which is lower than that recommended for congenital adrenal hyperplasia in Japan, proved to be excessive.

摘要

对于细胞色素P450氧化还原酶缺乏症(PORD)患者,建议在应激状态时进行类固醇替代治疗。然而,这些患者体内激素如何应对实际的身体应激尚不清楚。我们报告了一名患有PORD并伴有安特利-比克斯勒综合征表型的女婴。她的尿类固醇谱显示CYP17A1和CYP21A2活性存在缺陷,促肾上腺皮质激素(ACTH)刺激试验显示可能存在肾上腺功能不全。对实际身体应激的激素反应如下:采血时剧烈哭闹很少影响血清皮质醇水平。急性病毒性肠胃炎导致血液中ACTH和17α-羟孕酮水平随疾病严重程度显著升高。血清皮质醇水平也对这种应激产生反应,但反应可能有所减弱。关于围手术期类固醇替代治疗,即使静脉注射氢化可的松的剂量为6mg/kg(低于日本针对先天性肾上腺皮质增生症推荐的剂量),也被证明过量了。

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