Clinical indications for the use of urinary steroid profiles in neonates and children

被引:24
作者
Honour, JW [1 ]
Brook, CGD [1 ]
机构
[1] UCL, SCH MED, MIDDLESEX HOSP, DEPT MED, LONDON W1N 8AA, ENGLAND
关键词
gas chromatography; congenital adrenal hyperplasia; electrolyte balance; adrenal function;
D O I
10.1177/000456329703400107
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
For a number of rare adrenal disorders, some of which are life threatening in childhood, laboratories need access to specialist endocrine investigations. Measurements of hormones in blood samples may be diagnostic in some cases but not all of the requisite steroid hormone assays are available. Multiple plasma steroid measurements may be required to prove the nature of a steroid biosynthetic disorder but in newborn children immunoassays, performed without prior solvent extraction, can be misleading. A urine steroid profile by gas chromatography coupled with mass spectrometry examines many steroid metabolites simultaneously and provides specific diagnostic information. A urine steroid profile can provide precise information of the secretory nature of tumours and causes of virilization, salt loss and hypertension often from a spot urine sample rather than a 24h collection. However, a steroid profile is not helpful in making a diagnosis in neonatal genetic males with poorly developed genitalia.
引用
收藏
页码:45 / 54
页数:10
相关论文
共 37 条
[31]   A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families [J].
Strautnieks, SS ;
Thompson, RJ ;
Gardiner, RM ;
Chung, E .
NATURE GENETICS, 1996, 13 (02) :248-250
[32]   SYNDROME OF APPARENT MINERALOCORTICOID EXCESS ASSOCIATED WITH DEFECTS IN THE PERIPHERAL METABOLISM OF CORTISOL [J].
ULICK, S ;
LEVINE, LS ;
GUNCZLER, P ;
ZANCONATO, G ;
RAMIREZ, LC ;
RAUH, W ;
ROSLER, A ;
BRADLOW, HL ;
NEW, MI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1979, 49 (05) :757-766
[33]   NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA - A PROGRAM BASED ON A NOVEL DIRECT RADIOIMMUNOASSAY FOR 17-HYDROXYPROGESTERONE IN BLOOD SPOTS [J].
WALLACE, AM ;
BEASTALL, GH ;
COOK, B ;
CURRIE, AJ ;
ROSS, AM ;
KENNEDY, R ;
GIRDWOOD, RWA .
JOURNAL OF ENDOCRINOLOGY, 1986, 108 (02) :299-308
[34]   ADRENAL STATUS DURING THE 1ST MONTH OF LIFE IN MATURE AND PREMATURE HUMAN INFANTS [J].
WALLACE, AM ;
BEESLEY, J ;
THOMSON, M ;
GILES, CA ;
ROSS, AM ;
TAYLOR, NF .
JOURNAL OF ENDOCRINOLOGY, 1987, 112 (03) :473-480
[35]  
WONG T, 1992, CLIN CHEM, V38, P1830
[36]   17-ALPHA-HYDROXYLASE 17,20-LYASE DEFICIENCY - FROM CLINICAL INVESTIGATION TO MOLECULAR DEFINITION [J].
YANASE, T ;
SIMPSON, ER ;
WATERMAN, MR .
ENDOCRINE REVIEWS, 1991, 12 (01) :91-108
[37]   NO EVIDENCE OF MUTATIONS IN THE GENES FOR TYPE-I AND TYPE-II 3-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) IN NONCLASSICAL 3-BETA-HSD DEFICIENCY [J].
ZERAH, M ;
RHEAUME, E ;
MANI, P ;
SCHRAM, P ;
SIMARD, J ;
LABRIE, F ;
NEW, MI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (06) :1811-1817