Hormonal disturbances due to severe and mild forms of congenital adrenal hyperplasia are already detectable in neonatal life. (17th November 2014)
- Record Type:
- Journal Article
- Title:
- Hormonal disturbances due to severe and mild forms of congenital adrenal hyperplasia are already detectable in neonatal life. (17th November 2014)
- Main Title:
- Hormonal disturbances due to severe and mild forms of congenital adrenal hyperplasia are already detectable in neonatal life
- Authors:
- Faurschou, Signe
Mouritsen, Annette
Johannsen, Trine H.
Hougaard, David M.
Cohen, Arieh
Duno, Morten
Juul, Anders
Main, Katharina M. - Abstract:
- <abstract abstract-type="main" id="apa12835-abs-0001"> <title>Abstract</title> <sec id="apa12835-sec-0001" sec-type="section"> <title>Aim</title> <p>National screening programmes for congenital adrenal hyperplasia now include measuring several adrenal metabolites using highly sensitive liquid chromatography–tandem mass spectrometry. The aim of this study was to compare neonatal hormonal profiles – whole blood concentrations of 17<italic>α</italic>‐hydroxyprogesterone, androstenedione, and cortisol – with genotypes in 21‐hydroxylase deficiency.</p> </sec> <sec id="apa12835-sec-0002" sec-type="section"> <title>Methods</title> <p>The study included 62 patients with congenital adrenal hyperplasia born between 1982 and 2012 and 61 random controls born in 1985 and 2005. Patients were grouped according to mutation‐based predictions of enzyme impairment. Groups Null and A were salt‐wasting (n = 35), Group B was simple virilising (n = 7) and Group C was nonclassic (n = 20). Dried blood spot samples were retrieved from the Danish Neonatal Screening Biobank.</p> </sec> <sec id="apa12835-sec-0003" sec-type="section"> <title>Results</title> <p>All patients with molecular verified 21‐hydroxylase deficiency had significantly higher concentrations of 17<italic>α</italic>‐hydroxyprogesterone (p &lt; 0.001), androstenedione (p &lt; 0.001) and a higher ratio [(17<italic>α</italic>‐hydroxyprogesterone + androstenedione)/cortisol, p &lt; 0.05] than controls. Androstenedione showed a higher<abstract abstract-type="main" id="apa12835-abs-0001"> <title>Abstract</title> <sec id="apa12835-sec-0001" sec-type="section"> <title>Aim</title> <p>National screening programmes for congenital adrenal hyperplasia now include measuring several adrenal metabolites using highly sensitive liquid chromatography–tandem mass spectrometry. The aim of this study was to compare neonatal hormonal profiles – whole blood concentrations of 17<italic>α</italic>‐hydroxyprogesterone, androstenedione, and cortisol – with genotypes in 21‐hydroxylase deficiency.</p> </sec> <sec id="apa12835-sec-0002" sec-type="section"> <title>Methods</title> <p>The study included 62 patients with congenital adrenal hyperplasia born between 1982 and 2012 and 61 random controls born in 1985 and 2005. Patients were grouped according to mutation‐based predictions of enzyme impairment. Groups Null and A were salt‐wasting (n = 35), Group B was simple virilising (n = 7) and Group C was nonclassic (n = 20). Dried blood spot samples were retrieved from the Danish Neonatal Screening Biobank.</p> </sec> <sec id="apa12835-sec-0003" sec-type="section"> <title>Results</title> <p>All patients with molecular verified 21‐hydroxylase deficiency had significantly higher concentrations of 17<italic>α</italic>‐hydroxyprogesterone (p &lt; 0.001), androstenedione (p &lt; 0.001) and a higher ratio [(17<italic>α</italic>‐hydroxyprogesterone + androstenedione)/cortisol, p &lt; 0.05] than controls. Androstenedione showed a higher sensitivity (72%) than 17<italic>α</italic>‐hydroxyprogesterone (12%) to correctly identify Groups B and C.</p> </sec> <sec id="apa12835-sec-0004" sec-type="section"> <title>Conclusion</title> <p>There were significant differences in neonatal hormonal profiles between all groups and controls. This confirms that hormonal disturbances are already detectable in both severe and mild forms of congenital adrenal hyperplasia in neonatal life.</p> </sec> </abstract> … (more)
- Is Part Of:
- Acta pædiatrica. Volume 104:Number 2(2015:Feb.)
- Journal:
- Acta pædiatrica
- Issue:
- Volume 104:Number 2(2015:Feb.)
- Issue Display:
- Volume 104, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 104
- Issue:
- 2
- Issue Sort Value:
- 2015-0104-0002-0000
- Page Start:
- e57
- Page End:
- e62
- Publication Date:
- 2014-11-17
- Subjects:
- Pediatrics -- Periodicals
Pediatrics
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1651-2227 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apa.12835 ↗
- Languages:
- English
- ISSNs:
- 0803-5253
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0642.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3668.xml