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Birth Weight in Different Etiologies of Disorders of Sex Development.

Authors :
Poyrazoglu S
Darendeliler F
Ahmed SF
Hughes I
Bryce J
Jiang J
Rodie M
Hiort O
Hannema SE
Bertelloni S
Lisa L
Guran T
Cools M
Desloovere A
Claahsen-van der Grinten HL
Nordenstrom A
Holterhus PM
Kohler B
Niedziela M
Krone N
Source :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2017 Mar 01; Vol. 102 (3), pp. 1044-1050.
Publication Year :
2017

Abstract

Context: It is well established that boys are heavier than girls at birth. Although the cause of birth weight (BW) difference is unknown, it has been proposed that it could be generated from prenatal androgen action.<br />Objective: The aim of the current study was to determine the BW of children with disorders of sex development (DSD) of different etiologies and to evaluate the effects of androgen action on BW.<br />Methods: Data regarding diagnosis, BW, gestational age, karyotype, and concomitant conditions were collected from the International Disorders of Sex Development (I-DSD) Registry (www.i-dsd). BW standard deviation score was calculated according to gestational age. Cases were evaluated according to disorder classification in I-DSD (i.e., disorders of gonadal development, androgen excess, androgen synthesis, androgen action, nonspecific disorder of undermasculinization groups, and Leydig cell defect).<br />Results: A total of 533 cases were available; 400 (75%) cases were 46,XY, and 133 (25%) cases were 46,XX. Eighty cases (15%) were born small for gestational age (SGA). Frequency of SGA was higher in the 46,XY group (17.8%) than in the 46,XX (6.7%) group (P = 0.001). Mean BW standard deviation scores of cases with androgen excess and androgen deficiency [in disorders of gonadal development, androgen synthesis, and Leydig cell defect groups and androgen receptor gene (AR) mutation-positive cases in disorders of androgen action groups] were similar to normal children with the same karyotype. SGA birth frequency was higher in the AR mutation-negative cases in disorders of androgen action group and in the nonspecific disorders of the undermasculinization group.<br />Conclusions: BW dimorphism is unlikely to be explained by fetal androgen action per se. 46,XY DSDs due to nonspecific disorders of undermasculinization are more frequently associated with fetal growth restriction, SGA, and concomitant conditions.<br /> (Copyright © 2017 by the Endocrine Society)

Details

Language :
English
ISSN :
1945-7197
Volume :
102
Issue :
3
Database :
MEDLINE
Journal :
The Journal of clinical endocrinology and metabolism
Publication Type :
Academic Journal
Accession number :
28359094
Full Text :
https://doi.org/10.1210/jc.2016-3460