Increased Number of Sex Chromosomes Affects Height in a Nonlinear Fashion: A Study of 305 Patients With Sex Chromosome Aneuploidy

被引:134
作者
Ottesen, Anne Marie [1 ]
Aksglaede, Lise [1 ]
Garn, Inger [1 ]
Tartaglia, Nicole [2 ]
Tassone, Flora [3 ]
Gravholt, Claus H. [4 ]
Bojesen, Anders [5 ]
Sorensen, Kaspar [1 ]
Jorgensen, Niels [1 ]
Meyts, Ewa Rajpert-De [1 ]
Gerdes, Tommy [6 ]
Lind, Anne-Marie [6 ]
Kjaergaard, Susanne [6 ]
Juul, Anders [1 ]
机构
[1] Rigshosp, Univ Dept Growth & Reprod, DK-2100 Copenhagen O, Denmark
[2] Univ Colorado, Sch Med, Childrens Hosp, Child Dev Unit, Aurora, CO USA
[3] Univ Calif Davis, Dept Biochem & Mol Med, Davis, CA 95616 USA
[4] Aarhus Univ Hosp, Med Dept Endocrinol & Diabet M, DK-8000 Aarhus, Denmark
[5] Vejle Hosp, Dept Clin Genet, Vejle, Denmark
[6] Rigshosp, Univ Dept Clin Genet, DK-2100 Copenhagen O, Denmark
基金
英国医学研究理事会;
关键词
Klinefelter syndrome; SHOX copy number; tall stature; X and Y chromosomes; XXY; LERI-WEILL DYSCHONDROSTEOSIS; SHORT STATURE; KLINEFELTERS-SYNDROME; Y-CHROMOSOME; GENE SHOX; GROWTH; REGION; DELETION; PHENOTYPES; FEATURES;
D O I
10.1002/ajmg.a.33334
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tall stature and eunuchoid body proportions characterize patients with 47,XXY Klinefelter syndrome, whereas patients with 45,X Turner syndrome are characterized by impaired growth. Growth is relatively well characterized in these two syndromes, while few studies describe the growth of patients with higher grade sex chromosome aneuploidies. It has been proposed that tall stature in sex chromosome aneuploidy is related to an overexpression of SHOX, although the copy number of SHOX has not been evaluated in previous studies. Our aims were therefore: (1) to assess stature in 305 patients with sex chromosome aneuploidy and (2) to determine the number of SHOX copies in a subgroup of these patients (n = 255) these patients and 74 healthy controls. Median height standard deviation scores in 46,XX males (n = 6) were -1.2 (-2.8 to 0.3), +0.9 (-2.2 to +4.6) in 47,XXY (n = 129), +1.3 (-1.8 to +4.9) in 47,XYY (n = 44), +1.1 (-1.9 to +3.4) in 48,XXYY (n = 45), +1.8 (-2.0 to +3.2) in 48,XXXY (n = 9), and -1.8 (-4.2 to -0.1) in 49,XXXXY (n = 10). Median height standard deviation scores in patients with 45,X (n = 6) were -2.6 (-4.1 to -1.6), +0.7 (-0.9 to +3.2) in 47,XXX (n = 40), -0.6 (-1.9 to +2.1) in 48,XXXX (n = 13), and -1.0 (-3.5 to -0.8) in 49,XXXXX (n = 3). Height increased with an increasing number of extra X or Y chromosomes, except in males with five, and in females with four or five sex chromosomes, consistent with a nonlinear effect on height. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1206 / 1212
页数:7
相关论文
共 29 条
[11]   Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome [J].
Kirsch, S ;
Weiss, B ;
Zumbach, K ;
Rappold, G .
HUMAN GENETICS, 2004, 114 (02) :173-181
[12]  
LINDEN MG, 1995, PEDIATRICS, V96, P672
[13]   The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes [J].
Marchini, A ;
Marttila, T ;
Winter, A ;
Caldeira, S ;
Malanchi, I ;
Blaschke, RJ ;
Häcker, B ;
Rao, E ;
Karperien, M ;
Wit, JM ;
Richter, W ;
Tommasino, M ;
Rappold, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (35) :37103-37114
[14]   BNP is a transcriptional target of the short stature homeobox gene SHOX [J].
Marchini, Antonio ;
Haecker, Beate ;
Marttila, Tiina ;
Hesse, Volker ;
Emons, Joyce ;
Weiss, Birgit ;
Karperien, Marcel ;
Rappold, Gudrun .
HUMAN MOLECULAR GENETICS, 2007, 16 (24) :3081-3087
[15]   SHOX haploinsufficiency and overdosage:: impact of gonadal function status [J].
Ogata, T ;
Matsuo, N ;
Nishimura, G .
JOURNAL OF MEDICAL GENETICS, 2001, 38 (01) :1-6
[16]   A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene [J].
Ottesen, A. M. ;
Garn, I. D. ;
Aksglaede, L. ;
Juul, A. ;
Meyts, E. Rajpert-De .
MOLECULAR HUMAN REPRODUCTION, 2007, 13 (10) :745-750
[17]   49,XXXXY: a distinct phenotype. Three new cases and review [J].
Peet, J ;
Weaver, DD ;
Vance, GH .
JOURNAL OF MEDICAL GENETICS, 1998, 35 (05) :420-424
[18]   FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes [J].
Rao, E ;
Weiss, B ;
Fukami, M ;
Mertz, A ;
Meder, J ;
Ogata, T ;
Heinrich, U ;
GarciaHeras, J ;
Schiebel, K ;
Rappold, GA .
HUMAN GENETICS, 1997, 100 (02) :236-239
[19]   Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome [J].
Rao, E ;
Weiss, B ;
Fukami, M ;
Rump, A ;
Niesler, B ;
Mertz, A ;
Muroya, K ;
Binder, G ;
Kirsch, S ;
Winkelmann, M ;
Nordsiek, G ;
Heinrich, U ;
Breuning, MH ;
Ranke, MB ;
Rosenthal, A ;
Ogata, T ;
Rappold, GA .
NATURE GENETICS, 1997, 16 (01) :54-63
[20]   THE PSEUDOAUTOSOMAL REGIONS OF THE HUMAN SEX-CHROMOSOMES [J].
RAPPOLD, GA .
HUMAN GENETICS, 1993, 92 (04) :315-324