Metabolic and cardiovascular risk factors in Klinefelter syndrome

被引:23
作者
Spaziani, Matteo [1 ,2 ]
Radicioni, Antonio F. [1 ,2 ]
机构
[1] Sapienza Univ Rome, Sect Med Pathophysiol Food Sci & Endocrinol, Dept Expt Med, Rome, Italy
[2] Policlin Umberto 1, Ctr Rare Dis, Rome, Italy
关键词
body composition; cardiovascular risk; Klinefelter syndrome; metabolic syndrome; visceral obesity; ENDOTHELIAL PROGENITOR CELLS; HORMONE-BINDING GLOBULIN; TESTOSTERONE TREATMENT; REPLACEMENT THERAPY; INSULIN-RESISTANCE; LEG ULCERS; YOUNG MAN; MEN; PHENOTYPE; HYPOGONADISM;
D O I
10.1002/ajmg.c.31792
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Klinefelter syndrome (KS), which normally presents with a 47,XXY karyotype, is the most common sex chromosome disorder in males. It is also the most common genetic cause of male infertility. KS subjects are typically tall, with small and firm testes, gynecomastia, broad hips, and sparse body hair, although a less evident presentation is also possible. KS is also characterized by a high prevalence of hypogonadism, metabolic syndrome (MetS) and cardiovascular disease. The aim of this article is to systematically review metabolic and the cardiovascular risk factors in KS patients. Hypogonadism has an important role in the pathogenesis of the changes in body composition (particularly visceral obesity) and hence of insulin resistance and MetS, but the association between KS and MetS may go beyond hypogonadism alone. From childhood, KS patients may show an increase in visceral fat with a reduction in lean body mass and an increase in glucose and impaired fat metabolism. Their increased incidence of congenital anomalies, epicardial adipose tissue, and thromboembolic disease suggests they have a higher risk of cardiovascular disease. There is conflicting evidence on the effects of testosterone therapy on body composition and metabolism.
引用
收藏
页码:334 / 343
页数:10
相关论文
共 78 条
[1]  
Abramsky L, 1997, PRENATAL DIAG, V17, P363, DOI 10.1002/(SICI)1097-0223(199704)17:4<363::AID-PD79>3.0.CO
[2]  
2-O
[3]  
Ahmed S, 2009, JCPSP-J COLL PHYSICI, V19, P520, DOI 08.2009/JCPSP.520522
[4]   Normal bone mineral content but unfavourable muscle/fat ratio in Klinefelter syndrome [J].
Aksglaede, L. ;
Molgaard, C. ;
Skakkebaek, N. E. ;
Juul, A. .
ARCHIVES OF DISEASE IN CHILDHOOD, 2008, 93 (01) :30-34
[5]   Left ventricular dysfunction in Klinefelter syndrome is associated to insulin resistance, abdominal adiposity and hypogonadism [J].
Andersen, N. H. ;
Bojesen, A. ;
Kristensen, K. ;
Birkebaek, N. H. ;
Fedder, J. ;
Bennett, P. ;
Christiansen, J. S. ;
Gravholt, C. H. .
CLINICAL ENDOCRINOLOGY, 2008, 69 (05) :785-791
[6]   Recurrent deep vein thrombosis and pulmonary embolism in a young man with Klinefelter's syndrome and heterozygous mutation of MTHFR-677C&gt;T and 1298A&gt;C [J].
Angel, Joel R. ;
Parker, Stacey ;
Sells, Ryan E. ;
Atallah, Ehab .
BLOOD COAGULATION & FIBRINOLYSIS, 2010, 21 (04) :372-375
[7]  
BECKER KL, 1972, FERTIL STERIL, V23, P568
[8]   Morbidity in Klinefelter syndrome:: A Danish register study based on hospital discharge diagnoses [J].
Bojesen, A ;
Juul, S ;
Birkebæk, NH ;
Gravholt, CH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (04) :1254-1260
[9]   Genotype and phenotype in Klinefelter syndrome - impact of androgen receptor polymorphism and skewed X inactivation [J].
Bojesen, A. ;
Hertz, J. M. ;
Gravholt, C. H. .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2011, 34 (06) :E642-E648
[10]   Prenatal and postnatal prevalence of Klinefelter syndrome: A national registry study [J].
Bojesen, A ;
Juul, S ;
Gravholt, CH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (02) :622-626