Morbidity and mortality in Klinefelter syndrome (47,XXY)

被引:76
作者
Bojesen, Anders [1 ]
Gravholt, Claus H. [2 ,3 ]
机构
[1] Vejle Hosp, Dept Clin Genet, DK-7100 Sygehus Lillebaelt, Denmark
[2] Aarhus Univ Hosp, Dept Endocrinol & Internal Med, Aarhus Sygehus NBG, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Med Res Labs, Aarhus Sygehus NBG, DK-8000 Aarhus C, Denmark
关键词
47; XXY; Klinefelter syndrome; Morbidity; Mortality; Prevalence; SEX-CHROMOSOME ABNORMALITIES; SYSTEMIC-LUPUS-ERYTHEMATOSUS; MALE BREAST-CANCER; METABOLIC SYNDROME; NEWBORN-INFANTS; XYY SYNDROME; HORMONE; COHORT; MEN; ASSOCIATION;
D O I
10.1111/j.1651-2227.2011.02274.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Klinefelter syndrome (KS) (47,XXY) is the most common sex chromosome disorder in man and is a relatively common cause of male infertility and hypogonadism. The syndrome has been known since 1942, and many reports of different diseases associated with KS have been reported since that, but a more systematic knowledge about the long-term outcome was not described until the last decade, where nation-wide epidemiological studies were reported from Britain and Denmark. We here review the epidemiological data from two cohorts of patients with KS in Denmark and Britain, showing a significant increase in both mortality and morbidity from a variety of different causes. Mortality was increased by 50% (SMR 1.5 or HR 1.4) corresponding to a median loss of approximately 2 years. The risk of being admitted to hospital with any diagnosis was increased by 70%. The underlying reason for the poorer health in KS may be caused by interaction of genetic, hormonal and socio-economic factors. Conclusion: Both morbidity and mortality are significantly increased in Klinefelter syndrome with a 50% increase in mortality risk and a 70% increase in risk of being admitted to hospital.
引用
收藏
页码:807 / 813
页数:7
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