The Metabolic Syndrome Is Frequent in Klinefelter’s Syndrome and Is Associated With Abdominal Obesity and Hypogonadism

  1. Anders Bojesen, MD, PHD12,
  2. Kurt Kristensen, MD, PHD3,
  3. Niels H. Birkebaek, MD, PHD3,
  4. Jens Fedder, MD, PHD4,
  5. Leif Mosekilde, MD, DMSCI5,
  6. Paul Bennett, MD6,
  7. Peter Laurberg, MD, DMSCI7,
  8. Jan Frystyk, MD, DMSCI1,
  9. Allan Flyvbjerg, MD, DMSCI1,
  10. Jens S. Christiansen, MD, DMSCI1 and
  11. Claus H. Gravholt, MD, DMSCI1
  1. 1Medical Department M, Endocrinology and Diabetes, and Medical Research Laboratories, Clinical Institute, Aarhus University Hospital, Aarhus, Denmark
  2. 2Department of Clinical Genetics, Vejle Hospital, Vejle, Denmark
  3. 3Department of Pediatrics, Aarhus University Hospital, Skejby Hospital, Aarhus, Denmark
  4. 4Fertility Clinic and Scientific Unit, Braedstrup Hospital, Braedstrup, Denmark
  5. 5Medical Department C, Aarhus University Hospital, Aarhus, Denmark
  6. 6Department of Clinical Biochemistry, Statens Serum Institut, Copenhagen, Denmark
  7. 7Department of Endocrinology, Aalborg University Hospital, Aalborg, Denmark
  1. Address correspondence and reprint requests to Anders Bojesen, MD, Medical Department M, Endocrinology and Diabetes, Aarhus University Hospital, Noerrebrogade 42-44, DK-8000, Aarhus C, Denmark. E-mail: anders.bojesen{at}dadlnet.dk

Abstract

OBJECTIVE—Klinefelter’s syndrome is associated with an increased prevalence of diabetes, but the pathogenesis is unknown. Accordingly, the aim of this study was to investigate measures of insulin sensitivity, the metabolic syndrome, and sex hormones in patients with Klinefelter’s syndrome and an age-matched control group.

RESEARCH DESIGN AN METHODS—In a cross-sectional study, we examined 71 patients with Klinefelter’s syndrome, of whom 35 received testosterone treatment, and 71 control subjects. Body composition was evaluated using dual-energy X-ray absorptiometry scans. Fasting blood samples were analyzed for sex hormones, plasma glucose, insulin, C-reactive protein (CRP), and adipocytokines. We analyzed differences between patients with untreated Klinefelter’s syndrome and control subjects and subsequently analyzed differences between testosterone-treated and untreated Klinefelter’s syndrome patients.

RESULTS—Of the patients with Klinefelter’s syndrome, 44% had metabolic syndrome (according to National Cholesterol Education Program/Adult Treatment Panel III criteria) compared with 10% of control subjects. Insulin sensitivity (assessed by homeostasis model assessment 2 modeling), androgen, and HDL cholesterol levels were significantly decreased, whereas total fat mass and LDL cholesterol, triglyceride, CRP, leptin, and fructosamine levels were significantly increased in untreated Klinefelter’s syndrome patients. In treated Klinefelter’s syndrome patients, LDL cholesterol and adiponectin were significantly decreased, whereas no difference in body composition was found in comparison with untreated Klinefelter’s syndrome patients. Multivariate analyses showed that truncal fat was the major determinant of metabolic syndrome and insulin sensitivity.

CONCLUSIONS—The prevalence of metabolic syndrome was greatly increased, whereas insulin sensitivity was decreased in Klinefelter’s syndrome. Both correlated with truncal obesity. Hypogonadism in Klinefelter’s syndrome may cause an unfavorable change in body composition, primarily through increased truncal fat and decreased muscle mass. Testosterone treatment in Klinefelter’s syndrome only partly corrected the unfavorable changes observed in untreated Klinefelter’s syndrome, perhaps due to insufficient testosterone doses.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    • Accepted April 18, 2006.
    • Received January 20, 2006.
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