Literature DB >> 22489599

Reduced artery diameters in Klinefelter syndrome.

C Foresta1, N Caretta, P Palego, A Ferlin, D Zuccarello, A Lenzi, R Selice.   

Abstract

Various epidemiological studies in relatively large cohorts of patients with Klinefelter syndrome (KS) described the increased morbidity and mortality in these subjects. Our aim was to study the structure and function of arteries in different districts to investigate in these subjects possible alterations. A total of 92 patients having non-mosaic KS, diagnosed in Centre for Human Reproduction Pathology at the University of Padova, and 50 age-matched healthy male controls were studied. Klinefelter syndrome subjects and controls evaluation included complete medical history, physical examination, measurement of concentrations of the reproductive hormones, lipidic and glycidic metabolism, AR function and sensitivity, ultrasound examinations (diameters, carotid intima-media thickness and brachial flow-mediated dilation) of brachial, common carotid and common femoral artery and abdominal aorta. Klinefelter syndrome patients showed significantly reduced artery diameters in all districts evaluated. On the contrary no statistically significant difference was found in cIMT and brachial FMD values between KS patients and controls. Furthermore, we found no statistically significant correlation of artery diameters with reproductive hormones, metabolic parameters, anthropometric measures and weighted CAG repeats. To our knowledge, this is the first study finding a reduced artery diameter in several districts in KS patients compared with that of normal male subjects and overlapping to that of female subjects. We have not an explanation for this phenomenon, even if a possible involvement of genes controlling the development of vascular system might be hypothesized, and further research is required to verify this hypothesis.
© 2012 The Authors. International Journal of Andrology © 2012 European Academy of Andrology.

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Year:  2012        PMID: 22489599     DOI: 10.1111/j.1365-2605.2012.01269.x

Source DB:  PubMed          Journal:  Int J Androl        ISSN: 0105-6263


  8 in total

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Review 2.  Morbidity in Klinefelter syndrome and the effect of testosterone treatment.

Authors:  Simon Chang; Anne Skakkebaek; Shanlee M Davis; Claus H Gravholt
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Review 3.  Klinefelter syndrome: the commonest form of hypogonadism, but often overlooked or untreated.

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Journal:  Dtsch Arztebl Int       Date:  2013-05-17       Impact factor: 5.594

Review 4.  Klinefelter syndrome: cardiovascular abnormalities and metabolic disorders.

Authors:  A E Calogero; V A Giagulli; L M Mongioì; V Triggiani; A F Radicioni; E A Jannini; D Pasquali
Journal:  J Endocrinol Invest       Date:  2017-03-03       Impact factor: 4.256

5.  Deregulation of sertoli and leydig cells function in patients with Klinefelter syndrome as evidenced by testis transcriptome analysis.

Authors:  Marco D'Aurora; Alberto Ferlin; Marta Di Nicola; Andrea Garolla; Luca De Toni; Sara Franchi; Giandomenico Palka; Carlo Foresta; Liborio Stuppia; Valentina Gatta
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Review 6.  Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.

Authors:  M Bonomi; V Rochira; D Pasquali; G Balercia; E A Jannini; A Ferlin
Journal:  J Endocrinol Invest       Date:  2016-09-19       Impact factor: 4.256

7.  Aberrant ocular architecture and function in patients with Klinefelter syndrome.

Authors:  Cristin Brand; Michael Zitzmann; Nicole Eter; Sabine Kliesch; Joachim Wistuba; Maged Alnawaiseh; Peter Heiduschka
Journal:  Sci Rep       Date:  2017-10-13       Impact factor: 4.379

8.  Hypogonadism Makes Dyslipidemia in Klinefelter's Syndrome.

Authors:  Hyo Serk Lee; Chan Woo Park; Joong Shik Lee; Ju Tae Seo
Journal:  J Korean Med Sci       Date:  2017-11       Impact factor: 2.153

  8 in total

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