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Endocrine Abstracts (2019) 63 P319 | DOI: 10.1530/endoabs.63.P319

1University of Campania “L. Vanvitelli, Naples, Italy; 2University of Padoa, Padoa, Italy; 3Università della Campania “L. Vanvitelli, Napoli, Italy; 4University of Brescia, Brescia, Italy; 5University of Florence, Florence, Italy; 6Endocrinology, Bologna, Italy; 7University of Torino, Torino, Italy; 8University of Modena & Reggio Emilia, Modena, Italy; 9University of Catania, Catania, Italy; 10Endocrinology, Bari, Italy; 11University of Milano and IRCCS Istituto Auxologico Italiano, Milano, Italy; 12University Federico II, Naples, Italy; 13University of Marche, Ancona, Italy; 14IRCCS, Istituto Clinico Humanitas, Rozzano-Milano, Italy; 15Santa Maria Goretti Hospital, Latina, Italy; 16University of Catanzaro, Catanzaro, Italy; 17University of l’Aquila, l’Aquila, Italy.


Introduction: Klinefelter syndrome (KS) is the most frequent chromosomal disorders, occurring in 1:500 to 1:1000 live male births, associated to male infertility. Although significant research has been conducted, KS remains frustratingly underdiagnosed with a remarkable portion of cases being unidentified. Under diagnosis may be due to man’s hesitancy about seeking medical counseling, low awareness of KS among health professionals, and failure by health professionals to perform routine genital examinations in adult men.

Aim: Our purpose was to describe the phenotypic characteristics and the hormonal patterns of a cohort of patients currently attending a national network of academic or general hospitals of the Klinefelter Italian Group (KING). Moreover, we focused our interest on the geographical distribution, and age at diagnosis of KS in Italy.

Methods: A multicenter, observational study of 594 KS was performed among the patients regularly attending the KING centers, after written informed consent has been obtained.

Results: The mean age was 37.4±13.4 years (median IQR 28–46). The mean testicular volume was 3 ml in both testis, BMI was 26.6±5.5.8 and 25.5% of KS meet the diagnostic criteria for metabolic syndrome (Mets). Mean total testosterone was 350±9.1 ng/dl, LH and FSH mean levels were 16.6 (median IQR 8.8–22.5) and 28.5 (median IQR (17.5–39), respectively. A descriptive analysis performed in 594 KS, showed that 329 KS were referred to KING centers of Northern Italy, 65 and 200 KS patients to KING facilities in Central and Southern Italy, respectively. Analysis of variance showed significant statistical differences (P<00000) between the age at diagnosis of the KS of the three geographical groups. In particular, the age of KS patients was significantly lower in Southern Italy (33.3±13 S.D.) compared to Central and Northern Italy (40.2±12.5 S.D. and 39.2±13.3 S.D.).

Conclusions: Our preliminary data showed that KS is highly underdiagnosed in Italy, raising the question of the true prevalence of KS. Our patients presented with a wide spectrum of the classical Klinefelter symptoms. KS were overweight and, surprisingly, only 25.5% of them were diagnosed with Mets. This figure is very close to the Mets prevalence in the Italian general population quoted around 26%. In adulthood, two features were consistently present in every subject: small testes and high FSH and LH/testosterone ratio, despite normal testosterone levels. The differences of KS age between Italian geographical regions highlight the need for increased awareness leading to timely detection.

Volume 63

21st European Congress of Endocrinology

Lyon, France
18 May 2019 - 21 May 2019

European Society of Endocrinology 

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