دورية أكاديمية

Detection and characterization of male sex chromosome abnormalities in the UK Biobank study.

التفاصيل البيبلوغرافية
العنوان: Detection and characterization of male sex chromosome abnormalities in the UK Biobank study.
المؤلفون: Zhao, Yajie, Gardner, Eugene J, Tuke, Marcus A, Zhang, Huairen, Pietzner, Maik, Koprulu, Mine, Jia, Raina Y, Ruth, Katherine S, Wood, Andrew R, Beaumont, Robin N, Tyrrell, Jessica, Jones, Samuel E, Lango Allen, Hana, Day, Felix R, Langenberg, Claudia, Frayling, Timothy M, Weedon, Michael N, Perry, John RB, Ong, Ken K, Murray, Anna
بيانات النشر: Elsevier BV
MRC Epidemiology Unit
//dx.doi.org/10.1016/j.gim.2022.05.011
Genet Med
سنة النشر: 2022
المجموعة: Apollo - University of Cambridge Repository
مصطلحات موضوعية: 47,XYY, Disorders of sexual development, Endocrinology, Klinefelter syndrome, Thrombosis, Type 2 diabetes, Biological Specimen Banks, Diabetes Mellitus, Type 2, Humans, Male, Sex Chromosome Aberrations, United Kingdom, XYY Karyotype
الوصف: PURPOSE: The study aimed to systematically ascertain male sex chromosome abnormalities, 47,XXY (Klinefelter syndrome [KS]) and 47,XYY, and characterize their risks of adverse health outcomes. METHODS: We analyzed genotyping array or exome sequence data in 207,067 men of European ancestry aged 40 to 70 years from the UK Biobank and related these to extensive routine health record data. RESULTS: Only 49 of 213 (23%) of men whom we identified with KS and only 1 of 143 (0.7%) with 47,XYY had a diagnosis of abnormal karyotype on their medical records or self-report. We observed expected associations for KS with reproductive dysfunction (late puberty: risk ratio [RR] = 2.7; childlessness: RR = 4.2; testosterone concentration: RR = -3.8 nmol/L, all P < 2 × 10-8), whereas XYY men appeared to have normal reproductive function. Despite this difference, we identified several higher disease risks shared across both KS and 47,XYY, including type 2 diabetes (RR = 3.0 and 2.6, respectively), venous thrombosis (RR = 6.4 and 7.4, respectively), pulmonary embolism (RR = 3.3 and 3.7, respectively), and chronic obstructive pulmonary disease (RR = 4.4 and 4.6, respectively) (all P < 7 × 10-6). CONCLUSION: KS and 47,XYY were mostly unrecognized but conferred substantially higher risks for metabolic, vascular, and respiratory diseases, which were only partially explained by higher levels of body mass index, deprivation, and smoking. ; Y.Z., E.J.G., M.P., M.K., R.Y.J., H.L.A., F.R.D., C.L., J.R.B.P. and K.K.O. are supported by the Medical Research Council (Unit programs: MC_UU_00006/1 and MC_UU_00006/2). M.K. is supported by a Gates Fellowship. A.R.W. and J.T. hold Academy of Medical Sciences (AMS) Springboard awards [SBF004\1079 and SBF006\1134], which are supported by the AMS, the Wellcome Trust, the Government Department of Business, Energy and Industrial strategy, the British Heart Foundation and Diabetes UK. R.N.B. and A.M. are supported by the Medical Research Council (MR/T00200X/1). K.S.R. is supported by Cancer Research ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://www.repository.cam.ac.uk/handle/1810/338670Test
DOI: 10.17863/CAM.86083
الإتاحة: https://doi.org/10.17863/CAM.86083Test
https://www.repository.cam.ac.uk/handle/1810/338670Test
حقوق: Attribution 4.0 International ; https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.12E10123
قاعدة البيانات: BASE