Publication:
Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease

dc.contributor.authorSuttikarn Santiwatanaen_US
dc.contributor.authorPat Mahachoklertwattanaen_US
dc.contributor.authorChanin Limwongseen_US
dc.contributor.authorPatcharin Khlairiten_US
dc.contributor.authorSarunyu Pongratanakulen_US
dc.contributor.authorEkkapong Roothumnongen_US
dc.contributor.authorKanjana Prangphanen_US
dc.contributor.authorLulin Choubtumen_US
dc.contributor.authorDuantida Songdejen_US
dc.contributor.authorPreamrudee Poomthavornen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.date.accessioned2019-08-23T10:24:31Z
dc.date.available2019-08-23T10:24:31Z
dc.date.issued2018-12-01en_US
dc.description.abstract© 2018 John Wiley & Sons Ltd Objective: Skewed X chromosome inactivation (XCI) was associated with female predominance in adult autoimmune thyroid disease (ATD). In normal females, skewed XCI is increased with age. Whether early-onset skewed XCI is associated with childhood ATD remains unknown. This study aimed to determine XCI skewing in paediatric ATD. Design, Patients and Measurements: Ninety-one female ATD patients, aged 3-20 years and 57 age-matched, female controls were enrolled. XCI was analysed by enzymatic digestion of DNA with methylation-sensitive enzymes followed by PCR of the polymorphic CAG repeat in the androgen receptor gene. Skewed XCI was defined as having 80% or greater of the cells preferentially inactivated on the same X chromosome. XCI pattern of the enrolled patients and parental origin of the skewed XCI were determined. Results: After exclusion of samples with homozygous CAG repeats, skewed XCI was analysed in 83 patients (57 Graves' disease and 26 Hashimoto thyroiditis) and 52 controls. There was an increased frequency of skewed XCI in ATD patients as compared with the controls (23% vs 8%, P = 0.022). Patients with Hashimoto thyroiditis had greater frequency of skewed XCI than patients with Graves' disease (38% vs 16%, P = 0.023). There were no differences in clinical parameters between patients with skewed and random XCI. Analysis of 7 patients with skewed XCI showed a preferential inactivation of paternal X chromosome in 6 patients (86%). Conclusions: Frequency of skewed XCI was increased in childhood ATD. This observation suggests a possible association of skewed XCI in the development of paediatric ATD.en_US
dc.identifier.citationClinical Endocrinology. Vol.89, No.6 (2018), 863-869en_US
dc.identifier.doi10.1111/cen.13857en_US
dc.identifier.issn13652265en_US
dc.identifier.issn03000664en_US
dc.identifier.other2-s2.0-85055150156en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/44971
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055150156&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleSkewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055150156&origin=inwarden_US

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