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Campo DC Valor Lengua/Idioma
dc.creatorScalco, Renata C.-
dc.creatorHwa, Vivian-
dc.creatorDomene, Horacio Mario-
dc.creatorJasper, Hector Guillermo-
dc.creatorBelgorosky, Alicia-
dc.creatorMarino, Roxana-
dc.creatorPereira, Alberto M.-
dc.creatorTonelli, Carlos A.-
dc.creatorWit, Jan M.-
dc.creatorRosenfeld, Ron G.-
dc.creatorJorge, Alexander A. L.-
dc.date2016-11-16T21:25:37Z-
dc.date2016-11-16T21:25:37Z-
dc.date2015-06-
dc.date2016-11-11T16:51:10Z-
dc.date.accessioned2019-04-29T15:51:33Z-
dc.date.available2019-04-29T15:51:33Z-
dc.date.issued2015-06-
dc.identifierScalco, Renata C.; Hwa, Vivian; Domene, Horacio Mario; Jasper, Hector Guillermo; Belgorosky, Alicia; et al.; STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability.; Bioscientifica; European Journal Of Endocrinology; 173; 3; 6-2015; 1-17-
dc.identifier0804-4643-
dc.identifierhttp://hdl.handle.net/11336/8275-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/303909-
dc.descriptionContext and objective: GH insensitivity with immune dysfunction caused by STAT5B mutations is an autosomal recessivecondition. Heterozygous mutations in other genes involved in growth regulation were previously associated with a mildheight reduction. Our objective was to assess for the first time the phenotype of heterozygous STAT5B mutations.Methods: We genotyped and performed clinical and laboratory evaluations in 52 relatives of two previously describedBrazilian brothers with homozygous STAT5B c.424_427del mutation (21 heterozygous). Additionally, we obtained heightdata and genotype from 1104 adult control individuals from the same region in Brazil and identified five additional familiesharboring the same mutation (18 individuals, 11 heterozygous). Furthermore, we gathered the available height data fromfirst-degree relatives of patients with homozygous STAT5B mutations (17 individuals from seven families). Data fromheterozygous individuals and non-carriers were compared.Results: Individuals carrying heterozygous STAT5B c.424_427del mutation were 0.6 SDS shorter than their non-carrierrelatives (PZ0.009). Heterozygous subjects also had significantly lower SDS for serum concentrations of IGF1 (PZ0.028) andIGFBP3 (PZ0.02) than their non-carrier relatives. The 17 heterozygous first-degree relatives of patients carrying homozygousSTAT5B mutations had an average height SDS of K1.4G0.8 when compared with population-matched controls (P! 0.001).Conclusions: STAT5B mutations in the heterozygous state have a significant negative impact on height (w3.9 cm). This effectis milder than the effect seen in the homozygous state, with height usually within the normal range. Our results support thehypothesis that heterozygosity of rare pathogenic variants contributes to normal height heritability.-
dc.descriptionFil: Scalco, Renata C.. Universidade de Sao Paulo; Brasil-
dc.descriptionFil: Hwa, Vivian. Cincinnati Center for Growth Disorders; Estados Unidos-
dc.descriptionFil: Domene, Horacio Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones Endocrinológicas; Argentina-
dc.descriptionFil: Jasper, Hector Guillermo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones Endocrinológicas; Argentina-
dc.descriptionFil: Belgorosky, Alicia. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina-
dc.descriptionFil: Marino, Roxana. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina-
dc.descriptionFil: Pereira, Alberto M.. Leiden University Medical Center; Países Bajos-
dc.descriptionFil: Tonelli, Carlos A.. Universidade do Extremo Sul Catarinense; Brasil-
dc.descriptionFil: Wit, Jan M.. Leiden University Medical Center; Países Bajos-
dc.descriptionFil: Rosenfeld, Ron G.. Oregon Health and Science University; Estados Unidos-
dc.descriptionFil: Jorge, Alexander A. L. . Universidade de Sao Paulo; Brasil-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherBioscientifica-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898761/-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1530/EJE-15-0398-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.eje-online.org/content/173/3/291.long-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectSTAT5B-
dc.subjectheterozygous-
dc.subjectmutations-
dc.subjectEndocrinología y Metabolismo-
dc.subjectMedicina Clínica-
dc.subjectCIENCIAS MÉDICAS Y DE LA SALUD-
dc.titleSTAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability.-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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