INVESTIGADORES
FERNANDEZ DO PORTO Dario Augusto
congresos y reuniones científicas
Título:
Idiopatic short stature: The impact of polymorphic markers of genes encoding the 150 kDa circulating IGFs ternary complex
Autor/es:
H DOMENÉ;; P SCAGLIA; A MARTÍNEZ; A KESELMAN; D FERNÁNDEZ DO PORTO; V PIPMAN; S BENGOLEA; L KARABATAS; G ROPELATO; G BALLERINI; J HEINRICH; H JASPER
Lugar:
Estambul
Reunión:
Congreso; 47th Annual Meeting, European Society for Pediatric Endocrinology; 2008
Institución organizadora:
European Society for Pediatric Endocrinology
Resumen:
Abstract Title       Idiopathic short stature: The impact of polymorphic markers of genes encoding the 150-kDa circulating IGFs ternary complex.       Abstract Text        Idiopathic short stature (ISS) is a heterogeneous clinical condition, probably comprising several etiologies. Different studies have shown reduced IGF-I levels in a significant proportion of these subjects. Our aim was to determine: 1) if the distribution of some polymorphic markers of the genes encoding for GHR, IGF-I, IGFBP-3, and ALS in ISS differs from normal; 2) if the distribution of these markers differ using two different classifications of ISS: with low or normal IGF-I levels, or with (F-ISS) or without (NF-ISS) family background of short stature. We enrolled 191 normal children, height above -2.0 SDS, aged 5.1 to 16.6 years, and 82 ISS, height below -2.2 SDS, aged 2.0 to 17.6 years, with normal GH response after provocative tests (>7.0 µg/L). Height, IGF-I (RIA), IGFBP-3 (IRMA), ALS (RIA), and ternary complex formation (TCF, size exclusion chromatography) were expressed in SDS. Single nucleotide polymorphisms (SNPs) were determined by RFLP: two in the promoter region of IGFBP3 gene (rs2854744 and rs13241830), one in the 3´-UTR of IGF1 gene (rs6220), and one in the coding region of IGFALS gene (rs3751893), and a GHR gene polymorphism by multiplex PCR (full length or exon 3 deletion). ISS children showed a more frequent reduction (