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Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis.
Vázquez-Mosquera, María E; González-Vioque, Emiliano; Barbosa-Gouveia, Sofía; Bellido-Guerrero, Diego; Tejera-Pérez, Cristina; Martinez-Olmos, Miguel A; Fernández-Pombo, Antía; Castaño-González, Luis A; Chans-Gerpe, Roi; Couce, María L.
Afiliação
  • Vázquez-Mosquera ME; Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain.
  • González-Vioque E; Instituto de Investigación Sanitaria de Santiago (IDIS), Santiago de Compostela, Spain.
  • Barbosa-Gouveia S; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain.
  • Bellido-Guerrero D; Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
  • Tejera-Pérez C; European Reference Network for Hereditary Metabolic Disorders (MetabERN), Padova, Italy.
  • Martinez-Olmos MA; Division of Clinical Biochemistry, Hospital Universitario Puerta de Hierro-Majadahonda, Madrid, Spain.
  • Fernández-Pombo A; Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain.
  • Castaño-González LA; Instituto de Investigación Sanitaria de Santiago (IDIS), Santiago de Compostela, Spain.
  • Chans-Gerpe R; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain.
  • Couce ML; Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
Orphanet J Rare Dis ; 17(1): 105, 2022 03 04.
Article em En | MEDLINE | ID: mdl-35246208
BACKGROUND: Diagnosis of mature-onset diabetes of the young (MODY), a non-autoimmune monogenic form of diabetes mellitus, is confirmed by genetic testing. However, a positive genetic diagnosis is achieved in only around 50% of patients with clinical characteristics of this disease. RESULTS: We evaluated the diagnostic utility of transcriptomic analysis in patients with clinical suspicion of MODY but a negative genetic diagnosis. Using Nanostring nCounter technology, we conducted transcriptomic analysis of 19 MODY-associated genes in peripheral blood samples from 19 patients and 8 healthy controls. Normalized gene expression was compared between patients and controls and correlated with each patient's biochemical and clinical variables. Z-scores were calculated to identify significant changes in gene expression in patients versus controls. Only 7 of the genes analyzed were detected in peripheral blood. HADH expression was significantly lower in patients versus controls. Among patients with suspected MODY, GLIS3 expression was higher in obese versus normal-weight patients, and in patients aged < 25 versus > 25 years at diabetes onset. Significant alteration with respect to controls of any gene was observed in 57.9% of patients. CONCLUSIONS: Although blood does not seem to be a suitable sample for transcriptomic analysis of patients with suspected MODY, in our study, we detected expression alterations in some of the genes studied in almost 58% of patients. That opens the door for future studies that can clarify the molecular cause of the clinic of these patients and thus be able to maintain a more specific follow-up and treatment in each case.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article