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2.
Diabetes Care ; 27(5): 1164-70, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15111539

RESUMEN

OBJECTIVE: Connective tissue growth factor (CTGF) is strongly upregulated in fibrotic disorders and has been hypothesized to play a role in the development and progression of diabetes complications. The aim of the present study was to investigate the possible association of plasma CTGF levels in type 1 diabetic patients with markers relevant to development of diabetes complications. RESEARCH DESIGN AND METHODS: Plasma CTGF levels (full-length and NH2-terminal fragments) were determined in 62 well-characterized patients with type 1 diabetes and in 21 healthy control subjects. Correlations of these plasma CTGF levels with markers of glycemic control, platelet activation, endothelial activation, nephropathy, and retinopathy were investigated. RESULTS: -Elevated plasma NH2-terminal fragment of CTGF (CTGF-N) levels were detected in a subpopulation of type 1 diabetic patients and were associated with diabetic nephropathy. Stepwise regression analysis revealed contribution of albuminuria, creatinine clearance, and duration of diabetes as predictors of plasma CTGF-N level. Elevation of plasma CTGF-N levels in patients with retinopathy was probably due to renal comorbidity. CONCLUSIONS: Plasma CTGF-N levels are elevated in type 1 diabetic patients with nephropathy and appear to be correlated with proteinuria and creatinine clearance. Further studies will be needed to determine the relevance of plasma CTGF as a clinical marker and/or pathogenic factor in diabetic nephropathy.


Asunto(s)
Diabetes Mellitus Tipo 1/sangre , Nefropatías Diabéticas/sangre , Proteínas Inmediatas-Precoces/sangre , Péptidos y Proteínas de Señalización Intercelular/sangre , Adulto , Biomarcadores/sangre , Factor de Crecimiento del Tejido Conjuntivo , Creatinina/metabolismo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proteinuria , Valores de Referencia , Análisis de Regresión , Factor de Crecimiento Transformador beta/sangre
3.
Lancet Diabetes Endocrinol ; 3(9): 746, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25617948
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