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J Clin Endocrinol Metab ; 97(3): E409-13, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22205710

ABSTRACT

CONTEXT: Latent autoimmune diabetes of adults (LADA) is a form of autoimmune diabetes that has been classified as part of type 1 diabetes or as a distinct clinical entity. Its precise place as a disease category is therefore controversial. OBJECTIVE: The objective of this study was to further examine this issue by comparing the phenotypes of LADA and type 1 diabetes in a predominately minority population. PATIENTS AND METHODS: We studied 126 subjects who were anti-glutamic acid decarboxylase antibody-positive in two separate studies--63 subjects in an outpatient study (study 1), and 63 inpatients after resolution of ketoacidosis (study 2). Clinical and biochemical phenotyping was performed in all patients in each group. RESULTS: Few significant differences were found in the clinical or biochemical phenotypes in patients classified as LADA when compared with type 1 diabetes. Adiposity, body mass index, waist/hip ratio, fasting plasma C-peptide, serum high-density lipoprotein cholesterol, and triglycerides were all similar. The only distinguishing feature was a history of hypertension (study 1) or systolic blood pressure (study 2). Also, a history of ketoacidosis did not influence the phenotype of LADA in the outpatients in any discernable way. CONCLUSIONS: We conclude that LADA and type 1 diabetes are phenotypically indistinguishable in this predominantly minority population with a mean duration of glutamic acid decarboxylase antibody-positive diabetes of about 8 yr.


Subject(s)
Autoantibodies/immunology , Autoimmune Diseases/diagnosis , Diabetes Mellitus, Type 1/diagnosis , Glutamate Decarboxylase/immunology , Adult , Age of Onset , Autoimmune Diseases/immunology , Autoimmune Diseases/physiopathology , Blood Glucose , Diabetes Mellitus, Type 1/immunology , Diabetes Mellitus, Type 1/physiopathology , Female , Humans , Ketosis/diagnosis , Ketosis/immunology , Ketosis/physiopathology , Male , Middle Aged , Minority Health , Phenotype
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