Literature DB >> 11375362

Idiopathic type 1 diabetes in Dallas, Texas: a 5-year experience.

A Piñero-Piloña1, P Litonjua, L Aviles-Santa, P Raskin.   

Abstract

OBJECTIVE: To describe the clinical course of individuals with idiopathic type 1 diabetes after a mean of 5 years from diagnosis and to compare glycemic control between those treated with diet and/or oral agents and those treated with insulin at follow-up. RESEARCH DESIGN AND METHODS: Medical records of patients with new-onset diabetes, who presented with unprovoked diabetic ketoacidosis, were reviewed. A total of 54 of these individuals were traceable and had relevant data collected within the past 2 years. All patients had nonsusceptibility HLA haplotypes and no serological evidence of autoimmune type 1 diabetes. Most of these patients were male (41 men and 13 women), were non-Caucasian, were obese at the time of diagnosis (BMI 31.6 +/- 6.3 kg/m(2)), reported weight loss (12.8 +/- 9.8 kg), had a family history of type 2 diabetes, and had acanthosis nigricans. At follow-up, 33 patients were still taking insulin and 21 were on diet and/or oral-agent therapy.
RESULTS: Both treatment groups were similar in clinical presentation and demographics at diagnosis. After 4.8 +/- 1.6 years of follow-up, the 33 patients that were receiving insulin had a lower HbA(1c) than the 21 patients who were using therapies other than insulin (7.8 +/- 2.4 vs. 11.1 +/- 3.5%, P = 0.009; 95% CI 1.0-6.5%). There was a high correlation between change in weight and change in HbA(1c) at follow-up (r = 0.45, P < 0.001, n = 54). There were no differences in the rate of diabetes complications or in the episodes of recurrent diabetic ketoacidosis.
CONCLUSIONS: Idiopathic type 1 diabetes occurs more frequently in male African-American patients but also occurs in other ethnic groups. Patients with idiopathic type 1 diabetes who continued to use insulin had better glycemic control than patients using therapies other than insulin. Regained weight is a good clinical marker for improvement in glycemic control. Individuals with this type of diabetes should not be switched to therapies other than insulin.

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Year:  2001        PMID: 11375362     DOI: 10.2337/diacare.24.6.1014

Source DB:  PubMed          Journal:  Diabetes Care        ISSN: 0149-5992            Impact factor:   19.112


  17 in total

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2.  Male predominance in ketosis-prone diabetes mellitus.

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Journal:  Biomed Rep       Date:  2015-05-08

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Review 4.  Type 1 diabetes in Japan.

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Journal:  Diabetologia       Date:  2006-03-28       Impact factor: 10.122

5.  Update on diagnosis, pathogenesis and management of ketosis-prone Type 2 diabetes mellitus.

Authors:  Dawn Smiley; Prakash Chandra; Guillermo E Umpierrez
Journal:  Diabetes Manag (Lond)       Date:  2011-11-01

6.  PAX4 gene variations predispose to ketosis-prone diabetes.

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Journal:  Hum Mol Genet       Date:  2004-10-27       Impact factor: 6.150

Review 7.  Syndromes of ketosis-prone diabetes mellitus.

Authors:  Ashok Balasubramanyam; Ramaswami Nalini; Christiane S Hampe; Mario Maldonado
Journal:  Endocr Rev       Date:  2008-02-21       Impact factor: 19.871

8.  Atypical diabetes in children: ketosis-prone type 2 diabetes.

Authors:  Atul Vaibhav; Mathew Mathai; Shaun Gorman
Journal:  BMJ Case Rep       Date:  2013-01-08

9.  Prevalence and clinical characteristics of carotid atherosclerosis in newly diagnosed patients with ketosis-onset diabetes: a cross-sectional study.

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Journal:  Cardiovasc Diabetol       Date:  2013-01-16       Impact factor: 9.951

10.  Comparison between New-Onset and Old-Diagnosed Type 2 Diabetes with Ketosis in Rural Regions of China.

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Journal:  Int J Endocrinol       Date:  2016-02-04       Impact factor: 3.257

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