Factors associated with early relapse to insulin dependence in unprovoked A-β plus ketosis-prone diabetes

被引:14
作者
Gaba, Ruchi [1 ,2 ]
Gambhire, Dhiraj [3 ]
Uy, Natalie [1 ]
Gonzalez, Erica V. [1 ,2 ]
Iyer, Dinakar [1 ]
Hampe, Christiane S. [4 ]
Ram, Nalini [1 ,2 ]
Balasubramanyam, Ashok [1 ,2 ]
机构
[1] Baylor Coll Med, Diabet Res Ctr, Translat Metab Unit, Div Diabet Endocrinol & Metab, Houston, TX 77030 USA
[2] Ben Taub Gen Hosp, Endocrine Serv, Houston, TX 77030 USA
[3] Univ Texas Sch Publ Hlth, Houston, TX USA
[4] Univ Washington, Dept Med, Seattle, WA USA
关键词
Ketoacidosis; Beta-cell; HLA; Multivariate; Insulin-dependence; CLASS-II ALLELES; CLASSIFICATION; KETOACIDOSIS; MELLITUS; PATHOGENESIS;
D O I
10.1016/j.jdiacomp.2015.04.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Unprovoked "A-beta+" Ketosis-Prone Diabetes (KPD), a unique diabetic syndrome of adult-onset, obesity and proneness to ketoacidosis, is associated with rapid recovery of beta cell function and insulin-independence. Whereas most patients experience prolonged remission, a subset relapses early to insulin dependence. We sought to define factors associated with early relapse. Methods: We utilized a prospective, longitudinal database to analyze 50 unprovoked A-beta+ KPD patients with >2 measurements of beta cell function and glycemia following baseline assessment. Results: 19 patients (38%) relapsed to insulin dependence <1 year after the index DKA episode, while 31(62%) remained insulin-independent for >1 year (median 4.2 years). Younger age at baseline (OR = 0.947, P = 0.033), and lower HOMA2-%beta (OR = 0.982, P = 0.001), lower HOMA2-IR (OR = 0.582, P = 0.046) and higher HbA1c at 1 year (OR = 1.71, P = 0.002) were associated with early relapse. A multivariate model with these variables and the interaction of HOMA-4%beta and HbA1c at 1 year provided a good fit (P<0.05). Conclusions: Relapse to insulin dependence in unprovoked A-beta+ KPD patients is associated with younger age and, after I year, lack of robust increase in beta cell functional reserve, and suboptimal glycemic control. Measurements of these parameters 1 year after the index DKA episode can be used to assess the need for insulin therapy. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:918 / 922
页数:5
相关论文
共 14 条
[1]   Syndromes of ketosis-prone diabetes mellitus [J].
Balasubramanyam, Ashok ;
Nalini, Ramaswami ;
Hampe, Christiane S. ;
Maldonado, Mario .
ENDOCRINE REVIEWS, 2008, 29 (03) :292-302
[2]   Accuracy and predictive value of classification schemes for ketosis-prone diabetes [J].
Balasubramanyam, Ashok ;
Garza, Gilberto ;
Rodriguez, Lucille ;
Hampe, Christiane S. ;
Gaur, Lakshmi ;
Lernmark, Ake ;
Maldonado, Mario R. .
DIABETES CARE, 2006, 29 (12) :2575-2579
[3]   GAD ANTIBODY NEGATIVE NIDDM IN ADULT BLACK SUBJECTS WITH DIABETIC-KETOACIDOSIS AND INCREASED FREQUENCY OF HUMAN-LEUKOCYTE ANTIGEN DR3 AND DR4 - FLATBUSH DIABETES [J].
BANERJI, MA ;
CHAIKEN, RL ;
HUEY, H ;
TUOMI, T ;
NORIN, AJ ;
MACKAY, IR ;
ROWLEY, MJ ;
ZIMMET, PZ ;
LEBOVITZ, HE .
DIABETES, 1994, 43 (06) :741-745
[4]   Islet-Specific T-Cell Responses and Proinflammatory Monocytes Define Subtypes of Autoantibody-Negative Ketosis-Prone Diabetes [J].
Brooks-Worrell, Barbara M. ;
Iyer, Dinakar ;
Coraza, Ivonne ;
Hampe, Christiane S. ;
Nalini, Ramaswami ;
Ozer, Kerem ;
Narla, Radhika ;
Palmer, Jerry P. ;
Balasubramanyam, Ashok .
DIABETES CARE, 2013, 36 (12) :4098-4103
[5]   Ketosis-prone diabetes:: Dissection of a heterogeneous syndrome using an immunogenetic and β-cell functional classification, prospective analysis, and clinical outcomes [J].
Maldonado, M ;
Hampe, CS ;
Gaur, LK ;
D'Amico, S ;
Iyer, D ;
Hammerle, LP ;
Bolgiano, D ;
Rodriguez, L ;
Rajan, A ;
Lernmark, Å ;
Balasubramanyam, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (11) :5090-5098
[6]   Ketosis-prone type 2 diabetes in patients of sub-Saharan African origin -: Clinical pathophysiology and natural history of β-cell dysfunction and insulin resistance [J].
Mauvais-Jarvis, F ;
Sobngwi, E ;
Porcher, R ;
Riveline, JP ;
Kevorkian, JP ;
Vaisse, C ;
Charpentier, G ;
Guillausseau, PJ ;
Vexiau, P ;
Gautier, JF .
DIABETES, 2004, 53 (03) :645-653
[7]   HLA class II alleles specify phenotypes of ketosis-prone diabetes [J].
Nalini, Ramaswami ;
Gaur, Lakshmi K. ;
Maldonado, Mario ;
Hampe, Christiane S. ;
Rodriguez, Lucille ;
Garza, Gilberto ;
Lernmark, Ake ;
Balasubramanyam, Ashok .
DIABETES CARE, 2008, 31 (06) :1195-1200
[8]   Presence or absence of a known diabetic ketoacidosis precipitant defines distinct syndromes of "A-β plus " ketosis-prone diabetes based on long-term β-cell function, human leukocyte antigen class II alleles, and sex predilection [J].
Nalini, Ramaswami ;
Ozer, Kerem ;
Maldonado, Mario ;
Patel, Sanjeet G. ;
Hampe, Christiane S. ;
Guthikonda, Anu ;
Villanueva, Jesus ;
Smith, E. O'Brian ;
Gaur, Lakshmi K. ;
Balasubramanyam, Ashok .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2010, 59 (10) :1448-1455
[9]   Pathogenesis of A-β+ Ketosis-Prone Diabetes [J].
Patel, Sanjeet G. ;
Hsu, Jean W. ;
Jahoor, Farook ;
Coraza, Ivonne ;
Bain, James R. ;
Stevens, Robert D. ;
Iyer, Dinakar ;
Nalini, Ramaswami ;
Ozer, Kerem ;
Hampe, Christiane S. ;
Newgard, Christopher B. ;
Balasubramanyam, Ashok .
DIABETES, 2013, 62 (03) :912-922
[10]   Idiopathic Type 1 diabetes [J].
Piñero-Piloña, A ;
Raskin, P .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2001, 15 (06) :328-335