Smoking and the Risk of LADA: Results From a Swedish Population-Based Case-Control Study

Author:

Rasouli Bahareh1,Andersson Tomas12,Carlsson Per-Ola3,Grill Valdemar45,Groop Leif6,Martinell Mats7,Storm Petter6,Tuomi Tiinamaija8,Carlsson Sofia1

Affiliation:

1. Epidemiology Unit, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

2. Center for Occupational and Environmental Medicine, Stockholm County Council, Stockholm, Sweden

3. Department of Medical Sciences, Uppsala University, Uppsala, Sweden

4. NTNU Institute of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway

5. Department of Endocrinology, Trondheim University Hospital, Trondheim, Norway

6. Department of Clinical Sciences in Malmö, Clinical Research Centre, Lund University, Malmö, Sweden

7. Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden

8. Division of Endocrinology, Helsinki University Hospital; Finnish Institute for Molecular Medicine and Research Program for Diabetes and obesity, University of Helsinki; and Folkhalsan Research Center, Helsinki, Finland

Abstract

OBJECTIVE Smoking is an established risk factor for type 2 diabetes. In contrast, it has been proposed that smoking may reduce the risk of latent autoimmune diabetes in adults (LADA), but studies are scarce. We aimed to study the impact of smoking on LADA and type 2 diabetes risks. RESEARCH DESIGN AND METHODS We used data from a Swedish case-control study including incident case patients with LADA (GAD antibody [GADA] positive, n = 377) and type 2 diabetes (GADA negative, n = 1,188) and control subjects randomly selected from the population (n = 1,472). We calculated odds ratios (ORs) with 95% CIs by logistic regression, adjusted for age, sex, BMI, family history of diabetes, and alcohol consumption. RESULTS There was no indication of reduced risk of LADA in smokers; instead, heavy smoking was associated with an increased risk of LADA (OR 1.37, 95% CI 1.02–1.84). Heavy smokers had higher levels of HOMA of insulin resistance (9.89 vs. 4.38, P = 0.0479) and HOMA of β-cell function (55.7 vs. 42.5, P = 0.0204), but lower levels of GADA (75 vs. 250, P = 0.0445), compared with never smokers. Smokers also displayed an increased risk of type 2 diabetes (OR in ever smokers 1.53, 95% CI 1.25–1.88). CONCLUSIONS In this large population of LADA patients, we did not observe a protective effect of smoking on autoimmunity and the risk of LADA. A protective effect could possibly be masked by a smoking-induced aggravation of insulin resistance, akin to the diabetogenic effect seen in individuals with type 2 diabetes.

Funder

Swedish Medical Research Council

,

The Swedish Research Council for Health, Working life and Welfare

AFA Insurance Company

The Swedish Diabetes Association

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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