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Association of plasma ceramides with prevalent and incident type 2 diabetes mellitus in middle and older aged adults.
Dugani, Sagar B; Christenson, Luke R; Aakre, Jeremiah A; Bui, Hai H; Vella, Adrian; Mielke, Michelle M.
Affiliation
  • Dugani SB; Division of Hospital Internal Medicine, Mayo Clinic, Rochester, MN, United States; Division of Health Care Delivery Research, Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN, United States.
  • Christenson LR; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
  • Aakre JA; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
  • Bui HH; Eli Lilly and Company, Indianapolis, IN, United States.
  • Vella A; Division of Endocrinology, Mayo Clinic, Rochester, MN, United States.
  • Mielke MM; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States; Department of Neurology, Mayo Clinic, Rochester, MN, United States. Electronic address: mielke.michelle@mayo.edu.
Diabetes Res Clin Pract ; 179: 108991, 2021 Sep.
Article in En | MEDLINE | ID: mdl-34333058
ABSTRACT

AIMS:

The role of ceramides in the pathogenesis of type 2 diabetes mellitus (T2DM) is incompletely characterized. Given that ceramides represent therapeutic targets to disrupt the euglycemia-T2DM transition, we aimed to characterize their association with prevalent and incident T2DM in a novel cohort.

METHODS:

We examined the cross-sectional and longitudinal association of baseline ceramides with prevalent and incident T2DM among 1423 adults (47% women; median (range) baseline age 72 (51-95) years) in the Mayo Clinic Study of Aging cohort. We examined the associations of ceramides with prevalent T2DM (adjusted odds ratio [95% confidence interval]) at baseline and incident T2DM (adjusted hazard ratio [95% confidence interval]) during median follow-up of 6.2 years, after adjusting for demographic and metabolic factors.

RESULTS:

Among 1423 adults, there were 222 prevalent and 37 incident cases of T2DM. In cross-sectional analyses, higher levels of ceramide C160 were associated with lower odds of prevalent T2DM (aOR 0.84 [0.71-0.99];P = 0.03) whereas C180 (aOR 1.27 [1.06-1.42];P = 0.01), C180/160 (aOR 1.41 [1.22-1.62]; P < 0.001) and C180/240 (aOR 1.22 [1.05-1.41]; P = 0.01) were associated with higher odds. In Cox hazard regression models, C180/160 (aHR 1.63 [1.26-2.10];P < 0.001) and C180 (aHR 1.53 [1.12-2.08];P = 0.01) were associated with increased risk of incident T2DM.

CONCLUSIONS:

In this prospective population-based cohort, ceramides were associated with prevalent T2DM (C160,C180, C180/C160 ratio, C180/C240 ratio) and incident T2DM (C180, C180/C160 ratio) and could suggest targets for the primary and secondary prevention of T2DM.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Diabetes Res Clin Pract Journal subject: ENDOCRINOLOGIA Year: 2021 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Diabetes Res Clin Pract Journal subject: ENDOCRINOLOGIA Year: 2021 Document type: Article Affiliation country: Estados Unidos
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