Association of Type 2 Diabetes Subgroups With Cognitive Status Without Modification From Lifestyle Intervention

Author:

Bancks Michael P1ORCID,Lovato James2,Balasubramanyam Ashok3,Coday Mace4,Johnson Karen C4ORCID,Munshi Medha5,Rebello Candida6,Wagenknecht Lynne E7,Espeland Mark A8ORCID

Affiliation:

1. Department of Epidemiology and Prevention, Wake Forest University School of Medicine , Winston-Salem, NC 27157 , USA

2. Department of Biostatistics and Data Science, Wake Forest University School of Medicine , Winston-Salem, NC 27157 , USA

3. Department of Medicine, Baylor College of Medicine , Houston, TX 77030 , USA

4. Department of Preventive Medicine, University of Tennessee Health Science Center , Memphis, TN 38163 , USA

5. Joslin Diabetes Center, Harvard Medical School, and Division of Gerontology, Beth Israel Deaconess Medical Center , Boston, MA 02445 , USA

6. Pennington Biomedical Research Center, Louisiana State University System , Baton Rouge, LA 70808 , USA

7. Division of Public Health Sciences, Wake Forest University School of Medicine , Winston-Salem, NC 27157 , USA

8. Departments of Internal Medicine-Gerontology and Geriatric Medicine and Biostatistics and Data Science, Wake Forest University School of Medicine , Winston-Salem, NC 27157 , USA

Abstract

Abstract Context Type 2 diabetes is a risk factor for incident dementia but whether risk and treatment/prevention strategies differ by diabetes subgroup is unknown. Objective We assessed (1) whether specific type 2 diabetes (T2D) subgroups are associated with mild cognitive impairment (MCI) or probable dementia (PD), and (2) whether T2D subgroups modified the association of the Action for Health in Diabetes (Look AHEAD) multidomain intensive lifestyle intervention (ILI) with MCI/PD. Methods We included 3760 Look AHEAD participants with T2D and overweight or obesity randomly assigned to 10 years of ILI or diabetes support and education. We used k-means clustering techniques with data on age of diabetes diagnosis, body mass index, waist circumference, and glycated hemoglobin (HbA1c) to characterize diabetes subgroups at randomization. Prevalent MCI/PD were centrally adjudicated based on standardized cognitive tests and other health information 10 to 13 years after randomization. We estimated marginal probabilities for prevalent MCI/PD among T2D subgroups with adjustment for potential confounders and attrition and examined whether ILI modified any associations. Results Four distinct T2D subgroups were identified, characterized by older age at diabetes onset (43% of sample), high HbA1c (13%), severe obesity (23%), and younger age at onset (22%). Unadjusted prevalence of MCI/PD (314 cases, 8.4%) differed across T2D subgroup (older onset = 10.5%, severe obesity = 9.0%, high HbA1c = 7.9%, and younger onset = 4.0%). Adjusted probability for MCI/PD within T2D subgroup was highest for the severe obesity subgroup and lowest for the younger onset subgroup but did not differ by ILI arm (interaction P value = 0.84). Conclusions Among individuals with T2D and overweight or obesity, probability of MCI/PD differed by T2D subgroup. Probability of MCI/PD was highest for a subgroup characterized by severe obesity. Clinicaltrials.gov Identifier NCT00017953

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Rationale, design, and cohort characteristics of the Action for Health in Diabetes Aging study;Alzheimer's & Dementia: Translational Research & Clinical Interventions;2023-10

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