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Family typology for adults with type 2 diabetes: Longitudinal stability and validity for diabetes management and wellbeing

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posted on 2023-09-14, 19:55 authored by Lindsay S. Mayberry, Shilin Zhao, McKenzie K. Roddy, Andrew J. Spieker, Cynthia A. Berg, Lyndsay A. Nelson, Robert A. Greevy

Objective: We validated longitudinally a typology of diabetes-specific family functioning (Collaborative and Helpful, Satisfied with Low Involvement, Want More Involvement, Critically Involved) in adults with type 2 diabetes.

Research Design and Methods: We conducted k-means cluster analysis with nine dimensions to determine if the typology replicated in a diverse sample and type assignment was robust to variations in sampling and included dimensions. In a subsample with repeated assessments over 9 months, we examined stability and validity of the typology. We also applied a multinomial logistic regression approach to make the typology usable at the individual-level, like a diagnostic tool.

Results: Participants (N=717) were 51% male, over one-third reported minoritized race or ethnicity, mean age was 57 and mean HbA1c was 7.9% (63 mmol/mol) [8.7% (72 mmol/mol) for longitudinal subsample]. The typology replicated with respect to the number of types and dimension patterns. Type assignment was robust to sampling variations (97% consistent across simulations). Type had an average 52% stability over time within participants; instability was not explained by measurement error. Over 9 months, type was independently associated with HbA1c, diabetes self-efficacy, diabetes medication adherence, diabetes distress, and depressive symptoms (all p-values<0.05).

Conclusions: The typology of diabetes-specific family functioning replicated, and longitudinal analyses suggest type is more a dynamic state than stable trait. However, type varies with diabetes self-management and wellbeing over time as a consistent independent indicator of outcomes. The typology is ready to be applied to further precision medicine approaches to behavioral and psychosocial diabetes research and care.

Funding

This study was funded by a grant from the National Institutes of Health (R01-DK119282-S1).

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