The Contemporary Prevalence of Diabetic Neuropathy in Type 1 Diabetes: Findings From the T1D Exchange

Medientyp: E-Artikel

Titel: The Contemporary Prevalence of Diabetic Neuropathy in Type 1 Diabetes: Findings From the T1D Exchange

Beteiligte: Mizokami-Stout, Kara R.; Li, Zoey; Foster, Nicole C.; Shah, Viral; Aleppo, Grazia; McGill, Janet B.; Pratley, Richard; Toschi, Elena; Ang, Lynn; Pop-Busui, Rodica; Weinstock, Ruth; Izquierdo, Roberto; Sheikh, Umair; Conboy, Patricia; Bulger, Jane; Bzdick, Suzan; Klingensmith, Georgeanna; Banion, Carolyn; Barker, Jennifer; Cain, Cindy; Nadeau, Kristen; Rewers, Marian; Rewers, Arleta; Slover, Robert; [...]

Erschienen: American Diabetes Association, 2020

Sprache: Englisch

DOI: 10.2337/dc19-1583

ISSN: 1935-5548; 0149-5992

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Beschreibung: OBJECTIVE To evaluate the contemporary prevalence of diabetic peripheral neuropathy (DPN) in participants with type 1 diabetes in the T1D Exchange Clinic Registry throughout the U.S. RESEARCH DESIGN AND METHODS DPN was assessed with the Michigan Neuropathy Screening Instrument Questionnaire (MNSIQ) in adults with ≥5 years of type 1 diabetes duration. A score of ≥4 defined DPN. Associations of demographic, clinical, and laboratory factors with DPN were assessed. RESULTS Among 5,936 T1D Exchange participants (mean ± SD age 39 ± 18 years, median type 1 diabetes duration 18 years [interquartile range 11, 31], 55% female, 88% non-Hispanic white, mean glycated hemoglobin [HbA1c] 8.1 ± 1.6% [65.3 ± 17.5 mmol/mol]), DPN prevalence was 11%. Compared with those without DPN, DPN participants were older, had higher HbA1c, had longer duration of diabetes, were more likely to be female, and were less likely to have a college education and private insurance (all P &lt; 0.001). DPN participants also were more likely to have cardiovascular disease (CVD) (P &lt; 0.001), worse CVD risk factors of smoking (P = 0.008), hypertriglyceridemia (P = 0.002), higher BMI (P = 0.009), retinopathy (P = 0.004), reduced estimated glomerular filtration rate (P = 0.02), and Charcot neuroarthropathy (P = 0.002). There were no differences in insulin pump or continuous glucose monitor use, although DPN participants were more likely to have had severe hypoglycemia (P = 0.04) and/or diabetic ketoacidosis (P &lt; 0.001) in the past 3 months. CONCLUSIONS The prevalence of DPN in this national cohort with type 1 diabetes is lower than in prior published reports but is reflective of current clinical care practices. These data also highlight that nonglycemic risk factors, such as CVD risk factors, severe hypoglycemia, diabetic ketoacidosis, and lower socioeconomic status, may also play a role in DPN development.

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