The presence of cerebral white matter lesions and lower skin microvascular perfusion predicts lower cognitive performance in type 1 diabetes patients with retinopathy but not in healthy controls-A longitudinal study.

Anna L Emanuel, Eelco van Duinkerken, Mike P Wattjes, Martin Klein, Frederik Barkhof, Frank J Snoek, Michaela Diamant, Etto C Eringa, Richard G IJzerman, Erik H Serné

Journal: Microcirculation (New York, N.Y. : 1994) 2019;26(3):e12530

PMID: 30659710

Abstract

OBJECTIVE

Cognitive impairments in type 1 diabetes may result from hyperglycemia-associated cerebral microangiopathy. We aimed to identify cerebral microangiopathy and skin microvascular dysfunction-as a surrogate marker for generalized microvascular function-as predictors of cognitive performance over time.

METHODS

In this prospective cohort study, 25 type 1 diabetes patients with proliferative retinopathy and 25 matched healthy controls underwent neurocognitive testing at baseline and after follow-up (3.8 ± 0.8 years). At baseline, 1.5-T cerebral magnetic resonance imaging was used to detect WML and cerebral microbleeds. Skin capillary perfusion was assessed by means of capillary microscopy.

RESULTS

In type 1 diabetes patients, but not in healthy controls, the presence of WML (ß = -0.419; P = 0.037) as well as lower skin capillary perfusion (baseline: ß = 0.753; P < 0.001; peak hyperemia: ß = 0.743; P = 0.001; venous occlusion: ß = 0.675; P = 0.003; capillary recruitment: ß = 0.549; P = 0.022) at baseline was associated with lower cognitive performance over time, independent of age, sex, HbA1c, and severe hypoglycemia. The relationship between WML and lower cognitive performance was significantly reduced after adjusting for capillary perfusion.

CONCLUSIONS

These data fit the hypothesis that cerebral microangiopathy is a manifestation of generalized microvascular dysfunction, leading to lower cognitive performance.

© 2019 The Authors. Microcirculation Published by John Wiley & Sons Ltd.

Address: Diabetes Center, Department of Internal Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.; Department of Internal Medicine, Amstelland Hospital, Amstelveen, The Netherlands.; Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.; Department of Diagnostic and Interventional Neuroradiology, Hannover Medical School, Hannover, Germany.; Department of Medical Psychology, Amsterdam University Medical Center, Amsterdam, The Netherlands.; Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.; Diabetes Center, Department of Internal Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.; Department of Physiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
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