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Cardiovascular autonomic dysfunction predicts increasing albumin excretion in type 1 diabetes
Author(s) -
Lu Liangjian,
Marcovecchio M Loredana,
Dalton R Neil,
Dunger David
Publication year - 2018
Publication title -
pediatric diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.678
H-Index - 75
eISSN - 1399-5448
pISSN - 1399-543X
DOI - 10.1111/pedi.12614
Subject(s) - medicine , valsalva maneuver , blood pressure , cardiology , prospective cohort study , heart rate , diabetes mellitus , type 2 diabetes , renal function , nephropathy , autonomic function , endocrinology , heart rate variability
Objective To determine the potential role of cardiovascular autonomic dysfunction in the development of renal complications in young people with type 1 diabetes (T1D). Methods In this prospective study, 199 children and adolescents recruited to the Oxford Regional Prospective Study underwent assessment of autonomic function ~5 years after diagnosis, and were subsequently followed with longitudinal assessments of HbA 1c and urine albumin‐creatinine ratio (ACR) over 8.6 ± 3.4 years. Autonomic function was assessed with 4 standardized tests of cardiovascular reflexes: heart rate (HR) response to (1) Valsalva Maneuver, (2) deep breathing, (3) standing, and (4) blood pressure (BP) response to standing. Linear mixed models were used to assess the association between autonomic parameters and future changes in ACR. Results Independent of HbA 1c , each SD increase in HR response to Valsalva Maneuver predicted an ACR increase of 2.16% [95% CI: 0.08; 4.28] per year ( P  = .04), while each SD increase in diastolic BP response to standing predicted an ACR increase of 2.55% [95% CI: 0.37; 4.77] per year ( P  = .02). The effect of HR response to standing on ACR reached borderline significance (−2.07% [95% CI: −4.11; 0.01] per year per SD increase, P  = .051). Conclusions In this cohort of young people with T1D, enhanced cardiovascular reflexes at baseline predicted future increases in ACR. These results support a potential role for autonomic dysfunction in the pathogenesis of diabetic nephropathy.

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