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DOI 10.1111/pedi.12614

Медицинская библиотека · Pediatric diabetes · 2017

Cardiovascular autonomic dysfunction predicts increasing albumin excretion in type 1 diabetes.

Lu Liangjian, Marcovecchio M Loredana, Dalton R Neil, Dunger David

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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 HbA1c 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 HbA1c , 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.

Для цитирования: Lu Liangjian, Marcovecchio M Loredana, Dalton R Neil, Dunger David. Cardiovascular autonomic dysfunction predicts increasing albumin excretion in type 1 diabetes.. Pediatric diabetes. 2017. DOI: 10.1111/pedi.12614.

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