
Lipid profile as a predictor of Neuropathy: The Sheffield Prospective Diabetes Study
Author(s) -
Satyan Rajbhandari,
Fahad Syed Hamid,
Nigel Harris,
Solomon Tesfaye
Publication year - 2018
Publication title -
journal of diabetes and endocrinology association of nepal
Language(s) - English
Resource type - Journals
eISSN - 2631-2107
pISSN - 2594-3367
DOI - 10.3126/jdean.v2i2.22361
Subject(s) - medicine , prospective cohort study , diabetes mellitus , etiology , type 2 diabetes , diabetic neuropathy , complication , epidemiology , lipid profile , endocrinology , gastroenterology , surgery
Background : Despite being a very common complication, the aetiology and potential risk factors of diabetic neuropathy (DN) have not been clearly determined in a prospective study. Aims: The aim of Sheffield Prospective Diabetes Study was to identify the abnormalities of physiological, biochemical, haemorrhelogical and cellular function for complications of diabetes in type 1 diabetes.
Materials and Methods: 66 newly diagnosed type 1 diabetic subjects (mean age 31 ± 9 (SD) duration (3 years ± 2) were identified and followed for 9 years. They had detailed neurological assessment (symptoms and signs score, nerve conduction, vibration perception threshold, warm thermal discrimination threshold and autonomic function tests) and blood samples taken for detail biochemical and haemorrheological analysis at base line and at follow up.
Results: At the 9 years follow up, 51 subjects were studied of whom 18 were found to have DN using Dyck’s criteria. As expected subjects with DN had significantly higher (p <0.01) mean HbA1 over 9 years of follow up (11.8% vs 9.8%), but it was not significantly different at base line (10.2% vs 8.9%; p= 0.37). In addition, total cholesterol and LDL cholesterol at baseline were found to be risk factors for the development of neuropathy (5.9 vs 4.7 mmol; p=0.01 and 3.7 vs 2.8 mmol; p=0.03 respectively).
Conclusions: This prospective study confirms the findings of recent large epidemiological studies linking cardiovascular risk factors to the development of DN, and perhaps suggest a vascular aetiology for DN. Improvement of potentially modifiable risk factors for neuropathy may be useful for the development of risk reduction strategies.