Professor
Søren Sindrup
Department of Neurology, Odense University Hospital
Projekt styring | ||
Projekt status | Active | |
Data indsamlingsdatoer | ||
Start | 01.11.2015 | |
Slut | 31.12.2018 | |
Chronic polyneuropathy is a common neurological disorder in which there is a generalized affection of peripheral nerves. It can be caused by diseases such as diabetes, and toxic substances such as alcohol and certain drugs. However, quite often the cause cannot be determined. In clinical practice the evaluation of patients with polyneuropathy is a complicated two stage procedure, which first determines the presence and pattern of peripheral nerve affection, and then seeks to establish the cause of the neuropathy. Currently, the procedure includes measuring nerve conduction and doing blood tests, and in selected cases determination of nerve fibre density in skin biopsies.
This research program will implement nerve fibre density determined in skin biopsies in all cases of suspected polyneuropathy, and introduce confocal microscopy of the cornea to study small nerve fibres as a diagnostic test. Further, the programme will do extra blood testing and imaging to determine the aetiology of polyneuropathy. Finally, it will establish a biobank with blood, serum and skin biopsies for all participants. Comprehensive information on the participants with regard to history, clinical findings, scoring of neuropathy severity, and diagnostic test results will be entered into a research database. The biobank material can e.g. be used to search for serum factors causing neuropathy and alternative staining of nerve fibres in skin biopsies.
The rationale of the study is that by obtaining detailed information on a large number of patients with suspected polyneuropathy we will be able to:
Patients referred to the neuromuscular team at Department of Neurology for examination for chronic polyneuropathy.
We consecutively include patients aged 18+ with suspected polyneuropathy. Study data will collected at study entry and the patients will be re-examined 2 and 5 years after being diagnosed with polyneuropathy.
Clinical data concerning diagnosis, symptoms, neurological signs, scores of disease severity and quality of life, risk factors for neuropathy and cardiovascular diseases.
Results of neurophysiology examination, intra-epidermal nerve fibre density in skin biopsies, quantitative sensory examination and confocal microscopy of the cornea.
Blood (DNA), serum, spinal fluid.
Skin biopsies.
Photos of corneal nerve fibers obtained during microscopy.
Department of Neurology, Odense University Hospital
Department of Clinical Pathology, Odense University Hospital