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Peripheral and central nervous contribution to gastrointestinal symptoms in diabetic patients with autonomic neuropathy
Author(s) -
Brock C.,
Graversen C.,
Frøkjær J.B.,
Søfteland E.,
Valeriani M.,
Drewes A.M.
Publication year - 2013
Publication title -
european journal of pain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.305
H-Index - 109
eISSN - 1532-2149
pISSN - 1090-3801
DOI - 10.1002/j.1532-2149.2012.00254.x
Subject(s) - peripheral , sensation , medicine , peripheral neuropathy , stimulation , central nervous system , electroencephalography , autonomic nervous system , gastroenterology , diabetes mellitus , endocrinology , psychology , neuroscience , blood pressure , heart rate , psychiatry
Background & Aims Long‐term diabetes mellitus ( DM ) has been associated with neuronal changes in the enteric, peripheral and/or central nervous system. Moreover, abnormal visceral sensation and gastrointestinal ( GI ) symptoms are seen in up to 75% of patients. To explore the role of diabetic autonomic neuropathy ( DAN ) in patients with long‐standing DM , we investigated psychophysical responses and neuronal activity recorded as evoked brain potentials and dipolar source modelling. Methods Fifteen healthy volunteers and 14 type‐1 DM patients with DAN were assessed with a symptom score index characterizing upper GI abnormalities. Multichannel (62) electroencephalography was recorded during painful electrical stimulation of the lower oesophagus. Brain activity to painful stimulations was modelled using Brain Electrical Source Analysis ( besa ). Results Diabetic patients had higher stimulus intensities to evoke painful sensation ( p ≤ 0.001), longer latencies of N 2 and P 2 components (both p ≤ 0.001), and lower amplitudes of P1‐N2 and N2‐P2 complexes ( p ≤ 0.001; p = 0.02). Inverse modelling of brain sources showed deeper bilateral insular dipolar source localization ( p = 0.002). Symptom score index was negatively correlated with the depth of insular activity ( p = 0.004) and positively correlated with insular dipole strength ( p = 0.03). Conclusion DM patients show peripheral and central neuroplastic changes. Moreover, the role of abnormal insular processing may explain the appearance and persistence of GI symptoms related to DAN . This enhanced understanding of DAN may have future clinical and therapeutical implications.