Malik R A, Kumar S, Boulton A J
Department of Medicine, Manchester Royal Infirmary, UK.
J Neurol Neurosurg Psychiatry. 1995 Apr;58(4):493-5. doi: 10.1136/jnnp.58.4.493.
The pathogenesis of human diabetic neuropathy remains unclear. Mendenhall's syndrome is characterised by a mutation in the insulin receptor gene with consequent lifelong uncontrolled hyperglycaemia. The sural nerve biopsy from a patient with Mendenhall's syndrome showed a gross loss of myelinated fibres that was comparable with the degree of fibre loss in a case matched diabetic patient with established neuropathy. The biopsy from the patient with Mendenhall's syndrome showed only a very mild degree of microangiopathy, however, which failed to relate to the degree of nerve fibre loss and also did not compare with the advanced degree of microangiopathy seen in the diabetic patient. Thus hyperglycaemia itself did not result in appreciable microangiopathy. Furthermore the presence of severe neuropathy without advanced microangiopathy suggests an important and independent role for metabolic factors in the pathogenesis of neuropathy.
人类糖尿病性神经病变的发病机制仍不清楚。门登霍尔综合征的特征是胰岛素受体基因突变,导致终身血糖控制不佳。一名门登霍尔综合征患者的腓肠神经活检显示,有髓纤维大量丧失,这与一名匹配的已确诊糖尿病性神经病变患者的纤维丧失程度相当。然而,门登霍尔综合征患者的活检仅显示出非常轻微的微血管病变,这与神经纤维丧失程度无关,也与糖尿病患者所见的严重微血管病变程度不同。因此,高血糖本身并不会导致明显的微血管病变。此外,存在严重神经病变但无严重微血管病变表明代谢因素在神经病变发病机制中起重要且独立的作用。