کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5627051 | 1579664 | 2017 | 7 صفحه PDF | دانلود رایگان |
- Up-to-date findings from published clinical trials and meta-analyses regarding neurological outcomes from diabetes trials.
- A timely overview of the benefits of antidiabetic therapy from a neurologist's point of view.
- Therapy for diabetes mellitus type I effectively prevents polyneuropathy.
- Semaglutide is still the only drug proven to reduce stroke incidence as a separate endpoint.
- Antidiabetic therapy does not modify the risk of dementia.
Considering the causative or contributory effects of diabetes mellitus on common neurological diseases such as polyneuropathy, stroke and dementia, modern antidiabetic drugs may be expected to reduce incidence or progression of these conditions. Nevertheless, most observed benefits have been small, except in the context of therapy for diabetes mellitus type I and new-onset polyneuropathy. Recently, semaglutide, a GLP-1 analog, has been shown to significantly reduce stroke incidence in a randomized controlled trial. Beneficial effects of antidiabetic drugs on stroke severity or outcome have been controversial, though. The level of risk conferred by diabetes mellitus, the complex pathophysiology of neurological diseases, issues of trial design, side-effects of antidiabetic drugs as well as co-medication might be interacting factors that determine the performance of antidiabetic therapy with respect to neurological outcomes. It might be speculated that early treatment of prediabetes might prevent cerebral arteriosclerosis, cognitive decline or polyneuropathy more effectively, but this remains to be demonstrated.
Journal: Clinical Neurology and Neurosurgery - Volume 158, July 2017, Pages 60-66