Hypoglycaemia in type 2 diabetes exacerbates amyloid‐related proteins associated with dementia. Issue 2 (25th October 2020)
- Record Type:
- Journal Article
- Title:
- Hypoglycaemia in type 2 diabetes exacerbates amyloid‐related proteins associated with dementia. Issue 2 (25th October 2020)
- Main Title:
- Hypoglycaemia in type 2 diabetes exacerbates amyloid‐related proteins associated with dementia
- Authors:
- Moin, Abu Saleh Md
Al‐Qaissi, Ahmed
Sathyapalan, Thozhukat
Atkin, Stephen L.
Butler, Alexandra E. - Abstract:
- Abstract: Aims: Hypoglycaemia in diabetes (T2D) may increase the risk of Alzheimer's disease (AD). We hypothesized that hypoglycaemia‐induced amyloid‐related protein changes would be exacerbated in T2D. Materials and methods: A prospective, parallel study in T2D (n = 23) and controls (n = 23). Subjects underwent insulin‐induced hypoglycaemia with blood sampling at baseline, hypoglycaemia and post‐hypoglycaemia; proteomic analysis of amyloid‐related proteins was undertaken. Results: At baseline, amyloid‐precursor protein (APP) ( P < .01) was elevated and alpha‐synuclein (SNCA) ( P < .01) reduced in T2D. At hypoglycaemia, amyloid P‐component ( P < .01) was elevated and SNCA ( P < .05) reduced in T2D; APP ( P < .01) and noggin ( P < .05) were elevated and SNCA ( P < .01) reduced in controls. In the post‐hypoglycaemia follow‐up period, APP and microtubule‐associated protein tau normalized in controls but showed a below‐baseline decrease in T2D; noggin normalized in both; SNCA normalized in T2D, with a below‐baseline decrease in controls. Conclusion: The AD‐associated protein pattern found in T2D, with basal elevated APP and reduced SNCA, was exaggerated by hypoglycaemia with increased APP and decreased SNCA. Additional AD‐associated protein levels that changed in response to hypoglycaemia, particularly in T2D, included amyloid P‐component, microtubule‐associated protein tau, apolipoproteins A1 and E3, pappalysin and noggin. These results are in accordance with theAbstract: Aims: Hypoglycaemia in diabetes (T2D) may increase the risk of Alzheimer's disease (AD). We hypothesized that hypoglycaemia‐induced amyloid‐related protein changes would be exacerbated in T2D. Materials and methods: A prospective, parallel study in T2D (n = 23) and controls (n = 23). Subjects underwent insulin‐induced hypoglycaemia with blood sampling at baseline, hypoglycaemia and post‐hypoglycaemia; proteomic analysis of amyloid‐related proteins was undertaken. Results: At baseline, amyloid‐precursor protein (APP) ( P < .01) was elevated and alpha‐synuclein (SNCA) ( P < .01) reduced in T2D. At hypoglycaemia, amyloid P‐component ( P < .01) was elevated and SNCA ( P < .05) reduced in T2D; APP ( P < .01) and noggin ( P < .05) were elevated and SNCA ( P < .01) reduced in controls. In the post‐hypoglycaemia follow‐up period, APP and microtubule‐associated protein tau normalized in controls but showed a below‐baseline decrease in T2D; noggin normalized in both; SNCA normalized in T2D, with a below‐baseline decrease in controls. Conclusion: The AD‐associated protein pattern found in T2D, with basal elevated APP and reduced SNCA, was exaggerated by hypoglycaemia with increased APP and decreased SNCA. Additional AD‐associated protein levels that changed in response to hypoglycaemia, particularly in T2D, included amyloid P‐component, microtubule‐associated protein tau, apolipoproteins A1 and E3, pappalysin and noggin. These results are in accordance with the reported detrimental effects of hypoglycaemia. … (more)
- Is Part Of:
- Diabetes, obesity & metabolism. Volume 23:Issue 2(2021)
- Journal:
- Diabetes, obesity & metabolism
- Issue:
- Volume 23:Issue 2(2021)
- Issue Display:
- Volume 23, Issue 2 (2021)
- Year:
- 2021
- Volume:
- 23
- Issue:
- 2
- Issue Sort Value:
- 2021-0023-0002-0000
- Page Start:
- 338
- Page End:
- 349
- Publication Date:
- 2020-10-25
- Subjects:
- Alzheimer's disease -- amyloid‐related proteins -- dementia -- hypoglycaemia -- type 2 diabetes
Diabetes -- Periodicals
Obesity -- Periodicals
Metabolism -- Disorders -- Periodicals
Clinical pharmacology -- Periodicals
616.462 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1462-8902&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1463-1326 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dom.14220 ↗
- Languages:
- English
- ISSNs:
- 1462-8902
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.601970
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22312.xml