2022
DOI: 10.1016/j.tem.2021.10.008
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Common pathways in dementia and diabetic retinopathy: understanding the mechanisms of diabetes-related cognitive decline

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Cited by 56 publications
(28 citation statements)
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“…Reports indicate that a history of amputation or ulceration, 68 peripheral edema, 69 foot pressure, 70 plantar callus formation, 71 nephropathy, 72 poor glucose control, 73 ischemia, 74 retinopathy 75 and prolonged diabetes 76 is an important predisposing factor leading to the development of DFUs. Recent studies have reported that diabetic wounds exhibit a prolonged inflammatory phase due to impairment of phagocytes and macrophages, resulting in the excessive release of MMPs (matrix metalloproteinases), causing degradation of collagen and extracellular matrix (ECM).…”
Section: Pathophysiology Of Diabetic Foot Ulcers (Dfus)mentioning
confidence: 99%
“…Reports indicate that a history of amputation or ulceration, 68 peripheral edema, 69 foot pressure, 70 plantar callus formation, 71 nephropathy, 72 poor glucose control, 73 ischemia, 74 retinopathy 75 and prolonged diabetes 76 is an important predisposing factor leading to the development of DFUs. Recent studies have reported that diabetic wounds exhibit a prolonged inflammatory phase due to impairment of phagocytes and macrophages, resulting in the excessive release of MMPs (matrix metalloproteinases), causing degradation of collagen and extracellular matrix (ECM).…”
Section: Pathophysiology Of Diabetic Foot Ulcers (Dfus)mentioning
confidence: 99%
“…Thus, the presence of DR has been associated with the development of macrovascular complications of diabetes, specifically, cerebrovascular complications, cardiovascular complications and vascular peripheral complications [ 4 ]. Moreover, the evaluation of retinal neurodegeneration could help to identify patients which are at risk of cognitive impairment, an emerging complication of the type 2 diabetes [ 5 , 6 ].…”
Section: Introductionmentioning
confidence: 99%
“…BBB breakdown was suggested to be involved in the pathophysiology of several neurological disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis and multiple sclerosis [12]. However, the mechanisms driving barrier breakdown and their link to pathophysiology of neurodegenerative diseases are not yet fully characterized [13]. Pre-clinical studies in animal models poorly translate to humans and represent a major hurdle in the drug discovery pipeline, since 80% of potential treatments fail in clinical trials [14].…”
Section: Introductionmentioning
confidence: 99%