Abstract:Background
Low insulin-like growth factor 1 (IGF-1) have been associated with increased risk of atherosclerosis and atrial fibrillation in cross-sectional studies. Yet, prospective data linking IGF-1 levels to the development of ischemic stroke remain inconclusive. We examined prospectively the association between serum IGF-1 levels and incident ischemic stroke.
Methods
We measured serum IGF-1 levels in 757 elderly individuals (mean age 79±5, 62% women), free of prevalent stroke, from the Framingham original… Show more
“…Insulin‐like growth factor 1 (IGF‐1) plays an important role in brain development and normal growth . IGF‐1 reduces the progression of atherosclerosis, and in cross‐sectional studies, low circulating IGF‐1 is associated with increased risk of ischemic stroke . In humans, low levels of IGF‐1 are associated with stroke risk factors such as diabetes, hypertension, and coronary artery disease .…”
Section: Introductionmentioning
confidence: 99%
“…1 IGF-1 reduces the progression of atherosclerosis, and in cross-sectional studies, low circulating IGF-1 is associated with increased risk of ischemic stroke. 2 In humans, low levels of IGF-1 are associated with stroke risk factors such as diabetes, hypertension, and coronary artery disease. [3][4][5] Previous studies regarding stroke patients have suggested that low IGF-1 levels in the circulation are related with higher stroke severity, poor outcome, and less rates of survival after stroke.…”
The data showed that low serum IGF-1 levels at admission are associated with a high risk of developing PSD, suggesting that these alterations might be involved in the pathophysiology of depression symptoms in stroke patients.
“…Insulin‐like growth factor 1 (IGF‐1) plays an important role in brain development and normal growth . IGF‐1 reduces the progression of atherosclerosis, and in cross‐sectional studies, low circulating IGF‐1 is associated with increased risk of ischemic stroke . In humans, low levels of IGF‐1 are associated with stroke risk factors such as diabetes, hypertension, and coronary artery disease .…”
Section: Introductionmentioning
confidence: 99%
“…1 IGF-1 reduces the progression of atherosclerosis, and in cross-sectional studies, low circulating IGF-1 is associated with increased risk of ischemic stroke. 2 In humans, low levels of IGF-1 are associated with stroke risk factors such as diabetes, hypertension, and coronary artery disease. [3][4][5] Previous studies regarding stroke patients have suggested that low IGF-1 levels in the circulation are related with higher stroke severity, poor outcome, and less rates of survival after stroke.…”
The data showed that low serum IGF-1 levels at admission are associated with a high risk of developing PSD, suggesting that these alterations might be involved in the pathophysiology of depression symptoms in stroke patients.
“…The levels of IGF-1 are associated with cardiovascular disease risk. 30, 31 It is known that IGF-1 activates the PI3K/Akt pathway and promotes the synthesis of nitric oxide to prevent cardiovascular disease. 32, 33 Several studies…”
Section: Papp-a Knockdown Suppresses the Production Of Inflammatory Cmentioning
Background:Recent studies have suggested that pregnancy-associated plasma protein-A (PAPP-A) is involved in the pathogenesis of atherosclerosis. This study aim is to investigate the role and mechanisms of PAPP-A in reverse cholesterol transport (RCT) and inflammation during the development of atherosclerosis.
Methods and Results:PAPP-A was silenced in apolipoprotein E (apoE −/− ) mice with administration of PAPP-A shRNA. Oil Red O staining of the whole aorta root revealed that PAPP-A knockdown reduced lipid accumulation in aortas. Oil Red O, hematoxylin and eosin (HE) and Masson staining of aortic sinus further showed that PAPP-A knockdown alleviated the formation of atherosclerotic lesions. It was found that PAPP-A knockdown reduced the insulin-like growth factor 1 (IGF-1) levels and repressed the PI3K/Akt pathway in both aorta and peritoneal macrophages. The expression levels of LXRα, ABCA1, ABCG1, and SR-B1 were increased in the aorta and peritoneal macrophages from apoE −/− mice administered with PAPP-A shRNA. Furthermore, PAPP-A knockdown promoted RCT from macrophages to plasma, the liver, and feces in apoE −/− mice. In addition, PAPP-A knockdown elevated the expression and secretion of monocyte chemoattractant protein-1 (MCP-1), interleukin-6 (IL-6), tumor necrosis factor-α, and interleukin-1β through the nuclear factor kappa-B (NF-κB) pathway.
Conclusions:The present study results suggest that PAPP-A promotes the development of atherosclerosis in apoE −/− mice through reducing RCT capacity and activating an inflammatory response.
“…A case-control study of ischaemic stroke (IS) in a Korean population observed that common variants in IGF1 genes (rs2162679 and rs6214) exhibited protective effects on the development of IS [12]. Epidemiological studies revealed that the levels of circulating IGF1 and IGFBP3 below normal range were associated with the increased morbidity and mortality from ischaemic heart disease and stroke [13][14][15]. In addition, evidence supported that the prevalence of hypertension-induced cerebral haemorrhages and acute ischaemic stroke dramatically increased in people with a declining circulating IGF1 [16][17][18].…”
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