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Type 2 diabetes mellitus acts as a risk factor for cardiovascular disease. It has been hypothesized that control of plasma glucose levels would reduce cardiovascular disease in type 2 diabetic patients--thus lowering parameters such as mortality rate, myocardial infarction or stroke. A narrative review was carried out looking at data on mortality and cardiovascular disease outcomes, including myocardial infarction and stroke, associated with hypoglycemic therapy in type 2 diabetic patients, starting with the University Group Diabetes Trial (1970-1978) and ending with the Veterans Affairs Diabetes Trial (2009). The data reviewed in the present text fail to confirm the hypothesis presented above. No consistent relation between lowering plasma glucose and favorable effects either on mortality rate or on major cardiovascular disease has been clearly shown to exist. However, there are interesting data concerning drugs that lower plasma insulin levels, particularly metformin, but also, to a certain degree, pioglitazone. Also of interest are data on a possible legacy effect observed in the long-term follow-up of patients previously under intensive plasma glucose control. Consistent evidence in favor of lowering glycated hemoglobin levels to values under 7% also seems to be lacking at present, at least concerning mortality and cardiovascular outcomes. For the time being, it can be argued that efforts should be centered on interventions with clear evidence of benefit, such as treatment of hypertension or excessive weight, as well as the use of statins.
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BMC Psychiatry
September 2025
Department of Cardiovascular, The Second Affiliated Hospital of Nanchang University, No. 1 Minde Road, Jiangxi, Nanchang, 330006, China.
Infect Dis Ther
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School of Biomedical Sciences, The Chinese University of Hong Kong (CUHK), Hong Kong SAR, China.
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Paris Cité University, INSERM UMR-S 970, Paris Cardiovascular Research Centre, Paris, France.
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View Article and Find Full Text PDFMol Syst Biol
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Department of Medicine, Division of Cardiovascular Medicine, Stanford University, Stanford, CA, USA.
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Pediatric Intensive Care Unit, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences); Department of Immunology, School of Basic Medical Sciences; Department of Clinical Laboratory, the Third Affiliated Hospital of Southern Medical University, Southern Medical University, Gua
Communication between group 3 innate lymphoid cells (ILC3) and other immune cells, as well as intestinal epithelial cells, is pivotal in regulating intestinal inflammation. This study, for the first time, underscores the importance of crosstalk between intestinal endothelial cells (ECs) and ILC3. Our single-cell transcriptome analysis combined with protein expression detection revealed that ECs significantly increased the population of interleukin (IL)-22 ILC3 through interactions mediated by endothelin-1 (ET-1) and its receptor endothelin A receptor (EDNRA).
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