TREM-1; Is It a Pivotal Target for Cardiovascular Diseases?
AbstractCardiovascular diseases (CVDs) are as menacing as ever and still continue to kill adults worldwide, notwithstanding tremendous efforts to decrease their consequent mortality and morbidity. Lately, a growing body of research indicated that inflammation plays a pivotal role in the pathogenesis and complications of CVDs. A receptor of the immunoglobulin superfamily, triggering receptors expressed on myeloid cells-1 (TREM-1) was shown to induce and amplify the inflammation in both acute and chronic disease’ pathogenesis and progression, which hence makes it one of the most important complication factors of CVDs. Thus, studies endeavored to investigate the role played by TREM-1 in CVDs with respect to their etiologies, complications, and possible therapeutics. We examined here, for the first time, the most relevant studies regarding TREM-1 involvement in CVDs. We critically analyzed and summarized our findings and made some suggestions for furtherance of the investigations with the aim to utilize TREM-1 and its pathways for diagnostic, management, and prognosis of CVDs. Overall, TREM-1 was found to be involved in the pathogenesis of acute and chronic cardiovascular conditions, such as acute myocardial infarction (AMI) and atherosclerosis. Although most therapeutic approaches are yet to be elucidated, our present research outcome displays a promising future to utilizing the TREM-1 pathway as a potential target for understanding and managing CVDs. View Full-Text
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Kouassi, K.T.; Gunasekar, P.; Agrawal, D.K.; Jadhav, G.P. TREM-1; Is It a Pivotal Target for Cardiovascular Diseases? J. Cardiovasc. Dev. Dis. 2018, 5, 45.
Kouassi KT, Gunasekar P, Agrawal DK, Jadhav GP. TREM-1; Is It a Pivotal Target for Cardiovascular Diseases? Journal of Cardiovascular Development and Disease. 2018; 5(3):45.Chicago/Turabian Style
Kouassi, Kouassi T.; Gunasekar, Palanikumar; Agrawal, Devendra K.; Jadhav, Gopal P. 2018. "TREM-1; Is It a Pivotal Target for Cardiovascular Diseases?" J. Cardiovasc. Dev. Dis. 5, no. 3: 45.
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