Consideration of T-Cell Profile in the Examination of Statin Efficacy in Inflammatory Diseases, Neurodegeneration, and Neurocognitive Performance.

Matthew A Hintermayer, Daniel Mendelson, Jae Hyun Byun
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Abstract

Statins are a cornerstone in the medical management of cardiovascular disease, yet their efficacy varies greatly between individuals. In this commentary, we outline the evidence for the role of CD4+CD28null T-cell expansion as a critical moderator of the effects of statins in preventing cardiovascular events via the reduction of pathological inflammation. Given this relationship, we argue that T-cell profiles should be considered as a patient characteristic in clinical and preclinical studies examining statin efficacy in other age- and inflammation-related pathologies. We discuss the implications this may have for studies of statin use in numerous disease processes-notably, dementia and neurocognitive dysfunction-and the potential for T-cell profiles to be used as a prognosticator for statin efficacy in rheumatoid arthritis, Alzheimer's disease, and multiple sclerosis.

在研究他汀类药物对炎症性疾病、神经变性和神经认知能力的疗效时考虑 T 细胞特征。
他汀类药物是治疗心血管疾病的基石,但其疗效却因人而异。在这篇评论中,我们概述了 CD4+CD28 空 T 细胞扩增作为他汀类药物通过减少病理炎症预防心血管事件效果的关键调节因子所起作用的证据。鉴于这种关系,我们认为,在对他汀类药物对其他年龄和炎症相关病症的疗效进行临床和临床前研究时,应将 T 细胞特征作为患者特征加以考虑。我们讨论了这可能对他汀类药物用于多种疾病过程(尤其是痴呆症和神经认知功能障碍)的研究产生的影响,以及 T 细胞特征作为他汀类药物对类风湿性关节炎、阿尔茨海默病和多发性硬化症疗效的预后指标的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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