Fisetin for COVID-19 in skilled nursing facilities: Senolytic trials in the COVID era

被引:41
作者
Verdoorn, Brandon P. [1 ,2 ]
Evans, Tamara K. [1 ]
Hanson, Gregory J. [1 ,2 ]
Zhu, Yi [1 ]
Langhi Prata, Larissa G. P. [1 ]
Pignolo, Robert J. [1 ,2 ]
Atkinson, Elizabeth J. [3 ]
Wissler-Gerdes, Erin O. [1 ]
Kuchel, George A. [4 ]
Mannick, Joan B. [5 ]
Kritchevsky, Stephen B. [6 ]
Khosla, Sundeep [1 ,7 ]
Rizza, Stacey A. [8 ]
Walston, Jeremy D. [9 ]
Musi, Nicolas [10 ]
Lipsitz, Lewis A. [11 ,12 ,13 ]
Kiel, Douglas P. [11 ,12 ,13 ]
Yung, Raymond [14 ,15 ,16 ,17 ]
LeBrasseur, Nathan K. [1 ,18 ]
Singh, Ravinder J. [19 ]
McCarthy, Teresa [20 ]
Puskarich, Michael A. [20 ]
Niedernhofer, Laura J. [20 ]
Robbins, Paul D. [20 ]
Sorenson, Matthew [21 ]
Tchkonia, Tamara [1 ]
Kirkland, James L. [1 ,2 ]
机构
[1] Mayo Clin, Robert & Arlene Kogod Ctr Aging, Rochester, MN 55901 USA
[2] Mayo Clin, Div Geriatr & Gerontol, Rochester, MN 55901 USA
[3] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN USA
[4] Univ Connecticut, Ctr Aging, UConn Hlth, Farmington, CT USA
[5] Life Biosci, Boston, MA USA
[6] Sticht Ctr Healthy Aging & Alzheimers Prevent, Winston Salem, NC USA
[7] Mayo Clin, Dept Med, Div Endocrinol, Rochester, MN USA
[8] Mayo Clin, Div Infect Dis, Dept Med, Rochester, MN USA
[9] Johns Hopkins Univ, Dept Med, Div Geriatr Med & Gerontol, Baltimore, MD USA
[10] Univ Texas Hlth Sci Ctr San Antonio, Barshop Inst Longev & Aging Studies, San Antonio, TX 78229 USA
[11] Hebrew Senior Life, Hinda & Arthur Marcus Inst Aging Res, Boston, MA USA
[12] Beth Israel Deaconess Med Ctr, Div Gerontol, Boston, MA 02215 USA
[13] Harvard Med Sch, Boston, MA 02115 USA
[14] Univ Michigan, Geriatr Ctr, Ann Arbor, MI 48109 USA
[15] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
[16] VA Ann Arbor Geriatr Res Educ & Clin Ctr, Ann Arbor, MI USA
[17] Univ Michigan, Div Geriatr & Palliat Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[18] Mayo Clin, Dept Phys Med & Rehabil, Rochester, MN USA
[19] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[20] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Inst Biol Aging & Metab, Minneapolis, MN USA
[21] Mayo Clin, Legal Contract Adm, Rochester, MN USA
关键词
cellular senescence; facility for geroscience analysis; SARS-CoV-2; senolytics; Translational Geroscience Network; SENESCENT CELLS; UNITED-STATES; CORONAVIRUS;
D O I
10.1111/jgs.17416
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The burden of senescent cells (SnCs), which do not divide but are metabolically active and resistant to death by apoptosis, is increased in older adults and those with chronic diseases. These individuals are also at the greatest risk for morbidity and mortality from SARS-CoV-2 infection. SARS-CoV-2 complications include cytokine storm and multiorgan failure mediated by the same factors as often produced by SnCs through their senescence-associated secretory phenotype (SASP). The SASP can be amplified by infection-related pathogen-associated molecular profile factors. Senolytic agents, such as Fisetin, selectively eliminate SnCs and delay, prevent, or alleviate multiple disorders in aged experimental animals and animal models of human chronic diseases, including obesity, diabetes, and respiratory diseases. Senolytics are now in clinical trials for multiple conditions linked to SnCs, including frailty; obesity/diabetes; osteoporosis; and cardiovascular, kidney, and lung diseases, which are also risk factors for SARS-CoV-2 morbidity and mortality. A clinical trial is underway to test if senolytics decrease SARS-CoV-2 progression and morbidity in hospitalized older adults. We describe here a National Institutes of Health-funded, multicenter, placebo-controlled clinical trial of Fisetin for older adult skilled nursing facility (SNF) residents who have been, or become, SARS-CoV-2 rtPCR-positive, including the rationale for targeting fundamental aging mechanisms in such patients. We consider logistic challenges of conducting trials in long-term care settings in the SARS-CoV-2 era, including restricted access, consent procedures, methods for obtaining biospecimens and clinical data, staffing, investigational product administration issues, and potential solutions for these challenges. We propose developing a national network of SNFs engaged in interventional clinical trials.
引用
收藏
页码:3023 / 3033
页数:11
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