The Value of Ursodeoxycholic Acid and Mesenchymal Stem Cells in the Treatment of Severe COVID-19

被引:1
作者
Zheng, Qi [1 ]
Li, Yuetong [1 ]
Sheng, Guoping [2 ]
Li, Lanjuan [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Natl Clin Res Ctr Infect Dis, Natl Med Ctr Infect Dis,Sch Med,Collaborat Innovat, 79 Qingchun Rd, Hangzhou 310003, Peoples R China
[2] Zhejiang Shuren Univ, Shulan Int Med Coll, Dept Infect Dis, Shulan Hangzhou Hosp, Hangzhou 310022, Peoples R China
关键词
UDCA; MSCs; COVID-19; prognosis;
D O I
10.3390/microorganisms12071269
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Objective: The objective of this study was to evaluate the therapeutic efficacy of ursodeoxycholic acid (UDCA) and mesenchymal stem cells (MSCs) in patients with severe COVID-19. Methods: We included severe COVID-19 patients hospitalized at Shulan (Hangzhou) Hospital between December 2022 and June 2023. We used a logistic regression model to compare the use of UDCA and MSCs in the two distinct groups of improved and poor outcomes. It is noteworthy that the deterioration group encompassed instances of both death and abandonment of treatment. The receiver operating characteristic (ROC) curve was plotted to assess the performance of the model. The aim was to assess the therapeutic effect of UDCA and MSCs on the outcome of severe COVID-19 patients. Results: A total of 167 patients with severe COVID-19 were included in this study. The analysis revealed that out of 42 patients (25.1%), 17 patients (10.2%) had taken UDCA, and 17 patients (10.2%) had used MSCs. Following a multivariable logistic regression, the results indicated a negative association between UDCA treatment (OR = 0.38 (0.16-0.91), p = 0.029), MSCs treatment (OR = 0.21 (0.07-0.65), p = 0.007), and the risk of severe COVID-19 mortality. Additionally, age showed a positive association with the risk of mortality (OR = 1.03 (1.01-1.07), p = 0.025). Conclusions: UDCA and MSCs have shown potential in improving the prognosis of severe COVID-19 patients and could be considered as additional treatments for COVID-19 in the future.
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页数:10
相关论文
共 29 条
[1]   Ursodeoxycholic acid as a candidate therapeutic to alleviate and/or prevent COVID-19-associated cytokine storm [J].
Abdulrab, Saleem ;
Al-Maweri, Sadeq ;
Halboub, Esam .
MEDICAL HYPOTHESES, 2020, 143
[2]   FXR inhibition may protect from SARS-CoV-2 infection by reducing ACE2 [J].
Brevini, Teresa ;
Maes, Mailis ;
Webb, Gwilym J. ;
John, Binu, V ;
Fuchs, Claudia D. ;
Buescher, Gustav ;
Wang, Lu ;
Griffiths, Chelsea ;
Brown, Marnie L. ;
Scott, William E., III ;
Pereyra-Gerber, Pehuen ;
Gelson, William T. H. ;
Brown, Stephanie ;
Dillon, Scott ;
Muraro, Daniele ;
Sharp, Jo ;
Neary, Megan ;
Box, Helen ;
Tatham, Lee ;
Stewart, James ;
Curley, Paul ;
Pertinez, Henry ;
Forrest, Sally ;
Mlcochova, Petra ;
Varankar, Sagar S. ;
Darvish-Damavandi, Mahnaz ;
Mulcahy, Victoria L. ;
Kuc, Rhoda E. ;
Williams, Thomas L. ;
Heslop, James A. ;
Rossetti, Davide ;
Tysoe, Olivia C. ;
Galanakis, Vasileios ;
Vila-Gonzalez, Marta ;
Crozier, Thomas W. M. ;
Bargehr, Johannes ;
Sinha, Sanjay ;
Upponi, Sara S. ;
Fear, Corrina ;
Swift, Lisa ;
Saeb-Parsy, Kourosh ;
Davies, Susan E. ;
Wester, Axel ;
Hagstrom, Hannes ;
Melum, Espen ;
Clements, Darran ;
Humphreys, Peter ;
Herriott, Jo ;
Kijak, Edyta ;
Cox, Helen .
NATURE, 2023, 615 (7950) :134-+
[3]  
Cabrera D, 2019, HANDB EXP PHARMACOL, V256, P237, DOI 10.1007/164_2019_241
[4]  
Cao B, 2020, NEW ENGL J MED, V382, P1787, DOI [10.1056/NEJMoa2001282, 10.1056/NEJMc2008043]
[5]   Clinical Study of Mesenchymal Stem Cell Treatment for Acute Respiratory Distress Syndrome Induced by Epidemic Influenza A (H7N9) Infection: A Hint for COVID-19 Treatment [J].
Chen, Jiajia ;
Hu, Chenxia ;
Chen, Lijun ;
Tang, Lingling ;
Zhu, Yixin ;
Xu, Xiaowei ;
Chen, Lu ;
Gao, Hainv ;
Lu, Xiaoqing ;
Yu, Liang ;
Dai, Xiahong ;
Xiang, Charlie ;
Li, Lanjuan .
ENGINEERING, 2020, 6 (10) :1153-1161
[6]   Ursodeoxycholic Acid Does Not Improve COVID-19 Outcome in Hospitalized Patients [J].
Colapietro, Francesca ;
Angelotti, Giovanni ;
Masetti, Chiara ;
Shiffer, Dana ;
Pugliese, Nicola ;
De Nicola, Stella ;
Carella, Francesco ;
Desai, Antonio ;
Ormas, Monica ;
Calatroni, Marta ;
Omodei, Paolo ;
Ciccarelli, Michele ;
Aliberti, Stefano ;
Reggiani, Francesco ;
Bartoletti, Michele ;
Cecconi, Maurizio ;
Lleo, Ana ;
Aghemo, Alessio ;
Voza, Antonio .
VIRUSES-BASEL, 2023, 15 (08)
[7]   Systematic review and meta-analysis of cell therapy for COVID-19: global clinical trial landscape, published safety/efficacy outcomes, cell product manufacturing and clinical delivery [J].
Couto, Pedro S. ;
Al-Arawe, Nada ;
Filgueiras, Igor S. ;
Fonseca, Dennyson L. M. ;
Hinterseher, Irene ;
Catar, Rusan A. ;
Chinnadurai, Raghavan ;
Bersenev, Alexey ;
Cabral-Marques, Otavio ;
Moll, Guido ;
Verter, Frances .
FRONTIERS IN IMMUNOLOGY, 2023, 14
[8]   Mesenchymal Stem Cells [J].
Ding, Dah-Ching ;
Shyu, Woei-Cherng ;
Lin, Shinn-Zong .
CELL TRANSPLANTATION, 2011, 20 (01) :5-14
[9]   Characterisation of SARS-CoV-2 genomic variation in response to molnupiravir treatment in the AGILE Phase IIa clinical trial [J].
Donovan-Banfield, I'ah ;
Penrice-Randal, Rebekah ;
Goldswain, Hannah ;
Rzeszutek, Aleksandra M. ;
Pilgrim, Jack ;
Bullock, Katie ;
Saunders, Geoffrey ;
Northey, Josh ;
Dong, Xiaofeng ;
Ryan, Yan ;
Reynolds, Helen ;
Tetlow, Michelle ;
Walker, Lauren E. ;
FitzGerald, Richard ;
Hale, Colin ;
Lyon, Rebecca ;
Woods, Christie ;
Ahmad, Shazaad ;
Hadjiyiannakis, Dennis ;
Periselneris, Jimstan ;
Knox, Emma ;
Middleton, Calley ;
Lavelle-Langham, Lara ;
Shaw, Victoria ;
Greenhalf, William ;
Edwards, Thomas ;
Lalloo, David G. ;
Edwards, Christopher J. ;
Darby, Alistair C. ;
Carroll, Miles W. ;
Griffiths, Gareth ;
Khoo, Saye H. ;
Hiscox, Julian A. ;
Fletcher, Thomas .
NATURE COMMUNICATIONS, 2022, 13 (01)
[10]   Recent SARS-CoV-2 Outlook and Implications in a COVID-19 Vaccination Era [J].
Ehianeta, Teddy ;
Mzee, Said Abdulrahman Salim ;
Adebisi, Muslimat Kehinde ;
Ehianeta, Oluwayemisi .
INFECTIOUS MICROBES & DISEASES, 2021, 3 (03) :125-133