Clinical Significance of COVID-19 and Diabetes: In the Pandemic Situation of SARS-CoV-2 Variants including Omicron (B.1.1.529)

被引:10
|
作者
Yonekawa, Akiko [1 ]
Shimono, Nobuyuki [2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Med & Biosyst Sci, Fukuoka 8128582, Japan
[2] Kyushu Univ Hosp, Dept Gen Internal Med, Fukuoka 8128582, Japan
[3] Kyushu Univ Hosp, Ctr Study Global Infect, Fukuoka 8128582, Japan
来源
BIOLOGY-BASEL | 2022年 / 11卷 / 03期
关键词
SARS-CoV-2; COVID-19; diabetes; hyperinflammation; hyperglycemia; new-onset diabetes; Omicron variant; SARS CORONAVIRUS; HOSPITALIZED-PATIENTS; FUNCTIONAL RECEPTOR; INSULIN-TREATMENT; TYPE-2; RISK; MORTALITY; OUTCOMES; ACE2; ASSOCIATION;
D O I
10.3390/biology11030400
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Simple Summary Amidst the dual pandemics of diabetes and coronavirus disease 2019 (COVID-19), with the constant emergence of novel variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a vicious cycle has been created, i.e., a hyperglycemic state contributes to the severe clinical course of COVID-19, which in turn has deleterious effects on glycometabolism and in some cases causes new-onset diabetes. Here, we present a comprehensive review of the current literature on the clinical and experimental findings associated with the interrelationship between diabetes and COVID-19. To control disease outcomes and glucometabolic complications in COVID-19, this issue is still being investigated. The coronavirus disease 2019 (COVID-19) global pandemic, which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), remains uncontrolled, with the spread of emerging variants. According to accumulating evidence, diabetes is one of the leading risk factors for a severe COVID-19 clinical course, depending on the glycemic state before admission and during COVID-19 hospitalization. Multiple factors are thought to be responsible, including an altered immune response, coexisting comorbidity, and disruption of the renin-angiotensin system through the virus-host interaction. However, the precise underlying mechanisms remain under investigation. Alternatively, the focus is currently on the diabetogenic and ketosis-prone potential of SARS-CoV-2 itself, even for probable triggers of stress and steroid-induced hyperglycemia in COVID-19. In this article, we present a comprehensive review of the recent literature on the clinical and experimental findings associated with diabetes and COVID-19, and we discuss their bidirectional relationship, i.e., the risk for an adverse prognosis and the deleterious effects on glycometabolism. Accurate assessments of the incidence of new-onset diabetes induced by COVID-19 and its pathogenicity are still unknown, especially in the context of the circulation of SARS-CoV-2 variants, such as Omicron (B.1.1.529), which is a major challenge for the future.
引用
收藏
页数:18
相关论文
共 50 条
  • [1] SARS-CoV-2 Omicron (B.1.1.529) Variant: A Challenge with COVID-19
    Afshar, Zeinab Mohseni
    Pirzaman, Ali Tavakoli
    Karim, Bardia
    Anaraki, Shiva Rahimipour
    Hosseinzadeh, Rezvan
    Pireivatlou, Elaheh Sanjari
    Babazadeh, Arefeh
    Hosseinzadeh, Dariush
    Miri, Seyed Rouhollah
    Sio, Terence T.
    Sullman, Mark J. M.
    Barary, Mohammad
    Ebrahimpour, Soheil
    [J]. DIAGNOSTICS, 2023, 13 (03)
  • [2] COVID-19 vaccination and SARS-CoV-2 Omicron (B.1.1.529) variant: a at the end of the tunnel?
    Mattiuzzi, Camilla
    Henry, Brandon M.
    Lippi, Giuseppe
    [J]. INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2022, 118 : 167 - 168
  • [3] Epidemic waves caused by SARS-CoV-2 omicron (B.1.1.529) and pessimistic forecasts of the COVID-19 pandemic duration
    Nesteruk, Igor
    [J]. MEDCOMM, 2022, 3 (01):
  • [4] Neutralizing potency of COVID-19 vaccines against the SARS-CoV-2 Omicron (B.1.1.529) variant
    Lippi, Giuseppe
    Mattiuzzi, Camilla
    Henry, Brandon M.
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2022, 94 (05) : 1799 - 1802
  • [5] Havoc caused by the SARS-CoV-2 Omicron (B.1.1.529)
    NAGARAjAN, PRiTHiviRAj
    RANGARAjAlU, Kumar
    [J]. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2022, 16 (07) : BL1 - BL2
  • [6] Emerging evidence on Omicron (B.1.1.529) SARS-CoV-2 variant
    Sharma, Vineet
    Rai, Himanshu
    Gautam, Dev N. S.
    Prajapati, Pradeep K.
    Sharma, Rohit
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2022, 94 (05) : 1876 - 1885
  • [7] Omicron (B.1.1.529): constellation of unusual mutations in SARS-CoV-2
    Kashyap, Abhishek
    Banerjee, Indrajit
    [J]. AFRICAN HEALTH SCIENCES, 2023, 23 (02) : 1 - 2
  • [8] The SARS-CoV-2 Omicron (B.1.1.529) variant and the re-emergence of COVID-19 in Europe: An alarm for Bangladesh
    Islam, Md. Rabiul
    [J]. HEALTH SCIENCE REPORTS, 2022, 5 (02)
  • [9] Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron
    Shuai, Huiping
    Chan, Jasper Fuk-Woo
    Hu, Bingjie
    Chai, Yue
    Yuen, Terrence Tsz-Tai
    Yin, Feifei
    Huang, Xiner
    Yoon, Chaemin
    Jing-Chu Hu
    Liu, Huan
    Shi, Jialu
    Liu, Yuanchen
    Zhu, Tianrenzheng
    Zhang, Jinjin
    Hou, Yuxin
    Wang, Yixin
    Lu, Lu
    Jian-Piao Cai
    Zhang, Anna Jinxia
    Zhou, Jie
    Yuan, Shuofeng
    Brindley, Melinda A.
    Bao-Zhong Zhang
    Jian-Dong Huang
    To, Kelvin Kai-Wang
    Kwok-Yung Yuen
    Chu, Hin
    [J]. NATURE, 2022, 603 (7902) : 693 - +
  • [10] Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron
    Huiping Shuai
    Jasper Fuk-Woo Chan
    Bingjie Hu
    Yue Chai
    Terrence Tsz-Tai Yuen
    Feifei Yin
    Xiner Huang
    Chaemin Yoon
    Jing-Chu Hu
    Huan Liu
    Jialu Shi
    Yuanchen Liu
    Tianrenzheng Zhu
    Jinjin Zhang
    Yuxin Hou
    Yixin Wang
    Lu Lu
    Jian-Piao Cai
    Anna Jinxia Zhang
    Jie Zhou
    Shuofeng Yuan
    Melinda A. Brindley
    Bao-Zhong Zhang
    Jian-Dong Huang
    Kelvin Kai-Wang To
    Kwok-Yung Yuen
    Hin Chu
    [J]. Nature, 2022, 603 : 693 - 699