Evidence map›Paper›PMID 33232783›Full record

ReviewVirus research2021

Putative roles of vitamin D in modulating immune response and immunopathology associated with COVID-19.

Raman Kumar, Himani Rathi, Afrozul Haq, Sunil J Wimalawansa, Alpana Sharma

Open access · greenAbstract readReview
In one paragraph

Review in Virus research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

80 citing papers in PubMed, 2 syntheses or guidelines pooled it, 156 citations in OpenAlex.

  1. Pooled it
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  5. The effects of SARS-CoV-2 on bone homeostasis.Frontiers in endocrinology · 2026
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  7. Article
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  13. Vitamin D Status and Cardiovascular Disease in College Athletes After SARS-CoV-2 Infection.Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine · 2024
    Article
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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Raman KumarDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), New Delhi, India; Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), Rishikesh, India.
Himani RathiDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Rishikesh, India.
Afrozul HaqDepartment of Food Technology, Jamia Hamdard, New Delhi, India.
Sunil J WimalawansaCardio-Metabolic & Endocrine Institute, North Brunswick, NJ, USA.
Alpana SharmaDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), New Delhi, India. Electronic address: dralpanasharma@gmail.com.
All India Institute of Medical Sciences Rishikesh · INAll India Institute of Medical Sciences · INJamia Hamdard · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The first incidence of COVID-19 was reported in the Wuhan city of Hubei province in China in late December 2019. Because of failure in timely closing of borders of the affected region, COVID-19 spread across like a wildfire through air travel initiating a pandemic. It is a serious lower respiratory track viral infection caused by highly contagious, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Coronavirus including COVID-19 causing SARS-CoV-2 causes zoonotic diseases and thought to be originated from bats. Since its first incidence, the virus has spread all across the world, causing serious human casualties, economic losses, and disrupting global supply chains. As with SARS-CoV, COVID-19 causing SARS-CoV-2 follows a similar path of airborne infection, but is less lethal and more infectious than SARS and MERS. This review focusses on the pathogenesis of SARS-CoV-2, especially on the dysfunctional immune responses following a cytokine storm in severely affected persons. The mode of entry of SARS-CoV-2 is via the angiotensin converting enzyme 2 (ACE-2) receptors present on the epithelial lining of lungs, gastrointestinal tract, and mucus membranes. Older persons with weaker immune system and associated co-morbidities are more vulnerable to have dysfunctional immune responses, as most of them concomitantly have severe hypovitaminosis D. Consequently, causing severe damage to key organs of the body including lungs and the cardiovascular system. Since, vast majority of persons enters to the intensive care units and died, had severe vitamin D deficiency, thus, this area must be investigated seriously. In addition, this article assesses the role of vitamin D in reducing the risk of COVID-19. Vitamin D is a key regulator of the renin-angiotensin system that is exploited by SARS-CoV-2 for entry into the host cells. Further, vitamin D modulates multiple mechanisms of the immune system to contain the virus that includes dampening the entry and replication of SARS-CoV-2, reduces concentration of pro-inflammatory cytokines and increases levels of anti-inflammatory cytokines, enhances the production of natural antimicrobial peptide and activates defensive cells such as macrophages that could destroy SARS-CoV-2. Thus, this article provides the urgency of needed evidences through large population based randomized controlled trials and ecological studies to evaluate the potential role of vitamin D in COVID-19.

Indexed as

Adaptive ImmunityAnimalsClinical Trials as TopicCOVID-19Cytokine Release SyndromeDisease ManagementHumansImmunity, InnateImmunologic FactorsInflammationSARS-CoV-2Vitamin DZoonosesImmunologic FactorsVitamin DAcute respiratory distress syndrome (ARDS)CoronavirusCOVID-19Cytokine stormDexamethasoneImmune responseSARS-CoV-2TreatmentVitamin D

Identifiers

PMID33232783
PMCPMC7680047
OpenAlexW3108002574

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.