The Relationship Between Vitamin D Levels, Inflammatory Parameters and Disease Severity of COVID-19 Infection

The Relationship Between Vitamin D Levels, Inflammatory Parameters and Disease Severity of COVID-19 Infection: A Retrospective Study

Vitamin D deficiency increases the susceptibility to respiratory virus infections and the severity of infections. Inflammation plays a key role in pathogenesis in COVID19 while identifying clinical course and prognosis COVID19.The aim of this study was to determine the relationship between 25OH vitamin D levels, inflammatory laboratory parameters of neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR), C-reactive protein (CRP) levels and disease severity of COVID19 infection.

Study Overview

Detailed Description

In this retrospective study 300 patients diagnosed with COVID19 were included. According to clinical classification of cases with COVID19 the patients were divided into three groups; mild (Group1), moderate (Group2) and severe/critical (Group3). The 25OH vitamin D values below 20 ng/ml were defined as deficiency, 21-29 ng/ml were defined as insufficiency, and 30 ng/ml and above were defined as normal. Patients' age, gender, comorbid diseases and laboratory values were recorded

Study Type

Observational

Enrollment (Actual)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey, 34752
        • Gulcan Ozturk

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 97 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

COVID19 infection positive patients whose polymerase chain reaction (PCR) test positive patients and whose 25-OH vitamin D levels were measured in the last 6 months

Description

Inclusion Criteria:

  • The study included 300 polymerase chain reaction (PCR) test positive patients and whose 25-OH vitamin D levels were measured in the last 6 months

Exclusion Criteria:

  • Patients with COVID-19 whose 25-OH vitamin D levels were not measured in the last 6 months before the COVID-19 diagnosis were excluded from the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Experimental: Mild Clinical Group
patients showing mild clinical symptoms without pneumonia.
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl
Experimental: Moderate Clinical Group
patients with fever, other respiratory symptoms, and pneumonia findings based on radiological imaging
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl
Experimental: severe/critical clinical group
severe one of these as follows; patients with hypoxia (≤93% oxygen saturation), respiratory distress (RR >30 times per minute), partial pressure of arterial blood oxygen (PaO 2 )/the fraction of inspired oxygen (FiO 2 ) ≤ 300 mmHg, patients whose chest imaging shows that lung damage develops significantly within 24 to 48 hours, or critical one of these as follows; respiratory failure requiring mechanical ventilation, signs of septic shock with multiple organ failure requiring intensive care unit admission.
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
25-OH vitamin D
Time Frame: 1 day
laboratory measurement in unit of ng/ml
1 day
White blood cell count
Time Frame: 1 day
laboratory measurement in unit of x103/uL
1 day
neutrophil count
Time Frame: 1 day
laboratory measurement in unit of x103/uL
1 day
neutrophil ratio
Time Frame: 1 day
laboratory measurement in unit of %
1 day
lymphocyte count
Time Frame: 1 day
x103/uL
1 day
lymphocyte ratio
Time Frame: 1 day
laboratory measurement in unit of %
1 day
platelet count
Time Frame: 1 day
laboratory measurement in unit of x103/uL
1 day
hemoglobin count
Time Frame: 1 day
laboratory measurement in unit of g/dl
1 day
C-reactive protein levels
Time Frame: 1 day
laboratory measurement in unit of mg/dL
1 day
neutrophil to lymphocyte ratio
Time Frame: 1 day
laboratory measurement in unit of %
1 day
platelet to lymphocyte ratio
Time Frame: 1 day
laboratory measurement in unit of %
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2020

Primary Completion (Actual)

August 1, 2020

Study Completion (Actual)

August 1, 2020

Study Registration Dates

First Submitted

June 6, 2021

First Submitted That Met QC Criteria

June 28, 2021

First Posted (Actual)

June 30, 2021

Study Record Updates

Last Update Posted (Actual)

June 30, 2021

Last Update Submitted That Met QC Criteria

June 28, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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