Alcohol Misuse: An Independent Risk Factor that Increases the Incidence and Severity of COVID-19
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 3R24AA026801-02S1
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Key facts
Disease
COVID-19Start & end year
20192024Known Financial Commitments (USD)
$313,862Funder
National Institutes of Health (NIH)Principal Investigator
Ali KeshavarzianResearch Location
United States of AmericaLead Research Institution
Rush University Medical CenterResearch Priority Alignment
N/A
Research Category
Epidemiological studies
Research Subcategory
Disease susceptibility
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Not applicable
Broad Policy Alignment
Pending
Age Group
Adults (18 and older)
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
Abstract: The coronavirus disease 2019 (COVID-19) pandemic has resulted in unprecedented morbidity and mortality.Risk factors like age, obesity, and comorbidity impact the rate of SARS-CoV-2 infection and severity of COVID-19 leading to hospital ICU admission and death. Additional risk factors that promote exaggerated immune andinflammatory response to the virus leading to severe disease or death must exist. One such risk factor couldbe alcohol consumption because: (1) Alcohol is the most frequently used drug in the United States. (2) Patientshospitalized for pneumonia who have an alcohol use disorder (AUD) are at greater risk for developing AcuteRespiratory Distress Syndrome (ARDS) (the primary cause of death in COVID-19) than non-AUD patients; and(3) Alcohol negatively impacts function of the immune system and results in an inappropriate response topathogens (a primary mechanism of severe COVID-19 and ARDS); and (4) Alcohol disrupts the intestinalmicrobiome (dysbiosis) and intestinal and lung barriers which can both further promote inflammation andcontribute to ARDS. Accordingly, we hypothesize that alcohol misuse is an independent risk factor thatincreases the incidence and severity of COVID-19 by promoting exaggerated and dysregulated immune-inflammatory responses to SARS-CoV-2. We will leverage our COVID-19 data and biorepository at RushUniversity Medical Center (RUMC), which has tested over 22,000 patients (68% minority) with over 6000patients testing positive, over 1000 hospitalized, over 600 critically ill. Currently, all patients arriving at RUMCare screened for alcohol use with AUDIT. Our COVID-19 biorepository has banked nasopharyngeal swabs,serum/plasma, and peripheral blood mononuclear cells (PBMC). We will address the following Specific Aims:Aim 1: Determine if alcohol use or misuse increases severity of COVID-19 and elucidate interactionswith other risk factors. In this cross sectional study, we will use a machine learning classifier to determine ifincreased alcohol use/misuse are associated with more severe clinical presentation and poorer COVID-19health outcomes (in 12,000 RUMC, 6000 COVID-19+) patients. Aim 2. Determine the impact of alcohol useand misuse on COVID-19 disease course and the impact of COVID-19 on alcohol consumption. In thislongitudinal study, we will conduct longitudinal analysis of alcohol use in 6000 patients positive for COVID-19to determine: (2a) if alcohol use/misuse is associated with slower recovery from COVID-19-associatedsymptoms. Aim 3. Determine if alcohol misuse results in exaggerated immune-inflammatory responseto SARS-CoV-2 infection and more organ dysfunction in COVID-19 patients and explore themechanisms. In this mechanistic Aim, we will compare COVID-19 patients with different disease severity todetermine if alcohol misuse is associated with: (3a) altered immune/inflammatory response. (3b) disruptedintestinal barrier integrity. We will use machine learning and other advanced informatics approaches toinvestigate these Aims to discover new mechanisms for alcohol-COVID-19 interactions for prevention andtherapeutic targets for COVID-19.