Obesity, Insulin Resistance, and PASC: Persistent SARS-CoV-2

Sponsor
Stanford University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05833217
Collaborator
(none)
55
2
3
32
27.5
0.9

Study Details

Study Description

Brief Summary

The investigators are studying the pathophysiologic links between obesity, insulin resistance (IR), adipose tissue infection, and post-acute sequelae of COVID-19 (PASC). This study looks at whether adipose (fat) tissue contributes to PASC by driving chronic inflammation or by serving as a reservoir for SARS-CoV-2 persistence. The results will not only determine whether obesity and IR are risk factors for PASC, but will also define fundamental biology that sets the stage for the investigation of novel or existing therapies that target the causal pathways identified.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Adipose Tissue Biopsy
  • Diagnostic Test: Steady State Plasma Glucose (SSPG) Test
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
55 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Obesity, Insulin Resistance, and PASC: Persistent SARS-CoV-2 Infection and Inflammation in Human Adipose Tissue
Anticipated Study Start Date :
May 2, 2023
Anticipated Primary Completion Date :
May 2, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Chart Review (not actively recruiting)

Chart review of previously consented participants from the entire NIH RECOVER cohort, comprised of 15,000 infected and 2,600 noninfected patients across the country.

Experimental: COVID infected and healthy controls

Participants will perform a needle fat biopsy for tissue harvesting in the subacute phase (15-30d) of Covid-19 infection or as a healthy control. Our goal is 20 COVID-19 infected participants and 10 healthy controls.

Procedure: Adipose Tissue Biopsy
After an overnight fast, approximately 1-2 grams of subcutaneous fat will be removed by a needle. Participants will have a local anesthetic prior to the procedure. The needle fat biopsy will be repeated at quarterly intervals for one year (every 3 months). We will also draw 1 10mL tube of blood at each biopsy for measurement of inflammatory cytokines.

Experimental: Healthy Controls Only

We are looking for 20 healthy controls for 2 in-person visits on separate days. An Insulin Sensitivity Test (SSPG: Steady State Plasma Glucose) is performed to determine if the participant is insulin-sensitive or insulin resistant. A Needle Fat Biopsy: After an overnight fast, approximately 1-2 grams of subcutaneous fat will be removed by a needle. Patients will have a local anesthetic prior to the procedure.

Procedure: Adipose Tissue Biopsy
After an overnight fast, approximately 1-2 grams of subcutaneous fat will be removed by a needle. Participants will have a local anesthetic prior to the procedure. The needle fat biopsy will be repeated at quarterly intervals for one year (every 3 months). We will also draw 1 10mL tube of blood at each biopsy for measurement of inflammatory cytokines.

Diagnostic Test: Steady State Plasma Glucose (SSPG) Test
An Insulin Sensitivity Test (SSPG: Steady State Plasma Glucose) is performed to determine if participants are insulin sensitive or insulin resistant. This test is approximately 5-6 hours in length. Participants will be asked to fast for 12 hours. The insulin sensitivity test is designed to measure how well your cells remove glucose from your blood in response to insulin. During this test participants will have two small catheters (tubing) placed in their veins (I.V. lines). The total amount of blood that will be drawn during this test will be 140 mL of blood (approximately 9.5 tablespoons). Insulin is a natural hormone, and octreotide (a synthetic hormone) is a drug that temporarily blocks the secretion of insulin from your pancreas. A member of the research team is present and monitoring the results along with the nursing staff.
Other Names:
  • Insulin Sensitivity Test
  • Outcome Measures

    Primary Outcome Measures

    1. Triglyceride/HDL-cholesterol ratio [2 years]

      Investigate the relationship between insulin resistance, as described by triglyceride/HDL-cholesterol ratio, and incident PASC (long COVID).

    2. Concentration of Viral RNA in Adipose Tissue [2 years]

      Investigate the expression of viral RNA in adipose tissue in response to COVID-19 infection. Compare adipose tissue transcripts such as known MODY transcription factors measured by PCR between COVID-19 infected participants and healthy controls.

    3. Rate of Inflammatory Response [2 years]

      Investigate inflammatory response to PPARgamma agonist (drug) and other compounds tested in vitro in human fat cells. Compare plasma inflammatory cytokine levels in serum samples as measured by Luminex immunoassay between participants identified as Insulin Sensitive (IS) and Insulin Resistant (IR) using the 2-stage Steady State Plasma Glucose test.

    4. Rate of Inflammatory Gene Expression in Adipose Tissue [2 years]

      Investigate the expression of inflammatory genes in adipose tissue in response to COVID-19 infection. Compare adipose tissue transcripts such as defensin chemokine receptors and platelet activation factors measured by PCR between COVID-19 infected participants and healthy controls.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Ages 18 to 80

    • BMI ≥ 25 kg/m2

    • not currently pregnant

    Exclusion Criteria:

    Arm 2 (Adipose Tissue Biopsy) exclusions include

    • pregnancy

    • prior liposuction

    • recent change in weight (> 2 kg in one month)

    • bleeding disorders

    • anticoagulant use

    Arm 3 (healthy controls only) exclusions include patients with

    • major organ disease

    • diabetes

    • history of liposuction

    • bariatric surgery

    • eating disorders

    • psychiatric disorders

    • pregnancy or lactation

    • recent change in weight (over the past 12 weeks),

    • use of weight loss medication or oral steroids

    • hematocrit < 33%

    • fasting glucose >= 126 mg/dL

    • blood pressure >160/100 mmHg

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Clinical and Translational Research Unit Palo Alto California United States 94304
    2 Stanford Health Palo Alto California United States 94305

    Sponsors and Collaborators

    • Stanford University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tracey McLaughlin, Professor of Medicine, Stanford University
    ClinicalTrials.gov Identifier:
    NCT05833217
    Other Study ID Numbers:
    • 69063
    First Posted:
    Apr 27, 2023
    Last Update Posted:
    May 1, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 1, 2023