Post-acute sequelae of COVID-19 and longitudinal antibody levels in a community-based cohort

PLoS One. 2023 Sep 8;18(9):e0291259. doi: 10.1371/journal.pone.0291259. eCollection 2023.

Abstract

Background: Coronavirus disease 2019 (COVID-19) infection invokes variable immune responses and poses a risk of post-acute sequelae SARS-CoV-2 infection (PASC) symptoms; however, most data on natural history are derived from patients with severe infection. Further data are needed among patients with mild infection, who comprise most cases.

Methods: The Dallas Fort-Worth (DFW) COVID-19 Prevalence Study included 21,597 community-dwelling adults (ages 18-89) who underwent COVID-19 PCR and anti-nucleocapsid antibody testing between July 2020 and March 2021. We invited participants with positive COVID-19 results (cases) and a subset with negative results (controls), matched on age, sex, race/ethnicity, and ZIP code, to complete a follow-up questionnaire for PASC symptoms and repeat anti-nucleocapsid testing, and anti-spike antibody testing between July and December 2021.

Results: Of 3,917 adults invited to participate, 2260 (57.7%) completed the questionnaire- 1150 cases and 1110 controls. Persistent symptoms were reported in 21.1% of cases, with the most common being shortness of breath, fatigue, and loss of taste or smell. Among 292 cases with asymptomatic infection, >15% reported new fatigue and 8-10% reported new loss of taste/smell, myalgias, or headache. Median anti-nucleocapsid levels in cases decreased from 3.5U to 0.7U over a median follow-up of 8.6 months. Anti-spike antibody levels at 6-7 months post-vaccination in cases were similar to that of controls.

Conclusions: More than 1 in 5 patients with COVID-19 infection, including those with mild infection, reported persistent symptoms during follow-up. Both nucleocapsid and spike protein antibody levels decreased within six months following a COVID-19 infection and vaccination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Ageusia*
  • COVID-19* / complications
  • Disease Progression
  • Fatigue / etiology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nucleocapsid
  • SARS-CoV-2
  • Young Adult

Grants and funding

This work was supported by generous funding from the State of Texas, the City and County of Dallas, Tarrant County, and community philanthropy including Lyda Hill Philanthropies, W.W. Caruth, Jr. Fund at Communities Foundation of Texas, Harry S. Moss Heart Trust, Bank of America, N.A., Trustee, and many others. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.