Evidence map›Paper›PMID 40585077›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Assessing Neuropsychiatric Symptoms in Long COVID: A Retrospective Cohort Study from a South Texas Long COVID Clinic.

Anne Marie Wells, Summer Rolin, Barbara Robles-Ramamurthy, Gabriela Gibson-Lopez, Martin Goros, Jonathan A Gelfond, Stephen Gelfond, Philip Balfanz, Melissa Deuter, Donald McGeary and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Anne Marie WellsSouth Texas Medical Scientist Training Program, UT Health San Antonio, San Antonio, TX, USA.ORCID 0000-0002-4032-673X
Summer RolinDepartment of Rehabilitation Medicine, UT Health San Antonio, TX, USA.
Barbara Robles-RamamurthySouth Texas Psychiatry Practice-Based Research Network (PBRN), San Antonio, TX, USA.
Gabriela Gibson-LopezDepartment of Family & Community Medicine, UT Health San Antonio, San Antonio, TX, USA.
Martin GorosDepartment of Population Health Sciences, UT Health San Antonio, San Antonio, TX, USA.
Jonathan A GelfondDepartment of Population Health Sciences, UT Health San Antonio, San Antonio, TX, USA.
Stephen GelfondSouth Texas Psychiatry Practice-Based Research Network (PBRN), San Antonio, TX, USA.
Philip BalfanzSouth Texas Psychiatry Practice-Based Research Network (PBRN), San Antonio, TX, USA.
Melissa DeuterSouth Texas Psychiatry Practice-Based Research Network (PBRN), San Antonio, TX, USA.
Donald McGearyDepartment of Psychiatry & Behavioral Health Sciences, UT Health San Antonio, San Antonio, TX, USA.
Monica Verduzco-GutierrezDepartment of Rehabilitation Medicine, UT Health San Antonio, TX, USA.

Funding

Institute for Integration of Medicine & Science: A Partnership to Improve HealthUM1TR004538 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ROBERT A CLARK, Kenneth M Hargreaves · 2023 to 2026
$22.3M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ROBERT A CLARK · 2015 to 2026
$14.1M
Next-Generation Neuroscience Scholars ProgramR25NS089462 · NINDS · SOCIETY FOR NEUROSCIENCE · PI Karina Alvina, EDUARDO ROSA-MOLINAR · 2014 to 2026
$3.5M
South Texas Medical Scientist Training Program (STX-MSTP)T32GM145432 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jose E Cavazos, Ratna K Vadlamudi · 2023 to 2026
$2.3M
Integrated Graduate Training Program in Neuroscience, UTHSCSAT32NS082145 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI David A Morilak · 2013 to 2026
$1.5M
South Texas Medical Scientist Training Program (STX-MSTP)T32GM113896 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CAVAZOS, JOSE E · 2018 to 2022
$1.1M
Identifying a critical developmental period for cognitive speed in a mouse model for neurodevelopmental disordersF30MH134482 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WELLS, ANNE MARIE · 2024 to 2025
$84k
NCATS NIH HHS UM1 TR004538NIA NIH HHS P30 AG044271NIGMS NIH HHS T32 GM113896NIGMS NIH HHS T32 GM145432NIMH NIH HHS F30 MH134482NINDS NIH HHS R25 NS089462NINDS NIH HHS T32 NS082145
6 · The paper itself

Abstract

Long COVID, previously known as Post-Acute Sequelae of SARS-CoV-2 (PASC), refers to prolonged symptoms or diagnosable conditions following COVID-19 infection. The neuropsychiatric profile of Long COVID patients remains ambiguous. This study aimed to assess neuropsychiatric symptoms in a retrospective cohort of Long COVID patients (N = 162) at a Rehabilitation Medicine clinic in South Texas. Clinical data from patient records were used to calculate a Symptom Score, and screening tools for stress/PTSD (PCL-5), depression (PHQ-9), anxiety (GAD-7), and quality of life (SWL) were employed to evaluate if Long COVID duration and severity could predict neuropsychiatric outcomes. The majority were female (71%) and Hispanics (53%) who presented for treatment of Long COVID symptoms during the study period, including fatigue (93%), coughing/shortness of breath (81%), fever (67%), anosmia (58%), ageusia (54%), and weight loss (56%). A minority of participants were hospitalized (N = 49) or required ventilator support (N = 5) during acute infection. There was a high burden of neuropsychiatric symptoms, including subjective cognitive impairment (79%), headache (74%), and insomnia (58%). Symptom Score (median = 9, IQR [8,11]) was significantly correlated with increased depression (PHQ-9; p < 0.05), anxiety (GAD-7; p < 0.05) and elevated stress/PTSD (PCL-5; p < 0.05) symptoms. Long COVID patients taking stimulants or mood stabilizers had higher GAD-7 (p < 0.031, p < 0.035) and PHQ-9 (p < 0.034, p < 0.009) scores but not PCL-5 scores. Importantly, duration of Long COVID symptomatology also did not predict PCL-5 scores. No patient factors (e.g., sex, age, BMI, ethnicity) mediated Symptom Score. Nonetheless, historically marginalized groups, such as women and Hispanics, have been disproportionately affected by COVID-19. This study is the first to utilize validated screening tools to determine the presence and severity of neuropsychiatric symptoms in Long COVID patients. These findings may guide clinical management and future research on Long COVID, especially in historically excluded populations.

Indexed as

anxietydepressionGAD-7Long COVIDPASCPCL-5PHQ-9PTSDstress

Identifiers

PMID40585077
PMCPMC12204276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.