Evidence map›Paper›PMID 40021517›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2026

Objectifying persistent subjective cognitive impairment following COVID-19 infection: cross-sectional data from an outpatient memory-clinic in Germany.

Luca Tarantini, Corina Möller, Victoria Schiestl, Sabrina Sordon, Michael Noll-Hussong, Miriam Wittemann, Nicole Menzie, Matthias Riemenschneider

Abstract read
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Luca TarantiniDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany. luca.tarantini@uks.eu.ORCID http://orcid.org/0009-0005-2929-0763
Corina MöllerDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.
Victoria SchiestlDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0000-0002-8067-4704
Sabrina SordonDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0009-0002-8848-7978
Michael Noll-HussongDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0000-0002-9734-0161
Miriam WittemannDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0009-0003-7144-715X
Nicole MenzieDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0009-0008-0346-9425
Matthias RiemenschneiderDepartment of Psychiatry and Psychotherapy, Saarland University Medical Center, Kirrberger Straße, Building 90, 66421, Homburg, Germany.ORCID http://orcid.org/0000-0001-7658-1022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSubjective cognitive impairment is frequently reported by patients experiencing Post-COVID symptoms. This study aims to assess objective impairment in attention, memory, and executive functions among these patients. Further, we investigated potential determinants of objective cognitive impairment.

methodsIn this cross-sectional study, standardized neuropsychological testing (Vienna Testing System), assessment of cognitive symptom aggravation, psychiatric anamnesis, and psychometrics (BDI-II, Fatigue Severity Scale) were conducted in 229 patients who voluntarily presented to our outpatient memory-clinic due to subjective cognitive impairment following COVID-19. Blood-samples were collected to assess peripheral immune markers (IL-6, CRP) and APOE-ε4 genotype.

resultsObjective cognitive impairment in at least one domain was present in 39% of the patients and 47% showed symptoms of moderate or severe depression. The APOE-ε4 allele was present in 32% of the patients. Higher rates of depressive symptoms (OR = 1.41, 95%-CI = 1.02-1.95) and higher burden of the APOE-ε4 allele (OR = 3.29, 95%-CI = 1.51-7.40) predicted objective cognitive impairment, regardless of age, sex, years of formal education, time since infection, and medication for diabetes or hypertension. Fatigue severity, acute COVID-19 severity or inflammation markers had no impact.

conclusionsIn our study, subjective cognitive impairment following COVID-19 was more likely associated with high rates of depression rather than relatively low rates of objective cognitive performance. Thus, the study emphasizes the necessity for extensive neuropsychological testing and evaluation of depression when examining Post-COVID patients in clinical practice. Further, the link between objective cognitive impairment, depression and APOE-ε4 does not appear to be specific to Post-COVID symptoms. Therefore, depression- and APOE-ε4-mediated neurodegenerative pathomechanisms might be a promising therapeutical target.

Indexed as

Cognitive DysfunctionCOVID-19DepressionAdultAgedApolipoprotein E4Cross-Sectional StudiesExecutive FunctionFemaleGermanyHumansMaleMiddle AgedNeuropsychological TestsApolipoprotein E4APOE-ε4Cognitive complaintsCognitive impairmentCOVID-19DepressionPost-COVID

Identifiers

PMID40021517
PMCPMC12904877

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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.