ReviewAdvances in experimental medicine and biology2026
Cognition in Treatment-Resistant Depression: Obstacles and Challenges?
Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Treatment-resistant depression (TRD) is usually defined as an insufficient response to ≥1 treatment considered adequate in terms of dosage, duration, and compliance, or the failure to respond to electroconvulsive therapy (ECT). Cognitive disturbances are the core symptoms of depression and TRD, and they significantly contribute to the poor functional outcomes and treatment resistance. Patients with TRD have moderate to large cognitive deficits in executive function, verbal learning and memory, attention, visual perception, conceptual transformation, attention conversion, logic reasoning, and problem-solving, in processing speed compared to non-TRD patients. The biological underpinning of cognitive deterioration in TRD is diverse, including alterations in different brain regions and circuits, lower levels of N-acetyl aspartate and the important role of inflammatory processes, while animal studies reveal the involvement of 5-HT1A and 5-HT2 serotonergic and α2C-AR adrenergic receptors. It is important to better elucidate the biological background of cognitive dysfunction in TRD to develop more personalized and targeted treatments. Some therapeutic strategies of cognitive dysfunction in TRD include pharmacotherapy, neuromodulation, psychotherapy, and cognitive remediation. Cognitive disturbances in TRD correspond to both obstacles and challenges, but future studies should incorporate cognitive measurements and therapeutic strategies with individual approach to specifically target cognitive impairment in TRD.
Indexed as
Identifiers
42036567What OpenQuestion holds
Registered trials
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.