ReviewLung2026
Underlying Mechanisms of Comorbidity between Chronic Cough and Depression: A Review.
Review in Lung, 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
8 authors.
Funding
Abstract
There is a complex bidirectional association between chronic cough and depression, which constitutes a significant medical challenge. Epidemiological studies have shown that the incidence of depression in patients with chronic cough is as high as 33-53%, while the risk of new-onset chronic cough is significantly increased in patients with depression. Specifically, the risk of cough in individuals with severe depression is 3.32 times than those without depressive symptoms. Pathophysiological mechanisms underlying this bidirectional association include the following. From the perspective of neural pathways, the cough reflex and emotional regulation share neural pathways, including the vagus nerve, brainstem, limbic system, prefrontal cortex, and other brain regions. Both patients with chronic cough and depression exhibit abnormal functional connectivity and remodeling of the aforementioned neural pathways, as well as imbalanced levels of key neurotransmitters such as serotonin, glutamate, and γ-aminobutyric acid. From the perspective of the immune-inflammatory dimension, chronic inflammatory mediators such as IL-6 and TNF-α form a vicious cycle between peripheral inflammation and central inflammation, further exacerbating the comorbidity process. Elucidating the pathophysiological mechanism of this bidirectional association is of great theoretical and practical significance for optimizing clinical diagnosis and treatment strategies for comorbid patients, as well as improving their prognosis.
Indexed as
Identifiers
41936621What Socratic 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 Socratic graph.