ArticleClinics (Sao Paulo, Brazil)2026
Amyloidosis and risk of psychiatric disorders-insights from a real-world nationwide registry.
Article in Clinics (Sao Paulo, Brazil), 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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThis is a National Health Insurance (NHI) database research investigating the association between amyloidosis and psychiatric disorders risk.
methodsThe amyloidosis cohort was identified from insured individuals with amyloidosis, who were newly diagnosed from 2009 to 2019. Both cohorts were followed up and the subsequent psychiatric disorder was the major outcome event for the research. The multivariable model were used to examine the effect of amyloidosis and risk factor on the risk of developing psychiatric disorder.
resultsThe psychiatric disorder incidence was higher in the amyloidosis than in the comparison cohort (11.3 vs. 10.3 per 1000 person-years, crude HR = 1.10, 95% CI 1.02-1.19), with adjusted HR (aHR) of 1.26 (95% CI 1.16-1.36). After controlling for the confounders, amyloidosis cohort had a 1.38- fold higher risk of senile and pre-senile organic psychotic conditions (95% CI 1.22‒1.57), 1.26-fold higher risk of bipolar affective disorder (95% CI 1.10‒1.45), and 1.16-fold higher risk of other organic psychotic conditions than comparison cohort (95% CI 1.01-1.32).
conclusionsThe authors found that compared to a matched amyloidosis naïve cohort, psychiatric disorders risk was significantly higher in patients with amyloidosis. Among different psychiatric disorders, risks of senile and pre-senile organic psychotic conditions, bipolar affective disorder and other organic psychotic conditions were higher among people with amyloidosis.
Indexed as
Identifiers
42887292What 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.