Evidence map›Paper›PMID 42590136›Full record

ReviewJournal of clinical medicine2026

Transthyretin Cardiac Amyloidosis in Women: Underdiagnosis, Sex-Specific Phenotypic Expression and Therapeutic Response.

Federico Barocelli, Eleonora Canu, Giovanni Tassoni, Angelo Mastrangelo, Nicolò Pasini, Antonio Crocamo, Filippo Luca Gurgoglione, Laura Torlai Triglia, Francesca Russo, Angela Guidorossi and 4 more

Abstract readReview
In one paragraph

Review in Journal of clinical medicine, 2026. 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

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

14 authors.

Federico BarocelliCardiology Division, Parma University Hospital, 43126 Parma, Italy.ORCID 0000-0002-1412-4747
Eleonora CanuCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Giovanni TassoniCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Angelo MastrangeloCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Nicolò PasiniCardiology Division, Parma University Hospital, 43126 Parma, Italy.ORCID 0009-0007-2895-4219
Antonio CrocamoCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Filippo Luca GurgoglioneCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Laura Torlai TrigliaCardiology Division, Parma University Hospital, 43126 Parma, Italy.ORCID 0000-0002-0645-8974
Francesca RussoCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Angela GuidorossiCardiology Division, Parma University Hospital, 43126 Parma, Italy.ORCID 0009-0005-7450-9365
Maria Francesca NotarangeloCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Gian Luca GonziCardiology Division, Parma University Hospital, 43126 Parma, Italy.
Nicola GaibazziCardiology Division, Parma University Hospital, 43126 Parma, Italy.ORCID 0000-0002-2207-3388
Giampaolo NiccoliCardiology Division, Parma University Hospital, 43126 Parma, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transthyretin cardiac amyloidosis (ATTR-CA) is an increasingly recognized cause of cardiac dysfunction in adults, resulting from extracellular deposition of misfolded transthyretin fibrils and progressive myocardial impairment. Clinical expression and diagnostic yield differ substantially between sexes, contributing to systematic underdiagnosis in women, who often present with subtler myocardial remodeling, heart failure with preserved ejection fraction (HFpEF)-dominant phenotypes, and nonspecific systemic manifestations that fall below conventional diagnostic thresholds, particularly in early disease stages. Female patients, particularly those with ATTRwt, tend to present at older ages and more frequently show HFpEF-dominant phenotypes and nonspecific extracardiac manifestations. Carpal tunnel syndrome (CTS) is an important extracardiac red flag for ATTR-CM, but its interpretation in women requires caution because of the high background prevalence of idiopathic CTS in the general population. Evidence also suggests sex-related differences in diastolic function, right ventricular involvement, and overall progression. Despite these biological and phenotypic distinctions, women are markedly underrepresented in trials of disease-modifying therapies, limiting conclusions about sex-specific treatment effects and leaving uncertainty about whether current pharmacologic interventions provide comparable benefit. Hormonal influences, genetic background, and age-related mechanisms, comorbidities, and diagnostic pathways may contribute to the distinctive female phenotype, but underlying mechanisms remain insufficiently defined. This narrative review examines sex-associated differences in ATTR-CA, focusing on mechanisms of underdiagnosis, principal clinical and imaging features, and implications for therapeutic response, with the goal of improving diagnostic accuracy, guiding individualized management, and ultimately enhancing outcomes for women and all affected patients worldwide in clinical practice.

Indexed as

cardiac amyloidosisdiagnostic accuracyhormonal and genetic factorssex differencestransthyretin cardiac amyloidosis

Identifiers

PMID42590136
PMCPMC13467367

What Socratic holds

Textmetadata
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 Socratic graph.