Evidence map›Paper›PMID 39219298›Full record

ArticleESC heart failure2024

First report of the clinical characteristics and outcomes of cardiac amyloidosis in Saudi Arabia.

Omar Ahmad, Mohamed H Omer, Mohammed Janjua, Islam Alayary, Ahmed Fathala, Hani Alsergani, Bandar Alamro, Thibaud Damy, Bahaa Fadel, Dania Mohty

Abstract read
In one paragraph

Article in ESC heart failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 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

10 authors.

Omar AhmadCollege of Medicine, Al Faisal University, Riyadh, Saudi Arabia.
Mohamed H OmerSchool of Medicine, Cardiff University, Cardiff, UK.
Mohammed JanjuaCollege of Medicine, Al Faisal University, Riyadh, Saudi Arabia.
Islam AlayaryRare Diseases Medical Affairs, Pfizer Inc., Jeddah, Saudi Arabia.
Ahmed FathalaDepartment of Radiology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hani AlserganiCollege of Medicine, Al Faisal University, Riyadh, Saudi Arabia.
Bandar AlamroHeart Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Thibaud DamyDepartment of Cardiology, French Referral Center for Cardiac Amyloidosis, Henri Mondor University Hospital, Assistance-Publique Hôpitaux de Paris (APHP), Créteil, France.
Bahaa FadelCollege of Medicine, Al Faisal University, Riyadh, Saudi Arabia.
Dania MohtyCollege of Medicine, Al Faisal University, Riyadh, Saudi Arabia.

Funding

Pfizer 55437631
6 · The paper itself

Abstract

aimsCardiac amyloidosis (CA) is a potentially fatal multisystemic disease that remains significantly underdiagnosed, particularly in the Middle East. This study aims to evaluate the prevalence and clinical characteristics of CA in a high-risk population at a tertiary centre in Saudi Arabia.

methodsThis cross-sectional, retrospective, single-centre study was conducted at a tertiary hospital in Riyadh, Saudi Arabia. We reviewed the medical records of heart failure patients seen between August 2018 and July 2022 who exhibited red flags for CA and subsequently underwent CA screening. Red flags that prompted the workup included at least two of the following factors: the presence of unilateral or bilateral carpal tunnel syndrome, a family history of transthyretin amyloid (ATTR) amyloidosis and specific electrocardiographic features (relative/absolute low QRS voltage, pseudoinfarct pattern and atrioventricular/interventricular conduction abnormalities). Echocardiographic red flags included mainly increased wall thickness (≥12 mm), significant diastolic dysfunction, reduced left ventricular (LV) longitudinal function, right ventricular (RV) dysfunction and elevated right atrial (RA)/pulmonary artery (PA) pressure. Cardiac magnetic resonance (CMR) red flags included aspects similar to those in an echocardiogram as well as a subendocardial or transmural late gadolinium enhancement (LGE) pattern. These patients were assessed for CA through technetium-99m pyrophosphate ([

resultsA total of 177 patients were screened, of which 21.0 (11.9%) patients were diagnosed with transthyretin amyloid CA (ATTR-CA) and 13 (7.3%) patients were diagnosed with light chain CA (AL-CA). Compared with patients with negative/equivocal [

conclusionsThis is the first study to describe the clinical characteristics and outcomes of CA in the Middle East and Saudi Arabia. The prevalence of CA among screened heart failure patients here aligns with major international studies, suggesting significant underdiagnosis in the region. Therefore, larger multicentric studies and regional screening programmes are urgently needed to accurately characterize the epidemiology and outcomes of CA in the Middle East.

Indexed as

AmyloidosisCardiomyopathiesEchocardiographyMagnetic Resonance Imaging, CineAgedAmyloid Neuropathies, FamilialCross-Sectional StudiesElectrocardiographyFemaleFollow-Up StudiesHeart FailureHumansMaleMiddle AgedPrevalenceRetrospective Studiescardiac amyloidosisheart failureheart failure with preserved ejection fractionlight chainrestrictive cardiomyopathiestransthyretin

Identifiers

PMID39219298
PMCPMC11631269

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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.