Evidence map›Paper›PMID 40580092›Full record

ArticleAmyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis2025

Impact of autonomic dysfunction on cardiovascular outcomes among patients with ATTR cardiomyopathy: insights from the COMPASS-31.

Ariel Weinsaft, Sergio Teruya, Alfonsina Mirabal Santos, Stephen Helmke, Karan Wats, Juliana Levy, Dimitrios Bampatsias, Mathew S Maurer

Abstract read
In one paragraph

Article in Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2025. 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
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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

8 authors.

Ariel WeinsaftCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Sergio TeruyaCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Alfonsina Mirabal SantosCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Stephen HelmkeCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Karan WatsCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Juliana LevyCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Dimitrios BampatsiasCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.
Mathew S MaurerCardiac Amyloidosis Program, Division of Cardiology, Columbia University Irving Medical Center, New York, USA.

Funding

SCAN-MP (Screening for Cardiac Amyloidosis with Nuclear imaging in Minority Populations) COVID-19 SuppplementR01HL139671 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAURER, MATHEW S, RUBERG, FREDERICK LIEF · 2019 to 2023
$7.4M
Analysis of Lumbar Spine Stenosis Specimens for Identification of Transthyretin Cardiac AmyloidosisR01AG081582 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MATHEW S MAURER · 2023 to 2026
$2.8M
NHLBI NIH HHS R01 HL139671NIA NIH HHS R01 AG081582
6 · The paper itself

Abstract

backgroundATTR is a systemic disease, causing significant morbidity and mortality, manifesting with symptoms affecting both the heart and nervous system. This study employed the Composite Autonomic Symptom Scale 31 (COMPASS-31) to assess autonomic symptoms in relation to ATTR-CM subtypes and the impact of dysfunction on prognosis.

methodsThis study included contemporary ATTR-CM patients enrolled in an institutional registry from 7/21-6/24. Demographic information, patient-reported outcomes (COMPASS-31 and Kansas City Cardiomyopathy Questionnaire (KCCQ)), 6-min walk test, and clinical data (hospitalisations, mortality) were collected and compared between ATTR-CM sub-types (ATTRwt, ATTRv-Val122Ile, ATTRv-non Val122Ile).

results240 ATTR-CM patients (81% ATTRwt, 11% Val-122Ile, 8% non-Val122Ile) were studied. Following adjustment for age, significant COMPASS-31 score differences were observed between ATTRwt and ATTRv-nonV122I variant patients. "High" COMPASS-31 scores (≥35.42) were associated with later Columbia stage, lower exercise tolerance, and poorer quality of life (QOL) (all

conclusionsAmong ATTR-CM patients, autonomic dysfunction assessed

Indexed as

Amyloid Neuropathies, FamilialAutonomic Nervous System DiseasesCardiomyopathiesAgedAged, 80 and overAutonomic Nervous SystemFemaleHospitalizationHumansMaleMiddle AgedPrognosisQuality of LifeRegistriesSurveys and QuestionnairesAutonomic neuropathyCOMPASS-31neuropathytransthyretin amyloid cardiomyopathy

Identifiers

PMID40580092
PMCPMC12313188

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Registered trials

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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.