Evidence map›Paper›PMID 35579098›Full record

ArticleESC heart failure2022

The association between cardiac involvement and long-term clinical outcomes in patients with Duchenne muscular dystrophy.

Jung-Joon Cha, In-Soo Kim, Jong-Youn Kim, Eui-Young Choi, Pil-Ki Min, Young Won Yoon, Byoung Kwon Lee, Bum-Kee Hong, Hyuck Moon Kwon, Han Eol Cho and 3 more

Abstract read
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Article in ESC heart failure, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

13 authors.

Jung-Joon ChaDepartment of Cardiology, Cardiovascular Centre, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Korea.
In-Soo KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Jong-Youn KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Eui-Young ChoiDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Pil-Ki MinDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Young Won YoonDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Byoung Kwon LeeDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Bum-Kee HongDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Hyuck Moon KwonDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Han Eol ChoRehabilitation Institute of Neuromuscular Disease, Yonsei University College of Medicine, Seoul, Korea.
Won Ah ChoiRehabilitation Institute of Neuromuscular Disease, Yonsei University College of Medicine, Seoul, Korea.
Seong-Woong KangRehabilitation Institute of Neuromuscular Disease, Yonsei University College of Medicine, Seoul, Korea.
Se-Joong RimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsDespite advances in contemporary cardiopulmonary therapies, cardiomyopathy remains the leading cause of death in patients with Duchenne muscular dystrophy (DMD). Also, the long-term clinical outcomes of patients with DMD and cardiomyopathy is unknown. This study investigated long-term clinical outcomes and their associated factors in patients with late-stage DMD. METHODS AND

resultsA total of 116 patients with late-stage DMD (age > 15 years) were enrolled in this retrospective study. All enrolled patients were followed up at a single tertiary referral hospital. LV systolic dysfunction was dichotomously defined as reduced [left ventricular ejection fraction (LVEF) ≤ 40%] vs. preserved [>40%] based on the initial echocardiographic result. The primary endpoint was all-cause death. The secondary endpoint was a composite event defined as death or unexpected hospitalization due to cardiovascular reasons including chest pain, dyspnoea, and generalized oedema. The patients were divided into preserved (n = 84, 72.4%) and reduced LVEF groups (n = 32, 27.6%). The mean age was 20.8 ± 5.9 years, the mean disease duration, 8.8 ± 3.7 years, and the mean follow-up duration, 1708 ± 659 days. For primary endpoint, the reduced LVEF group showed a lower rate of overall survival (Reduced LVEF vs. Preserved LVEF; 81.3% vs. 98.8%, log-rank P = 0.005). In the multivariable Cox regression analysis, brain-natriuretic peptide (BNP) level (adjusted hazard ratio [HR] 1.088, 95% confidence interval [CI] 1.019-1.162, P = 0.011) and diuretic use (adjusted HR 9.279, 95%CI 1.651-52.148, P = 0.011) were significant predictors of all-cause death in patients with DMD. For the secondary endpoint, the reduced LVEF group had a lower rate of freedom from composite events than the preserved LVEF group (65.6% vs. 86.9%, log-rank P = 0.005). In the multivariable Cox regression analysis, BNP level (adjusted HR 1.057, 95%CI 1.005-1.112, P = 0.032) and diuretic use (adjusted HR 4.189, 95% CI 1.704-10.296, P = 0.002) were significant predictors of the composite event in patients with DMD.

conclusionsPatients with DMD and reduced LVEF had worse clinical outcomes than those with preserved LVEF. BNP level and diuretic use were associated with adverse clinical outcomes in patients with late-stage DMD, irrespective of LVEF.

Indexed as

CardiomyopathiesMuscular Dystrophy, DuchenneVentricular Dysfunction, LeftAdolescentAdultDiureticsHumansRetrospective StudiesStroke VolumeVentricular Function, LeftYoung AdultDiureticsBrain-natriuretic peptideDiureticsDuchenne muscular dystrophyLong-term clinical outcomeLV systolic dysfunction

Identifiers

PMID35579098
PMCPMC9288783

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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.