Evidence map›Paper›PMID 31419965›Full record

ArticleBMC nephrology2019

Cardiac function assessed by myocardial deformation in adult polycystic kidney disease patients.

Mats C H Lassen, Atif N Qasim, Tor Biering-Sørensen, Jacob L T Reeh, Terry Watnick, Stephen L Seliger, Huanwen Chen, Mariem A Sawan, Daniel Nguyen, Yongfang Li and 2 more

Abstract read
In one paragraph

Article in BMC nephrology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Cardiovascular Manifestations and Management in ADPKD.Kidney international reports · 2023
    Review
  2. Article
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

12 authors.

Mats C H LassenDepartment of Cardiology, Herlev & Gentofte Hospital, University of Copenhagen, Niels Andersens vej 65, DK-2900, Post 835, Copenhagen, Denmark. mcha@live.dk.ORCID 0000-0002-2255-582X
Atif N QasimDivision of Cardiology, University of California, San Francisco (UCSF), 505 Parnassus Ave, San Francisco, CA, 94143, USA.
Tor Biering-SørensenDepartment of Cardiology, Herlev & Gentofte Hospital, University of Copenhagen, Niels Andersens vej 65, DK-2900, Post 835, Copenhagen, Denmark.
Jacob L T ReehDepartment of Cardiology, Herlev & Gentofte Hospital, University of Copenhagen, Niels Andersens vej 65, DK-2900, Post 835, Copenhagen, Denmark.
Terry WatnickDivision of Nephrology, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Stephen L SeligerDivision of Nephrology, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Huanwen ChenDivision of Nephrology, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Mariem A SawanDivision of Cardiovascular Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Daniel NguyenDivision of Cardiovascular Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Yongfang LiDivision of Cardiovascular Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Susie N HongDivision of Cardiovascular Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD, 21201, USA.
Meyeon ParkDivision of Nephrology, University of California, San Francisco (UCSF), 505 Parnassus Ave, San Francisco, CA, 94143, USA.

Funding

Research BaseP30DK090868 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI SELIGER, STEPHEN L. · 2010 to 2019
$11.1M
Why do patients with cardiovascular disease develop kidney injury and disease?K23DK099238 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PARK, MEYEON · 2013 to 2017
$928k
NIDDK NIH HHS K23 DK099238NIDDK NIH HHS P30 DK090868
6 · The paper itself

Abstract

backgroundPatients with autosomal dominant polycystic kidney disease (ADPKD) have an increased risk of cardiovascular morbidity and mortality. Impaired left ventricular (LV) global longitudinal strain (GLS) can be a sign of subclinical cardiac dysfunction even in patients with otherwise preserved ejection fraction (EF). Transmitral early filling velocity to early diastolic strain rate (E/SRe) is a novel measure of LV filling pressure, which is often affected early in cardiac disease.

methodsA total of 110 ADPKD patients not on dialysis were included in this prospective study. All patients underwent an extensive echocardiographic examination including two-dimensional speckle tracking. GLS and strain rates were measured. The distribution of GLS and E/SRe was determined and patient characteristics were compared by median levels of GLS (- 17.8%) and E/SRe (91.4 cm). Twenty healthy participants were included as control group.

resultsThere was a significantly worse GLS in the ADPKD patients (mean: - 17.8 ± 2.5%) compared to the healthy controls (mean: - 21.9 ± 1.9%), p < 0.001. The same was true for E/SRe (mean: 10.0 ± 0.3 cm) compared to the control group (mean: 6.5 ± 0.3 cm), p < 0.001. In simple logistic regression, male gender (OR: 4.74 [2.10-10.71], p < 0.001), fasting glucose (odds ratio (OR) 1.05 [1.01-1.10], p = 0.024), htTKV (OR: 1.07 [1.01-1.13], p = 0.013), HDL cholesterol (OR: 0.97 [0.94, 0.996], p = 0.025), triglycerides (OR: 1.01 [1.00-1.02], p = 0.039), hemoglobin (OR: 1.50 [1.11-2.04], p = 0.009), and β-blocker use (OR: 1.07 [1.01, 1.13], p = 0.013) were all associated with higher GLS. After multivariate logistic regression with backward model selection, only male gender (OR: 5.78 [2.27-14.71], p < 0.001) and β-blocker use (OR: 14.00 [1.60, 122.51], p = 0.017) remained significant. In simple logistic regression models, BMI (OR: 1.11 [1.02-1.20], p = 0.015), systolic blood pressure (OR: 1.03 [1.00-1.06], p = 0.027) and β-blocker use (OR: 17.12 [2.15-136.20], p = 0.007) were associated with higher E/SRe - a novel measure of left ventricular filling pressure. After backward elimination, only β-blocker use (OR: 17.22 [2.16, 137.14], p = 0.007) remained significant.

conclusionHigher GLS and E/SRe are common in ADPKD patients, even in patients with preserved eGFR and normal left ventricular EF. GLS and E/SRe may aid in cardiovascular risk stratification in patients with ADPKD as they represent early markers of cardiac dysfunction.

Indexed as

AdultCase-Control StudiesCross-Sectional StudiesEchocardiographyFemaleHumansMaleMiddle AgedMyocardial ContractionPolycystic Kidney, Autosomal DominantProspective StudiesRegression AnalysisSex FactorsStroke VolumeVentricular Dysfunction, LeftAutosomal dominant polycystic kidney diseaseGlobal longitudinal StrainTwo-dimensional speckle tracking echocardiography

Identifiers

PMID31419965
PMCPMC6697983

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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.