Evidence map›Paper›PMID 40929648›Full record

ArticleAnnals of the American Thoracic Society2026

Morning Larks and Night Owls: Considering Chronotype in Evaluation of Patients with Pulmonary Hypertension.

Cyrus Vahdatpour, Shiza Virk, Haocheng Ding, Samuel Epstein, Kirk Jones, Omar Alneser, Muhammad Albanna, Christina Eagan, Katherine Fu, Oluwafemi Ossunuga and 11 more

Abstract read
In one paragraph

Article in Annals of the American Thoracic Society, 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

21 authors.

Cyrus VahdatpourDivision of Pulmonary & Critical Care Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Shiza VirkDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Haocheng DingDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Samuel EpsteinDivision of Pulmonary & Critical Care Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California.
Kirk JonesDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Omar AlneserDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Muhammad AlbannaAscension Saint Francis Hospital, Evanston, Illinois; and.
Christina EaganDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Katherine FuDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Oluwafemi OssunugaDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Lauran ZaineddineDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Jeffrey S AnnisDivision of Cardiovascular Medicine, School of Medicine, Vanderbilt University, Nashville, Tennessee.
Elnaz EbrahimiDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Ali AtayaDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.ORCID 0000-0001-8505-1680
Saminder KalraDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Evan L BrittainDivision of Cardiovascular Medicine, School of Medicine, Vanderbilt University, Nashville, Tennessee.
Megan M LoweryDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Susheela HadigalDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Karyn A EsserDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Zhiguang HuoDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Andrew J BryantDivision of Pulmonary & Critical Care Medicine, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.ORCID 0000-0001-9433-3049

Funding

Role of CXCR2-mediated cell trafficking in pulmonary vascular remodelingR01HL142776 · NHLBI · UNIVERSITY OF FLORIDA · PI BRYANT, ANDREW JUSTIN · 2019 to 2023
$1.9M
National Heart, Lung and Blood Institute R01HL142776NHLBI NIH HHS R01 HL142776Pulmonary Hypertension Accelerated Bayer Award
6 · The paper itself

Abstract

rationalePulmonary hypertension (PH) is a systemic illness with increasingly subtle disease manifestations, including sleep disruption. Patients with PH are at increased risk for disturbances in circadian biology, although, to date, there are no data on "morningness" or "eveningness" in pulmonary vascular disease.

objectivesOur group studied circadian rhythms in patients with PH, on the basis of chronotype analysis, to explore whether there is a link between circadian parameters and physiological risk-stratifying factors to inform novel treatment strategies in patients with PH.

methodsWe serially recruited participants from July 2022 to March 2024 by administering the Munich Chronotype Questionnaire in clinic. We then compared free-day sleep measurements in patients with PH and bed-partner control subjects (BPCs), investigating associations with survival predictors. In exploratory analysis, we looked for associations between known single-nucleotide polymorphism (SNP) variants of core clock genes and cardiopulmonary hemodynamics. Finally, we performed circadian analysis of time-stamped heart rate variation from a PH cohort compared with control subjects.

resultsIn this pilot study, we recruited 103 patients with PH and 38 BPCs, ages 20 to 86 years. Compared with BPCs, patients with PH had longer sleep duration and less social jet lag (SJL), with no clear difference in chronotype. Within the PH cohort, sleep duration was associated with worse functional class, whereas SJL was associated with a low risk for disease progression and more severe signs of right ventricular dysfunction. However, a later chronotype was associated with a decrease in mean pulmonary artery pressure. In an independent cohort of patients with PH, there was a relationship between functionally distinct core clock gene SNP variants and relevant hemodynamic parameters. Patients with PH exhibited a distinct delayed phase shift in circadian HR variation.

conclusionsPH in adults is associated with significant changes in sleep duration and SJL, corroborated by both genomic and physiologic data. Dependence between circadian variables, SNP data, and disease characteristics suggest that findings may directly relate to disease pathogenesis through derangement in the molecular core clock.

Indexed as

Circadian RhythmHypertension, PulmonarySleepAdultAgedAged, 80 and overChronotypeFemaleHeart RateHumansMaleMiddle AgedPilot ProjectsPolymorphism, Single NucleotideSurveys and QuestionnairesYoung Adultchronotypecircadianpulmonary hypertensionsleepsleep-wake disorders

Identifiers

PMID40929648
PMCPMC12983450

What OpenQuestion holds

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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 OpenQuestion graph.