Evidence map›Paper›PMID 36528682›Full record

ArticleJournal of human hypertension2023

Vascular phenotypes in early hypertension.

Eleanor C Murray, Christian Delles, Patryk Orzechowski, Pawel Renc, Arkadiusz Sitek, Joost Wagenaar, Tomasz J Guzik

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of human hypertension, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04015635 (A Study of the Roles of the Immune and Inflammatory Systems in Hypertension), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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.

NCT04015635 unknown statusnot on this map

A Study of the Roles of the Immune and Inflammatory Systems in Hypertension

TypeobservationalSponsorUniversity of GlasgowRan2019 to 2021Enrolled160ConditionsHypertension, Inflammation, Vascular DiseasesArmsNone involved
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Immune and inflammatory mechanisms in hypertension.Nature reviews. Cardiology · 2024
    Review
  6. Review
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

7 authors at 5 institutions in 3 countries.

Eleanor C MurraySchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK. Eleanor.Murray3@nhs.scot.ORCID 0000-0002-4837-4840
Christian DellesSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.ORCID 0000-0003-2238-2612
Patryk OrzechowskiDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Pawel RencSano Centre for Computational Science, Krakow, Poland.ORCID 0000-0002-0487-7454
Arkadiusz SitekMassachusetts General Hospital, Harvard Medical School, Harvard University Boston, Boston, MA, USA.ORCID 0000-0002-0677-4002
Joost WagenaarDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Tomasz J GuzikSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK. tguzik@ed.ac.uk.
AGH University of Krakow · PLUniversity of Glasgow · GBHarvard University · USJagiellonian University · PLUniversity of Pennsylvania · US

Funding

British Heart Foundation FS/4YPHD/F/20/34127 ABritish Heart Foundation PG/19/84/34771British Heart Foundation PG/21/10541British Heart Foundation RE/18/6/34217
6 · The paper itself

Abstract

The study characterises vascular phenotypes of hypertensive patients utilising machine learning approaches. Newly diagnosed and treatment-naïve primary hypertensive patients without co-morbidities (aged 18-55, n = 73), and matched normotensive controls (n = 79) were recruited (NCT04015635). Blood pressure (BP) and BP variability were determined using 24 h ambulatory monitoring. Vascular phenotyping included SphygmoCor® measurement of pulse wave velocity (PWV), pulse wave analysis-derived augmentation index (PWA-AIx), and central BP; EndoPAT™-2000® provided reactive hyperaemia index (LnRHI) and augmentation index adjusted to heart rate of 75bpm. Ultrasound was used to analyse flow mediated dilatation and carotid intima-media thickness (CIMT). In addition to standard statistical methods to compare normotensive and hypertensive groups, machine learning techniques including biclustering explored hypertensive phenotypic subgroups. We report that arterial stiffness (PWV, PWA-AIx, EndoPAT-2000-derived AI@75) and central pressures were greater in incident hypertension than normotension. Endothelial function, percent nocturnal dip, and CIMT did not differ between groups. The vascular phenotype of white-coat hypertension imitated sustained hypertension with elevated arterial stiffness and central pressure; masked hypertension demonstrating values similar to normotension. Machine learning revealed three distinct hypertension clusters, representing 'arterially stiffened', 'vaso-protected', and 'non-dipper' patients. Key clustering features were nocturnal- and central-BP, percent dipping, and arterial stiffness measures. We conclude that untreated patients with primary hypertension demonstrate early arterial stiffening rather than endothelial dysfunction or CIMT alterations. Phenotypic heterogeneity in nocturnal and central BP, percent dipping, and arterial stiffness observed early in the course of disease may have implications for risk stratification.

Indexed as

HypertensionVascular StiffnessBlood PressureBlood Pressure Monitoring, AmbulatoryCarotid Intima-Media ThicknessHumansPhenotypePulse Wave Analysis

Identifiers

PMID36528682
PMCPMC9758678
OpenAlexW4312065282

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.