Evidence map›Paper›PMID 32829661›Full record

ArticleHypertension (Dallas, Tex. : 1979)2020

Heritability and the Genetic Correlation of Heart Rate Variability and Blood Pressure in >29 000 Families: The Lifelines Cohort Study.

Balewgizie S Tegegne, Tengfei Man, Arie M van Roon, Nigus G Asefa, Harriëtte Riese, Ilja Nolte, Harold Snieder

Open access · hybridAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 8% 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.

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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  8. Proteome-Wide Genetic Investigation of Large Artery Stiffness.JACC. Basic to translational science · 2024
    Article
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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

7 authors at 1 institution in 1 country.

Balewgizie S TegegneFrom the Department of Epidemiology (B.S.T., T.M., N.G.A., I.N., H.S.), University Medical Center Groningen, University of Groningen, the Netherlands.
Tengfei ManFrom the Department of Epidemiology (B.S.T., T.M., N.G.A., I.N., H.S.), University Medical Center Groningen, University of Groningen, the Netherlands.
Arie M van RoonDepartment of Vascular Medicine (A.M.v.R.), University Medical Center Groningen, University of Groningen, the Netherlands.
Nigus G AsefaFrom the Department of Epidemiology (B.S.T., T.M., N.G.A., I.N., H.S.), University Medical Center Groningen, University of Groningen, the Netherlands.
Harriëtte RieseDepartment of Psychiatry, Interdisciplinary Center Psychopathology and Emotion Regulation (H.R.), University Medical Center Groningen, University of Groningen, the Netherlands.
Ilja NolteFrom the Department of Epidemiology (B.S.T., T.M., N.G.A., I.N., H.S.), University Medical Center Groningen, University of Groningen, the Netherlands.
Harold SniederFrom the Department of Epidemiology (B.S.T., T.M., N.G.A., I.N., H.S.), University Medical Center Groningen, University of Groningen, the Netherlands.
University Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of the cardiac autonomic nervous system, as indexed by reduced heart rate variability (HRV), has been associated with the development of high blood pressure (BP). However, the underlying pathological mechanisms are not yet fully understood. This study aimed to estimate heritability of HRV and BP and to determine their genetic overlap. We used baseline data of the 3-generation Lifelines population-based cohort study (n=149 067; mean age, 44.5). In-house software was used to calculate root mean square of successive differences and SD of normal-to-normal intervals as indices of HRV based on 10-second resting ECGs. BP was recorded with an automatic BP monitor. We estimated heritabilities and genetic correlations with variance components methods in ASReml software. We additionally estimated genetic correlations with bivariate linkage disequilibrium score regression using publicly available genome-wide association study data. The heritability (SE) estimates were 15.6% (0.90%) for SD of normal-to-normal intervals and 17.9% (0.90%) for root mean square of successive differences. For BP measures, they ranged from 24.4% (0.90%) for pulse pressure to 30.3% (0.90%) for diastolic BP. Significant negative genetic correlations (all

Indexed as

AdultAutonomic Nervous SystemBlood PressureCohort StudiesFemaleGenome-Wide Association StudyHeart RateHumansLinkage DisequilibriumMaleMiddle AgedYoung Adultblood pressureheart ratehumansrestsoftwarevariability

Identifiers

PMID32829661
PMCPMC7480943
OpenAlexW3081082235

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.