Evidence map›Paper›PMID 22025373›Full record

ArticleHypertension (Dallas, Tex. : 1979)2011

Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study.

Mervi Oikonen, Emmi Tikkanen, Jonna Juhola, Tarja Tuovinen, Ilkka Seppälä, Markus Juonala, Leena Taittonen, Vera Mikkilä, Mika Kähönen, Samuli Ripatti and 13 more

Open access · bronzeAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.1field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Sex Differences in Genetic Risk for Hypertension.Hypertension (Dallas, Tex. : 1979) · 2021
    Article
  11. Genetic Risk Scores for Complex Disease Traits in Youth.Circulation. Genomic and precision medicine · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Genetic Programming of Hypertension.Frontiers in pediatrics · 2017
    Review
  17. Prediction of Blood Pressure and Blood Pressure Change With a Genetic Risk Score.Journal of clinical hypertension (Greenwich, Conn.) · 2016
    Article
  18. Review
  19. Familial aggregation and childhood blood pressure.Current hypertension reports · 2015
    Review
  20. 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

23 authors at 1 institution in 1 country.

Mervi OikonenResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, PO Box 52, FI-20521 Turku, Finland. mervi.oikonen@utu.fi
Emmi Tikkanen
Jonna Juhola
Tarja Tuovinen
Ilkka Seppälä
Markus Juonala
Leena Taittonen
Vera Mikkilä
Mika Kähönen
Samuli Ripatti
Jorma Viikari
Terho Lehtimäki
Aki S Havulinna
Frank Kee
Christopher Newton-Cheh
Leena Peltonen
Nicholas J Schork
Sarah S Murray
Gerald S Berenson
Wei Chen
Sathanur R Srinivasan
Veikko Salomaa
Olli T Raitakari
Tampere University Hospital · FI

Funding

EVOLUTION OF CARDIOVASCULAR RISK WITH NORMAL AGINGR01AG016592 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, WEI · 2000 to 2015
$11.7M
Genetic Modulation on the Relationship of Low Birth Weight to Metabolic SyndromeR03HD061437 · NICHD · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, WEI · 2010 to 2011
$146k
Birth Weight, Postnatal Growth, Blood Pressure and Subclinical Cardiovascular DisR03HD062783 · NICHD · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, WEI · 2010 to 2011
$146k
NIA NIH HHS AG-16592NIA NIH HHS R01 AG016592NICHD NIH HHS HD-061437NICHD NIH HHS HD-062783NICHD NIH HHS R03 HD061437NICHD NIH HHS R03 HD062783Wellcome Trust
6 · The paper itself

Abstract

Clinical relevance of a genetic predisposition to elevated blood pressure was quantified during the transition from childhood to adulthood in a population-based Finnish cohort (N=2357). Blood pressure was measured at baseline in 1980 (age 3-18 years) and in follow-ups in 1983, 1986, 2001, and 2007. Thirteen single nucleotide polymorphisms associated with blood pressure were genotyped, and 3 genetic risk scores associated with systolic and diastolic blood pressures and their combination were derived for all of the participants. Effects of the genetic risk score were 0.47 mm Hg for systolic and 0.53 mm Hg for diastolic blood pressures (both P<0.01). The combination genetic risk score was associated with diastolic blood pressure from age 9 years onward (β=0.68 mm Hg; P=0.015). Replications in 1194 participants of the Bogalusa Heart Study showed essentially similar results. The participants in the highest quintile of the combination genetic risk score had a 1.82-fold risk of hypertension in adulthood (P<0.0001) compared with the lowest quintile, independent of a family history of premature hypertension. These findings show that genetic variants are associated with preclinical blood pressure traits in childhood; individuals with several susceptibility alleles have, on average, a 0.5-mm Hg higher blood pressure, and this trajectory continues from childhood to adulthood.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAge FactorsBlood PressureBody Mass IndexChildChild, PreschoolCohort StudiesCross-Sectional StudiesFemaleFinlandFollow-Up StudiesGenotypeHumansHypertensionSodium, Dietary

Identifiers

PMID22025373
PMCPMC3247907
OpenAlexW2167053513

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.