Evidence map›Paper›PMID 24029162›Full record

ArticleAmerican journal of hypertension2014

Body mass index modulates blood pressure heritability: the Family Blood Pressure Program.

Jeannette Simino, Gang Shi, Alan Weder, Eric Boerwinkle, Steven C Hunt, Dabeeru C Rao

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of hypertension, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Systolic Blood Pressure Mediates Body Mass Index and Non-alcoholic Fatty Liver Disease: A Population-Based Study.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2021
    Article
  4. 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

6 authors at 4 institutions in 1 country.

Jeannette SiminoDivision of Biostatistics, Washington University in St. Louis, School of Medicine, St. Louis, Missouri.
Gang Shi
Alan Weder
Eric Boerwinkle
Steven C Hunt
Dabeeru C Rao
Washington University in St. Louis · USMichigan Medicine · USThe University of Texas Health Science Center at Houston · USUniversity of Utah · US

Funding

The Family Blood Pressure Program (Program Data Center)U01HL054473 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2000 to 2008
$5.8M
Post-Doctoral Research Training in Genetic EpidemiologyT32HL091823 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2008 to 2017
$2.1M
RESEARCH PROJECT IN GENETIC EPIDEMIOLOGYR01GM028719 · NIGMS · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 1985 to 2008
$2.0M
EXPLORING A NEW DIRECTION TO GENE DISCOVERY FOR HYPERTENSION IN THE LARGE FBPPR21HL095054 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2009 to 2010
$303k
NHLBI NIH HHS R21 HL095054NHLBI NIH HHS T32 HL091823NHLBI NIH HHS U01 HL054473NHLBI NIH HHS U01 HL54473NIGMS NIH HHS R01 GM028719NIGMS NIH HHS R01 GM28719
6 · The paper itself

Abstract

backgroundCandidate gene and twin studies suggest that interactions between body mass index (BMI) and genes contribute to the variability of blood pressure (BP). To determine whether there is evidence for gene-BMI interactions, we investigated the modulation of BP heritability by BMI using 4,153 blacks, 1,538 Asians, 4,013 whites, and 2,199 Hispanic Americans from the Family Blood Pressure Program.

methodsTo capture the BP heritability dependence on BMI, we employed a generalized variance components model incorporating linear and Gaussian interactions between BMI and the genetic component. Within each race and network subgroup, we used the Akaike information criterion and likelihood ratio test to select the appropriate interaction function for each BP trait (systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP), and pulse pressure (PP)) and determine interaction significance, respectively.

resultsBP heritabilities were significantly modified by BMI in the GenNet and SAPPHIRe Networks, which contained the youngest and least-obese participants, respectively. GenNet Whites had unimodal SBP, MAP, and PP heritabilities that peaked between BMI values of 33 and 37kg/m(2). The SBP and MAP heritabilities in GenNet Hispanic Americans, as well as the PP heritability in GenNet blacks, were increasing functions of BMI. The DBP and SBP heritabilities in the SAPPHIRe Chinese and Japanese, respectively, were decreasing functions of BMI.

conclusionsBP heritability differed by BMI in the youngest and least-obese networks, although the shape of this dependence differed by race. Use of nonlinear gene-BMI interactions may enhance BP gene discovery efforts in individuals of European ancestry.

Indexed as

Body Mass IndexAdultAsian PeopleBlack PeopleBlood PressureFemaleHispanic or LatinoHumansMaleMiddle AgedObesityWhite Peopleblood pressureBMIFBPPheritabilityhypertensioninteractions.

Identifiers

PMID24029162
PMCPMC3958601
OpenAlexW2140819433

What OpenQuestion holds

Textmetadata
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.