Evidence map›Paper›PMID 28732058›Full record

ArticlePloS one2017

The role of a FADS1 polymorphism in the association of fatty acid blood levels, BMI and blood pressure in young children-Analyses based on path models.

Maike Wolters, Carmen Dering, Alfonso Siani, Paola Russo, Jaakko Kaprio, Patrizia Risé, Luis A Moreno, Stefaan De Henauw, Kirsten Mehlig, Toomas Veidebaum and 8 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Bioactive lipids in hypertension.Advances in pharmacology (San Diego, Calif.) · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. 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

18 authors at 11 institutions in 9 countries.

Maike WoltersLeibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.ORCID http://orcid.org/0000-0002-4943-2141
Carmen DeringLeibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.
Alfonso SianiEpidemiology and Population Genetics, Institute of Food Sciences, National Research Council, Avellino, Italy.
Paola RussoEpidemiology and Population Genetics, Institute of Food Sciences, National Research Council, Avellino, Italy.
Jaakko KaprioInstitute for Molecular Medicine FIMM, University of Helsinki, Helsinki, Finland.
Patrizia RiséDiSFeB, Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.
Luis A MorenoGENUD (Growth, Exercise, Nutrition and Development) Research Group, Instituto Agroalimentario de Aragón (IA2), Instituto de Investigación Sanitaria Aragón (IIS Aragón), Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y Nutrición (CIBERObn), University of Zaragoza, Zaragoza, Spain.
Stefaan De HenauwDepartment of Public Health, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Kirsten MehligSection for Epidemiology and Social Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Toomas VeidebaumNational Institute for Health Development, Tallinn, Estonia.
Denés MolnárNational Institute of Health Promotion, University of Pécs, Pécs, Hungary.
Michael TornaritisResearch and Education Institute of Child Health, Strovolos, Cyprus.
Licia IacovielloDepartment of Epidemiology and Prevention, IRCCS Istituto Neurologico Mediterraneo Neuromed, Pozzilli (IS), Italy.
Yannis PitsiladisUniversity of Brighton, Eastbourne, United Kingdom.
Claudio GalliDiSFeB, Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.
Ronja ForaitaLeibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.
Claudia BörnhorstLeibniz Institute for Prevention Research and Epidemiology-BIPS, Bremen, Germany.
IDEFICS and I. Family consortia
Leibniz Institute for Prevention Research and Epidemiology - BIPS · DEInstitute of Food Science · ITUniversity of Milan · ITGhent University · BEIstituto Neurologico Mediterraneo · ITNational Institute for Health Development · EEUniversidad de Zaragoza · ESUniversity of Brighton · GBUniversity of Gothenburg · SEUniversity of Helsinki · FIUniversity of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe recent obesity epidemic in children also showed an increase in the prevalence of hypertension. As blood pressure (BP) is associated with (long-chain) polyunsaturated fatty acids (LC PUFA), genetic variation in desaturase enzymes being involved in the synthesis of LC PUFA may be associated with BP. This study aimed to investigate the direct effects (independent of mediating variables) and indirect effects (mediated through intermediate variables) of a common variant in the FADS1 gene, rs174546, known to affect delta-5 desaturase (D5D) activity on PUFA level, body mass index (BMI) and BP.

methodsA subsample of the IDEFICS (Identification and prevention of dietary- and lifestyle-induced health effects in children and infants) baseline survey including 520 children aged 2 to <10 years from six European countries was included. The association between rs174546 (T<C) and BP z-score as well as the mediating effects of selected key PUFA levels (dihomo-gamma-linolenic acid, DGLA; arachidonic acid, ARA; eicosapentaenoic acid, EPA) or estimated D5D activity (D5D index) and BMI z-score were investigated through path model analyses, adjusting for sex, age, educational level of parents, family history of hypertension, lifestyle factors and blood levels of saturated and monounsaturated fatty acids, triglycerides and low density lipoprotein cholesterol. Whole blood fatty acids were measured by a validated gas chromatographic method and recorded as percentage of weight of all fatty acids detected.

resultsMinor allele carriers of the SNP rs174546 had significantly higher DGLA and lower ARA and EPA levels as well as a lower D5D index. Via ARA and BMI z-score, the polymorphism had an indirect lowering effect on systolic BP z-score for each additional T allele (standardized effect estimate -0.057, p = 0.007). For DGLA, EPA and D5D index, the indirect effects of rs174546 on systolic BP were also negative but did not reach significance. DGLA and EPA had an increasing indirect effect on systolic BP via BMI. Results for diastolic BP were in general similar but effect estimates were lower compared to systolic BP.

conclusionGenetic variation in FADS1 influences BP via ARA and BMI indicating a favorable effect of the minor allele in SNP rs174546. Thus, polymorphisms with an impact on the D5D activity may play a role for the BP level mediated through PUFA and BMI. Therefore, health effects of dietary n-6 and n-3 PUFA may vary depending on genetic FADS1 variants.

Indexed as

Body Mass IndexGenetic Predisposition to DiseasePolymorphism, Single NucleotideBlood PressureBlood Pressure DeterminationChildChild, PreschoolChromatography, GasCohort StudiesCross-Sectional StudiesDelta-5 Fatty Acid DesaturaseEuropeFatty Acid DesaturasesFatty AcidsFemaleGenotyping TechniquesDelta-5 Fatty Acid DesaturaseFADS1 protein, humanFatty Acid DesaturasesFatty Acids

Identifiers

PMID28732058
PMCPMC5521833
OpenAlexW2739099339

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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.