Evidence map›Paper›PMID 26018448›Full record

ArticleBMC genetics2015

Exploring the relationship between lifestyles, diets and genetic adaptations in humans.

Cristina Valente, Luis Alvarez, Sarah J Marks, Ana M Lopez-Parra, Walther Parson, Ockie Oosthuizen, Erica Oosthuizen, António Amorim, Cristian Capelli, Eduardo Arroyo-Pardo and 2 more

Abstract read
In one paragraph

Article in BMC genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
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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

12 authors.

Cristina ValenteIPATIMUP, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal. csantos@ipatimup.pt.
Luis AlvarezIPATIMUP, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal. lfernandez@ipatimup.pt.
Sarah J MarksDepartment of Zoology, University of Oxford, Oxford, UK. sarah.marks@live.co.uk.
Ana M Lopez-ParraDepartamento de Toxicología y Legislación Sanitaria, Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain. amlopezparra@med.ucm.es.
Walther ParsonInstitute of Legal Medicine, Innsbruck Medical University, Innsbruck, Austria. walther.parson@i-med.ac.at.
Ockie OosthuizenSchool of Medicine, University of Namibia, Windhoek, Namibia. dr-ockie@iway.na.
Erica OosthuizenSchool of Medicine, University of Namibia, Windhoek, Namibia. ericao@iway.na.
António AmorimIPATIMUP, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal. aamorim@ipatimup.pt.
Cristian CapelliDepartment of Zoology, University of Oxford, Oxford, UK. cristian.capelli@zoo.ox.ac.uk.
Eduardo Arroyo-PardoDepartamento de Toxicología y Legislación Sanitaria, Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain. earroyop@med.ucm.es.
Leonor GusmãoIPATIMUP, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal. lgusmao@ipatimup.pt.
Maria J PrataIPATIMUP, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal. mprata@ipatimup.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne of the most important dietary shifts underwent by human populations began to occur in the Neolithic, during which new modes of subsistence emerged and new nutrients were introduced in diets. This change might have worked as a selective pressure over the metabolic pathways involved in the breakdown of substances extracted from food. Here we applied a candidate gene approach to investigate whether in populations with different modes of subsistence, diet-related genetic adaptations could be identified in the genes AGXT, PLRP2, MTRR, NAT2 and CYP3A5.

resultsAt CYP3A5, strong signatures of positive selection were detected, though not connected to any dietary variable, but instead to an environmental factor associated with the Tropic of Cancer. Suggestive signals of adaptions that could indeed be connected with differences in dietary habits of populations were only found for PLRP2 and NAT2. Contrarily, the demographic history of human populations seemed enough to explain patterns of diversity at AGXT and MTRR, once both conformed the evolutionary expectations under selective neutrality.

conclusionsAccumulated evidence indicates that CYP3A5 has been under adaptive evolution during the history of human populations. PLRP2 and NAT2 also appear to have been modelled by some selective constrains, although clear support for that did not resist to a genome wide perspective. It is still necessary to clarify which were the biological mechanisms and the environmental factors involved as well as their interactions, to understand the nature and strength of the selective pressures that contributed to shape current patterns of genetic diversity at those loci.

Indexed as

DietGenetic Association StudiesLife StyleAdaptation, BiologicalAllelesBiological EvolutionCytochrome P-450 CYP3AFerredoxin-NADP ReductaseGene FrequencyHumansLinkage DisequilibriumLipaseQuantitative Trait LociSelection, GeneticTransaminasesAlanine-glyoxylate transaminaseCytochrome P-450 CYP3AFerredoxin-NADP ReductaseLipasemethionine synthase reductasepancreatic lipase related protein 2Transaminases

Identifiers

PMID26018448
PMCPMC4445807

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Registered trials

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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.