Evidence map›Paper›PMID 28650999›Full record

ArticlePloS one2017

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.

Tokiho Akiyama, Takafumi Katsumura, Shigeki Nakagome, Sang-Il Lee, Keiichiro Joh, Hidenobu Soejima, Kazuma Fujimoto, Ryosuke Kimura, Hajime Ishida, Tsunehiko Hanihara and 4 more

Open access · goldAbstract read
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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. The next stage of physiological anthropology.Journal of physiological anthropology · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. 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

14 authors at 6 institutions in 2 countries.

Tokiho AkiyamaDepartment of Anatomy, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.ORCID http://orcid.org/0000-0002-9050-1014
Takafumi KatsumuraDepartment of Anatomy, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Shigeki NakagomeDepartment of Mathematical Analysis and Statistical Inference, The Institute of Statistical Mathematics, Tachikawa, Tokyo, Japan.
Sang-Il LeeDepartment of Human Science, Faculty of Design, Kyushu University, Minami-ku Fukuoka, Japan.
Keiichiro JohDivision of Molecular Genetics and Epigenetics, Department of Biomolecular Science, Faculty of Medicine, Saga University, Nabeshima, Saga, Japan.
Hidenobu SoejimaDivision of Molecular Genetics and Epigenetics, Department of Biomolecular Science, Faculty of Medicine, Saga University, Nabeshima, Saga, Japan.
Kazuma FujimotoDepartment of Internal Medicine, Faculty of Medicine, Saga University, Nabeshima, Saga, Japan.
Ryosuke KimuraDepartment of Human Biology and Anatomy, Faculty of Medicine, University of the Ryukyus, Nishihara-cho, Okinawa, Japan.
Hajime IshidaDepartment of Human Biology and Anatomy, Faculty of Medicine, University of the Ryukyus, Nishihara-cho, Okinawa, Japan.
Tsunehiko HaniharaDepartment of Anatomy, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Akira YasukouchiDepartment of Human Science, Faculty of Design, Kyushu University, Minami-ku Fukuoka, Japan.
Yoko SattaDepartment of Evolutionary Studies of Biosystems, SOKENDAI (The Graduate University for Advanced Studies), Hayama, Kanagawa, Japan.
Shigekazu HiguchiDepartment of Human Science, Faculty of Design, Kyushu University, Minami-ku Fukuoka, Japan.
Hiroki OotaDepartment of Anatomy, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kitasato University · JPKyushu University · JPSaga University · JPThe Graduate University for Advanced Studies, SOKENDAI · JPUniversity of the Ryukyus · JPUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Humans show various responses to the environmental stimulus in individual levels as "physiological variations." However, it has been unclear if these are caused by genetic variations. In this study, we examined the association between the physiological variation of response to light-stimulus and genetic polymorphisms. We collected physiological data from 43 subjects, including light-induced melatonin suppression, and performed haplotype analyses on the clock genes, PER2 and PER3, exhibiting geographical differentiation of allele frequencies. Among the haplotypes of PER3, no significant difference in light sensitivity was found. However, three common haplotypes of PER2 accounted for more than 96% of the chromosomes in subjects, and 1 of those 3 had a significantly low-sensitive response to light-stimulus (P < 0.05). The homozygote of the low-sensitive PER2 haplotype showed significantly lower percentages of melatonin suppression (P < 0.05), and the heterozygotes of the haplotypes varied their ratios, indicating that the physiological variation for light-sensitivity is evidently related to the PER2 polymorphism. Compared with global haplotype frequencies, the haplotype with a low-sensitive response was more frequent in Africans than in non-Africans, and came to the root in the phylogenetic tree, suggesting that the low light-sensitive haplotype is the ancestral type, whereas the other haplotypes with high sensitivity to light are the derived types. Hence, we speculate that the high light-sensitive haplotypes have spread throughout the world after the Out-of-Africa migration of modern humans.

Indexed as

AllelesGene FrequencyHaplotypesPolymorphism, Single NucleotideAdolescentFemaleGenetic Association StudiesGenotypeHumansLightMaleMelatoninPeriod Circadian ProteinsPhylogenySalivaYoung AdultMelatoninPER2 protein, humanPeriod Circadian Proteins

Identifiers

PMID28650999
PMCPMC5484468
OpenAlexW2698521989

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.