Evidence map›Paper›PMID 40440257›Full record

ArticlePloS one2025

SNP associations in the L-citrulline metabolic pathway and vascular aging in the Japanese population.

Dai Nogimura, Kazuki Moriyasu, Sachiko Ishida, Masakazu Kohda, Takayuki Yazawa, Masahiko Morita

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

6 authors.

Dai NogimuraInstitute of Health Sciences, Kirin Holdings Company, Ltd., Fujisawa, Kanagawa, Japan.ORCID https://orcid.org/0009-0008-8477-288X
Kazuki MoriyasuInstitute of Health Sciences, Kirin Holdings Company, Ltd., Fujisawa, Kanagawa, Japan.
Sachiko IshidaDeNA Life Science, Inc., R&D Group, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6463-3059
Masakazu KohdaDeNA Life Science, Inc., R&D Group, Tokyo, Japan.
Takayuki YazawaDeNA Life Science, Inc., R&D Group, Tokyo, Japan.
Masahiko MoritaInstitute of Health Sciences, Kirin Holdings Company, Ltd., Fujisawa, Kanagawa, Japan.ORCID https://orcid.org/0009-0007-9394-6135

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decreased nitric oxide (NO) production from the vascular endothelium is a major factor for vascular aging. Because vascular aging has few specific subjective symptoms, assessing the susceptibility to vascular aging is beneficial for its early detection and improvement. Therefore, this study evaluated the associations between single nucleotide polymorphisms (SNPs) on L-citrulline (Cit) pathways essential for NO production and the health characteristics involved in vascular aging using a candidate gene approach. Associations with a significance level included those between the KCNMB4 rs17108108 C allele and tendency to gain weight, the ADCY8 rs6470860 G allele and numbness of limbs, the NOS1 rs2271987 T allele and lower back pain, and the PDE9A rs2284972 G allele and body pain with negative mood states. A genome-wide association study was also conducted to analyze SNPs more extensively across genes related to Cit and NO metabolism, which revealed genome-wide significant associations between the PRMT6 rs12028323 C allele and mood disturbance. These significant associations could be explained by the change in downstream NO signaling, supporting the relationship between the investigated traits and vascular function. These traits can be manifested as subjective symptoms of vascular aging. Therefore, the identified SNPs could predict susceptibility to the subjective symptoms of vascular aging, which could lead to genotype-based personalized interventions of Cit for an efficient improvement of vascular health.

Indexed as

AgingCitrullineMetabolic Networks and PathwaysPolymorphism, Single NucleotideAdultAgedAllelesEast Asian PeopleFemaleGenome-Wide Association StudyHumansJapanMaleMiddle AgedNitric OxideCitrullineNitric Oxide

Identifiers

PMID40440257
PMCPMC12121766

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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.