Evidence map›Paper›PMID 29162152›Full record

ArticleHuman genomics2017

The peptidylglycine-α-amidating monooxygenase (PAM) gene rs13175330 A>G polymorphism is associated with hypertension in a Korean population.

Hye Jin Yoo, Minjoo Kim, Minkyung Kim, Jey Sook Chae, Sang-Hyun Lee, Jong Ho Lee

Open access · goldAbstract read
In one paragraph

Article in Human genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Peptidylglycine α-amidating monooxygenase is required for atrial secretory granule formation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
  9. Review
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 2 institutions in 1 country.

Hye Jin YooNational Leading Research Laboratory of Clinical Nutrigenetics/Nutrigenomics, Department of Food and Nutrition, College of Human Ecology, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul, 03722, South Korea.
Minjoo KimResearch Center for Silver Science, Institute of Symbiotic Life-TECH, Yonsei University, Seoul, 03722, South Korea.
Minkyung KimResearch Center for Silver Science, Institute of Symbiotic Life-TECH, Yonsei University, Seoul, 03722, South Korea.
Jey Sook ChaeResearch Center for Silver Science, Institute of Symbiotic Life-TECH, Yonsei University, Seoul, 03722, South Korea.
Sang-Hyun LeeDepartment of Family Practice, National Health Insurance Corporation, Ilsan Hospital, Goyang, 10444, South Korea.
Jong Ho LeeNational Leading Research Laboratory of Clinical Nutrigenetics/Nutrigenomics, Department of Food and Nutrition, College of Human Ecology, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul, 03722, South Korea. jhleeb@yonsei.ac.kr.
Yonsei University · KRNational Health Insurance Service · KR

Funding

Ministry of Science, ICT and Future Planning NRF-2012M3A9C4048762Ministry of Science, ICT and Future Planning NRF-2016R1A2B4011662
6 · The paper itself

Abstract

backgroundPeptidylglycine-α-amidating monooxygenase (PAM) may play a role in the secretion of atrial natriuretic peptide (ANP), which is a hormone involved in the maintenance of blood pressure (BP). The objective of the present study was to determine whether PAM is a novel candidate gene for hypertension (HTN).

resultsA total of 2153 Korean participants with normotension and HTN were included. Genotype data were obtained using the Korean Chip. The rs13175330 polymorphism of the PAM gene was selected from the ten single nucleotide polymorphisms (SNPs) most strongly associated with BP. The presence of the G allele of the PAM rs13175330 A>G SNP was associated with a higher risk of HTN after adjustments for age, sex, BMI, smoking, and drinking [OR 1.607 (95% CI 1.220-2.116), p = 0.001]. The rs13175330 G allele carriers in the HTN group treated without antihypertensive therapy (HTN w/o therapy) had significantly higher systolic and diastolic BP than the AA carriers, whereas the G allele carriers in the HTN group treated with antihypertensive therapy (HTN w/ therapy) showed significantly higher diastolic BP. Furthermore, rs13175330 G allele carriers in the HTN w/o therapy group had significantly increased levels of insulin, insulin resistance, and oxidized low-density lipoprotein (LDL) and significantly decreased LDL-cholesterol levels and LDL particle sizes compared to the AA carriers.

conclusionThese results suggest that the PAM rs13175330 A>G SNP is a novel candidate gene for HTN in the Korean population. Additionally, the PAM rs13175330 G allele might be associated with insulin resistance and LDL atherogenicity in patients with HTN.

Indexed as

Polymorphism, Single NucleotideAdultAgedAged, 80 and overAmidine-LyasesAsian PeopleBlood PressureCase-Control StudiesCholesterol, HDLFemaleGenetic Predisposition to DiseaseHumansHypertensionInsulinInsulin ResistanceLipoproteins, LDLAmidine-LyasesCholesterol, HDLInsulinLipoproteins, LDLMixed Function Oxygenasesoxidized low density lipoproteinPAM protein, humanAtrial natriuretic peptideGenetic associationGenetic polymorphismsHypertensionLDL atherogenicityPeptidylglycine-α-amidating monooxygenase

Identifiers

PMID29162152
PMCPMC5696732
OpenAlexW2770281322

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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.