Evidence map›Paper›PMID 23935855›Full record

ArticlePloS one2013

Genetic polymorphism of human Y chromosome and risk factors for cardiovascular diseases: a study in WOBASZ cohort.

Grażyna Kostrzewa, Grażyna Broda, Magdalena Konarzewska, Paweł Krajewki, Rafał Płoski

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. The Y chromosome: a blueprint for men's health?European journal of human genetics : EJHG · 2017
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Grażyna KostrzewaDepartment of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
Grażyna Broda
Magdalena Konarzewska
Paweł Krajewki
Rafał Płoski

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variants of Y chromosome predispose to hypertension in rodents, whereas in humans the evidence is conflicting. Our purpose was to study the distribution of a panel of Y chromosome markers in a cohort from a cross-sectional population-based study on the prevalence of cardiovascular risk factors in Poland (WOBASZ study). The HindIII, YAP Y chromosome variants, previously shown to influence blood pressure, lipid traits or height, as well as SNPs defining main Y chromosome haplogroups, were typed in 3026, 2783 and 2652 samples, respectively. In addition, 4 subgroups (N~100 each) representing extremes of LDL concentration or blood pressure (BP) were typed for a panel of 17 STRs. The HindIII and YAP polymorphism were not associated with any of the studied traits. Analysis of the haplogroup distribution showed an association between higher HDL level and hg I-M170 (P = 0.02), higher LDL level and hg F*(xI-M170, J2-M172, K-M9) (P = 0.03) and lower BMI and hg N3-Tat (P = 0.04). Analysis of STRs did not show statistically significant differences. Since all these associations lost statistical significance after Bonferroni correction, we conclude that a major role of Y chromosome genetic variation (defined by HindIII, YAP or main Y chromosome haplogroups) in determining cardiovascular risk in Poles is unlikely.

Indexed as

Chromosomes, Human, YPolymorphism, GeneticAdultAgedBlood PressureCardiovascular DiseasesCholesterol, LDLCohort StudiesCross-Sectional StudiesFemaleHaplotypesHumansMaleMiddle AgedPhenotypePolandCholesterol, LDL

Identifiers

PMID23935855
PMCPMC3723826

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