Evidence map›Paper›PMID 25673673›Full record

ArticleProceedings. Biological sciences2015

Apolipoprotein E (ApoE) polymorphism is related to differences in potential fertility in women: a case of antagonistic pleiotropy?

Grazyna Jasienska, Peter T Ellison, Andrzej Galbarczyk, Michal Jasienski, Malgorzata Kalemba-Drozdz, Maria Kapiszewska, Ilona Nenko, Inger Thune, Anna Ziomkiewicz

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.0field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. The physiological effects of APOE genotype in healthy young/middle-aged individuals.Biological reviews of the Cambridge Philosophical Society · 2026
    Article
  3. Apolipoprotein E Polymorphism and Reproductive Patterns Among Postreproductive Women.American journal of human biology : the official journal of the Human Biology Council · 2026
    Article
  4. Transcriptome Sequencing and Identification ofAnimals : an open access journal from MDPI · 2026
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  6. Impact ofProceedings of the National Academy of Sciences of the United States of America · 2025
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  11. Review
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  13. Science advances · 2023
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  14. Review
  15. Article
  16. The influence of 17q21.31 andFrontiers in aging neuroscience · 2022
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  17. Dissociable effects ofNature aging · 2021
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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

9 authors at 6 institutions in 3 countries.

Grazyna JasienskaDepartment of Environmental Health, Jagiellonian University Medical College, Krakow, Poland jasienska@post.harvard.edu.
Peter T EllisonDepartment of Human Evolutionary Biology, Harvard University, Cambridge, MA, USA.
Andrzej GalbarczykDepartment of Environmental Health, Jagiellonian University Medical College, Krakow, Poland.
Michal JasienskiCenter for Innovatics, Nowy Sacz Business School-National-Louis University, Zielona 27, 33-300 Nowy Sacz, Poland.
Malgorzata Kalemba-DrozdzAndrzej Frycz Modrzewski Krakow University, Krakow, Poland.
Maria KapiszewskaAndrzej Frycz Modrzewski Krakow University, Krakow, Poland.
Ilona NenkoDepartment of Environmental Health, Jagiellonian University Medical College, Krakow, Poland.
Inger ThuneDepartment of Community Medicine, Faculty of Health Sciences, University of Tromsø, Tromsø, Norway The Cancer Center, Oslo University Hospital, Oslo, Norway.
Anna ZiomkiewiczPolish Academy of Sciences, Unit of Anthropology in Wroclaw, Poland.
Jagiellonian University · PLAndrzej Frycz Modrzewski Krakow University · PLHarvard University · USNational-Louis University · PLPolish Academy of Sciences · PLUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The alleles that are detrimental to health, especially in older age, are thought to persist in populations because they also confer some benefits for individuals (through antagonistic pleiotropy). The ApoE4 allele at the ApoE locus, encoding apolipoprotein E (ApoE), significantly increases risk of poor health, and yet it is present in many populations at relatively high frequencies. Why has it not been replaced by natural selection with the health-beneficial ApoE3 allele? ApoE is a major supplier of cholesterol precursor for the production of ovarian oestrogen and progesterone, thus ApoE has been suggested as the potential candidate gene that may cause variation in reproductive performance. Our results support this hypothesis showing that in 117 regularly menstruating women those with genotypes with at least one ApoE4 allele had significantly higher levels of mean luteal progesterone (144.21 pmol l(-1)) than women with genotypes without ApoE4 (120.49 pmol l(-1)), which indicates higher potential fertility. The hormonal profiles were based on daily data for entire menstrual cycles. We suggest that the finding of higher progesterone in women with ApoE4 allele could provide first strong evidence for an evolutionary mechanism of maintaining the ancestral and health-worsening ApoE4 allele in human populations.

Indexed as

Genetic PleiotropyPolymorphism, GeneticAdultAllelesApolipoprotein E3Apolipoprotein E4FemaleFertilityHumansMenstrual CycleProgesteroneReproductionSalivaApolipoprotein E3Apolipoprotein E4Progesteroneantagonistic pleiotropyApoEapolipoprotein polymorphismfertilityprogesterone

Identifiers

PMID25673673
PMCPMC4345437
OpenAlexW1975167118

What OpenQuestion holds

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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.