Evidence map›Paper›PMID 27538888›Full record

ArticleInternational journal of epidemiology2016

Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence.

Qin Wang, Peter Würtz, Kirsi Auro, Laure Morin-Papunen, Antti J Kangas, Pasi Soininen, Mika Tiainen, Tuulia Tynkkynen, Anni Joensuu, Aki S Havulinna and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in International journal of epidemiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
17.7field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 114 citations in OpenAlex.

  1. Pooled it
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  6. Impact of Estetrol Combined with Drospirenone on Blood Coagulation and Fibrinolysis in Patients with Endometriosis: A Multicenter, Randomized, Open-Label, Active-Controlled, Parallel-Group Study.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Trial
  7. Article
  8. Article
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  11. Sex-Specific Determinants of the Ketone Body β-Hydroxybutyrate in the General Population.The Journal of clinical endocrinology and metabolism · 2026
    Article
  12. Article
  13. Review
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  15. Observational
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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

25 authors at 11 institutions in 4 countries.

Qin WangComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Peter WürtzComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Kirsi Auro
Laure Morin-PapunenDepartment of Obstetrics and Gynecology, Oulu University Hospital, University of Oulu and Medical Research Center Oulu, Oulu, Finland.
Antti J KangasComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Pasi SoininenComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Mika TiainenComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Tuulia TynkkynenComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland.
Anni JoensuuNational Institute for Health and Welfare, Helsinki, Finland.
Aki S HavulinnaNational Institute for Health and Welfare, Helsinki, Finland.
Kristiina AaltoDepartment of Medical Microbiology and Immunology, University of Turku, Turku, Finland.
Marko SalmiDepartment of Medical Microbiology and Immunology, University of Turku, Turku, Finland.
Stefan BlankenbergClinic for General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
Tanja ZellerClinic for General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
Jorma ViikariDepartment of Medicine, University of Turku and Division of Medicine, Turku University Hospital, Finland.
Mika KähönenDepartment of Clinical Physiology, University of Tampere and Tampere University Hospital, Tampere, Finland.
Terho LehtimäkiDepartment of Clinical Chemistry, Fimlab Laboratories, School of Medicine, University of Tampere, Tampere, Finland.
Veikko SalomaaNational Institute for Health and Welfare, Helsinki, Finland.
Sirpa JalkanenDepartment of Medical Microbiology and Immunology, University of Turku, Turku, Finland.
Marjo-Riitta Järvelin
Markus PerolaNational Institute for Health and Welfare, Helsinki, Finland.
Olli T RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Debbie A LawlorMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK and.
Johannes Kettunen
Mika Ala-KorpelaComputational Medicine, Faculty of Medicine, University of Oulu & Biocenter Oulu, Oulu, Finland, mika.ala-korpela@com.
University of Oulu · FIFinnish Institute for Health and Welfare · FIUniversity of Eastern Finland · FIUniversity of Turku · FITurku University Hospital · FIGerman Centre for Cardiovascular Research · DETampere University · FITampere University Hospital · FIUniversität Hamburg · DEUniversity of Bristol · GBUniversity of Helsinki · FI

Funding

British Heart FoundationDepartment of Health NF-SI-0611-10196Medical Research Council G0500539Medical Research Council G0600705Medical Research Council MC_UU_12013/1Medical Research Council MC_UU_12013/5Wellcome Trust GR069224
6 · The paper itself

Abstract

backgroundHormonal contraception is commonly used worldwide, but its systemic effects across lipoprotein subclasses, fatty acids, circulating metabolites and cytokines remain poorly understood.

methodsA comprehensive molecular profile (75 metabolic measures and 37 cytokines) was measured for up to 5841 women (age range 24-49 years) from three population-based cohorts. Women using combined oral contraceptive pills (COCPs) or progestin-only contraceptives (POCs) were compared with those who did not use hormonal contraception. Metabolomics profiles were reassessed for 869 women after 6 years to uncover the metabolic effects of starting, stopping and persistently using hormonal contraception.

resultsThe comprehensive molecular profiling allowed multiple new findings on the metabolic associations with the use of COCPs. They were positively associated with lipoprotein subclasses, including all high-density lipoprotein (HDL) subclasses. The associations with fatty acids and amino acids were strong and variable in direction. COCP use was negatively associated with albumin and positively associated with creatinine and inflammatory markers, including glycoprotein acetyls and several growth factors and interleukins. Our findings also confirmed previous results e.g. for increased circulating triglycerides and HDL cholesterol. Starting COCPs caused similar metabolic changes to those observed cross-sectionally: the changes were maintained in consistent users and normalized in those who stopped using. In contrast, POCs were only weakly associated with metabolic and inflammatory markers. Results were consistent across all cohorts and for different COCP preparations and different types of POC delivery.

conclusionsUse of COCPs causes widespread metabolic and inflammatory effects. However, persistent use does not appear to accumulate the effects over time and the metabolic perturbations are reversed upon discontinuation. POCs have little effect on systemic metabolism and inflammation.

Indexed as

AdultCholesterol, HDLContraceptives, Oral, HormonalCross-Sectional StudiesCytokinesFatty AcidsFemaleFinlandHumansLinear ModelsLongitudinal StudiesMetabolomeMetabolomicsProgestinsRisk FactorsTriglyceridesCholesterol, HDLContraceptives, Oral, HormonalCytokinesFatty AcidsProgestinsTriglyceridesamino acidscombined oral contraceptive pillscytokinesfatty acidshormonal contraceptionhormonesinflammationlipoproteinsmetabolomicsprogestin-only contraceptivesrisk factors

Identifiers

PMID27538888
PMCPMC5100613
OpenAlexW2511714506

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.