Evidence map›Paper›PMID 40991148›Full record

ArticleEuropean journal of epidemiology2025

Sex, male origin microchimerism, and mortality in a Danish cohort.

Gitte Lindved Petersen, Tri-Long Nguyen, Rune Lindahl-Jacobsen, Anne Tjønneland, Mads Kamper-Jørgensen

Abstract read
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Article in European journal of epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Gitte Lindved PetersenDepartment of Translational Type 1 Diabetes Research, Steno Diabetes Center Copenhagen, Herlev, Denmark. gitte.lindved.petersen@regionh.dk.ORCID http://orcid.org/0000-0001-8920-4015
Tri-Long NguyenSection of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-6376-7212
Rune Lindahl-JacobsenUnit of Epidemiology, Biostatistics and Biodemography, Department of Public Health, University of Southern Denmark, Odense, Denmark.ORCID http://orcid.org/0000-0002-4622-9826
Anne TjønnelandDanish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-4385-2097
Mads Kamper-JørgensenSection of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-6393-5258

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously demonstrated that women with detectable male cells in peripheral blood – male origin microchimerism (a presumed souvenir from pregnancy) – enjoy half the risk of all-cause mortality compared with women tested negative. However, such differences are vulnerable to confounding. Also, it is unknown whether better survival in women vs. men is confined to women testing male origin microchimerism positive. In this updated analysis, we first compared the survival of positive and negative women using prognostic score weighing to minimize potential confounding. Next, we compared the survival of women tested positive and negative for male origin microchimerism to men. Women (n = 766) and men (n = 1,000) from the Diet, Cancer, and Health cohort aged 50–64 years in 1993–1997 were followed until 2017 for all-cause mortality in national Danish registers. Based on predictors of death, we calculated prognostic scores for all women and compared mortality according to male origin microchimerism status by prognostic score weighted Cox regression adjusting for potential confounding. Next, we compared mortality across positive/negative women and men. Women who tested male origin microchimerism positive versus negative had a 50% lower mortality rate (adjusted HR = 0.50 [95% CI 0.32–0.77]). Compared with men, women who tested positive had a 51% lower mortality rate (HR = 0.49 [95% confidence interval (CI) 0.38–0.61]), whereas women who tested negative had a similar rate (HR = 0.83 [95% CI 0.63–1.09]). Women who tested positive for male origin microchimerism lived longer than their counterparts who tested negative, who appeared to have a similar survival pattern to that of men.

Indexed as

ChimerismMortalityCause of DeathCohort StudiesDenmarkFemaleHumansMaleMiddle AgedProportional Hazards ModelsRegistriesSex FactorsCausal inferenceDenmarkMale origin microchimerismMortalityPrognostic score weighingRestricted mean survival time difference

Identifiers

PMID40991148
PMCPMC12696143

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