Evidence map›Paper›PMID 33300155›Full record

ArticleAmerican journal of physical anthropology2021

Predictors of maternal-origin microchimerism in young women in the Philippines.

Tiffany D Pan, Sami B Kanaan, Nanette R Lee, Josephine L Avila, J Lee Nelson, Dan T A Eisenberg

Open access · greenAbstract read
In one paragraph

Article in American journal of physical anthropology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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 3 institutions in 2 countries.

Tiffany D PanDepartment of Anthropology, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-6646-8552
Sami B KanaanClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Nanette R LeeUSC-Office of Population Studies Foundation, Inc., Cebu City, Philippines.
Josephine L AvilaUSC-Office of Population Studies Foundation, Inc., Cebu City, Philippines.
J Lee NelsonClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Dan T A EisenbergDepartment of Anthropology, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-0812-1862
University of Washington · USUniversity of Southern Philippines Foundation · PHFred Hutch Cancer Center · US

Funding

Scientific/Technical CoreP2CHD042828 · NICHD · UNIVERSITY OF WASHINGTON · PI SARA R. CURRAN · 2017 to 2026
$6.3M
Microchimerism as AlloImmunityR01HL117737 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, J. LEE · 2014 to 2018
$2.4M
Population Research TrainingT32HD007543 · NICHD · UNIVERSITY OF WASHINGTON · PI CURRAN, SARA R. · 2002 to 2016
$2.3M
NHLBI NIH HHS R01 HL117737NICHD NIH HHS P2C HD042828NICHD NIH HHS T32 HD007543NIH HHS P2C HD042828NIH HHS R01 HL117737NIH HHS T32 HD007543
6 · The paper itself

Abstract

objectivesMicrochimerism is the presence of a small quantity of cells or DNA from a genetically distinct individual. This phenomenon occurs with bidirectional maternal-fetal exchange during pregnancy. Microchimerism can persist for decades after delivery and have long-term health implications. However, little is known about why microchimerism is detectable at varying levels in different individuals. We examine the variability and the following potential determinants of maternal-origin microchimerism (MMc) in young women in the Philippines: gestational duration (in utero exposure to MMc), history of being breastfed (postpartum exposure to MMc), maternal telomere length (maternal cells' ability to replicate and persist), and participant's pregnancies in young adulthood (effect of adding fetal-origin microchimerism to preexisting MMc). MATERIALS AND

methodsData are from the Cebu Longitudinal Health and Nutrition Survey, a population-based study of infant feeding practices and long-term health outcomes. We quantified MMc using quantitative PCR (qPCR) in 89 female participants, ages 20-22, and analyzed these data using negative binomial regression.

resultsIn a multivariate model including all predictors, being breastfed substantially predicted decreased MMc (detection rate ratio = 0.15, p = 0.007), and there was a trend of decreasing MMc in participants who had experienced more pregnancies (detection rate ratio = 0.55, p = 0.057). DISCUSSION: These results might be explained by breastfeeding having lasting impact on immune regulatory networks, thus reducing MMc persistence. MMc may also decrease in response to the introduction of fetal-origin microchimerism with pregnancies experienced in adulthood.

Indexed as

ChimerismAdultAnthropology, PhysicalBreast FeedingCohort StudiesDNAFemaleHumansImmune ToleranceMaternal-Fetal ExchangePhilippinesPregnancyTelomereYoung AdultDNAbiological inheritancedevelopmental originsimmune tolerance

Identifiers

PMID33300155
PMCPMC11753296
OpenAlexW3113279458

What OpenQuestion holds

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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.