Evidence map›Paper›PMID 35394678›Full record

Trial reportAmerican journal of reproductive immunology (New York, N.Y. : 1989)2022

Genital inflammatory status and the innate immune response to contraceptive initiation.

Nina Radzey, Rushil Harryparsad, Bahiah Meyer, Pai Lien Chen, Xiaoming Gao, Charles Morrison, Ongeziwe Taku, Anna-Lise Williamson, Celia Mehou-Loko, Florence Lefebvre d'Hellencourt and 10 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of reproductive immunology (New York, N.Y. : 1989), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
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  4. Genital inflammatory status and the innate immune response to contraceptive initiation.American journal of reproductive immunology (New York, N.Y. : 1989) · 2022
    Trial
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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

20 authors at 8 institutions in 3 countries.

Nina RadzeyInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Rushil HarryparsadInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Bahiah MeyerInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Pai Lien ChenFHI 360, Durham, North Carolina, USA.
Xiaoming GaoFHI 360, Durham, North Carolina, USA.
Charles MorrisonFHI 360, Durham, North Carolina, USA.
Ongeziwe TakuInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Anna-Lise WilliamsonInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Celia Mehou-LokoInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Florence Lefebvre d'HellencourtFHI 360, Durham, North Carolina, USA.
Gregory BuckVirginia Commonwealth University, Richmond, Virginia, USA.
Jennifer SmitMatCH Research Unit (MRU), Department of Obstetrics and Gynaecology, University of the Witwatersrand, Durban, South Africa.
Jerome StraussVirginia Commonwealth University, Richmond, Virginia, USA.
Kavita NandaFHI 360, Durham, North Carolina, USA.
Khatija AhmedSetshaba Research Centre, Tshwane, South Africa.
Mags BeksinskaMatCH Research Unit (MRU), Department of Obstetrics and Gynaecology, University of the Witwatersrand, Durban, South Africa.
Myrna SerranoVirginia Commonwealth University, Richmond, Virginia, USA.
Veronique BaileySetshaba Research Centre, Tshwane, South Africa.
Lindi MassonInstitute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town, South Africa.
Jennifer DeeseRTI International, Research Triangle Park, North Carolina, USA.
Family Health International 360 · USUniversity of Cape Town · ZAVirginia Commonwealth University · USWellcome Centre for Infectious Diseases Research in Africa · ZASetshaba Research Centre · ZAUniversity of the Witwatersrand · ZAMonash University · AURTI International · US

Funding

Soweto Clinical Trials UnitUM1AI069453 · NIAID · WITS HEALTH CONSORTIUM (PTY), LTD · PI Glenda E Gray, Lerato Mohapi · 2012 to 2026
$40.9M
Understanding the Impact of Lower Dose Medroxyprogesterone Acetate on Female Genital Tract Microbiome and ImmunologyR01HD096937 · NICHD · FAMILY HEALTH INTERNATIONAL · PI DEESE, JENNIFER CARAWAY, MASSON, LINDI · 2018 to 2022
$3.7M
NICHD NIH HHS R01 HD096937
6 · The paper itself

Abstract

problemData on the effects of contraceptives on female genital tract (FGT) immune mediators are inconsistent, possibly in part due to pre-existing conditions that influence immune mediator changes in response to contraceptive initiation.

methodsThis study included 161 South African women randomised to injectable depot medroxyprogesterone acetate (DMPA-IM), copper intrauterine device (IUD), or levonorgestrel (LNG) implant in the Evidence for Contraceptive Options and HIV Outcomes (ECHO) trial. We measured thirteen cytokines and antimicrobial peptides previously associated with HIV acquisition in vaginal swabs using Luminex and ELISA, before, and at 1 and 3 months after contraceptive initiation. Women were grouped according to an overall baseline inflammatory profile. We evaluated modification of the relationships between contraceptives and immune mediators by baseline inflammation, demographic, and clinical factors.

resultsOverall, LNG implant and copper IUD initiation were associated with increases in inflammatory cytokines, while no changes were observed following DMPA-IM initiation. However, when stratifying by baseline inflammatory profile, women with low baseline inflammation in all groups experienced significant increases in inflammatory cytokines, while those with a high baseline inflammatory profile experienced no change or decreases in inflammatory cytokines.

conclusionWe conclude that pre-contraceptive initiation immune profile modifies the effect of contraceptives on the FGT innate immune response.

Indexed as

Contraceptive Agents, FemaleHIV InfectionsCytokinesFemaleGenitaliaHumansImmunity, InnateInflammationIntrauterine Devices, CopperLevonorgestrelMedroxyprogesterone AcetateContraceptive Agents, FemaleCytokinesLevonorgestrelMedroxyprogesterone Acetatecontraceptioncoppercytokinesfemaleinflammationintrauterine deviceslevonorgestrelmedroxyprogesterone acetate

Identifiers

PMID35394678
PMCPMC10909525
OpenAlexW4224256190

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.