Evidence map›Paper›PMID 36516191›Full record

ArticlePloS one2022

Second trimester cytokine profiles associated with gestational diabetes and hypertensive disorders of pregnancy.

Paulina M B Hart, Nikki L Stephenson, Natalie V Scime, Suzanne C Tough, Donna M Slater, Kathleen H Chaput

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Paulina M B HartDepartment of Paediatrics, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-1534-2586
Nikki L StephensonDepartment of Community Health Sciences, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.ORCID 0000-0003-0124-7278
Natalie V ScimeDepartment of Community Health Sciences, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.
Suzanne C ToughDepartment of Paediatrics, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.
Donna M SlaterDepartment of Physiology and Pharmacology, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.
Kathleen H ChaputDepartment of Community Health Sciences, Cumming School of Medicine at University of Calgary, Calgary, AB, Canada.ORCID 0000-0001-7596-6019
University of Calgary · CA

Funding

CIHR 161362
6 · The paper itself

Abstract

Healthy pregnancy requires a coordinated immune response, yet complications can arise, putting both the mother's and child's health at risk. Hypertensive disorders of pregnancy (HDP) and gestational diabetes mellitus (GDM) are pregnancy-related complications that account for most maternal morbidity and mortality. Cytokines are proteins released as part of the immune response to disease or infection and regulate inflammation. Certain pregnancy complications cause localized and systemic inflammation; however, cytokine profiles specific to such complications are not well understood. This study aims to examine associations between pregnancy complications of HDP and GDM and cytokine profiles in the second trimester of pregnancy. Data was obtained from the All Our Families birth cohort in Calgary, Alberta, Canada. The cohort collected questionnaires at the time of participant enrollment and maternal blood samples at 17-23 weeks gestation. Cases of HDP (n = 27) and GDM (n = 31) were matched to controls on BMI, maternal age, and smoking status in the preconception period at a 1:3 ratio. Cytokine levels were measured in blood samples using Luminex xMAP technology using a panel of 42 cytokines. Using R software, a Classification and Regression Tree (CART) analysis was conducted to identify cytokine profiles and levels associated with each complication. Four cytokines were identified in the HDP CART (in descending order of importance): Monocyte Chemoattractant Protein-1 (cut-off: <480pg/mL), Macrophage Inflammatory Protein-1β (cut-off: ≥26pg/mL), Eotaxin (cut-off: <27/≥27&<36/≥36pg/mL), and Soluble Cluster of Differentiation 40 Ligand (cut-off: <1342pg/mL). Six cytokine levels were identified in the GDM CART: Interleukin-1 Receptor Antagonist (IL-1Ra; cut-off: <25pg/mL), Interleukin-5 (cut-off: ≥0.4pg/mL), Interferon-γ (cut-off: <4.9pg/mL), IL-1Ra (cut-off: ≥111pg/mL), Eotaxin (cut-off: ≥21pg/mL), and Interleukin-18 (cut-off: ≥155pg/mL). By examining the complex inter-relationships between cytokines, findings of cytokine profiles guide further research in identifying biomarkers of pregnancy complications relevant to the design of the future management or prevention of these conditions.

Indexed as

Diabetes, GestationalHypertension, Pregnancy-InducedPre-EclampsiaPregnancy ComplicationsAlbertaChildCytokinesFemaleHumansInflammationInterleukin 1 Receptor Antagonist ProteinPregnancyPregnancy Trimester, SecondCytokinesInterleukin 1 Receptor Antagonist Protein

Identifiers

PMID36516191
PMCPMC9749996
OpenAlexW4311438950

What OpenQuestion holds

Textmetadata
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.