Evidence map›Paper›PMID 31353785›Full record

Trial reportAmerican journal of reproductive immunology (New York, N.Y. : 1989)2019

High-mobility group box 1 at the time of parturition in women with gestational diabetes mellitus.

Ashley V Hill, Ramkumar Menon, Maria Perez-Patron, Genny Carrillo, Xiaohui Xu, Brandie D Taylor

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in American journal of reproductive immunology (New York, N.Y. : 1989), 2019. 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
0.6field-weighted citation impact, top 33% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Differences in cord blood extracellular vesicle cargo in preterm and term births.American journal of reproductive immunology (New York, N.Y. : 1989) · 2022
    Article
  9. High-mobility group box 1 is a driver of inflammation throughout pregnancy.American journal of reproductive immunology (New York, N.Y. : 1989) · 2021
    Review
  10. 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 5 institutions in 1 country.

Ashley V HillDepartment of Epidemiology and Biostatistics, Texas A&M University, College Station, TX, USA.ORCID 0000-0002-3535-1404
Ramkumar MenonDivision of Maternal-Fetal Medicine and Perinatal Research, Department of Obstetrics and Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA.ORCID 0000-0001-9213-6105
Maria Perez-PatronDepartment of Epidemiology and Biostatistics, Texas A&M University, College Station, TX, USA.
Genny CarrilloDepartment of Environmental and Occupational Health, Texas A&M University, College Station, TX, USA.
Xiaohui XuDepartment of Epidemiology and Biostatistics, Texas A&M University, College Station, TX, USA.
Brandie D TaylorDepartment of Epidemiology and Biostatistics, Texas A&M University, College Station, TX, USA.ORCID 0000-0002-8234-1815
Texas A&M University · USTemple University · USTexas A&M University System · USThe University of Texas Medical Branch at Galveston · USUniversity of Pittsburgh · US

Funding

Adolescent Research in Community Postdoctoral Training ProgramT32HD087162 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MILLER, ELIZABETH · 2016 to 2020
$1.2M
Discovery FoundationNICHD NIH HHS 5T32HD087162-03NICHD NIH HHS T32 HD087162
6 · The paper itself

Abstract

problemHigh-mobility group box 1 (HMGB1), a danger-associated molecular pattern marker, may indicate sterile inflammation through innate immune pathways. HMGB1 is implicated in hyperglycemia and excess glucose in trophoblast. Metabolic dysfunction and dyslipidemia are associated with gestational diabetes mellitus (GDM), but few studies examined associations between HMGB1 and GDM. We determined HMGB1 levels, and the ratio of HMGB1 to innate immune markers, in women with GDM at parturition. METHOD OF STUDY: This case-control study of 50 GDM pregnancies and 100 healthy controls utilized data and plasma samples from PeriBank. HMGB1, pentraxin-3, and interleukin (IL)-6 were measured by ELISA. Logistic regression calculated odds ratios (OR) and 95% confidence intervals (CI) adjusting for age, pre-pregnancy body mass index, and type of labor.

resultsThere were no significant associations between HMGB1 and GDM. The ratio of HMGB1 to pentraxin-3 and IL-6 did not alter the odds of GDM. There was a significant statistical interaction between HMGB1 and maternal age (P = .02). When associations were examined by age groups, HMGB1 was associated with reduced odds of HMGB1 among women ≤25 (AOR = 0.007 CI 95% <0.001-0.3). Odds ratios increased as age increased (AOR range 1.2-3.8) but results were not statistically significant.

conclusionHigh-mobility group box 1 was not associated with GDM. However, we found evidence that maternal age was a potential effect modifier of the relationship between HMGB1 and GDM. As there is growing evidence that HMGB1 may play important roles in reproduction, future studies should explore maternal factors that may alter HMGB1 levels.

Indexed as

Diabetes, GestationalHMGB1 ProteinParturitionC-Reactive ProteinFemaleHumansInterleukin-6PentraxinsPregnancySerum Amyloid P-ComponentC-Reactive ProteinHMGB1 ProteinHMGB1 protein, humanIL6 protein, humanInterleukin-6PentraxinsSerum Amyloid P-Componentgestational diabetes mellitushigh-mobility group box 1innate immunitypregnancy

Identifiers

PMID31353785
PMCPMC8135071
OpenAlexW2966868638

What OpenQuestion holds

Textmetadata
LicenceTDM
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.