Evidence map›Paper›PMID 35560012›Full record

ArticleF&S science2022

Vascular alterations impede fragile tolerance to pregnancy in type 1 diabetes.

Kelsey L McNew, Abin Abraham, Daniel E Sack, Charles Duncan Smart, Yasminye D Pettway, Alexander C Falk, Rolanda L Lister, Annika B Faucon, Cosmin A Bejan, John A Capra and 3 more

Open access · goldAbstract read
In one paragraph

Article in F&S science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 2 institutions in 1 country.

Kelsey L McNewDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee; Vanderbilt University Medical Scientist Training Program, Nashville, Tennessee.
Abin AbrahamVanderbilt University Medical Scientist Training Program, Nashville, Tennessee; Vanderbilt University School of Medicine, Vanderbilt University, Nashville, Tennessee.
Daniel E SackVanderbilt University Medical Scientist Training Program, Nashville, Tennessee; Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Charles Duncan SmartVanderbilt University Medical Scientist Training Program, Nashville, Tennessee; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Yasminye D PettwayVanderbilt University Medical Scientist Training Program, Nashville, Tennessee; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Alexander C FalkDivision of Pediatric Endocrinology, Vanderbilt University Medical Center, Nashville, Tennessee.
Rolanda L ListerDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee.
Annika B FauconDivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Vanderbilt Genetics Institute, Vanderbilt University, Nashville, Tennessee.
Cosmin A BejanDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.
John A CapraBakar Computational Health Sciences Institute and Department of Epidemiology and Biostatistics, University of California, San Francisco, California.
David M AronoffDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee; Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee; Division of Infectious Disease, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Kelli L BoydDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee; Gilead Science, Inc., Foster, California.
Daniel J MooreDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee; Division of Pediatric Endocrinology, Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: daniel.moore@vumc.org.
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Training Program on Genetic Variation and Human PhenotypesT32GM080178 · NIGMS · VANDERBILT UNIVERSITY · PI COX, NANCY J, SAMUELS, DAVID C · 2007 to 2021
$3.1M
Determining the contribution of zinc deficiency to perinatal Group B Streptococcus infectionsR01HD090061 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ARONOFF, DAVID M, GADDY, JENNIFER A · 2017 to 2021
$2.5M
The Role of macrophages in chorioamnionitis and group B streptococcal infectionsR01AI134036 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ARONOFF, DAVID M · 2017 to 2021
$2.4M
Automated Storage and Retrieval of Biological SystemsS10RR025141 · NCRR · VANDERBILT UNIVERSITY · PI RODEN, DAN M · 2008 to 2008
$988k
Intrauterine Programming of Diabetes Induced Cardiac EmbyropathyK01HL140278 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LISTER, ROLANDA LAMORA · 2018 to 2022
$616k
Leveraging Electronic Health Records and Genomic Biobanks for Kidney Stone DiseaseR21DK127075 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BEJAN, COSMIN ADRIAN, HSI, RYAN · 2021 to 2022
$476k
NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1 TR002243NCI NIH HHS P30 CA068485NCRR NIH HHS S10 RR025141NCRR NIH HHS UL1 RR024975NHLBI NIH HHS F30 HL151069NHLBI NIH HHS K01 HL140278NIAID NIH HHS R01 AI134036NICHD NIH HHS R01 HD090061NIDDK NIH HHS F30 DK121438NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R21 DK127075NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM080178NIH HHS S10 OD023475NIMH NIH HHS F30 MH123219
6 · The paper itself

Abstract

objectiveTo determine the impact of autoimmunity in the absence of glycemic alterations on pregnancy in type 1 diabetes (T1D).

designBecause nonobese diabetic (NOD) mice experience autoimmunity before the onset of hyperglycemia, we studied pregnancy outcomes in prediabetic NOD mice using flow cytometry and enzyme-linked immunosorbent assays. Once we determined that adverse events in pregnancy occurred in euglycemic mice, we performed an exploratory study using electronic health records to better understand pregnancy complications in humans with T1D and normal hemoglobin A1c levels.

settingUniversity Medical Center. PATIENT(S)/ANIMAL(S): Nonobese diabetic mice and electronic health records from Vanderbilt University Medical Center. INTERVENTION(S): Nonobese diabetic mice were administered 200 μg of an anti-interleukin 6 (IL-6) antibody every other day starting on day 5 of gestation. MAIN OUTCOME MEASURE(S): Changes in the number of abnormal and reabsorbed pups in NOD mice and odds of vascular complications in pregnancy in T1D in relation to A1c. RESULT(S): Prediabetic NOD mice had increased adverse pregnancy outcomes compared with nonautoimmune mice; blockade of IL-6, which was secreted by endothelial cells, decreased the number of reabsorbed and abnormal fetuses. Similarly, vascular complications were increased in pregnant patients with T1D across all A1c values. CONCLUSION(S): The vascular secretion of IL-6 drives adverse pregnancy outcomes in prediabetic NOD mice. Pregnant patients with T1D have increased vascular complications even with normal hemoglobin A1cs, indicating a potential effect of autoimmunity on the placental vasculature.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Prediabetic StateAnimalsEndothelial CellsFemaleGlycated HemoglobinHumansInterleukin-6MiceMice, Inbred NODPlacentaPregnancyGlycated HemoglobinInterleukin-6autoimmunityIL-6NOD micereproductive immunologyType 1 diabetes

Identifiers

PMID35560012
PMCPMC9850286
OpenAlexW4210668860

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.