A multidisciplinary Prematurity Research Cohort Study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 27 08 2021
accepted: 13 07 2022
entrez: 25 8 2022
pubmed: 26 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

Worldwide, 10% of babies are born preterm, defined as a live birth before 37 weeks of gestation. Preterm birth is the leading cause of neonatal death, and survivors face lifelong risks of adverse outcomes. New approaches with large sample sizes are needed to identify strategies to predict and prevent preterm birth. The primary aims of the Washington University Prematurity Research Cohort Study were to conduct three prospective projects addressing possible causes of preterm birth and provide data and samples for future research. Pregnant patients were recruited into the cohort between January 2017 and January 2020. Consenting patients were enrolled into the study before 20 weeks' gestation and followed through delivery. Participants completed demographic and lifestyle surveys; provided maternal blood, placenta samples, and cord blood; and participated in up to three projects focused on underlying physiology of preterm birth: cervical imaging (Project 1), circadian rhythms (Project 2), and uterine magnetic resonance imaging and electromyometrial imaging (Project 3). A total of 1260 participants were enrolled and delivered during the study period. Of the participants, 706 (56%) were Black/African American, 494 (39%) were nulliparous, and 185 (15%) had a previous preterm birth. Of the 1260 participants, 1220 (97%) delivered a live infant. Of the 1220 with a live birth, 163 (14.1%) had preterm birth, of which 74 (6.1%) were spontaneous preterm birth. Of the 1220 participants with a live birth, 841 participated in cervical imaging, 1047 contributed data and/or samples on circadian rhythms, and 39 underwent uterine magnetic resonance imaging. Of the 39, 25 underwent electromyometrial imaging. We demonstrate feasibility of recruiting and retaining a diverse cohort in a complex prospective, longitudinal study throughout pregnancy. The extensive clinical, imaging, survey, and biologic data obtained will be used to explore cervical, uterine, and endocrine physiology of preterm birth and can be used to develop novel approaches to predict and prevent preterm birth.

Sections du résumé

BACKGROUND
Worldwide, 10% of babies are born preterm, defined as a live birth before 37 weeks of gestation. Preterm birth is the leading cause of neonatal death, and survivors face lifelong risks of adverse outcomes. New approaches with large sample sizes are needed to identify strategies to predict and prevent preterm birth. The primary aims of the Washington University Prematurity Research Cohort Study were to conduct three prospective projects addressing possible causes of preterm birth and provide data and samples for future research.
STUDY DESIGN
Pregnant patients were recruited into the cohort between January 2017 and January 2020. Consenting patients were enrolled into the study before 20 weeks' gestation and followed through delivery. Participants completed demographic and lifestyle surveys; provided maternal blood, placenta samples, and cord blood; and participated in up to three projects focused on underlying physiology of preterm birth: cervical imaging (Project 1), circadian rhythms (Project 2), and uterine magnetic resonance imaging and electromyometrial imaging (Project 3).
RESULTS
A total of 1260 participants were enrolled and delivered during the study period. Of the participants, 706 (56%) were Black/African American, 494 (39%) were nulliparous, and 185 (15%) had a previous preterm birth. Of the 1260 participants, 1220 (97%) delivered a live infant. Of the 1220 with a live birth, 163 (14.1%) had preterm birth, of which 74 (6.1%) were spontaneous preterm birth. Of the 1220 participants with a live birth, 841 participated in cervical imaging, 1047 contributed data and/or samples on circadian rhythms, and 39 underwent uterine magnetic resonance imaging. Of the 39, 25 underwent electromyometrial imaging.
CONCLUSION
We demonstrate feasibility of recruiting and retaining a diverse cohort in a complex prospective, longitudinal study throughout pregnancy. The extensive clinical, imaging, survey, and biologic data obtained will be used to explore cervical, uterine, and endocrine physiology of preterm birth and can be used to develop novel approaches to predict and prevent preterm birth.

Identifiants

pubmed: 36006907
doi: 10.1371/journal.pone.0272155
pii: PONE-D-21-27892
pmc: PMC9409532
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0272155

Subventions

Organisme : NICHD NIH HHS
ID : P50 HD103525
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Comput Biol Med. 2020 Jan;116:103543
pubmed: 31786490
Lancet. 2017 Dec 17;388(10063):3027-3035
pubmed: 27839855
J Biomed Opt. 2018 Dec;23(12):1-4
pubmed: 30520276
Data Brief. 2020 Jan 03;28:105078
pubmed: 31956675
Med Biol Eng Comput. 2020 Aug;58(8):1651-1665
pubmed: 32458384
J Biol Rhythms. 2019 Jun;34(3):323-331
pubmed: 31018734
J Biomed Opt. 2018 Dec;23(12):1-6
pubmed: 30520275
Semin Fetal Neonatal Med. 2016 Apr;21(2):68-73
pubmed: 26794420
N Engl J Med. 2005 Jan 6;352(1):9-19
pubmed: 15635108
Sci Transl Med. 2019 Mar 13;11(483):
pubmed: 30867320
Trials. 2017 Oct 26;18(1):500
pubmed: 29073916
Lancet. 2012 Jun 9;379(9832):2162-72
pubmed: 22682464
Lancet Glob Health. 2013 Dec;1(6):e328-30
pubmed: 25104592
Eur J Epidemiol. 2007;22(12):831-7
pubmed: 17955333

Auteurs

Molly J Stout (MJ)

Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan, United States of America.

Jessica Chubiz (J)

Department of Obstetrics and Gynecology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Nandini Raghuraman (N)

Department of Obstetrics and Gynecology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Peinan Zhao (P)

Department of Obstetrics and Gynecology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Methodius G Tuuli (MG)

Department of Obstetrics and Gynecology, Brown University, Providence, Rhode Island, United States of America.

Lihong V Wang (LV)

Department of Medical Engineering, California Institute of Technology, Pasadena, California, United States of America.

Alison G Cahill (AG)

Department of Women's Health, University of Texas at Austin, Austin, Texas, United States of America.

Phillip S Cuculich (PS)

Department of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Yong Wang (Y)

Department of Obstetrics and Gynecology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Emily S Jungheim (ES)

Department of Obstetrics and Gynecology, Northwestern University, Chicago, Illinois, United States of America.

Erik D Herzog (ED)

Department of Biology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Justin Fay (J)

Department of Biology, University of Rochester, Rochester, New York, United States of America.

Alan L Schwartz (AL)

Department of Pediatrics, Washington University in St. Louis, St. Louis, Missouri, United States of America.

George A Macones (GA)

Department of Women's Health, University of Texas at Austin, Austin, Texas, United States of America.

Sarah K England (SK)

Department of Obstetrics and Gynecology, Washington University in St. Louis, St. Louis, Missouri, United States of America.

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