Placental Accelerated Aging in Antenatal Depression. (Record no. 13837)

MARC details
000 -LEADER
fixed length control field 05087nam a22004217a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 240122s20232023xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 2589-9333
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1016/j.ajogmf.2023.101237 [doi]
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code S2589-9333(23)00379-8 [pii]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 38012987
266 ## - Date added to catalog
Date added to catalog 2024-01-22
245 ## - TITLE STATEMENT
Title Placental Accelerated Aging in Antenatal Depression.
251 ## - Source
Source American Journal of Obstetrics & Gynecology MFM. :101237, 2023 Nov 25
252 ## - Abbreviated Source
Abbreviated source Am J Obstet Gynecol MFM. :101237, 2023 Nov 25
253 ## - Journal Name
Journal name American journal of obstetrics & gynecology MFM
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2023
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Manufacturer FY2024
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Publication date 2023 Nov 25
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Publication status aheadofprint
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Medline status Publisher
520 ## - SUMMARY, ETC.
Abstract BACKGROUND: Antenatal maternal depression is associated with poor pregnancy outcomes and long-term effects on offspring. Previous studies have identified links between antenatal depression and placental DNA methylation and between placental epigenetic aging and poor pregnancy outcomes such as preterm labor and preeclampsia. It is possible that the relationship between antenatal depression and poor pregnancy outcomes is partly mediated via placental aging.
520 ## - SUMMARY, ETC.
Abstract CONCLUSION: Antenatal depressive symptoms during second trimester was associated with an average of 0.41 weeks increased placental age acceleration. Accelerated placental aging may play important role in underlying mechanism linking antenatal depression to pregnancy complications related to placental dysfunction. Copyright © 2023. Published by Elsevier Inc.
520 ## - SUMMARY, ETC.
Abstract OBJECTIVE: To investigate whether antenatal depressive symptoms are associated with placental epigenetic age acceleration, an epigenetic aging clock measure derived from the difference between methylation age and gestational age at delivery.
520 ## - SUMMARY, ETC.
Abstract RESULTS: There were 31 (10.3%) women with depressive symptoms (i.e., EDPS score >=10) in first trimester, 48 (16%) in second trimester, and 49 (16.4%) in third trimester. Of these, 21 (7.2%) women had sustained first and second trimester depressive symptoms, 19 (7%) had sustained second and third trimester depressive symptoms, and 12 (4.8%) had sustained depressive symptoms throughout pregnancy. Women with depressive symptoms in second trimester had 0.41 weeks higher placental age acceleration compared to women without depressive symptoms during second trimester (beta=0.21 weeks, 95% CI [-0.17, 0.58], P=.28 during 1st trimester; beta=0.41 weeks, 95% CI [0.10, 0.71], P=.009 during 2nd trimester; beta=0.17 weeks, 95% CI [-0.14, 0.47], P=.29 during 3rd trimester). Sustained first and second trimester depressive symptoms were associated with 0.72 weeks higher placental age acceleration (95% CI [0.29, 1.15], P=.001) compared to no depressive symptoms in the two trimesters. The association between second trimester depressive symptoms and higher placental epigenetic age acceleration strengthened in analysis of pregnancies with male fetuses (beta=0.53 weeks, 95% CI [0.06, 1.08], P=.03) but was not significant in pregnancies with female fetuses.
520 ## - SUMMARY, ETC.
Abstract STUDY DESIGN: The study included 301 women who provided placenta samples at delivery as part of the NICHD Fetal Growth Studies - Singletons that recruited participants from diverse race/ethnic groups at 12 U.S. clinical sites (2009 - 2013). Women underwent depression screening using the Edinburgh Postnatal Depression Scale up to 6 times across the three trimesters of pregnancy. Depressive symptoms status was determined for each pregnancy trimester using an Edinburgh Postnatal Depression Scale score, in which a score >=10 was defined as having depressive symptoms and <10 as not depressed. Placental DNA methylation was profiled from placenta samples. Placental epigenetic age was estimated using a methylation-based age estimator (placental "epigenetic clock") that has previously been found to have high placental gestational age prediction accuracy for uncomplicated term pregnancies. Placental age acceleration was defined to be the residual upon regressing the estimated epigenetic age on gestational age at delivery. Associations between EDPS score >=10 compared with <10 in the first, second, and third trimester (i.e., depressive symptoms compared to none in each trimester) and placental age acceleration were tested using multivariable linear regression adjusting for maternal age, parity, race/ethnicity, and employment.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Washington Hospital Center
656 ## - INDEX TERM--OCCUPATION
Department Maternal - Fetal Medicine & Genetics Fellowship
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Department Obstetrics and Gynecology/Maternal-Fetal Medicine
657 ## - INDEX TERM--FUNCTION
Medline publication type Journal Article
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors Grantz, Katherine L
Institution Code MWHC
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors Saeed, Haleema
Institution Code MWHC
Program Maternal - Fetal Medicine & Genetics Fellowship
Degree MBBS
790 ## - Authors
All authors Saeed H, Wu J, Tesfaye M, Grantz KL, Tekola-Ayele F
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.1016/j.ajogmf.2023.101237">https://dx.doi.org/10.1016/j.ajogmf.2023.101237</a>
Public note https://dx.doi.org/10.1016/j.ajogmf.2023.101237
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 01/22/2024   38012987 38012987 01/22/2024 01/22/2024 Journal Article

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