Cargando…

Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial

BACKGROUND: Several meta analyses have concluded n-3 fatty acids, including docosahexaenoic acid (DHA), reduce early preterm birth (EPB, < 34 weeks), however, the amount of DHA required is unclear. We hypothesized that 1000 mg DHA per day would be superior to 200 mg, the amount in most prenatal s...

Descripción completa

Detalles Bibliográficos
Autores principales: Carlson, Susan E, Gajewski, Byron J, Valentine, Christina J, Kerling, Elizabeth H, Weiner, Carl P, Cackovic, Michael, Buhimschi, Catalin S, Rogers, Lynette K, Sands, Scott A, Brown, Alexandra R, Mudaranthakam, Dinesh Pal, Crawford, Sarah A, DeFranco, Emily A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257993/
https://www.ncbi.nlm.nih.gov/pubmed/34308309
http://dx.doi.org/10.1016/j.eclinm.2021.100905
_version_ 1783718418271174656
author Carlson, Susan E
Gajewski, Byron J
Valentine, Christina J
Kerling, Elizabeth H
Weiner, Carl P
Cackovic, Michael
Buhimschi, Catalin S
Rogers, Lynette K
Sands, Scott A
Brown, Alexandra R
Mudaranthakam, Dinesh Pal
Crawford, Sarah A
DeFranco, Emily A
author_facet Carlson, Susan E
Gajewski, Byron J
Valentine, Christina J
Kerling, Elizabeth H
Weiner, Carl P
Cackovic, Michael
Buhimschi, Catalin S
Rogers, Lynette K
Sands, Scott A
Brown, Alexandra R
Mudaranthakam, Dinesh Pal
Crawford, Sarah A
DeFranco, Emily A
author_sort Carlson, Susan E
collection PubMed
description BACKGROUND: Several meta analyses have concluded n-3 fatty acids, including docosahexaenoic acid (DHA), reduce early preterm birth (EPB, < 34 weeks), however, the amount of DHA required is unclear. We hypothesized that 1000 mg DHA per day would be superior to 200 mg, the amount in most prenatal supplements. METHODS: This randomised, multicentre, double-blind, adaptive-design, superiority trial was conducted in three USA medical centres. Women with singleton pregnancies and 12 to 20 weeks gestation were eligible. randomization was generated in SAS® by site in blocks of 4. The planned adaptive design periodically generated allocation ratios favoring the better performing dose. Managing study personnel were blind to treatment until 30 days after the last birth. The primary outcome was EPB by dose and by enrolment DHA status (low/high). Bayesian posterior probabilities (pp) were determined for planned efficacy and safety outcomes using intention-to-treat. The study is registered with ClinicalTrials.gov (NCT02626299) and closed to enrolment. FINDINGS: Eleven hundred participants (1000 mg, n = 576; 200 mg, n = 524) were enrolled between June 8, 2016 and March 13, 2020 with the last birth September 5, 2020. 1032 (n = 540 and n = 492) were included in the primary analyses. The higher dose had a lower EPB rate [1.7% (9/540) vs 2.4% (12/492), pp=0.81] especially if participants had low DHA status at enrolment [2.0% (5/249) vs 4.1%, (9/219), pp=0.93]. Participants with high enrolment DHA status did not realize a dose effect [1000 mg: 1.4% (4/289); 200 mg: 1.1% (3/271), pp = 0.57]. The higher dose was associated with fewer serious adverse events (maternal: chorioamnionitis, premature rupture of membranes and pyelonephritis; neonatal: feeding, genitourinary and neurologic problems, all pp>0.90). INTERPRETATION: Clinicians could consider prescribing 1000 mg DHA daily during pregnancy to reduce EPB in women with low DHA status if they are able to screen for DHA. FUNDING: The National Institutes of Health Child Health and Human Development (NICHD) funded the study. Life's DHA™-S oil, DSM Nutritional Products LLC, Switzerland provided all capsules.
format Online
Article
Text
id pubmed-8257993
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-82579932021-07-23 Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial Carlson, Susan E Gajewski, Byron J Valentine, Christina J Kerling, Elizabeth H Weiner, Carl P Cackovic, Michael Buhimschi, Catalin S Rogers, Lynette K Sands, Scott A Brown, Alexandra R Mudaranthakam, Dinesh Pal Crawford, Sarah A DeFranco, Emily A EClinicalMedicine Research Paper BACKGROUND: Several meta analyses have concluded n-3 fatty acids, including docosahexaenoic acid (DHA), reduce early preterm birth (EPB, < 34 weeks), however, the amount of DHA required is unclear. We hypothesized that 1000 mg DHA per day would be superior to 200 mg, the amount in most prenatal supplements. METHODS: This randomised, multicentre, double-blind, adaptive-design, superiority trial was conducted in three USA medical centres. Women with singleton pregnancies and 12 to 20 weeks gestation were eligible. randomization was generated in SAS® by site in blocks of 4. The planned adaptive design periodically generated allocation ratios favoring the better performing dose. Managing study personnel were blind to treatment until 30 days after the last birth. The primary outcome was EPB by dose and by enrolment DHA status (low/high). Bayesian posterior probabilities (pp) were determined for planned efficacy and safety outcomes using intention-to-treat. The study is registered with ClinicalTrials.gov (NCT02626299) and closed to enrolment. FINDINGS: Eleven hundred participants (1000 mg, n = 576; 200 mg, n = 524) were enrolled between June 8, 2016 and March 13, 2020 with the last birth September 5, 2020. 1032 (n = 540 and n = 492) were included in the primary analyses. The higher dose had a lower EPB rate [1.7% (9/540) vs 2.4% (12/492), pp=0.81] especially if participants had low DHA status at enrolment [2.0% (5/249) vs 4.1%, (9/219), pp=0.93]. Participants with high enrolment DHA status did not realize a dose effect [1000 mg: 1.4% (4/289); 200 mg: 1.1% (3/271), pp = 0.57]. The higher dose was associated with fewer serious adverse events (maternal: chorioamnionitis, premature rupture of membranes and pyelonephritis; neonatal: feeding, genitourinary and neurologic problems, all pp>0.90). INTERPRETATION: Clinicians could consider prescribing 1000 mg DHA daily during pregnancy to reduce EPB in women with low DHA status if they are able to screen for DHA. FUNDING: The National Institutes of Health Child Health and Human Development (NICHD) funded the study. Life's DHA™-S oil, DSM Nutritional Products LLC, Switzerland provided all capsules. Elsevier 2021-05-17 /pmc/articles/PMC8257993/ /pubmed/34308309 http://dx.doi.org/10.1016/j.eclinm.2021.100905 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Carlson, Susan E
Gajewski, Byron J
Valentine, Christina J
Kerling, Elizabeth H
Weiner, Carl P
Cackovic, Michael
Buhimschi, Catalin S
Rogers, Lynette K
Sands, Scott A
Brown, Alexandra R
Mudaranthakam, Dinesh Pal
Crawford, Sarah A
DeFranco, Emily A
Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title_full Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title_fullStr Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title_full_unstemmed Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title_short Higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: A randomised, double-blind, adaptive-design superiority trial
title_sort higher dose docosahexaenoic acid supplementation during pregnancy and early preterm birth: a randomised, double-blind, adaptive-design superiority trial
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257993/
https://www.ncbi.nlm.nih.gov/pubmed/34308309
http://dx.doi.org/10.1016/j.eclinm.2021.100905
work_keys_str_mv AT carlsonsusane higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT gajewskibyronj higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT valentinechristinaj higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT kerlingelizabethh higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT weinercarlp higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT cackovicmichael higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT buhimschicatalins higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT rogerslynettek higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT sandsscotta higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT brownalexandrar higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT mudaranthakamdineshpal higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT crawfordsaraha higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial
AT defrancoemilya higherdosedocosahexaenoicacidsupplementationduringpregnancyandearlypretermbirtharandomiseddoubleblindadaptivedesignsuperioritytrial