Evidence map›Paper›PMID 39313480›Full record

ArticleArthritis care & research2025

Association Between 25-hydroxyvitamin D Levels and Adverse Pregnancy Outcomes in Systemic Lupus Erythematosus.

Nima Madanchi, Andrea Fava, Daniel W Goldman, Laurence S Magder, Michelle Petri

Abstract read
In one paragraph

Article in Arthritis care & research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Nima MadanchiJohns Hopkins University, Baltimore, Maryland.ORCID 0000-0002-2155-3283
Andrea FavaJohns Hopkins University, Baltimore, Maryland.ORCID 0000-0001-6738-4836
Daniel W GoldmanJohns Hopkins University, Baltimore, Maryland.ORCID 0000-0001-5003-3503
Laurence S MagderUniversity of Maryland, Baltimore.
Michelle PetriJohns Hopkins University, Baltimore, Maryland.ORCID 0000-0003-1441-5373

Funding

Hopkins Lupus CohortR01AR069572 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI PETRI, MICHELLE A · 2016 to 2020
$3.4M
Clinical applications of urine proteomics to lupus nephritisR01DK134625 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Andrea Fava · 2023 to 2026
$2.8M
NIAMS NIH HHS R01 AR069572NIDDK NIH HHS R01 DK134625NIH HHS R01AR069572NIH HHS R01DK134625
6 · The paper itself

Abstract

objectiveWe evaluated the association of 25-hydroxyvitamin D (25(OH)D) levels with adverse pregnancy outcomes in systemic lupus erythematosus (SLE).

methodsThe Hopkins Lupus Cohort includes visits of pregnant patients, including assessment of 25(OH)D levels at each visit. We examined the relationship between 25(OH)D levels and adverse pregnancy outcomes (miscarriage, preterm delivery, and small for gestational age). We also used a time-to-event analysis to assess whether time-varying of 25(OH)D levels were associated with time to miscarriage or preterm delivery.

resultsIn subgroups of patients defined by the average of 25(OH)D levels, we observed significantly different risks of miscarriage (P = 0.0045), preterm delivery (P = 0.0007), and the composite measure of all three adverse pregnancy outcomes (P = 0.011). The highest risks were observed among those with the lowest or highest levels of vitamin D. Nine of 10 pregnant patients with low vitamin D levels during the second trimester resulted in having a premature delivery. The time-to-event model confirmed the same U-shaped association after adjustment for SLE disease activity; however, the increased risk among those with highest levels of vitamin D was not statistically significant. Body mass index did not appear to be a confounding factor.

conclusionOur study is not able to prove causation, but the results strongly suggest an association of 25(OH)D at both lower and higher levels with adverse pregnancy outcomes. We recommend the monitoring of maternal serum 25(OH)D levels during SLE pregnancies, aiming for the ideal range of 40 to 59 ng/mL.

Indexed as

Lupus Erythematosus, SystemicPregnancy ComplicationsPregnancy OutcomePremature BirthVitamin DVitamin D DeficiencyAbortion, SpontaneousAdultBiomarkersCohort StudiesFemaleHumansInfant, Small for Gestational AgePregnancyRisk FactorsYoung Adult25-hydroxyvitamin DBiomarkersVitamin D

Identifiers

PMID39313480
PMCPMC11929614

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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.