Evidence map›Paper›PMID 38944975›Full record

ArticleSchizophrenia research2024

Maternal vitamin D levels during pregnancy and offspring schizophrenia.

Andre Sourander, Subina Upadhyaya, Heljä-Marja Surcel, Susanna Hinkka-Yli-Salomäki, Keely Cheslack-Postava, Sanju Silwal, Ian W McKeague, Alan S Brown

Abstract read
In one paragraph

Article in Schizophrenia research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Andre SouranderUniversity of Turku, Department of Child Psychiatry, Research Centre for Child Psychiatry, Turku, Finland; Turku University Hospital, Department of Child Psychiatry, Turku, Finland; University of Turku, INVEST Research Flagship, Finland; Department of Psychiatry, New York State Psychiatric Institute, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: andsou@utu.fi.
Subina UpadhyayaUniversity of Turku, Department of Child Psychiatry, Research Centre for Child Psychiatry, Turku, Finland.
Heljä-Marja SurcelFaculty of Medicine, University of Oulu, Finland; Biobank Borealis of Northern Finland, Oulu, Finland.
Susanna Hinkka-Yli-SalomäkiUniversity of Turku, Department of Child Psychiatry, Research Centre for Child Psychiatry, Turku, Finland.
Keely Cheslack-PostavaDepartment of Psychiatry, New York State Psychiatric Institute, Columbia University Irving Medical Center, New York, NY, USA.
Sanju SilwalUniversity of Turku, Department of Child Psychiatry, Research Centre for Child Psychiatry, Turku, Finland.
Ian W McKeagueDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York, NY, USA.
Alan S BrownDepartment of Psychiatry, New York State Psychiatric Institute, Columbia University Irving Medical Center, New York, NY, USA; Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA.

Funding

Prenatal Factors in Autism and other Psychiatric Outcomes in a National Birth CohortR01ES028125 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BROWN, ALAN STEWART · 2017 to 2021
$2.3M
NIEHS NIH HHS R01 ES028125
6 · The paper itself

Abstract

backgroundFindings from previous studies on maternal 25(OH)D levels during pregnancy and offspring schizophrenia are limited and inconsistent.

methodsWe used nationwide population-based register data with a nested case-control design to examine the association between maternal 25(OH)D levels during pregnancy and offspring schizophrenia. The cases of schizophrenia (n = 1145) were born from 1987 to 1997, and received a diagnosis of schizophrenia by 2017, and were matched with equal number of controls. A quantitative immunoassay was used to measure maternal 25(OH)D in archived maternal serum in the national biobank of the Finnish Maternity Cohort, collected during the first and early second trimesters. Conditional logistic regression models examined the association between maternal 25(OH)D levels and offspring schizophrenia.

resultsNo significant association was found between log-transformed maternal 25(OH)D levels and schizophrenia in unadjusted (OR 0.96, 95 % CI 0.78-1.17, p = 0.69) or adjusted analyses (aOR 0.98, 95 % CI 0.79-1.22, p = 0.89). Analyses by quintiles also revealed no association between the lowest quintile of maternal 25(OH)D levels and schizophrenia (OR 1.09, 95 % CI 0.81-1.45, p = 0.55; aOR 1.06, 95 % CI 0.78-1.45, p = 0.71). Maternal 25(OH)D levels, measured in categories, either in deficient category (OR 1.07 (0.85-1.35), p = 0.52; aOR 1.05 (0.81-1.34), p = 0.88) or insufficient category (OR 1.13, 95 % CI 0.92-1.40, p = 0.23; aOR 1.13, 95 % CI 0.90-1.41, p = 0.27) were also not associated with offspring schizophrenia.

conclusionsMaternal vitamin D levels in early pregnancy were not associated with offspring schizophrenia. Future studies measuring vitamin D during different stages of gestation are needed to draw firm conclusions.

Indexed as

Prenatal Exposure Delayed EffectsSchizophreniaVitamin DAdultCase-Control StudiesFemaleFinlandHumansMalePregnancyRegistriesVitamin D DeficiencyYoung Adult25-hydroxyvitamin DVitamin DAntenatalMaternalOffspringPregnancySchizophreniaVitamin D

Identifiers

PMID38944975
PMCPMC11412259

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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.