Maternal serum cytokine levels and risk of bipolar disorder
•Cases with bipolar disorder (BD) and matched controls were identified.•Nine cytokines were measured in archived prenatal maternal serum samples.•Among cases overall, the cytokine levels were not associated with risk of BD.•Lower levels of IL-4 and IL-6 were observed in BD cases without psychotic fe...
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Published in | Brain, behavior, and immunity Vol. 63; pp. 108 - 114 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.07.2017
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Abstract | •Cases with bipolar disorder (BD) and matched controls were identified.•Nine cytokines were measured in archived prenatal maternal serum samples.•Among cases overall, the cytokine levels were not associated with risk of BD.•Lower levels of IL-4 and IL-6 were observed in BD cases without psychotic features.•Findings varied by trimester.
Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal cytokines. The objective of this study was to determine the association between maternal levels of cytokines measured during each trimester of pregnancy and the risk of BD in offspring. We conducted a case-control study nested in the Child Health and Development Study, a birth cohort that enrolled pregnant women in 1959–1966. Potential cases with DSM-IV-TR bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features were ascertained through electronic medical records, a public agency database, and a mailing to the cohort. Diagnoses were confirmed by clinical interview. Nine cytokines (IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IFN-γ, TNF-α and GM-CSF) were measured simultaneously by Luminex assays in archived prenatal maternal serum samples from 85 cases and 170 matched controls. Data were analyzed using conditional logistic regression. In the overall study sample, there were no significant associations between prenatal maternal cytokine levels and BD after adjustment for confounders. The risk of BD without psychotic features was decreased among subjects with higher maternal levels of first trimester log-transformed IL-4 (OR (95% CI)=0.76 (0.58, 0.98); p=0.04) and third trimester log-transformed IL-6 (OR (95% CI)=0.64 (0.42, 0.98); p=0.04). In conclusion, higher levels of prenatal maternal cytokines were not associated with increased risk for BD. Further studies with larger samples are necessary to confirm the finding. |
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AbstractList | Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal cytokines. The objective of this study was to determine the association between maternal levels of cytokines measured during each trimester of pregnancy and the risk of BD in offspring. We conducted a case-control study nested in the Child Health and Development Study, a birth cohort that enrolled pregnant women in 1959-1966. Potential cases with DSM-IV-TR bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features were ascertained through electronic medical records, a public agency database, and a mailing to the cohort. Diagnoses were confirmed by clinical interview. Nine cytokines (IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IFN-γ, TNF-α and GM-CSF) were measured simultaneously by Luminex assays in archived prenatal maternal serum samples from 85 cases and 170 matched controls. Data were analyzed using conditional logistic regression. In the overall study sample, there were no significant associations between prenatal maternal cytokine levels and BD after adjustment for confounders. The risk of BD without psychotic features was decreased among subjects with higher maternal levels of first trimester log-transformed IL-4 (OR (95% CI)=0.76 (0.58, 0.98); p=0.04) and third trimester log-transformed IL-6 (OR (95% CI)=0.64 (0.42, 0.98); p=0.04). In conclusion, higher levels of prenatal maternal cytokines were not associated with increased risk for BD. Further studies with larger samples are necessary to confirm the finding.Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal cytokines. The objective of this study was to determine the association between maternal levels of cytokines measured during each trimester of pregnancy and the risk of BD in offspring. We conducted a case-control study nested in the Child Health and Development Study, a birth cohort that enrolled pregnant women in 1959-1966. Potential cases with DSM-IV-TR bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features were ascertained through electronic medical records, a public agency database, and a mailing to the cohort. Diagnoses were confirmed by clinical interview. Nine cytokines (IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IFN-γ, TNF-α and GM-CSF) were measured simultaneously by Luminex assays in archived prenatal maternal serum samples from 85 cases and 170 matched controls. Data were analyzed using conditional logistic regression. In the overall study sample, there were no significant associations between prenatal maternal cytokine levels and BD after adjustment for confounders. The risk of BD without psychotic features was decreased among subjects with higher maternal levels of first trimester log-transformed IL-4 (OR (95% CI)=0.76 (0.58, 0.98); p=0.04) and third trimester log-transformed IL-6 (OR (95% CI)=0.64 (0.42, 0.98); p=0.04). In conclusion, higher levels of prenatal maternal cytokines were not associated with increased risk for BD. Further studies with larger samples are necessary to confirm the finding. Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal cytokines. The objective of this study was to determine the association between maternal levels of cytokines measured during each trimester of pregnancy and the risk of BD in offspring. We conducted a case-control study nested in the Child Health and Development Study, a birth cohort that enrolled pregnant women in 1959-1966. Potential cases with DSM-IV-TR bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features were ascertained through electronic medical records, a public agency database, and a mailing to the cohort. Diagnoses were confirmed by clinical interview. Nine cytokines (IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IFN-γ, TNF-α and GM-CSF) were measured simultaneously by Luminex assays in archived prenatal maternal serum samples from 85 cases and 170 matched controls. Data were analyzed using conditional logistic regression. In the overall study sample, there were no significant associations between prenatal maternal cytokine levels and BD after adjustment for confounders. The risk of BD without psychotic features was decreased among subjects with higher maternal levels of first trimester log-transformed IL-4 (OR (95% CI)=0.76 (0.58, 0.98); p=0.04) and third trimester log-transformed IL-6 (OR (95% CI)=0.64 (0.42, 0.98); p=0.04). In conclusion, higher levels of prenatal maternal cytokines were not associated with increased risk for BD. Further studies with larger samples are necessary to confirm the finding. •Cases with bipolar disorder (BD) and matched controls were identified.•Nine cytokines were measured in archived prenatal maternal serum samples.•Among cases overall, the cytokine levels were not associated with risk of BD.•Lower levels of IL-4 and IL-6 were observed in BD cases without psychotic features.•Findings varied by trimester. Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal cytokines. The objective of this study was to determine the association between maternal levels of cytokines measured during each trimester of pregnancy and the risk of BD in offspring. We conducted a case-control study nested in the Child Health and Development Study, a birth cohort that enrolled pregnant women in 1959–1966. Potential cases with DSM-IV-TR bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features were ascertained through electronic medical records, a public agency database, and a mailing to the cohort. Diagnoses were confirmed by clinical interview. Nine cytokines (IL-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IFN-γ, TNF-α and GM-CSF) were measured simultaneously by Luminex assays in archived prenatal maternal serum samples from 85 cases and 170 matched controls. Data were analyzed using conditional logistic regression. In the overall study sample, there were no significant associations between prenatal maternal cytokine levels and BD after adjustment for confounders. The risk of BD without psychotic features was decreased among subjects with higher maternal levels of first trimester log-transformed IL-4 (OR (95% CI)=0.76 (0.58, 0.98); p=0.04) and third trimester log-transformed IL-6 (OR (95% CI)=0.64 (0.42, 0.98); p=0.04). In conclusion, higher levels of prenatal maternal cytokines were not associated with increased risk for BD. Further studies with larger samples are necessary to confirm the finding. Highlights • Cases with bipolar disorder (BD) and matched controls were identified. • Nine cytokines were measured in archived prenatal maternal serum samples. • Among cases overall, the cytokine levels were not associated with risk of BD. • Lower levels of IL-4 and IL-6 were observed in BD cases without psychotic features. • Findings varied by trimester. |
Author | Cremers, Serge Schaefer, Catherine A. Bao, Yuanyuan Brown, Alan S. Cheslack-Postava, Keely Shen, Ling |
AuthorAffiliation | b Pathology and Cell Biology, Columbia University Medical Center, New York, NY a Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, United States c KPNC Permanente Division of Research, Oakland, CA, United States d Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, United States |
AuthorAffiliation_xml | – name: c KPNC Permanente Division of Research, Oakland, CA, United States – name: d Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, United States – name: a Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, United States – name: b Pathology and Cell Biology, Columbia University Medical Center, New York, NY |
Author_xml | – sequence: 1 givenname: Keely surname: Cheslack-Postava fullname: Cheslack-Postava, Keely email: kc2497@cumc.columbia.edu organization: Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, United States – sequence: 2 givenname: Serge surname: Cremers fullname: Cremers, Serge organization: Pathology and Cell Biology, Columbia University Medical Center, New York, NY, United States – sequence: 3 givenname: Yuanyuan surname: Bao fullname: Bao, Yuanyuan organization: Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, United States – sequence: 4 givenname: Ling surname: Shen fullname: Shen, Ling organization: KPNC Permanente Division of Research, Oakland, CA, United States – sequence: 5 givenname: Catherine A. surname: Schaefer fullname: Schaefer, Catherine A. organization: KPNC Permanente Division of Research, Oakland, CA, United States – sequence: 6 givenname: Alan S. surname: Brown fullname: Brown, Alan S. organization: Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, United States |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27477922$$D View this record in MEDLINE/PubMed |
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Keywords | Prenatal Maternal Cytokines Immune IL-4 Bipolar disorder IL-6 |
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Snippet | •Cases with bipolar disorder (BD) and matched controls were identified.•Nine cytokines were measured in archived prenatal maternal serum samples.•Among cases... Highlights • Cases with bipolar disorder (BD) and matched controls were identified. • Nine cytokines were measured in archived prenatal maternal serum samples.... Prenatal exposure to influenza has previously been associated with increased risk of bipolar disorder (BD), an association that may be mediated by maternal... |
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SubjectTerms | Allergy and Immunology Bipolar disorder Bipolar Disorder - immunology Case-Control Studies Cohort Studies Cytokines Cytokines - blood Female Humans IL-4 IL-6 Immune Influenza, Human - complications Interleukin-4 - blood Interleukin-6 - blood Maternal Pregnancy Pregnancy Complications, Infectious - immunology Prenatal Prenatal Exposure Delayed Effects Psychiatry Risk Factors |
Title | Maternal serum cytokine levels and risk of bipolar disorder |
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