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TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study

OBJECTIVES: To compare levels of a marker of lipid peroxidation (thiobarbituric acid reactive substances, TBARS) and brain-derived neurotrophic factor (BDNF) in umbilical cord blood (UCB) between newborns exposed to crack/cocaine in utero (exposed newborns [EN], n=57) and non-exposed newborns (NEN,...

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Autores principales: Mardini, Victor, Rohde, Luis A., Ceresér, Keila M., Gubert, Carolina M., da Silva, Emily G., Xavier, Fernando, Parcianello, Rodrigo, Röhsig, Liane M., Pechansky, Flávio, Szobot, Claudia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Psiquiatria 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111386/
https://www.ncbi.nlm.nih.gov/pubmed/28273279
http://dx.doi.org/10.1590/1516-4446-2016-2035
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author Mardini, Victor
Rohde, Luis A.
Ceresér, Keila M.
Gubert, Carolina M.
da Silva, Emily G.
Xavier, Fernando
Parcianello, Rodrigo
Röhsig, Liane M.
Pechansky, Flávio
Szobot, Claudia M.
author_facet Mardini, Victor
Rohde, Luis A.
Ceresér, Keila M.
Gubert, Carolina M.
da Silva, Emily G.
Xavier, Fernando
Parcianello, Rodrigo
Röhsig, Liane M.
Pechansky, Flávio
Szobot, Claudia M.
author_sort Mardini, Victor
collection PubMed
description OBJECTIVES: To compare levels of a marker of lipid peroxidation (thiobarbituric acid reactive substances, TBARS) and brain-derived neurotrophic factor (BDNF) in umbilical cord blood (UCB) between newborns exposed to crack/cocaine in utero (exposed newborns [EN], n=57) and non-exposed newborns (NEN, n=99), as well as in maternal peripheral blood at delivery. METHODS: This was a cross-sectional study. Potential confounders, including perinatal parameters, psychopathology, and use of other substances, were assessed. RESULTS: After adjusting for potential confounders, adjusted mean BDNF was significantly higher in EN (3.86 ng/mL, 95% confidence interval [95%CI] 2.29-5.43) than in NEN (0.85 ng/mL, 95%CI 0.47-1.23; p < 0.001; Cohen effect size: 1.12), and significantly lower in crack/cocaine mothers than in control mothers (4.03 ng/mL, 95%CI 2.87-5.18 vs. 6.67 ng/mL, 95%CI 5.60-7.74; p = 0.006). The adjusted mean TBARS level was significantly lower in EN (63.97 µM MDA, 95%CI 39.43-88.50) than NEN (177.04 µM MDA, 95%CI 140.93-213.14; p < 0.001; effect size = 0.84), with no difference between mother groups (p = 0.86). CONCLUSIONS: The changes in TBARS levels observed in EN suggest that fetuses exposed to cocaine mobilize endogenous antioxidant routes since very early stages of development. The increase in BDNF levels in EN might indicate changes in fetal development, whereas the changes in BDNF levels in mothers provide evidence of the complex metabolic processes involved in drug use during pregnancy.
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spelling pubmed-71113862020-04-02 TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study Mardini, Victor Rohde, Luis A. Ceresér, Keila M. Gubert, Carolina M. da Silva, Emily G. Xavier, Fernando Parcianello, Rodrigo Röhsig, Liane M. Pechansky, Flávio Szobot, Claudia M. Braz J Psychiatry Brief Communication OBJECTIVES: To compare levels of a marker of lipid peroxidation (thiobarbituric acid reactive substances, TBARS) and brain-derived neurotrophic factor (BDNF) in umbilical cord blood (UCB) between newborns exposed to crack/cocaine in utero (exposed newborns [EN], n=57) and non-exposed newborns (NEN, n=99), as well as in maternal peripheral blood at delivery. METHODS: This was a cross-sectional study. Potential confounders, including perinatal parameters, psychopathology, and use of other substances, were assessed. RESULTS: After adjusting for potential confounders, adjusted mean BDNF was significantly higher in EN (3.86 ng/mL, 95% confidence interval [95%CI] 2.29-5.43) than in NEN (0.85 ng/mL, 95%CI 0.47-1.23; p < 0.001; Cohen effect size: 1.12), and significantly lower in crack/cocaine mothers than in control mothers (4.03 ng/mL, 95%CI 2.87-5.18 vs. 6.67 ng/mL, 95%CI 5.60-7.74; p = 0.006). The adjusted mean TBARS level was significantly lower in EN (63.97 µM MDA, 95%CI 39.43-88.50) than NEN (177.04 µM MDA, 95%CI 140.93-213.14; p < 0.001; effect size = 0.84), with no difference between mother groups (p = 0.86). CONCLUSIONS: The changes in TBARS levels observed in EN suggest that fetuses exposed to cocaine mobilize endogenous antioxidant routes since very early stages of development. The increase in BDNF levels in EN might indicate changes in fetal development, whereas the changes in BDNF levels in mothers provide evidence of the complex metabolic processes involved in drug use during pregnancy. Associação Brasileira de Psiquiatria 2017-03-02 /pmc/articles/PMC7111386/ /pubmed/28273279 http://dx.doi.org/10.1590/1516-4446-2016-2035 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Mardini, Victor
Rohde, Luis A.
Ceresér, Keila M.
Gubert, Carolina M.
da Silva, Emily G.
Xavier, Fernando
Parcianello, Rodrigo
Röhsig, Liane M.
Pechansky, Flávio
Szobot, Claudia M.
TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title_full TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title_fullStr TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title_full_unstemmed TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title_short TBARS and BDNF levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
title_sort tbars and bdnf levels in newborns exposed to crack/cocaine during pregnancy: a comparative study
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111386/
https://www.ncbi.nlm.nih.gov/pubmed/28273279
http://dx.doi.org/10.1590/1516-4446-2016-2035
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