The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder

Abstract Brain-derived neurotrophic factor (BDNF), a key peptide in neurocognitive development, has been reported to be elevated in the serum of children with autism spectrum disorder (ASD). In a few studies, however, no differences or the converse have been documented. As a secondary analysis of a...

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Autores principales: Cristan A. Farmer, Audrey E. Thurm, Bianca Honnekeri, Paul Kim, Susan E. Swedo, Joan C. Han
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:b30d12340fc9469184346d72304286de2021-12-02T18:50:48ZThe contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder10.1038/s41598-021-97367-42045-2322https://doaj.org/article/b30d12340fc9469184346d72304286de2021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-97367-4https://doaj.org/toc/2045-2322Abstract Brain-derived neurotrophic factor (BDNF), a key peptide in neurocognitive development, has been reported to be elevated in the serum of children with autism spectrum disorder (ASD). In a few studies, however, no differences or the converse have been documented. As a secondary analysis of a natural history study, we examined differences in ELISA serum BDNF between a group of children aged 1 to 9 years (69% white) with ASD (n = 94) and those with typical development (n = 52) or non-ASD developmental delay (n = 21), while accounting for the potential confounding effects of platelet quantity. Platelet counts were measured within 4 h of blood draw using an automated cell counter. Taqman single nucleotide polymorphism (SNP) assays were used to genotype 11 SNPs within the BDNF locus. Unadjusted mean BDNF concentration was higher in children with ASD than in children with typical development (standardized mean difference = 0.23; 95% CI 0.07, 0.38), but not children with non-ASD developmental delay. The magnitude of this difference was reduced after adjusting for platelet count (standardized mean difference = 0.18; 95% CI 0.02, 0.33). Although some BDNF SNPs were related to BDNF concentration, the distributions of these genotypes did not differ across diagnostic groups. This study replicates previous work suggesting that average serum BDNF concentration is higher in ASD compared to typical development, and extends that work by highlighting the potentially confounding role of platelet counts. The etiology of platelet count differences warrants further elucidation. Nonetheless, our results suggest that elevation in BDNF may be partially explained by higher platelet counts in children with ASD, an association that should be considered in future analysis and interpretation. Registration: NCT00298246Cristan A. FarmerAudrey E. ThurmBianca HonnekeriPaul KimSusan E. SwedoJoan C. HanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Cristan A. Farmer
Audrey E. Thurm
Bianca Honnekeri
Paul Kim
Susan E. Swedo
Joan C. Han
The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
description Abstract Brain-derived neurotrophic factor (BDNF), a key peptide in neurocognitive development, has been reported to be elevated in the serum of children with autism spectrum disorder (ASD). In a few studies, however, no differences or the converse have been documented. As a secondary analysis of a natural history study, we examined differences in ELISA serum BDNF between a group of children aged 1 to 9 years (69% white) with ASD (n = 94) and those with typical development (n = 52) or non-ASD developmental delay (n = 21), while accounting for the potential confounding effects of platelet quantity. Platelet counts were measured within 4 h of blood draw using an automated cell counter. Taqman single nucleotide polymorphism (SNP) assays were used to genotype 11 SNPs within the BDNF locus. Unadjusted mean BDNF concentration was higher in children with ASD than in children with typical development (standardized mean difference = 0.23; 95% CI 0.07, 0.38), but not children with non-ASD developmental delay. The magnitude of this difference was reduced after adjusting for platelet count (standardized mean difference = 0.18; 95% CI 0.02, 0.33). Although some BDNF SNPs were related to BDNF concentration, the distributions of these genotypes did not differ across diagnostic groups. This study replicates previous work suggesting that average serum BDNF concentration is higher in ASD compared to typical development, and extends that work by highlighting the potentially confounding role of platelet counts. The etiology of platelet count differences warrants further elucidation. Nonetheless, our results suggest that elevation in BDNF may be partially explained by higher platelet counts in children with ASD, an association that should be considered in future analysis and interpretation. Registration: NCT00298246
format article
author Cristan A. Farmer
Audrey E. Thurm
Bianca Honnekeri
Paul Kim
Susan E. Swedo
Joan C. Han
author_facet Cristan A. Farmer
Audrey E. Thurm
Bianca Honnekeri
Paul Kim
Susan E. Swedo
Joan C. Han
author_sort Cristan A. Farmer
title The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
title_short The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
title_full The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
title_fullStr The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
title_full_unstemmed The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder
title_sort contribution of platelets to peripheral bdnf elevation in children with autism spectrum disorder
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b30d12340fc9469184346d72304286de
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