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Conflict of interest: EHC has served on the Scientific Advisory Board for Impel Pharmaceuticals, anticipates research support from Jazz Pharmaceuticals, and receives an editorial stipend from Springer. JVV has consulted or served on advisory boards for Novartis, Roche Pharmaceuticals, and SynapDx; has received research funding from Novartis, Roche Pharmaceuticals, Forest, Seaside Therapeutics, Janssen, SynapDx, Yamo Pharmaceuticals, MapLight, and Acadia; and has received an editorial stipend from Springer and Wiley.
Figures
Figure 1. Comparative maternal, proband, and paternal…
Figure 1. Comparative maternal, proband, and paternal WB5-HT levels between autism rare variant carriers and…
Figure 1. Comparative maternal, proband, and paternal WB5-HT levels between autism rare variant carriers and noncarriers.
We predicted that the mothers of probands carrying rare autism-associated variants would have lower WB5-HT than mothers of noncarrier probands. With the observation that 5-HT levels in mothers of ASD probands show an upward skew (2), we hypothesized that the mothers of noncarrier probands would not show this skew and would instead show a normal distribution that would largely overlap with the theoretical distribution of the general population (A). Although median maternal WB5-HT did not differ across groups, the distribution was significantly upward shifted in the autism rare-variant noncarriers (B). We observed no significant differences in proband (C) or paternal (D) WB5-HT.
Muller CL, et al. Impact of maternal serotonin transporter genotype on placental serotonin, fetal forebrain serotonin, and neurodevelopment. Neuropsychopharmacology. 2017;42(2):427–436. doi: 10.1038/npp.2016.166.
-
DOI
-
PMC
-
PubMed
Montgomery AK, et al. Maternal serotonin levels are associated with cognitive ability and core symptoms in autism spectrum disorder. J Am Acad Child Adolesc Psychiatry. 2018;57(11):867–875. doi: 10.1016/j.jaac.2018.06.025.
-
DOI
-
PMC
-
PubMed
Fu JM, et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nat Genet. 2022;54(9):1320–1331. doi: 10.1038/s41588-022-01104-0.
-
DOI
-
PMC
-
PubMed
Chen R, et al. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism. Mol Autism. 2017;8:14. doi: 10.1186/s13229-017-0130-3.
-
DOI
-
PMC
-
PubMed
Fischbach GD, Lord C. The Simons Simplex Collection: a resource for identification of autism genetic risk factors. Neuron. 2010;68(2):192–195. doi: 10.1016/j.neuron.2010.10.006.
-
DOI
-
PubMed