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Arginine vasopressin in cerebrospinal fluid is a marker of sociality in nonhuman primates

Version 2 2024-03-12, 17:17
Version 1 2024-03-01, 11:00
journal contribution
posted on 2024-03-12, 17:17 authored by K.J. Parker, J.P. Garner, S. Partap, A.Y. Hardan, E.H. Sherr, J.P. Capitanio, O. Oztan, E.R. Tarara, J. Li, Valentina SclafaniValentina Sclafani, L.A. Del Rosso, K. Chun, S.W. Berquist, M.G. Chez

Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by core social impairments. ASD remains poorly understood because of the difficulty in studying disease biology directly in patients and the reliance on mouse models that lack clinically relevant, complex social cognition abilities. We use ethological observations in rhesus macaques to identify male monkeys with naturally occurring low sociality. These monkeys showed differences in specific neuropeptide and kinase signaling pathways compared to socially competent male monkeys. Using a discovery and replication design, we identified arginine vasopressin (AVP) in cerebrospinal fluid (CSF) as a key marker of group differences in monkey sociality; we replicated these findings in an independent monkey cohort. We also confirmed in an additional monkey cohort that AVP concentration in CSF is a stable traitlike measure. Next, we showed in a small pediatric cohort that CSF AVP concentrations were lower in male children with ASD compared to age-matched male children without ASD (but with other medical conditions). We demonstrated that CSF AVP concentration was sufficient to accurately distinguish ASD cases from medical controls. These data suggest that AVP and its signaling pathway warrant consideration in future research studies investigating new targets for diagnostics and drug development in ASD. © 2018 The Authors.

History

School affiliated with

  • School of Psychology (Research Outputs)

Publication Title

Science Translational Medicine

Volume

10

Issue

439

Pages/Article Number

eaam9100

Publisher

American Association for the Advancement of Science

ISSN

1946-6234

eISSN

1946-6242

Date Submitted

2019-04-12

Date Accepted

2017-11-10

Date of First Publication

2018-05-02

Date of Final Publication

2018-05-02

Date Document First Uploaded

2019-02-01

ePrints ID

34824