TY - JOUR
T1 - Can the “female protective effect” liability threshold model explain sex differences in autism spectrum disorder?
AU - Dougherty, Joseph
AU - Marrus, Natasha
AU - Maloney, Susan E.
AU - Yip, Benjamin
AU - Sandin, Sven
AU - Turner, Tychele
AU - Selmanovic, Din
AU - Kroll, Kristen L.
AU - Gutmann, David H.
AU - Constantino, John
AU - Weiss, Lauren A.
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/10/19
Y1 - 2022/10/19
N2 - Male sex is a strong risk factor for autism spectrum disorder (ASD). The leading theory for a “female protective effect” (FPE) envisions males and females have “differing thresholds” under a “liability threshold model” (DT-LTM). Specifically, this model posits that females require either a greater number or larger magnitude of risk factors (i.e., greater liability) to manifest ASD, which is supported by the finding that a greater proportion of females with ASD have highly penetrant genetic mutations. Herein, we derive testable hypotheses from the DT-LTM for ASD, investigating heritability, familial recurrence, correlation between ASD penetrance and sex ratio, population traits, clinical features, the stability of the sex ratio across diagnostic changes, and highlight other key prerequisites. Our findings reveal that several key predictions of the DT-LTM are not supported by current data, requiring us to establish a different conceptual framework for evaluating alternate models that explain sex differences in ASD.
AB - Male sex is a strong risk factor for autism spectrum disorder (ASD). The leading theory for a “female protective effect” (FPE) envisions males and females have “differing thresholds” under a “liability threshold model” (DT-LTM). Specifically, this model posits that females require either a greater number or larger magnitude of risk factors (i.e., greater liability) to manifest ASD, which is supported by the finding that a greater proportion of females with ASD have highly penetrant genetic mutations. Herein, we derive testable hypotheses from the DT-LTM for ASD, investigating heritability, familial recurrence, correlation between ASD penetrance and sex ratio, population traits, clinical features, the stability of the sex ratio across diagnostic changes, and highlight other key prerequisites. Our findings reveal that several key predictions of the DT-LTM are not supported by current data, requiring us to establish a different conceptual framework for evaluating alternate models that explain sex differences in ASD.
UR - http://www.scopus.com/inward/record.url?scp=85140415234&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2022.06.020
DO - 10.1016/j.neuron.2022.06.020
M3 - Review article
C2 - 35868305
AN - SCOPUS:85140415234
SN - 0896-6273
VL - 110
SP - 3243
EP - 3262
JO - Neuron
JF - Neuron
IS - 20
ER -