E Kale Edmiston

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Associate Professor

Country flagUnited States

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Recent Grants

Grant: Close

Feed Forward Visual System Function in High Trait Anxiety

Open Date: 2019-04-15

Close Date: 2024-03-31

Grant: Close

Neuromodulation of Visual Cortex in Individuals At-Risk for Developing Anxiety Disorders

Open Date: 2019-01-15

Close Date: 2021-01-14

Articles (12)

Recent research in autism spectrum disorder (ASD) has suggested a higher prevalence of gender diversity in individuals diagnosed with ASD. Adolescence is a critical period for the consolidation of gender identity, yet the extent to which the experience of gender diversity is stable over adolescence and puberty in autistic youth is poorly understood. The aim of the study was to examine the consistency of gender diversity using the gender diversity screening questionnaire for self‐ and parent‐report of youth (GDSQ‐S, GDSQ‐P) over a four‐year longitudinal study of pubertal development in youth with ASD ( N = 140, 36 assigned‐female‐at birth (AFAB)) and typical development (TD, N = 104, 58 assigned‐male‐at‐birth [AMAB]) and their parents. The extent to which diagnosis (ASD vs. TD), assigned sex (AFAB vs. AMAB) and developmental level (age, puberty) predict GDSQ trajectory over time was explored. There was a significant diagnosis by sex‐assigned‐at‐birth by age interaction for GDSQ‐S Gender Diversity, p = 0.002, showing higher scores in autistic AFAB youth over adolescence, and TD AFAB showing initially lower, then increasing levels over adolescence. For GDSQ‐P, Gender Incongruence was significantly different between the groups, p = 0.032, showing higher incongruence for autistic AFAB around age 10, decreasing between age 12–14 before increasing again, while TD AFAB evidence the inverse trend. AMAB trends were stable. The significant diagnostic, developmental and sex‐based differences indicate AFAB youth experience greater gender diversity that evolves over development. Findings suggest gender identity formation is nuanced and may be influenced by pubertal progression, hormonal patterns, and psychosocial factors. Results underscore the need for enhanced understanding of the unique, dynamic profiles of females‐assigned‐at‐birth.

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Collaborators (6)

Joz Motmans

Ghent University Hospital

BELGIUM
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Simon Vandekar

-

UNITED STATES
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Rachael Muscatello

Research Assistant Professor

Vanderbilt University Medical Center

UNITED STATES
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Lejla Colic

Jena University Hospital

GERMANY
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Ulrika Nygren

Karolinska Institutet

SWEDEN
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Elizabeth Lippard

Assistant Professor

The University of Texas at Austin Dell Medical School

UNITED STATES
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