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The Relationship Between the Uncinate Fasciculus and Anxious Temperament Is Evolutionarily Conserved and Sexually
Do P M Tromp1, Andrew S Fox2, Jonathan A Oler3
1Department of Psychiatry, University of Wisconsin, Madison, Wisconsin; Neuroscience Training Program, University of Wisconsin, Madison, Wisconsin; HealthEmotion Research Institute, University of Wisconsin, Madison, Wisconsin.
Insights
Anxious temperament is linked to uncinate fasciculus (UF) microstructure changes in male monkeys, suggesting a conserved, sex-specific neural basis for anxiety. Environmental factors significantly influence UF microstructure, not just heritability.
Area of Science:
- Neuroscience
- Behavioral Genetics
- Developmental Psychology
Background:
- Anxious temperament (AT) is a heritable trait linked to anxiety and depressive disorders.
- Previous research identified alterations in the uncinate fasciculus (UF) in boys with anxiety disorders.
- The UF connects prefrontal and limbic regions, crucial for emotional regulation.
Purpose of the Study:
- To investigate the evolutionary conservation of sex-specific UF microstructure alterations in a nonhuman primate model of AT.
- To determine the contribution of heritable versus environmental factors to UF microstructure variation.
Main Methods:
- Diffusion tensor imaging (DTI) was used to assess UF microstructure (fractional anisotropy) in 581 young rhesus monkeys.
- Tract-based analyses examined the relationship between AT, UF microstructure, and sex.
- Oligogenic linkage analysis was employed to determine the heritability of UF microstructure.
Main Results:
- A significant negative correlation was found between AT and UF fractional anisotropy in male monkeys, but not in females (AT × sex interaction; p = .032).
- Heritability analyses indicated that variation in UF fractional anisotropy was primarily influenced by nonheritable (environmental) factors (h² = 0.185, p = .077).
Conclusions:
- The study demonstrates a conserved, male-specific association between UF microstructure and anxious temperament across species.
- Findings suggest environmental influences play a critical role in shaping UF microstructure, potentially mediating anxiety development.
- These results support the use of nonhuman primates as a translational model for understanding anxiety disorders and developing targeted treatments.
Background:
Anxious temperament (AT) is an early-life heritable trait that predisposes individuals to develop anxiety and depressive disorders. Our previous work in preadolescent children suggests alterations in the uncinate fasciculus (UF), the white matter tract that connects prefrontal with limbic regions, in boys with anxiety disorders. Here, using a nonhuman primate model of AT, we tested whether this sexually dimorphic finding is evolutionarily conserved and examined the extent to which heritable and environmental influences contribute to UF microstructure.
Methods:
Diffusion tensor images were collected in 581 young rhesus monkeys (1.89 ± 0.77 years old; 43.9% female). Using tract-based analyses, we assessed the relationship among AT, UF microstructure (as measured with fractional anisotropy), and sex. Heritability of tract microstructure was determined using oligogenic linkage analysis of this large multigenerational pedigree.
Results:
We predicted and found a negative relation between AT and UF fractional anisotropy in male but not female monkeys (AT × sex; p = .032, 1-tailed). Additionally, heritability analyses revealed that variation in UF fractional anisotropy was largely due to nonheritable factors (h2 = 0.185, p = .077).
Conclusions:
These results demonstrate a cross-species, male-specific relation between UF microstructure and anxiety and provide a potential substrate for anxiety-related prefrontal-limbic dysregulation. The heritability analyses point to the importance of environmental influences on UF microstructure, which could be important in mediating the nonheritable components of pathological anxiety. These findings have the potential to guide new treatment strategies for childhood anxiety disorders and further support the use of nonhuman primates as a translational model to discover mechanisms underlying the development of anxiety.
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