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Abstract Details

Structural Evolution of the Frontal Aslant Tract: Implications for Primate Vocalization and Human Speech
Aging, Dementia, and Behavioral Neurology
P3 - Poster Session 3 (5:00 PM-6:00 PM)
12-002

By investigating the frontal aslant tract (FAT) and its extended networks across non-human and human primates, we aim to establish how the possible inter-species variances may explain the emergence of human speech, and in turn to predict specific language deficits following lesions/degeneration in different FAT portions. 

Vocalization and speech rely on dorsomedial and ventrolateral frontal regions connected by the FAT. The involvement of the FAT in different aspects of speech is not completely understood.

We used spherical deconvolution tractography to dissect the FAT, its subsegments and its extended networks in 9 monkeys, 43 chimpanzees and 43 humans. We also dissect the dorsomedial/limbic (cingulum) and ventrolateral/auditory (arcuate fasciculus) FAT extended networks and compared the volumes of those tracts among the three species. We then correlated FAT subsegments degeneration and different language deficits in 98 PPA patients.

The FAT is different among the three species (W=88.7; p<0.001), enlarged in humans compared to non-human primates. Differences among the three species are present for both posterior (W=116.2; p<0.001) and anterior (W=479.5; p<0.001) FAT segments. The posterior FAT is reduced in chimpanzees and humans compared to monkeys, whereas the anterior FAT is enlarged in chimpanzees and even more so in humans.
In PPA, we found a posterior-to-anterior gradient for verbal fluency (Words Per Minute-WPM) and syntax (Northwestern Anagram Test-NAT). WPM showed a progressively weaker correlation from the posterior (r=0.397; p<0.001) to the anterior FAT (r=0.042; p=0.707). Conversely, NAT showed stronger correlation from the posterior (r=0.177; p=0.104) to the anterior FAT (r=0.318; p=0.004).

Unique aspects of human speech, including syntax, evolved from exaptation/remodeling of the FAT and its ventrolateral extended network. We can predict a spectrum of aphasia syndromes resulting from lesions in the motor FAT/FAT opercularis (aphemia spectrum); in the FAT opercularis/triangularis (posterior transcortical motor aphasia); in the FAT triangularis/orbitalis (agrammatic-anterior transcortical motor aphasia).

Authors/Disclosures
Salvatore Citro, MD
PRESENTER
Dr. Citro has nothing to disclose.
Matthew S. Dawson, PhD Dr. Dawson has nothing to disclose.
Ahmad Beyh, PhD Dr. Beyh has nothing to disclose.
Flavio DellAcqua, PhD Dr. DellAcqua has received personal compensation in the range of $0-$499 for serving as a Consultant for Nordic Imaging Lab. The institution of Dr. DellAcqua has received research support from ACimmune. Dr. DellAcqua has received intellectual property interests from a discovery or technology relating to health care. Dr. DellAcqua has received publishing royalties from a publication relating to health care.
Carlo Cavaliere, MD, PhD Dr. Cavaliere has nothing to disclose.
Tim Dyrby Prof. Dyrby has nothing to disclose.
Kristine Krug, DPhil The institution of Prof. Krug has received research support from Deutsche Forschungsgemeinschaft. The institution of Prof. Krug has received research support from Leibniz Foundation. The institution of Prof. Krug has received research support from German Federal Ministry of Research, Technology & Space.
Maurice PTITO, PhD Prof. PTITO has nothing to disclose.
Lorenzo Carnevale, PhD Prof. Carnevale has nothing to disclose.
Sergio Della Sala, MD, PhD Prof. Della Sala has nothing to disclose.
William Hopkins, PhD The institution of Dr. Hopkins has received research support from NIH.
M. M. Mesulam, MD, FAAN (Cogn Neur & Alzheimer Center, NW Univ) Dr. Mesulam has received publishing royalties from a publication relating to health care.
Marco Catani, MD, PhD Prof. Catani has received personal compensation in the range of $0-$499 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Elsevier.