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. 2026 Jan 13;273(1):79.
doi: 10.1007/s00415-025-13543-w.

Preferential age-related striatal volume preservation in cervical dystonia

Affiliations

Preferential age-related striatal volume preservation in cervical dystonia

M Owusu-Ansah et al. J Neurol. .

Abstract

Background and purpose: Previous research has shown inconsistent striatal volumetric differences in isolated, idiopathic dystonia. In healthy populations, progressive striatal volume loss occurs with advancing age. We investigated age-related striatal volume in participants with adult-onset cervical dystonia (CD) and other isolated, idiopathic focal dystonias.

Methods: High-resolution structural MRI was analyzed in 184 participants (92 focal dystonia: 33 CD, 18 laryngeal, 18 blepharospasm, 10 embouchure, 13 upper-limb; 92 healthy controls). Subcortical volumes (caudate, putamen, hippocampus, amygdala, ventricles) were quantified using FreeSurfer, adjusted for intracranial volume. Linear regression examined age-volume relationships controlling for sex and motion.

Results: CD showed significantly different age-related striatal trajectories versus controls. Putamen [F(1117) = 10.82, p = 0.001, η2 = 0.043] and caudate [F(1117) = 5.17, p = 0.025, η2 = 0.027] demonstrated significant group × age interactions after FDR correction. CD exhibited volume increases with age (β = + 37.4 mm3/year) while controls showed typical decline (β = -38.2 mm3/year). This pattern was striatum-specific; hippocampus, amygdala, and ventricles showed similar age-related changes between groups (p > 0.8). Other dystonia subtypes demonstrated age-related decline similar to controls. Among dystonias, only CD showed preserved putamen [F(4,78) = 3.11, p = 0.020, η2 = 0.048] and caudate [F(4,78) = 3.59, p = 0.010, η2 = 0.080] volumes. Disease duration and severity did not correlate with striatal volumes.

Conclusions: Our findings reveal selective preservation of caudate and putamen volume with age that is unique to CD among focal dystonia subtypes. This neuroanatomical distinction suggests different adaptive or pathophysiological mechanisms underlying CD. These results contribute to the conceptualization of both common and heterogeneous neurobiological substrates across dystonia subtypes, highlighting the importance of subtype-specific research approaches to consider age.

Keywords: Aging; Caudate; Cervical dystonia; Neuroplasticity; Putamen; Structural MRI.

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Conflict of interest statement

Declarations. Conflict of interest: The authors declare no competing interests. Ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by the Human Research Protection Office at Washington University School of Medicine (HRPO#: 201603081, 201102481, 201508100 for dystonia participants; HRPO #: 201501149, 201512032, 201103106 for healthy controls). Consent to participation: Informed consent was obtained from all individual participants included in the study in accordance with the Declaration of Helsinki. NIH rights statement: This research was supported by the National Institutes of Health. The accepted manuscript will be submitted to PubMed Central and made publicly available immediately upon publication in accordance with NIH Public Access Policy.

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