Scholarlink

Background <p>Tremor dominant Parkinson’s disease (TDPD) and postural instability and gait disturbance (PIGD) are clinically defined motor subtypes of PD with significant differences in clinical phenotype, prevalence of non-motor symptoms (NMS), rate of progression and underlying pathophysiology.</p> Objective <p>To evaluate white matter microstructural integrity in TDPD and PIGD motor subtypes of PD to ascertain subtype specific patterns of involvement.</p> Methods <p>Data was analysed for 162 subjects – TDPD (<i>n</i> = 74), PIGD (<i>n</i> = 54) and HC (<i>n</i> = 34) who were prospectively recruited. All subjects underwent detailed clinical assessment including the MDS-UPDRS, MDS-NMS, and motor subtyping was based on the ratio of mean TD/PIGD score (≥ 1.15:TD, ≤ 0.90: PIGD) from the MDS-UPDRS. 3T multi-shell diffusion weighted imaging data was acquired and processed. Diffusion metrics of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD) and radial diffusivity (RD) were considered for tract based spatial statistics and evaluation of whole tract measures.</p> Results <p>The PIGD group exhibited widespread reductions in FA and increases in MD, RD, and AD in motor, associative, and limbic tracts, consistent across voxel-wise and tract-level analyses. TDPD showed limited alterations. White matter changes in PIGD correlated with higher motor and non-motor symptom severity, particularly involving corticospinal, fronto-occipital, and cingulum tracts.</p> Conclusions <p>The PIGD variant of PD has significantly widespread alterations involving diffusion metrics of numerous dopaminergic and non-dopaminergic tracts involved in distinct motor and non-motor symptoms. These may be the basis for the phenotypic variations and differences in severity observed between these motor subtypes.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

White matter alterations in tremor-dominant and postural instability and gait disturbance subtypes of Parkinson’s disease

  • 期刊论文

  • 发表日期：

    2025年8月11日

查看全文
  • Shweta Prasad,
  • Tarunya Nagaraj,
  • Shubha GS Bhat,
  • Spurthi S Purushotham,
  • Ruchita Taneja,
  • Mahima Bhardwaj,
  • DK Samartha,
  • Shyam Sundar Aramugham,
  • Keshav J Kumar,
  • Pooja Mailankody,
  • Rohan R Mahale,
  • Vikram V Holla,
  • Nitish Kamble,
  • Ravi Yadav,
  • Jitender Saini,
  • Pramod Kumar Pal

摘要

Background

Tremor dominant Parkinson’s disease (TDPD) and postural instability and gait disturbance (PIGD) are clinically defined motor subtypes of PD with significant differences in clinical phenotype, prevalence of non-motor symptoms (NMS), rate of progression and underlying pathophysiology.

Objective

To evaluate white matter microstructural integrity in TDPD and PIGD motor subtypes of PD to ascertain subtype specific patterns of involvement.

Methods

Data was analysed for 162 subjects – TDPD (n = 74), PIGD (n = 54) and HC (n = 34) who were prospectively recruited. All subjects underwent detailed clinical assessment including the MDS-UPDRS, MDS-NMS, and motor subtyping was based on the ratio of mean TD/PIGD score (≥ 1.15:TD, ≤ 0.90: PIGD) from the MDS-UPDRS. 3T multi-shell diffusion weighted imaging data was acquired and processed. Diffusion metrics of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD) and radial diffusivity (RD) were considered for tract based spatial statistics and evaluation of whole tract measures.

Results

The PIGD group exhibited widespread reductions in FA and increases in MD, RD, and AD in motor, associative, and limbic tracts, consistent across voxel-wise and tract-level analyses. TDPD showed limited alterations. White matter changes in PIGD correlated with higher motor and non-motor symptom severity, particularly involving corticospinal, fronto-occipital, and cingulum tracts.

Conclusions

The PIGD variant of PD has significantly widespread alterations involving diffusion metrics of numerous dopaminergic and non-dopaminergic tracts involved in distinct motor and non-motor symptoms. These may be the basis for the phenotypic variations and differences in severity observed between these motor subtypes.