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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Independent Associations of Stroke and Sarcopenia-Related Phenotype with Lower-Limb Strength and Gait: A 1:2 Matched Cohort Analysis

  1. 1Neuromuscular Control Laboratory, School of Kinesiology, Yeungnam University, Gyeongsan 38541, Gyeongbuk, Republic of Korea
  2. 2Research Institute of Human Ecology, Yeungnam University, Gyeongsan 38541, Gyeongbuk, Republic of Korea

Abstract

Background/Objectives: Whether stroke and sarcopenia relate to the same components of lower-limb function is unclear. We estimated each exposure’s mutually adjusted association with strength, gait performance, and gait variability, and their interaction. Methods: Thirty-three stroke survivors were matched 1:2 to 66 controls (n = 99) and classified into operational sarcopenia-related phenotype groups by AWGS 2019 muscle-mass and gait-speed cut-offs, not diagnoses. Strength, spatiotemporal gait, and gait variability were analysed in rank-based additive MANCOVAs (Pillai’s trace; permutation within matched sets; Holm correction across domains). Further runs added gait speed, removed the phenotype, added weight, or substituted ASM/Ht2. Results: Stroke was associated with strength (Pillai’s V = 0.240, Holm p = 0.003) and gait variability (V = 0.096, Holm p = 0.044; not significant after adjustment for weight), but not with gait performance (Holm p = 0.133) unless the phenotype was removed (V = 0.194, Holm p < 0.001). The phenotype was associated with all three domains (Holm p ≤ 0.008) through its slow-gait group; the low-ASM group and ASM/Ht2 showed no associations. At a given gait speed, neither exposure was associated with gait (Holm p ≥ 0.247). Several judgements varied across matched datasets. Conclusions: In this cohort, lower-limb function followed strength and walking performance more closely than muscle mass. The stroke association with strength held across matched datasets and limb rules, and neither exposure’s gait association was detectable at a given walking speed. No interaction was detected, and the estimates are imprecise, particularly for strength. These are conditional cross-sectional associations.

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BibTeX
@article{shin2026independent,
  title = {{Independent Associations of Stroke and Sarcopenia-Related Phenotype with Lower-Limb Strength and Gait: A 1:2 Matched Cohort Analysis}},
  author = {Sunghoon Shin and Yungon Lee},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = oct,
  doi = {10.3390/jcm15207779},
  url = {https://www.mdpi.com/2077-0383/15/20/7779},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Independent Associations of Stroke and Sarcopenia-Related Phenotype with Lower-Limb Strength and Gait: A 1:2 Matched Cohort Analysis
AU  - Sunghoon Shin
AU  - Yungon Lee
PY  - 2026
DA  - 2026/10/09
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15207779
UR  - https://www.mdpi.com/2077-0383/15/20/7779
AB  - Background/Objectives: Whether stroke and sarcopenia relate to the same components of lower-limb function is unclear. We estimated each exposure’s mutually adjusted association with strength, gait performance, and gait variability, and their interaction. Methods: Thirty-three stroke survivors were matched 1:2 to 66 controls (n = 99) and classified into operational sarcopenia-related phenotype groups by AWGS 2019 muscle-mass and gait-speed cut-offs, not diagnoses. Strength, spatiotemporal gait, and gait variability were analysed in rank-based additive MANCOVAs (Pillai’s trace; permutation within matched sets; Holm correction across domains). Further runs added gait speed, removed the phenotype, added weight, or substituted ASM/Ht2. Results: Stroke was associated with strength (Pillai’s V = 0.240, Holm p = 0.003) and gait variability (V = 0.096, Holm p = 0.044; not significant after adjustment for weight), but not with gait performance (Holm p = 0.133) unless the phenotype was removed (V = 0.194, Holm p < 0.001). The phenotype was associated with all three domains (Holm p ≤ 0.008) through its slow-gait group; the low-ASM group and ASM/Ht2 showed no associations. At a given gait speed, neither exposure was associated with gait (Holm p ≥ 0.247). Several judgements varied across matched datasets. Conclusions: In this cohort, lower-limb function followed strength and walking performance more closely than muscle mass. The stroke association with strength held across matched datasets and limb rules, and neither exposure’s gait association was detectable at a given walking speed. No interaction was detected, and the estimates are imprecise, particularly for strength. These are conditional cross-sectional associations.
SN  - 2077-0383
ER  -