Lumbopelvic Muscle Mechanical Properties in Women with Multiple Sclerosis: A Cross-Sectional Case-Controlled Study
2024

Muscle Properties in Women with Multiple Sclerosis

Sample size: 44 publication 10 minutes Evidence: moderate

Author Information

Author(s): Cruz-Medel Inés, Peña-Toledo María Ángeles, Alburquerque-Sendín Francisco, Rodrigues-de-Souza Daiana Priscila, Conde-Gavilán Cristina, Jover-Sánchez Ana María, Carmona-Medialdea Claudia, Agüera-Morales Eduardo

Primary Institution: Reina Sofia University Hospital, University of Cordoba, Spain

Hypothesis

Women with MS exhibit altered mechanical properties in both the pelvic floor muscles and lumbar muscles, including reduced strength, elasticity, and coordination, due to the neurological damage associated with MS.

Conclusion

Women with MS have lower muscle tone and stiffness and increased elasticity in pelvic floor muscles compared to women without MS.

Supporting Evidence

  • Women with MS showed significant differences in pelvic floor muscle properties compared to women without MS.
  • Altered muscle properties may contribute to symptoms like incontinence in women with MS.
  • Correlation patterns between muscle properties and clinical characteristics differed by group.

Takeaway

Women with multiple sclerosis have weaker pelvic floor muscles than women who don't have the disease, which can lead to problems like incontinence.

Methodology

This cross-sectional observational study included 22 women with MS and 22 age- and BMI-matched women without MS, assessing muscle properties using a MyotonPRO device.

Potential Biases

Selection bias and recall bias may affect the validity of the results.

Limitations

The sample size may affect the statistical power and generalizability of the findings, and the use of subjective questionnaires may introduce variability.

Participant Demographics

22 women with MS and 22 age- and BMI-matched women without MS.

Statistical Information

P-Value

0.006

Confidence Interval

95% CI [2.12, 4.41]

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.3390/biomedicines12122925

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