Sensory and Motor Peripheral Nerve Function and Incident Mobility Disability

  • Rachel E. Ward
    Spaulding Rehabilitation Hospital Cambridge Massachusetts
  • Robert M. Boudreau
    Department of Epidemiology Graduate School of Public Health, University of Pittsburgh Pittsburgh Pennsylvania
  • Paolo Caserotti
    Institute of Sports Science and Clinical Biomechanics University of Southern Denmark Odense Denmark
  • Tamara B. Harris
    Laboratory of Epidemiology, Biometry, and Demography National Institute on Aging National Institutes of Health Bethesda Maryland
  • Sasa Zivkovic
    Department of Neurology School of Medicine University of Pittsburgh Pittsburgh Pennsylvania
  • Bret H. Goodpaster
    Department of Medicine School of Medicine University of Pittsburgh Pittsburgh Pennsylvania
  • Suzanne Satterfield
    Department of Preventive Medicine University of Tennessee Memphis Tennessee
  • Stephen B. Kritchevsky
    Division of Gerontology and Geriatric Medicine Department of Internal Medicine School of Medicine, Wake Forest Winston‐Salem North Carolina
  • Ann V. Schwartz
    Department of Epidemiology and Biostatistics University of California at San Francisco San Francisco California
  • Aaron I. Vinik
    Department of Neurobiology Eastern Virginia Medical School Norfolk Virginia
  • Jane A. Cauley
    Department of Epidemiology Graduate School of Public Health, University of Pittsburgh Pittsburgh Pennsylvania
  • Eleanor M. Simonsick
    Translational Gerontology Branch National Institute on Aging National Institutes of Health Baltimore Maryland
  • Anne B. Newman
    Department of Epidemiology Graduate School of Public Health, University of Pittsburgh Pittsburgh Pennsylvania
  • Elsa S. Strotmeyer
    Department of Epidemiology Graduate School of Public Health, University of Pittsburgh Pittsburgh Pennsylvania

説明

<jats:sec><jats:title>Objectives</jats:title><jats:p>To assess the relationship between sensorimotor nerve function and incident mobility disability over 10 years.</jats:p></jats:sec><jats:sec><jats:title>Design</jats:title><jats:p>Prospective cohort study with longitudinal analysis.</jats:p></jats:sec><jats:sec><jats:title>Setting</jats:title><jats:p>Two <jats:styled-content style="fixed-case">U</jats:styled-content>.<jats:styled-content style="fixed-case">S</jats:styled-content>. clinical sites.</jats:p></jats:sec><jats:sec><jats:title>Participants</jats:title><jats:p>Population‐based sample of community‐dwelling older adults with no mobility disability at 2000/01 examination (N = 1,680; mean age ± <jats:styled-content style="fixed-case">SD</jats:styled-content> 76.5 ± 2.9, body mass index 27.1 ± 4.6; 50.2% female, 36.6% black, 10.7% with diabetes mellitus).</jats:p></jats:sec><jats:sec><jats:title>Measurements</jats:title><jats:p>Motor nerve conduction amplitude (poor <1 <jats:styled-content style="fixed-case">mV</jats:styled-content>) and velocity (poor <40 m/s) were measured on the deep peroneal nerve. Sensory nerve function was measured using 10‐ and 1.4‐g monofilaments and vibration detection threshold at the toe. Lower extremity symptoms included numbness or tingling and aching or burning pain. Incident mobility disability assessed semiannually over 8.5 years (interquartile range 4.5–9.6 years) was defined as two consecutive self‐reports of a lot of difficulty or inability to walk one‐quarter of a mile or climb 10 steps.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Nerve impairments were detected in 55% of participants, and 30% developed mobility disability. Worse motor amplitude (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 1.29 per <jats:styled-content style="fixed-case">SD</jats:styled-content>, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.16–1.44), vibration detection threshold (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 1.13 per <jats:styled-content style="fixed-case">SD</jats:styled-content>, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.04–1.23), symptoms (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 1.65, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.26–2.17), two motor impairments (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 2.10, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.43–3.09), two sensory impairments (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 1.91, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.37–2.68), and three or more nerve impairments (<jats:styled-content style="fixed-case">HR</jats:styled-content> = 2.33, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> = 1.54–3.53) predicted incident mobility disability after adjustment. Quadriceps strength mediated relationships between certain nerve impairments and mobility disability, although most remained significant.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Poor sensorimotor nerve function independently predicted mobility disability. Future work should investigate modifiable risk factors and interventions such as strength training for preventing disability and improving function in older adults with poor nerve function.</jats:p></jats:sec>

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