TY - JOUR
T1 - Autonomic response to walk tests is useful for assessing outcome measures in people with multiple sclerosis
AU - Kontaxis, Spyridon
AU - Laporta, Estela
AU - Garcia, Esther
AU - Guerrero, Ana Isabel
AU - Zabalza, Ana
AU - Matteo, Martinis
AU - Lucia, Roselli
AU - Simblett, Sara
AU - Weyer, Janice
AU - Hotopf, Matthew
AU - Narayan, Vaibhav A
AU - Rashid, Zulqarnain
AU - Folarin, Amos A
AU - Dobson, Richard J B
AU - Buron, Mathias Due
AU - Leocani, Letizia
AU - Cummins, Nicholas
AU - Vairavan, Srinivasan
AU - Costa, Gloria Dalla
AU - Magyari, Melinda
AU - Sørensen, Per Soelberg
AU - Nos, Carlos
AU - Bailón, Raquel
AU - Comi, Giancarlo
AU - The Radar-Cns Consortium, null
N1 - Copyright © 2023 Kontaxis, Laporta, Garcia, Guerrero, Zabalza, Matteo, Lucia, Simblett, Weyer, Hotopf, Narayan, Rashid, Folarin, Dobson, Buron, Leocani, Cummins, Vairavan, Costa, Magyari, Sørensen, Nos, Bailón, Comi and the RADAR-CNS Consortium.
Funding Information:
The RADAR-CNS project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 115902. This Joint Undertaking receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA (www.imi.europa.eu). This communication reflects the views of the RADAR-CNS Consortium and neither IMI nor the European Union and EFPIA are liable for any use that may be made of the information contained herein. Morover, the work was supported by the Grant TED2021-131106B-I00 funded by MCIN/AEI/ 10.13039/501100011033 and by the “European Union NextGenerationEU/PRTR”.
Funding Information:
The RADAR-CNS project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 115902. This Joint Undertaking receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA ( www.imi.europa.eu ). This communication reflects the views of the RADAR-CNS Consortium and neither IMI nor the European Union and EFPIA are liable for any use that may be made of the information contained herein. Morover, the work was supported by the Grant TED2021-131106B-I00 funded by MCIN/AEI/ 10.13039/501100011033 and by the “European Union NextGenerationEU/PRTR”.
Publisher Copyright:
Copyright © 2023 Kontaxis, Laporta, Garcia, Guerrero, Zabalza, Matteo, Lucia, Simblett, Weyer, Hotopf, Narayan, Rashid, Folarin, Dobson, Buron, Leocani, Cummins, Vairavan, Costa, Magyari, Sørensen, Nos, Bailón, Comi and the RADAR-CNS Consortium.
PY - 2023
Y1 - 2023
N2 -
Objective: The aim of this study was to evaluate the association between changes in the autonomic control of cardiorespiratory system induced by walk tests and outcome measures in people with Multiple Sclerosis (pwMS).
Methods: Electrocardiogram (ECG) recordings of 148 people with Relapsing-Remitting MS (RRMS) and 58 with Secondary Progressive MS (SPMS) were acquired using a wearable device before, during, and after walk test performance from a total of 386 periodical clinical visits. A subset of 90 participants repeated a walk test at home. Various MS-related symptoms, including fatigue, disability, and walking capacity were evaluated at each clinical visit, while heart rate variability (HRV) and ECG-derived respiration (EDR) were analyzed to assess autonomic nervous system (ANS) function. Statistical tests were conducted to assess differences in ANS control between pwMS grouped based on the phenotype or the severity of MS-related symptoms. Furthermore, correlation coefficients (
r) were calculated to assess the association between the most significant ANS parameters and MS-outcome measures.
Results: People with SPMS, compared to RRMS, reached higher mean heart rate (HRM) values during walk test, and larger sympathovagal balance after test performance. Furthermore, pwMS who were able to adjust their HRM and ventilatory values, such as respiratory rate and standard deviation of the ECG-derived respiration, were associated with better clinical outcomes. Correlation analyses showed weak associations between ANS parameters and clinical outcomes when the Multiple Sclerosis phenotype is not taken into account. Blunted autonomic response, in particular HRM reactivity, was related with worse walking capacity, yielding
r = 0.36
r = 0.29 (RRMS) and
r > 0.5 (SPMS). A positive strong correlation
r > 0.7
r > 0.65 between cardiorespiratory parameters derived at hospital and at home was also found.
Conclusion: Autonomic function, as measured by HRV, differs according to MS phenotype. Autonomic response to walk tests may be useful for assessing clinical outcomes, mainly in the progressive stage of MS. Participants with larger changes in HRM are able to walk longer distance, while reduced ventilatory function during and after walk test performance is associated with higher fatigue and disability severity scores. Monitoring of disorder severity could also be feasible using ECG-derived cardiac and respiratory parameters recorded with a wearable device at home.
AB -
Objective: The aim of this study was to evaluate the association between changes in the autonomic control of cardiorespiratory system induced by walk tests and outcome measures in people with Multiple Sclerosis (pwMS).
Methods: Electrocardiogram (ECG) recordings of 148 people with Relapsing-Remitting MS (RRMS) and 58 with Secondary Progressive MS (SPMS) were acquired using a wearable device before, during, and after walk test performance from a total of 386 periodical clinical visits. A subset of 90 participants repeated a walk test at home. Various MS-related symptoms, including fatigue, disability, and walking capacity were evaluated at each clinical visit, while heart rate variability (HRV) and ECG-derived respiration (EDR) were analyzed to assess autonomic nervous system (ANS) function. Statistical tests were conducted to assess differences in ANS control between pwMS grouped based on the phenotype or the severity of MS-related symptoms. Furthermore, correlation coefficients (
r) were calculated to assess the association between the most significant ANS parameters and MS-outcome measures.
Results: People with SPMS, compared to RRMS, reached higher mean heart rate (HRM) values during walk test, and larger sympathovagal balance after test performance. Furthermore, pwMS who were able to adjust their HRM and ventilatory values, such as respiratory rate and standard deviation of the ECG-derived respiration, were associated with better clinical outcomes. Correlation analyses showed weak associations between ANS parameters and clinical outcomes when the Multiple Sclerosis phenotype is not taken into account. Blunted autonomic response, in particular HRM reactivity, was related with worse walking capacity, yielding
r = 0.36
r = 0.29 (RRMS) and
r > 0.5 (SPMS). A positive strong correlation
r > 0.7
r > 0.65 between cardiorespiratory parameters derived at hospital and at home was also found.
Conclusion: Autonomic function, as measured by HRV, differs according to MS phenotype. Autonomic response to walk tests may be useful for assessing clinical outcomes, mainly in the progressive stage of MS. Participants with larger changes in HRM are able to walk longer distance, while reduced ventilatory function during and after walk test performance is associated with higher fatigue and disability severity scores. Monitoring of disorder severity could also be feasible using ECG-derived cardiac and respiratory parameters recorded with a wearable device at home.
UR - http://www.scopus.com/inward/record.url?scp=85153848974&partnerID=8YFLogxK
U2 - 10.3389/fphys.2023.1145818
DO - 10.3389/fphys.2023.1145818
M3 - Article
C2 - 37089424
SN - 1664-042X
VL - 14
SP - 1145818
JO - Frontiers in Physiology
JF - Frontiers in Physiology
M1 - 1145818
ER -