Validity and reliability of VO2-max measurements in persons with multiple sclerosis
Introduction
Multiple sclerosis (MS) is an immune-mediated chronic inflammatory and neurodegenerative disorder of the central nervous system (CNS) with an elusive etiology [1], [2]. The progressively disabling nature of the disease manifests as sensory, motor, cerebellar, and cognitive dysfunctions that may limit physical activity in persons with MS (PwMS) with subsequent deconditioning [3]. The cardiorespiratory fitness is regarded as a crucial health indicator for PwMS, since a good physical fitness is associated with a lower mortality [4]. Direct measurement of the whole body maximal oxygen consumption during incremental exercise to exhaustion (VO2-max test) is considered the gold standard when assessing cardiorespiratory fitness [5]. The VO2-max is both an important health [6], [7] and performance [8] marker. Moreover, higher VO2-max is associated with better walking performance [9], improved cognitive processing speed [10], and a possible prophylactic influence on the structural decline of brain tissue in PwMS [11], while an impaired VO2-max is related to functional limitations that may hinder independent living in healthy populations [12].
VO2-max is measured directly by respiratory gas exchange measurements during incremental exercise. Several criteria have been proposed that should be attained before a measurement is regarded as valid [13], [14]. The primary validity criterion describes a plateau in oxygen uptake despite an increase in work rate, while the secondary criteria include: 1) an elevated respiratory exchange ratio (RER) above 1.15; 2) achievement of a fixed percentage of the age-predicted maximal heart rate (HR-max); 3) a high level of lactic acid in the blood in the minutes following the exercise test; and 4) subjective ratings of perceived exertion (RPE) indicating exhaustion [13], [14]. However, no study has yet assessed if all of these criteria are achieved in PwMS following a VO2-max test. This is a problem since obtaining an accurate and valid VO2-max value is of importance when evaluating patients' health and performance status in clinical practice and research [15]. Recent findings have questioned the ability of healthy populations to attain the commonly used primary validity criterion, by reporting that only 37–59% were able to do this [16], [17]. Consequently, it is possible that PwMS will not be able to attain the plateau criterion, but may be able to attain the secondary criteria.
Another important property of a test is the reliability of the test. In healthy people studies have shown a high test–retest reliability of the VO2-max test [18], [19], [20], [21]. However, day-to-day variation of VO2-max measurements has not yet been evaluated in PwMS.
Consequently, the objectives of the present study were: 1) to investigate the validity of the VO2-max test in ambulatory PwMS by evaluating primary and secondary criteria attainment and 2) to investigate the test–retest (day-to-day) reliability of the VO2-max test in PwMS. In addition the criteria attainment and the VO2-max measurements were analyzed in MS subgroups based on disability level, and were compared to those of healthy age-matched controls from our lab database.
It was hypothesized: 1) that most PwMS would not attain the primary VO2-max criterion but to a higher degree would be able to meet the secondary criteria, and 2) that the VO2-max test would show a low day-to-day variation in PwMS.
Section snippets
Study design
All PwMS completed two identical test sessions consisting of an incremental test of VO2-max. The second test session, which was used to examine test–retest variation, was performed within 2–8 days of the first session to ensure that no significant training adaptions would occur between sessions and at the same time allow full recovery between test sessions. Data from the present study in PwMS were gender and age matched with normative data from our lab-database, which covers data from n = 60
Demographics
Characteristics of the total sample and subgroups are reported in Table 1. There was no significant difference in age, height, sex, weight, body-mass-index (BMI), and fat percentage between the MS group and the CON group. Also, there was no significant difference in age, height, sex, weight, BMI, and fat percentage between the corresponding subgroups (MS1 vs. CON1 and MS2 vs. CON2). A significant difference in age and disease duration was observed between the mild (MS1) and moderate (MS2) MS
Discussion
This is the first study to investigate the validity and reliability of the VO2-max test in mild to moderately impaired PwMS. The present study demonstrates that only 40% of the PwMS were able to achieve the plateau criterion, which is regarded as the primary validity criterion for the VO2-max test. However, 65–95% of PwMS were able to achieve the secondary criteria age-predicted HR-max, RER ≥ 1.15, lactate > 8.0 mmol/L or RPE ≥ 17. No apparent effect of disability level on criteria achievement was
Limitations
The present study (and the VO2-max test) has several limitations. First, all of the traditional VO2-max criteria have individual limitations and there seems to be no consensus on the number of criteria that needs to be met, or how many criteria that should be applied to confirm the validity of the VO2-max test [27]. Second, post exercise lactate and RPE values were unfortunately not available for the matched healthy control subjects in this study, which weaken the conclusions regarding validity
Conclusion
In mild to moderately impaired PwMS less than half achieve the primary validity criterion when performing a VO2-max test. However, a high reliability and a better achievement of the secondary criteria imply that a valid VO2-max test can be performed, and the test validity was further shown to be comparable to that of healthy controls. The day-to-day variation implies that a change of more than 10% is required to be interpreted as a real change.
Disclosures
Ulrik Dalgas has received research support, travel grants and/or teaching honoraria from Biogen Idec, Merck Serono, Novartis and Sanofi Aventis and further serves as a principal investigator for an ongoing Biogen-sponsored study (ACTIMS). None of the other authors have any disclosures.
Funding
The present study was not based on any external funding.
Acknowledgments
The authors wish to thank Vivi Brandt and Thor Petersen, from the MS Clinic at Aarhus University Hospital, for skillful help with recruitment and handling of patients as well as handling of logistic matters.
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Cited by (0)
- 1
Martin Langeskov: Study conception and design, study coordination, data collection, data analysis, statistical analysis and manuscript writing.
- 2
Daniel Langeskov: Data analysis, statistical analysis and manuscript writing.
- 3
Kristian Overgaard: Study conception and design, data analysis and manuscript writing.
- 4
Andreas Møller: Study conception and design, and manuscript writing.
- 5
Ulrik Dalgas: Study conception and design, study coordination, data analysis, statistical analysis and manuscript writing.