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Relationship Between Patient-Reported Outcomes and Clinical Outcomes in Patients With Morquio A Syndrome

Abstract

This cross-sectional analysis assessed the correlation between patient-reported outcomes (PROs) and clinical outcomes in 24 German patients with Morquio A. Clinical outcomes included 6-minute walk test (6MWT), 3-minute stair climb (3MSC) test, and joint range of motion as measures for endurance/mobility, forced vital capacity (FVC) and maximum voluntary ventilation (MVV) as measures for respiratory function, and height as an important manifestation. The PROs included the EuroQoL (EQ) 5D-5L (EQ5D-5L), to measure health-related QoL (HRQoL), and patients’ rating of their ability to walk, climb, or breathe. In adults, endurance and pulmonary function measures and height showed strong and statistically significant correlation with the patients’ EQ5D-5L (6MWT: R = .884, 3MSC test: R = .852, FVC: R = .815, MVV: R = .825, height: R = .842). The adult patients’ rating of their ability to walk and climb also correlated strongly with 6MWT (R = .839) and 3MSC test (R = .700) results. Improvements in these clinical outcomes may be robust surrogate parameters of a better EQ5D-5L/HRQoL in patients with Morquio A.

Keywords
Morquio A; mucopolysaccharidosis IV; patient-reported outcomes; quality of life; EQ5D-5L; patient’s perception; 6MWT; 3MSC test; FVC; maximal voluntary ventilation; mobility; physical endurance; respiratory function tests

Introduction

Morquio A syndrome, or mucopolysaccharidosis (MPS) IVA (Online Mendelian Inheritance in Man [OMIM] 253000), is a rare lysosomal storage disorder inherited in an autosomal recessive fashion. The disease is caused by a deficiency in the enzyme .-acetylgalactosamine-6-sulfatase (GALNS) leading to impaired degradation of the glycosaminoglycans (GAGs) chondroitin-6-sulfate (CS) and keratan sulfate (KS)11 Neufeld, EF, Muenzer, J. The mucopolysaccharidoses. In: Scriver, CR, Beaudet, AL, Sly, WS, Valle, D, eds. The Metabolic and Molecular Bases of Inherited Disease. 8 ed. New York: McGraw-Hill Medical Publishing Division; 2001:3421–3452. and disruption of the extracellular matrix function. Morquio A is a multisystemic disease including cardiopulmonary manifestations, severe skeletal abnormalities, and compressive myelopathy. The skeletal manifestations are due to excessive deposition of GAGs in cartilage and bone, resulting in stunted growth with short trunk and neck, genu valgum, hip dysplasia, joint hypermobility/laxity, spinal abnormalities, and pectus carinatum.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61.44 Montaño, AM, Tomatsu, S, Gottesman, GS, Smith, M, Orii, T. International Morquio A Registry: clinical manifestation and natural course of Morquio A disease. J Inherit Metab Dis. 2007;30 (2):165–174. Altogether, these manifestations result in impaired endurance, walking ability, and gait.33 Hendriksz, CJ, Al-Jawad, M, Berger, KI. Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA. J Inherit Metab Dis. 2013;36 (2):309–22. Therefore, many patients with Morquio A will sooner or later need walking aids or a wheelchair to assist with mobility.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61.,44 Montaño, AM, Tomatsu, S, Gottesman, GS, Smith, M, Orii, T. International Morquio A Registry: clinical manifestation and natural course of Morquio A disease. J Inherit Metab Dis. 2007;30 (2):165–174. This progressive nature and the involvement of multiple organs result in significantly impaired functional capacity, endurance, and quality of life (QoL) in these patients. Frequent infections, impaired vision or hearing, frequent surgeries, and (joint) pain and/or fatigue further compromise the patient’s QoL.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61.,44 Montaño, AM, Tomatsu, S, Gottesman, GS, Smith, M, Orii, T. International Morquio A Registry: clinical manifestation and natural course of Morquio A disease. J Inherit Metab Dis. 2007;30 (2):165–174.,55 Tomatsu, S, Montaño, AM, Oikawa, H. Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment. Curr Pharm Biotechnol. 2011;12 (6):931–945.

As endurance is a measure of the level of effort required to perform an activity, including functional reserves of the cardiovascular, pulmonary, and/or musculoskeletal systems,66 Mocellin, R . Exercise testing in children with congenital heart disease. Pediatrician. 1986;13 (1):18–25.,77 McArdle, WD, Katch, FI, Katch, VL. The Physiologic Support Systems. Essentials of Exercise Physiology, Third ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:290–431. it can be used to gauge functional capacity in disorders with multiple organ system involvement. The 6-minute walk test (6MWT) is a measure of endurance used in a variety of patient populations, including those with moderate to severe heart and lung diseases, neurological disease, musculoskeletal diseases, and other MPS disorders.88 McDonald, A., Steiner, R, Kuehl, K., Turbeville, S. Clinical utility of endurance measures for evaluation of treatment in patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). J Pediatr Rehabil Med. 2010;3 (2):119–127.

Industry, clinicians, and regulatory authorities increasingly recognize the role of patient-reported measures of health-related QoL (HRQoL) in the evaluation of new therapies and strategies.99 Deshpande, PR, Rajan, S, Sudeepthi, BL, Abdul Nazir, CP. Patient-reported outcomes: A new era in clinical research. Perspect Clin Res. 2011;2 (4):137–144.1111 Food and Drug Administration (2009). Guidance for industry: Patient-Reported Outcome Measures: Use in Medical Product Development to Support Labeling Claims. US: Food and Drug Administration. Strong correlations were found between endurance and pulmonary function measures and the patients’ HRQoL in different disease areas such as cardiovascular,1212 Santos, JJAD, Plewka, JEA, Brofman, PRS. Quality of life and clinical indicators in heart failure: a multivariate analysis. Arq Bras Cardiol. 2009;93 (2):149–156. pulmonary,1313 Saad, IAB., Botega, NJ., Toro, IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J. 2007;125 (1):46–49. and musculoskeletal diseases.1414 Henricson, E, Abresch, R, Han, JJ. The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: longitudinal comparisons and clinically-meaningful changes over one year. PLoS Curr. 2013;5. This suggests that better clinical outcomes will possibly lead to corresponding better results in the patient’s HRQoL.

There are currently limited data on how Morquio A affects a patient’s HRQoL. One recent study, the patient-reported outcomes (PRO) survey, evaluated the global burden of disease among patients with Morquio A, underscoring mobility (not becoming fully dependent on a wheelchair) as the most important determinant for HRQoL.1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32. However, as far as we are aware, no studies have formally assessed the relationship between PRO and clinical outcomes in patients with Morquio A. The aim of this study was therefore to determine the correlation between PRO and clinical outcomes in a German cohort. We also examined whether these relationships are consistent in children (<18 years) as well as in adult (≥18 years) patients with Morquio A.

Methods

Study Design and Patient Selection

This cross-sectional analysis included the German patients who participated in the global burden of disease PRO survey in patients with Morquio A as described earlier1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32.; as such the PRO data were obtained from the PRO survey database. The clinical outcomes data of these patients were obtained from the Mainz Clinical database and for some patients from the Morquio Clinical Assessment Program (MorCAP) natural history study database.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61. Only German patients were included in the analysis because only for these patients clinical outcomes data were available within a 6-month time window of the PRO survey.

The Morquio A burden of disease survey in Germany was a voluntary, single-assessment, cross-sectional, paper-based survey administered in person via trusted local clinicians. The study population consisted of patients with Morquio A having a confirmed diagnosis of MPS IVA, based on genetic testing or reduced GALNS activity. Eligible patients had to be ≥7 years of age (some exceptions were made due to the limited number of patients) and able to speak, write, and understand their language. Ethics approval was obtained and all patients (or their caregivers) signed an informed consent/ascent form. Additional details have been described previously.1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32.

Patient-Reported Outcomes

In the PRO survey, HRQoL was assessed using the General Health-Related Quality of Life EuroQoL(EQ) 5D-5L questionnaire.1616 EuroQol Group . EQ-5D-5L User Guide. Web site. http://www.euroqol.org/fileadmin/user_upload/Documenten/PDF/Folders_Flyers/UserGuide_EQ-5D-5.pdf> Accessed February 2014. EuroQol Group. EQ-5D-5L User Guide. Web site. <http://www.euroqol.org/about-eq-5d/valuation-of-eq-5d.html> Accessed February 2014.
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This is a generic standardized measure of health status developed by the EuroQoL group and applicable to a wide range of health conditions and therapies. It comprises 5 dimensions (5D), namely, mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 levels (5L) coded from 1 to 5, namely, no problems (1), slight problems (2), moderate problems (3), severe problems and unable to function (mobility, self-care, and usual activities; 4), or extreme problems (pain/discomfort and anxiety/depression; 5), generating a total of 3125 combinations representing different health states. These EQ5D-5L health states can be converted into a single summary index value (utility) by applying a formula that essentially attaches weights to each of the levels in each dimension. This formula is based on the valuation of EQ-5D health states from general population samples.1616 EuroQol Group . EQ-5D-5L User Guide. Web site. http://www.euroqol.org/fileadmin/user_upload/Documenten/PDF/Folders_Flyers/UserGuide_EQ-5D-5.pdf> Accessed February 2014. EuroQol Group. EQ-5D-5L User Guide. Web site. <http://www.euroqol.org/about-eq-5d/valuation-of-eq-5d.html> Accessed February 2014.
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An EQ5D-5L utility value of “1” represents perfect health; a value of “0” represents death. Subsequent normalization to a healthy population can provide negative values indicating that the patient is feeling worse than death.

Next to EQ5D-5L, PROs included the following anchor questions: patient’s perception of the ability/strength to walk and climb stairs and the ability to breathe. These anchor questions were developed in a patient focus group to assess the minimal important difference perceptible to patients in the 6MWT, 3-minute stair-climb (3MSC) test, and pulmonary function tests, respectively. The strength to walk (long distances) or to climb stairs was rated from 1 (no strength, unable to walk without mobility aids or paralyzed) to 5 (a great deal of strength) with 2 implying minimal strength, 3 moderate strength, and 4 a good deal of strength. The ability to breathe was rated from 1 (very low) to 5 (very high).

Clinical Outcomes

Endurance/mobility was evaluated using the 6MWT (ATS statement 2002) and the 3MSC test.1717 Harmatz, P, Ketteridge, D, Giugliani, R. Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase. Pediatrics. 2005;115 (6):e681–e689. Respiratory function was investigated by measuring forced vital capacity (FVC)1818 Miller, MR, Hankinson, J, Brusasco, V. Standardisation of spirometry. Eur Respir J. 2005;26 (2):319–338. and maximum voluntary ventilation (MVV)1818 Miller, MR, Hankinson, J, Brusasco, V. Standardisation of spirometry. Eur Respir J. 2005;26 (2):319–338. during spirometry. In addition, the following joint range of motion (ROM) tests were measured using a double-armed goniometer as described previously1919 Tylki-Szymanska, A, Marucha, J, Jurecka, A, Syczewska, M, Czartoryska, B. Efficacy of recombinant human a-L-iduronidase (laronidase) on restricted range of motion of upper extremities in mucopolysaccharidosis type I patients. J Inherit Metab Dis. 2010;33 (2):151–157.,2020 Gerhardt, JJ, Rondinelli, RD. Goniometric techniques for range-of-motion assessment. Phys Med Rehabil Clin N Am. 2001;12 (3):507–527.: hip extension, wrist extension, and shoulder flexion. Since the range of active shoulder flexion may be influenced by spinal retroflexion, the test was done in the thorax plane rather than in the vertical plane. Hip extension was scored against normal. Shoulder flexion and wrist extension were expressed as actual values.

Statistical Analysis

The correlation between the PRO data from the Morquio A global burden of disease survey and the clinical outcomes data from the Mainz Clinical or MorCAP natural history databases was assessed using analysis of variance regression analysis providing Pearson’s coefficients (R), slopes as well as coefficients of determination (adjusted R2). R values >.7 were considered to demonstrate strong correlation; P values <.05 were considered statistically significant. Clinical outcome data obtained outside a 6-month time window from the PRO data were ruled out for analysis.

Results

Patient Characteristics

The analysis involved 24 German patients with Morquio A (14 adults aged ≥18 years and 10 children aged 10-17 years). Demographics and clinical characteristics of the participants are shown in Table 1. In all patients, the height varied between 94 and 170 cm with a mean height of 121.3 cm (123.9 cm in adults and 117.9 cm in children). The EQ5D-5L utility score varied between −.205 and 1 in all patients with a mean utility score of .552 (.422 in adults and .763 in children). In all patients, the 6MWT distance ranged from 0 (not able to walk) to 531.7 m with a mean of 212.9 m (131.3 m in adults and 317.8 m in children). For the 3MSC test, the results varied between 0 (not able to climb stairs) and 206 stairs with a mean of 106.1 stairs (72.0 stairs in adults and 140.3 stairs in children). Regarding the pulmonary function parameters in all patients, the mean FVC was 1.9 L and the mean MVV was 46.6 L/min.

Table 1
Patient Demographics and Clinical Characteristics.

Correlation Between Endurance and Pulmonary Function Measures and Height With HRQoL/EQ5D-5L

Table 2 shows the correlation between endurance and pulmonary function measures and height with the EQ5D-5L utility score in all patients with Morquio A and split for adults and children.

Table 2
Pearson’s Correlation and Regression Analysis Between Endurance and Pulmonary Function Measures and Height and the Patient’s EQ5D-5L/Health-Related Quality of Life.

A strong and statistically significant correlation was found between the 2 endurance parameters and the EQ5D-5L utility score in all patients: R = .713 (P = .0019) and R = .693 (P = .0060) for the correlation with the 6MWT and 3MSC test, respectively. For FVC and MVV, a moderate but statistically significant correlation with the EQ5D-5L utility score was shown in all patients: R = .521 (P = .0155) and R = .534 (P = .0126), respectively.

Strongest (and statistically significant) correlations were observed in adult patients, whereas only poor correlations were observed in children (Table 2). In adult patients, the Pearson’s coefficient R between the endurance measures and the QoL utility score was .884 for the 6MWT (P = .0016; Supplementary Figure 1a) and .852 for the 3MSC test (P = .0149; Supplementary Figure 1b). For pulmonary function measures, the Pearson’s coefficient R was .815 for the FVC (P = .0007; Supplementary Figure 1c) and .825 for the MVV (. = .0005; Supplementary Figure 1d). Regression analysis indicated that the 6MWT was most closely associated with EQ5D-5L (Supplementary Figure 1a). An increase of 100 m in the 6MWT distance was associated with a .2 increase in the EQ5D-5L utility score. This is consistent with the highest correlation found between the 6MWT and EQ5D-5L score.

A moderate but statistically significant correlation was also observed between height and EQ5D-5L utility score in all patients: R = .477 (P = .0289). In line with the results for endurance and pulmonary function measures, the correlation was strong and statistically significant in adult patients and poor and non-statistically significant in children: R = .842 (P = .0003) and R = .124 (P = .7702), respectively (Table 2).

Table 3
Pearson’s Correlation and Regression Analysis Between Skeletal Flex Extensions and the Patient’s EQ5D-5L/Health-Related Quality of Life.

Correlation Between Skeletal Flex Extensions and HRQoL/EQ5D-5L

The correlation and regression between flex extension tests of different joints and the EQ5D-5L utility score were also determined (Table 3). In all patients with Morquio A, none of the flex extension tests correlated statistically significantly with the EQ5D-5L utility score. Moderate correlation (R = .511, P = .0895) was observed between the EQ5D-5L utility score and hip extension, whereas the correlation with wrist extension and shoulder flexion was poor: R = .011 and R = .182, respectively. The same pattern was shown in adult patients: poor and nonsignificant correlation between EQ5D-5L and wrist extension and shoulder flexion (R = .360 with P = .3812 and R = .348 with P = .4439, respectively), whereas hip extension correlated moderately but not statistically significantly with EQ5D-5L (R = .565 with P = .1866). In children, the correlation pattern was opposite. Wrist extension and shoulder flexion correlated strongly (though probably due to small sample size not significantly) with the EQ5D-5L utility score (R = .841 with P = .1589 and R = .943 with P = .0566, respectively). However, only poor correlation was shown between hip extension and the EQ5D-5L utility score (R = .123; Table 3).

Correlation Between Patient’s Perception and Endurance and Pulmonary Function Measures

Finally, the correlation and regression fit between the patient’s perception ratings to perform a specific task and the endurance (6MWT and 3MSC test; Figure 1) and pulmonary function (FVC and MVV; Supplementary Table 1) measures was determined.

Figure 1
Pearson’s correlation and regression analysis between endurance measures and the patient’s perception of the ability/strength to walk or climb stairs in patients with Morquio A. 6MWT versus ability/strength to walk in (A) all patients, (B) adults, and (C) children; 3MSC test versus ability/strength to climb stairs in (D) all patients, (E) adults, and (F) children. The solid lines represent predicted regression lines between the patient’s perception scores and endurance measures. Please note that data from all patients may not be visible due to overlap of some data points (eg, 4 adult patients with a 6MWTD of 0 m rated their ability/strength to walk as 1, that is, no strength/unable to walk without mobility aids or paralyzed). Abbreviations: 6MWT(D), 6-minute walk test (distance); 3MSC, 3-minute stair climb test; R, Pearson’s coefficient; Adjusted R2, coefficient of determination; ANOVA, analysis of variance. P value determined by ANOVA test. The patient’s perception was scored using values ranging from 1 to 5 with 1 = no strength (or unable to perform the task or paralyzed), 2 = minimal strength, 3 = moderate strength, 4 = a good deal of strength, and 5 = a great deal of strength.

In all patients with Morquio A, a strong and statistically significant correlation was observed between both the patient’s perception of their ability/strength to walk and the 6MWT (N = 17, R = .815, P = .00007; Figure 1A) and the patient’s perception of their ability/strength to climb stairs and the 3MSC test (N = 16, R = .688, P = .00324; Figure 1D). This was confirmed in adults and children. For the 6MWT results, the Pearson’s coefficient R was .839 and .641 for adults (Figure 1B) and children (Figure 1C), respectively. This was statistically significant in adults (P = .0047) and approached significance in children (P = .0867). For the 3MSC test results, the Pearson’s coefficient R was .700 and .784 for adults (Figure 1E) and children (Figure 1F), respectively. This was statistically significant (P = .0214) in children and approached significance in adults (P = .0534).

In contrast with the results for endurance measures, only a moderate to poor and non-significant correlation was found between the pulmonary function test (FVC and MVV) results and the patient’s perception of the ability to breathe (Supplementary Table 1). In all patients with Morquio A, Pearson’s coefficients were .318 and .164 for FVC and MVV, respectively. Similar results were obtained in both age subgroups.

In addition to the correlation, the regression fit analysis was assessed for the clinical outcomes and the patient’s perception (Figure 1 and Supplementary Table 1). Best fit result was observed between the 6MWT and the adults’ perception of walking ability, which is in line with the result in the previous section (6MWT vs EQ5D-5L; Figure 1B).

Discussion

In this article, we evaluated the relationship between PRO from the Morquio A PRO global burden of disease study1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32. and clinical outcomes from the Mainz Clinical database and the MorCAP database.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61. Mean values showed impaired endurance and pulmonary function, markedly below that documented for healthy participants.2121 Li, AM, Yin, J, Au, JT. Standard reference for the six-minute-walk test in healthy children aged 7 to 16 years. Am J Respir Crit Care Med. 2007;176 (2):174–180.2323 Web site. http://www.cdc.gov/niosh/topics/spirometry/refcalculator.html. Last updated: July 2010, last accessed: February 2015.
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R values >.7 and P values <.05 show that height as well as endurance (6MWT and 3MSC test) and pulmonary function measures (FVC and MVV) have excellent correlation with EQ5D-5L in Morquio A, mainly in adult patients. This indicates that better results in clinical outcomes such as height, the 6MWT, 3MSC test, FVC, and MVV are likely to be associated with better EQ5D-5L/HRQoL in the patient. Only poor correlation was observed in children. This might be explained by large differences in disease progression in these young patients resulting in a very heterogeneous group with varying results.

Reduced height is regarded as one of the phenotypical characteristics of Morquio A. This was confirmed by impaired mean values of 123.9 cm in adults and 117.9 cm in children aged 10 to 17 years observed in our German patients, which are in line with previously published data in these age categories.2424 Montaño, AM, Tomatsu, S, Brusius, A, Smith, M, Orii, T. Growth charts for patients affected with Morquio A disease. Am J Med Genet A. 2008;146A (10):1286–1295. However, a big variability in height range was observed up to a value of 170 cm in adults and 156 cm in a male child in the 15- to 17-year age category (which was still within the 97th centile of previously published growth charts for male patients with Morquio A2424 Montaño, AM, Tomatsu, S, Brusius, A, Smith, M, Orii, T. Growth charts for patients affected with Morquio A disease. Am J Med Genet A. 2008;146A (10):1286–1295.). This variability in height range can possibly be explained by heterogeneity in disease phenotype. Height is (sometimes) considered to be related to mortality, to the aggressiveness of the disease, and therefore a reduced HRQoL. Our analysis shows that height does indeed seem to be correlated with the EQ5D-5L/HRQoL.

The results from our analysis are in line with studies in other disease areas.1212 Santos, JJAD, Plewka, JEA, Brofman, PRS. Quality of life and clinical indicators in heart failure: a multivariate analysis. Arq Bras Cardiol. 2009;93 (2):149–156.,1313 Saad, IAB., Botega, NJ., Toro, IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J. 2007;125 (1):46–49.,1414 Henricson, E, Abresch, R, Han, JJ. The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: longitudinal comparisons and clinically-meaningful changes over one year. PLoS Curr. 2013;5.,2525 Brown, CD, Benditt, JO, Sciurba, FC. Exercise testing in severe emphysema: association with quality of life and lung function. COPD. 2008;5 (2):117–124.,2626 Han, B, Yan, B, Zhao, N. The influence of the functional capacity on subjective well-being and quality of life of patients with silicosis. Aging Ment Health. 2013;17 (6):707–713. In patients with heart failure, FVC and MVV were shown to be predictors for QoL.1212 Santos, JJAD, Plewka, JEA, Brofman, PRS. Quality of life and clinical indicators in heart failure: a multivariate analysis. Arq Bras Cardiol. 2009;93 (2):149–156. In patients with Duchenne muscular dystrophy, strong correlation was observed between the 6MWT and the Pediatric Outcomes Data Collection Instrument domain score for transfer and basic mobility (R = .79).1414 Henricson, E, Abresch, R, Han, JJ. The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: longitudinal comparisons and clinically-meaningful changes over one year. PLoS Curr. 2013;5. Likewise, QoL was correlated with the 6MWT in pulmonary disorders1313 Saad, IAB., Botega, NJ., Toro, IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J. 2007;125 (1):46–49.,2525 Brown, CD, Benditt, JO, Sciurba, FC. Exercise testing in severe emphysema: association with quality of life and lung function. COPD. 2008;5 (2):117–124.,2626 Han, B, Yan, B, Zhao, N. The influence of the functional capacity on subjective well-being and quality of life of patients with silicosis. Aging Ment Health. 2013;17 (6):707–713. and with FVC in patients who underwent a pulmonary resection due to lung cancer.1313 Saad, IAB., Botega, NJ., Toro, IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J. 2007;125 (1):46–49.

We also examined the correlation between the ROM of various joints (hip, wrist, and shoulder) and the patient’s EQ5D-5L. In all patients with Morquio A, none of the flex extension tests correlated strongly or statistically significantly with the patient’s EQ5D-5L. However, hip extension correlated moderately (R = .511) with EQ5D-5L (P = .0895). The same patterns were found in adult patients. In contrast, children showed stronger correlation between wrist extension and shoulder flexion and EQ5D-5L. This might be explained by the involvement of the hip joint in mobility, which is possibly of greater importance for adult patients. On the other hand activities that include wrist and shoulder movements, such as writing and playing, seem to be key determinants for children’s EQ5D-5L. Alternatively, this result could reflect the relevance of these joints in terms of being able to use mobility aids (such as crutches).

In addition to the correlation with the EQ5D-5L utility scores, we also evaluated the correlation between the clinical outcomes and the patient’s perception to perform a specific task (walk or climb stairs). In line with the results for EQ5D-5L, a good to strong correlation was also found between the 6MWT and 3MSC test results and the patients’ rating of their ability/strength to walk and climb stairs. This (statistically significant) result was observed in all patients with Morquio A (P = .00007 for 6MWT; P = .00324 for 3MSC test correlation) as well as in adults (P = .0047 for 6MWT; P = .0534 for 3MSC test correlation) and children (P = .0214 for 3MSC test; P = .0867 for 6MWT correlation) separately, indicating that gains in these endurance outcomes are perceptible for all patients and translate into increased mobility. It should be noted that the correlation with the 3MSC test in adults and with the 6MWT in children may not have reached statistical significance because of the small patient numbers involved in the age subgroup analyses. Although both adults and children displayed a strong correlation between the 3MSC test and the ability to climb stairs, this relationship was even more prominent in children. This might be explained by the fact that improvements in the 3MSC test might be smaller in adult patients, possibly due to progressive skeletal damage leading to difficulties in climbing stairs.22 Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61.,55 Tomatsu, S, Montaño, AM, Oikawa, H. Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment. Curr Pharm Biotechnol. 2011;12 (6):931–945. This is underscored by the difference in mean values between children and adults for the 3MSC test results. In adult patients with Morquio A, the mean number of stairs climbed during the 3MSC test was 72, whereas it was 140 stairs in children. Moreover, the mean EQ5D-5L utility scores/HRQoL were higher for children (.763) compared to adults (.422), which might be explained by a less advanced disease and less wheelchair use in children.1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32.

In contrast to the strong correlations between endurance measures and the perception of patients how well they could walk or climb stairs, patients seem to have difficulties in effectively rating their pulmonary function. The poor correlation between the patients’ rating of their ability to breathe and the MVV and FVC readings indicates that changes in pulmonary function might not be perceptible by patients with Morquio A. This is in line with other PRO studies showing poor ability of patients to rate their lung function capacity,2727 Heuker, D., Lengele, B., Delecluse, V. Subjective and objective assessment of quality of life after chest wall resection. Eur J Cardiothorac Surg. 2011;39 (1):102–108. underlining the importance of dyspnea rating scales in patients with impaired lung function.2828 Cazzola, M, MacNee, W, Martinez, FJ. Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J. 2008;31 (2):416–469. Correlation between pulmonary function measures and the self-rated breathing ability was also greater in children than in adults. Again, this might be explained by the more advanced disease stage in adult patients with Morquio A leading to increased difficulty in breathing.55 Tomatsu, S, Montaño, AM, Oikawa, H. Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment. Curr Pharm Biotechnol. 2011;12 (6):931–945. Possibly, this should also be regarded in the light of the limited number of patients and large standard deviation.

Overall, our results show strong correlations in adult patients with Morquio A for measures that reflect the patient’s endurance/mobility: the 6MWT and the 3MSC test versus EQ5D-5L and the patient’s rating of their ability/strength to walk and climb stairs. Also, hip extension showed a good correlation with EQ5D-5L. Altogether the strong correlation with these mobility measures further supports the importance of mobility for the patient’s EQ5D-5L/HRQoL. This is in line with recently published data by Hendriksz CJ et al, pinpointing mobility as the key determinant for HRQoL in patients with Morquio A.1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32. The authors showed that HRQoL reduces dramatically if patients become always wheelchair dependent and that even a slight increase in mobility (wheelchair use only when needed) greatly improves HRQoL. Therefore, increased mobility will likely translate into greater independence and would lead to less dependence on caregivers for care and support in undertaking activities of daily living.2929 Hendriksz, CJ, Lavery, C, Coker, M. The burden endured by caregivers of patients with morquio a syndrome: results from an international patient-reported outcomes survey. J Inborn Error Metab Screen. 2014;2:1–8. However, greater mobility might not necessarily translate into improved independence in children as most children are not considered independent and require caregivers regardless of mobility level.1515 Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32. This might explain why there was a poor correlation between the endurance measures and pulmonary function tests with EQ5D-5L in children with Morquio A. Furthermore, the heterogeneity in this group further complicates the analysis and interpretation of these results.

It should be taken into account that only a small number of patients were included in this study (inherent to the ultra-rare nature of this disease) and that information was missing for some patients. Moreover, longitudinal data from a larger, international patient group are essential to confirm the findings from this cross-sectional analysis and would be the goal of future studies and publications. Validation of these findings would strengthen the value of the impact of changes in these measures on the patient’s HRQoL.

Conclusion

Strong correlations were observed between HRQoL, as measured by the EQ5D-5L, with endurance and pulmonary function measures and height in patients with Morquio A, in particular in adult patients. Also, the patient’s perception of the ability to walk or climb stairs correlated very well with the 6MWT and 3MSC test, independent of age. Therefore, increases in endurance and pulmonary function measures and height are likely to be associated with perceptible gains in mobility and/or HRQoL in patients with Morquio A.

Acknowledgments

We acknowledge the participation of all study patients and their families and the German MPS Society. We would also like to thank the expert assistance of all study site coordinators and personnel, with special thanks to Jörg Reinke, Seyfullah Gökce, David Mangold, and Stefan Klein of the Villa Metabolica team. The authors are also grateful to Ismar Healthcare NV for their writing assistance (which was funded by BioMarin Europe Ltd.) and IMS Health Corp. for their assistance in performing the study (which was funded by BioMarin Europe Ltd.).

Funding

  • The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The performance of this analysis and writing assistance was funded by BioMarin Europe Ltd.

References

  • 1
    Neufeld, EF, Muenzer, J. The mucopolysaccharidoses. In: Scriver, CR, Beaudet, AL, Sly, WS, Valle, D, eds. The Metabolic and Molecular Bases of Inherited Disease. 8 ed. New York: McGraw-Hill Medical Publishing Division; 2001:3421–3452.
  • 2
    Harmatz, P, Mengel, KE, Giugliani, R. The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab. 2013;109 (1):54–61.
  • 3
    Hendriksz, CJ, Al-Jawad, M, Berger, KI. Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA. J Inherit Metab Dis. 2013;36 (2):309–22.
  • 4
    Montaño, AM, Tomatsu, S, Gottesman, GS, Smith, M, Orii, T. International Morquio A Registry: clinical manifestation and natural course of Morquio A disease. J Inherit Metab Dis. 2007;30 (2):165–174.
  • 5
    Tomatsu, S, Montaño, AM, Oikawa, H. Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment. Curr Pharm Biotechnol. 2011;12 (6):931–945.
  • 6
    Mocellin, R . Exercise testing in children with congenital heart disease. Pediatrician. 1986;13 (1):18–25.
  • 7
    McArdle, WD, Katch, FI, Katch, VL. The Physiologic Support Systems. Essentials of Exercise Physiology, Third ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:290–431.
  • 8
    McDonald, A., Steiner, R, Kuehl, K., Turbeville, S. Clinical utility of endurance measures for evaluation of treatment in patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). J Pediatr Rehabil Med. 2010;3 (2):119–127.
  • 9
    Deshpande, PR, Rajan, S, Sudeepthi, BL, Abdul Nazir, CP. Patient-reported outcomes: A new era in clinical research. Perspect Clin Res. 2011;2 (4):137–144.
  • 10
    Patrick, DL, Burke, LB, Powers, JH. Patient-reported outcomes to support medical product labeling claims: FDA perspective. Value Health. 2007;10 (suppl 2):S125–S137.
  • 11
    Food and Drug Administration (2009). Guidance for industry: Patient-Reported Outcome Measures: Use in Medical Product Development to Support Labeling Claims. US: Food and Drug Administration.
  • 12
    Santos, JJAD, Plewka, JEA, Brofman, PRS. Quality of life and clinical indicators in heart failure: a multivariate analysis. Arq Bras Cardiol. 2009;93 (2):149–156.
  • 13
    Saad, IAB., Botega, NJ., Toro, IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J. 2007;125 (1):46–49.
  • 14
    Henricson, E, Abresch, R, Han, JJ. The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: longitudinal comparisons and clinically-meaningful changes over one year. PLoS Curr. 2013;5.
  • 15
    Hendriksz, CJ, Lavery, C, Coker, M. Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey. Orphanet J Rare Dis. 2014;9:32.
  • 16
    EuroQol Group . EQ-5D-5L User Guide. Web site. http://www.euroqol.org/fileadmin/user_upload/Documenten/PDF/Folders_Flyers/UserGuide_EQ-5D-5.pdf> Accessed February 2014. EuroQol Group. EQ-5D-5L User Guide. Web site. <http://www.euroqol.org/about-eq-5d/valuation-of-eq-5d.html> Accessed February 2014.
    » http://www.euroqol.org/fileadmin/user_upload/Documenten/PDF/Folders_Flyers/UserGuide_EQ-5D-5.pdf>
  • 17
    Harmatz, P, Ketteridge, D, Giugliani, R. Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase. Pediatrics. 2005;115 (6):e681–e689.
  • 18
    Miller, MR, Hankinson, J, Brusasco, V. Standardisation of spirometry. Eur Respir J. 2005;26 (2):319–338.
  • 19
    Tylki-Szymanska, A, Marucha, J, Jurecka, A, Syczewska, M, Czartoryska, B. Efficacy of recombinant human a-L-iduronidase (laronidase) on restricted range of motion of upper extremities in mucopolysaccharidosis type I patients. J Inherit Metab Dis. 2010;33 (2):151–157.
  • 20
    Gerhardt, JJ, Rondinelli, RD. Goniometric techniques for range-of-motion assessment. Phys Med Rehabil Clin N Am. 2001;12 (3):507–527.
  • 21
    Li, AM, Yin, J, Au, JT. Standard reference for the six-minute-walk test in healthy children aged 7 to 16 years. Am J Respir Crit Care Med. 2007;176 (2):174–180.
  • 22
    Casanova, C, Celli, BR, Barria, P. The 6-min walk distance in healthy subjects: reference standards from seven countries. Eur Respir J. 2011;37 (1):150–156.
  • 23
    Web site. http://www.cdc.gov/niosh/topics/spirometry/refcalculator.html Last updated: July 2010, last accessed: February 2015.
    » http://www.cdc.gov/niosh/topics/spirometry/refcalculator.html
  • 24
    Montaño, AM, Tomatsu, S, Brusius, A, Smith, M, Orii, T. Growth charts for patients affected with Morquio A disease. Am J Med Genet A. 2008;146A (10):1286–1295.
  • 25
    Brown, CD, Benditt, JO, Sciurba, FC. Exercise testing in severe emphysema: association with quality of life and lung function. COPD. 2008;5 (2):117–124.
  • 26
    Han, B, Yan, B, Zhao, N. The influence of the functional capacity on subjective well-being and quality of life of patients with silicosis. Aging Ment Health. 2013;17 (6):707–713.
  • 27
    Heuker, D., Lengele, B., Delecluse, V. Subjective and objective assessment of quality of life after chest wall resection. Eur J Cardiothorac Surg. 2011;39 (1):102–108.
  • 28
    Cazzola, M, MacNee, W, Martinez, FJ. Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J. 2008;31 (2):416–469.
  • 29
    Hendriksz, CJ, Lavery, C, Coker, M. The burden endured by caregivers of patients with morquio a syndrome: results from an international patient-reported outcomes survey. J Inborn Error Metab Screen. 2014;2:1–8.

Publication Dates

  • Publication in this collection
    19 June 2019
  • Date of issue
    2015
Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT) Rua Ramiro Barcelos, 2350, CEP: 90035-903, Porto Alegre, RS - Brasil, Tel.: 55-51-3359-6338, Fax: 55-51-3359-8010 - Porto Alegre - RS - Brazil
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