Next Article in Journal
SARS-CoV-2 Infection Causes Relapse of Kleine-Levin Syndrome: Case Report and Review of Literature
Previous Article in Journal
Median-to-Ulnar Nerve Communication in Carpal Tunnel Syndrome: An Electrophysiological Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis

by
Cristina Salvioni
1,*,
Adriana Leico Oda
1,
Marco Orsini
2,
Michele Pauli
1,
Luciana M. Frabasile
1,
Percilia C. L. Alves
1,
Rosana M. Borges
1,
Helena N. M. Sierra
1,
Gabriela Menegatti
1,
Márcio Ottoboni Pinho
1 and
Acary Souza Bulle Oliveira
1
1
Department of Clinical Neurology, Federal University of Sao Paulo, Sao Paulo 04023-900, Brazil
2
Department of Medicine, Iguacu University—UNIG and Master Program in Neurology—Vassouras University—USS, Rio de Janeiro 28300-000, Brazil
*
Author to whom correspondence should be addressed.
Submission received: 7 April 2021 / Revised: 1 June 2021 / Accepted: 7 July 2021 / Published: 19 July 2021

Abstract

:
Background: The influence of changes in body composition on swallowing in patients with Amyotrophic Lateral Sclerosis (ALS) is unknown. Understanding the interrelation between body compartments and dysphagia may establish specific treatments related to both nutritional aspects as to myofunctional ones designed to delay swallowing loss. Aim: The aim of the study was to evaluate the relationship between body composition and dysphagia during the course of the disease. Methods: The protocol of this study included assessments carried out quarterly for one year and included: analysis of body composition by multi-frequency segmental bioimpedance, nutritional diagnosis, maximum strength test of the tongue and lips, analysis of swallowing using the Functional Oral Intake Score (FOIS) and Swallowing Rating Scale of the American Speech-Language-Hearing Association (ASHA), speech intelligibility and analysis of disease severity. To measure the degree of relationship between quantitative variables, Spearman’s correlation was used. Results: Thirty-four patients were evaluated, 28 Spinal Group and 6 Bulbar Group. The results did not show any significant differences in the analysis of body composition between the groups. Positive associations were found between body compartments and swallowing analysis. The phase angle showed a strong correlation between the FOIS scales (r = 0.74, p < 0.01), ASHA (r = 0.77, p < 0.01) and tongue (r = 0.66, p < 0.01). Conclusions: Changes in body compartments were related to swallowing functionality and speech intelligibility in ALS patients, emphasizing the importance of analyzing body compartments for decision making by the interdisciplinary team. Although these preliminary data were collected in a small sample size, they serve to motivate future studies in this area.

1. Introduction

Amyotrophic Lateral Sclerosis (ALS) is a progressive degenerative disorder of the upper and lower motor neurons, causing weakness and wasting of muscles controlling limb movement, speech, swallowing and breathing. Eventual respiratory failure and malnutrition with dehydration are the primary cause of death [1]. Worldwide incidence ranges from 1.5 to 2.7:100,000 people/year [2].
ALS is presented in two main different forms: bulbar progressive paresis, (bulbar onset, 25–35% of patients) or spinal motor neuron injury (limb onset or peripheral onset) [3,4,5]. Almost 80% of ALS patients with bulbar onset will develop dysarthria and dysphagia. In a spinal or peripheral onset of the disease muscle weakness is the main symptom [1]. Mean survival of ALS is 3–5 years, with 5–10% living longer than 10 years [3].
During the course of the disease, a progressive decline in muscle function depends on both motor neuron degeneration and nutritional status. Malnutrition is an independent prognostic factor for survival [1,6,7,8,9]. Changes in the body compartments of these patients, regardless of weight reduction, with loss of fat-free mass were also associated with shorter survival [10], just as the increase in body fat has been identified as a protective factor in the evolution of the disease [7,11]. Desport et al. (2003) [12], validated the use of Bioelectrical Impedance (BIA) to assess body composition in ALS patients. Until today, the analysis of body composition has not been used frequently in clinical practice to monitor the progression of the disease and guide the conduct of the interdisciplinary team.
Nutritional aspects and swallowing are interrelated. Dysphagia, caused by weakness resulting from the flaccidity or spasticity of the muscles of the oropharyngeal region, is one of the most serious and debilitating symptoms of the disease [13] and it is the major cause of changes in the nutritional status of patients with ALS [14]. Understanding the interrelation between body compartments and dysphagia may establish specific treatments related to both nutritional and myofunctional aspects designed to delay swallowing loss. In the present study, therefore, we aim to assess the relationship between body composition and dysphagia during the course of the disease.

2. Methods

2.1. Study Participants

This is a longitudinal and observational study, with a convenience sample recruited from the Neuromuscular Diseases Research Sector at the Federal University of São Paulo. Patients diagnosed with ALS were included, following the criteria defined by El Escorial Criteria from the World Federation of Neurology [15], in regular follow-up with a team of nutritionists and speech therapists, therefore following the same medication protocol proposed by the institution’s medical team, without distinction between groups. Furthermore, patients who had an alternative feeding route at the time of the first evaluation, tracheostomy and who had a history of other neurological impairments were excluded. The study was approved by the institution’s Research Ethics Committee, under number 0288/2017.
Participants were divided into two groups, according to the form of the disease manifestation: Spinal Group (SG), with onset of the disease by upper or lower limbs, and Bulbar Group (BG), beginning with speech, swallowing or atrophy and tongue fasciculation and facial weakness.
The protocol of this study included nutritional assessment and aspects of swallowing performed quarterly for a period of one year, so that the follow-up could take place in four assessments carried out between the times (T1, T2, T3 and T4).

2.2. Nutritional Assessment

The patients were weighed on a platform scale (Toledo do Brasil) with a capacity of 500 kg. The height was estimated through the leg length, according to the equations proposed by CHUMLEA et al., 1985 [16] for patients who did not walk or evaluated with the individual standing with the aid of a fixed digital stadiometer HM-210D, with a 1 mm register (InBody Ottoboni®, HM-210D, InBody Co., Ltd., Seoul, Korea). The Body Mass Index (BMI) was calculated according to the formula BMI = weight/height2 and classified according to age [17,18]. The body composition assessment was performed with the patient in the supine position on a stretcher with a non-conductive surface using the InBody S10 multi-frequency segmental bioimpedance device (InBody Co., Ltd., Seoul, Korea), Ottoboni®. The measures evaluated by the BIA were: Body Fat Mass (BFM), Percent Body Fat (% BF), Visceral Fat Area (VFA), Fat Free Mass (FFM), Skeletal Muscle Mass (SMM), FFM of Trunk (t FFM) and Phase Angle (PA).

2.3. Swallowing Aspects

To obtain pressure and resistance measurements of the phono-articulatory structures, the Iowa Oral Performance Instrument (IOPI) was used [19]. The device consists of an air bulb connected to a pressure transducer and the values are displayed on the screen, measured in kPa. With the patient seated, instructions were given to measure the maximum pressure of the structures-lips and tongue. The bulb was placed in three positions: tongue on the anterior part against the anterior portion of the hard palate, and on the right and left labial commissures with the instruction to press as hard as possible. Each movement was performed three times with time intervals of 30 s and considered the largest measure. To assess the change in the individual’s functional swallowing and/or the ability to swallow over time, the Functional Oral Intake Score (FOIS) [20] and Swallowing Rating Scale of the American Speech-Language-Hearing Association (ASHA) [21] were used. Speech intelligibility was classified, according to the Yorkston proposal [22].

2.4. Disease Progression

The assessment of disease progression was performed using Amyotrophic Lateral Sclerosis Functional Rating (ALSFRS-R). The scale was analyzed by its total score (ALSFRS-R Total) and its subscale scores: bulbar subscale score, fine motor subscale score, gross motor subscale score and respiratory subscale score. ALSFRS-R total scores range from 0 to 48, with 48 indicating no impairment and 0 being most impaired; ALSFRS-R subscales scores range from 0 to 12 with 12 indicating no impairment and 0 being most impaired [23].

2.5. Statistical Analysis

The Shapiro–Wilk normality test was applied to continuous variables. As for longitudinal analyzes, that is, for comparison between follow-up times, Friedman’s nonparametric tests (when comparing all times) and Wilcoxon (when comparing only 2 times-T1 and T4)) were used. To measure the degree of relationship between quantitative variables, the Spearman’s correlation. The value of statistical significance adopted was p < 0.05 (bicaudal). Correction of significance was performed using the False Discovery Rate method (FDR). FDR is a method of conceptualizing the type I error rate in null hypothesis tests when conducting multiple comparisons. The analysis was performed with the aid of the statistical program Statistical Package for Social Science, version 26.0.

3. Results

Thirty-four patients diagnosed with ALS were included in the study, the categorical clinical variables are shown in Table 1.
Regarding the investigated subscale scores of the ALSFRS-R scale, SG patients had higher scores for the subscale bulbar (p = 0.02 at T1 and p = 0.04 at T4) while BG patients showed significantly higher scores on the fine motor subscale (p = 0.03 in T1 and T4). Even though the BG showed higher scores for the gross motor subscale at all times evaluated, only a statistically significant difference was observed in the final evaluation (p = 0.01). The respiratory subscale and the total score did not differ significantly between the diagnostic groups (Figure 1).
Figure 2 shows the averages of the total score of the functionality scale for the diagnostic groups and the whole cohort studied, without distinction of the diagnosis, over the follow-up period. In this analysis, there is, therefore, an average fall of 0.76 points/month for SG, 0.48 points/month for BG and 0.60 points/month for the whole cohort.
The classification of the nutritional status, according to the BMI, of patients at the time of assessment (T1) and at the end of the study (T4), is shown in Table 2. At the beginning of the research, there is a higher frequency of malnutrition among patients in BG compared to SG. On the other hand, at the end of the study, malnutrition remained constant in BG and there was an increase in SG.
Over the follow-up period, the comparison of body composition by BIA of the diagnostic groups did not show a statistically significant difference for any variable analyzed in this research. Figure 3 shows the variation in body weight, skeletal muscle mass, percent body fat and phase angle during follow-up.
Figure 4 shows the comparisons of speech-language assessment measures between groups. For the temporal analysis of the behavior of the FOIS and ASHA scale, there were no significant differences between the moments of the initial and final evaluations. Thus, there was no difference between the scales that sought to assess the functionality of swallowing for the groups. In the same graph, significant differences can be noticed for all variables of pressure and speech intelligibility scale.
The following analyzes sought to assess the association between body composition and clinical speech therapy assessment. For the SG, the FOIS and ASHA scales showed a significant positive association for BMI and body weight, while the Yorkston scale only for weight. Significant correlations were observed, directly proportional, between tongue pressure and right and left labial commissure and also weight, FFM, SMM and t FFM. In the BG, the FOIS, ASHA scales and tongue pressure showed significant correlations with the BP. For the SG, without the FDR, we obtained 16 rejected null hypotheses and with the FDR, 13 hypotheses. In BG, without FDR, 3 null hypotheses rejected and with FDR, 2 hypotheses. Thus, as there were 54 analyses, the proportion of SG decreased from 29.6% to 24.1% whereas BG decreased from 5.6% to 3.7% (Table 3).
For the SG, the clinical speech therapy findings were positively correlated with all subscales and for the total health of the ALSFRS-R. The correlation in the BG showed a direct association between the FOIS and ASHA scales and the bulbar and respiratory subscale scores. Regarding the pressure of phono-articulatory organs, only the right commissure showed a direct correlation with the total score; (r = 0.54) (p < 0.05). For the SG, without the FDR, we obtained 29 rejected null hypotheses and with the FDR, there were no changes in the analyses. For BG, without FDR, 5 null hypotheses rejected and with FDR 2 hypotheses. Thus, as there were 30 analyses, the proportion in SG remained at 96.7% and in BG, it decreased from 16.7% to 6.7% (Table 4).

4. Discussion

The results did not show significant differences in the analysis of body composition between the groups. Positive associations were found between body compartments and swallowing analysis. The demographic characterization of the sample agrees with the worldwide distribution reported in epidemiological studies [5,24].
The ALSFRS-R was evaluated not only by its total score, but also by its subscale scores. In the scales where there is a sum of points, it was observed that the total score does not reflect the particularity of each subscale, which becomes very relevant, depending on the analysis that is intended to be conducted [25,26]. When observing the differences between the groups evaluated with the subscale scores of the ALSFRS-R, as evidenced by the characteristic itself of the disease, bulbar change was more frequent and more severe in the BG, while changes in motor function initially compromised the SG.
In the analysis of the variation in the total score of the scale, over the follow-up period, it was possible to observe a fall of 0.76 points/month for the SG, 0.48 points/month for the BG and 0.60 points/month for the whole cohort (Figure 2). A study that provided a detailed description of the clinical trial database at ALS (PRO-ACT), in order to answer important questions about the natural history of the disease, observed a functional decline rate of 1.02 points/month of ALSFRS-R [27]. A recent study, controlled placebo and double blind, with lipid supplementation, found a reduction of 0.69 points/month in the supplemented group [28]. Given these results, the big question was: what would have caused the reduction in the scale found in this research to have been similar or less than that of controlled clinical trials? It is possible that the regular and systematic treatment carried out by an interdisciplinary team with expertise in the treatment of ALS has contributed to the achievement of such results [29,30]. However, a possible sample selection bias, with patients presenting the slowest evolution of the disease, could also have contributed to the achievement of these results.
Although the disease with bulbar onset can be considered a greater risk of malnutrition, in this study this was not proven. If inadequate caloric intake and weight loss are correlated with the severity of dysphagia [31,32], it is possible that the increased energy expenditure due to spasticity and fasciculations be a determining factor for nutritional risk also to occur with patients with onset appendicular [6]. Still, it is possible that the nutritional status of those studied was influenced by gastrostomy, more present in BG [33].
The findings of the swallowing functionality evaluated by the FOIS scale, are in line with the results found by ALVES et al. (2018) [34], in which the index obtained was lower for patients with bulbar onset of the disease. Like the FOIS scale, the functional measures of swallowing obtained by the ASHA scale also declined insignificantly over time. Because it is an evolutionary disease, in which the signs and symptoms appear progressively, patients develop strategies that help them maintain functionality, regardless of their muscular condition. Such strategies may involve swallowing maneuvers, the use of facilitative measures, the choice of certain utensils that favor the grasping and accommodation of food and also management of the environment, such as the elimination of distracting factors. Thus, it is observed that the functionality of swallowing and the adaptation of food consistency for meals remain stable in the analysis of the scales adopted, since the compensation used by patients is not considered in their analysis.
Speech intelligibility differentiated the groups from each other. The process of denervation of the bulbar musculature results in deterioration and eventual loss of the ability to swallow and speak. Therefore, dysarthria and dysphagia are common symptoms in patients with ALS [35], and they can coexist above all in patients with involvement of the bulbar musculature. At some point, communication is affected during the course of the disease [36], which would explain at the end of the study, the changes of speech having also marked the SA. Thereafter, it was possible to observe that, although the neuroanatomy functional basis is the same, the clinical evolution of dysarthria does not present the same linearity.
As for the pressure measurements of the evaluated structures, as in this study, other studies have also shown differences in tongue pressure, differentiating the evaluations [37,38]. In a recent study, ninety percent of patients with dysphagia had an average tongue pressure of less than 34.2 kPa [38]. The results obtained in the T4 of this research, showed impairment in the prominent swallowing for the BG. The decrease in tongue strength at the time of diagnosis has already been identified as an independent prognostic factor for the survival time in patients with ALS [37]. The increase of 1 kPa in the tongue pressure presented by the patients led to a 6% reduction in the probability of indicating PEG [39] elements that would justify the more striking presence of the alternative feeding route in the BG. As well as tongue pressure measurements, lip pressure measurements also showed a significant reduction with the worsening of ALS [39].
Positive associations were observed between the parameters analyzed in the speech therapy assessment and body composition. The justification of the relationship between the findings is based on the alignment of body segments and their biomechanics, whereas changes in body compartments, especially measures related to muscle mass, could compromise such structures. Axial muscle weakness can lead to postural changes in the trunk, considered to be the region of all static compensations, for having connected to it, the upper and lower limbs and the cervical [40]. In addition, the limb weakness itself could misalign this central axis, leading to two clinical conditions: changes in the cervical axis, which can directly interfere with the functioning of the structures connected to it, and the reduction of the base support, making it difficult for the muscles that have the action of pressure valves, as is the case of the lips and the soft palate [41,42]. Such placements would help justify the positive associations found between the measures of the evaluation of swallowing to skeletal muscle mass, free mass and fat and, mainly, fat free mass of the trunk, for SG. Still, the neck muscles contribute to the stabilization and protection of the cervical spine and, therefore, any impairment of these muscles could also cause problems in the swallowing process [43]. In ALS, a prospective and multicenter cohort study demonstrated that weakness of the neck flexors is a potent factor for predicting survival and for worsening activities of daily living, such as speech, swallowing, upper limb function, turning on bed and even walking [44]. Weakness in the neck as an initial symptom was also associated with a shorter survival time for these patients [45].
The loss of muscle mass associated with dysphagia has been established in other studies [46,47,48,49,50]. The decrease in skeletal muscle mass has been identified as a potential risk factor for dysphagia in sarcopenic patients [48]. Lip strength and tongue strength are also associated with sarcopenic dysphagia and are useful indexes for rehabilitation [51]. Wakabayashi et al. (2017) [50], assessed the prevalence of skeletal muscle mass loss and its association with swallowing function in patients with dysphagia after cardiovascular surgery. In the results, it was possible to observe that the prevalence of loss of skeletal muscle mass in these patients was very high and independently associated with the function of swallowing, after adjustment for tracheostomy tubes.
The analysis of the PA brought interesting results. The PA evaluated by the total body analysis was positively associated with the FOIS, ASHA scales and with the tongue pressure, but only for the BG. It must be determined, under the analysis of new studies, whether the PA will also be effective in verifying changes in swallowing for patients who start the disease by limbs. A study that evaluated the multi-dimensional electrical impedance myography of the tongue as a potential biomarker for ALS, observed that the PA, specifically of this organ, had lower values in the patients evaluated when compared to healthy adults [51].
The clinical measures chosen for the speech-language assessment of this study, despite the limited correlations found between the ALSFRS-R and the BG, proved to be relevant for monitoring the progression of the disease. The limited number of patients in the BG may have contributed to these results. As well as the results presented here, other studies have also found correlations between the same speech therapy measures used here with the ALSFRS-R [52,53].
Changes in body compartments were related to swallowing functionality and speech intelligibility in ALS patients. Although the results presented improve the understanding of the contribution that body composition could have in the loss of swallowing and dysphagia, being able to cause nutritional decline, the study is limited by its small sample size. However, the interrelation between nutritional aspects and swallowing deserves more attention in order to motivate further prospective studies in this area. Still, analyzing nutritional decline through the systematic assessment of the body composition of patients with ALS could assist in the clinical management of dysphagia, helping the decision making of the interdisciplinary team.
This study was approved by the relevant research ethics committee and informed consent was obtained from the research subjects.

Author Contributions

Conceptualization, C.S., A.L.O. and M.O.; methodology, C.S. and A.L.O.; software, M.O.P.; validation, C.S., A.L.O. and A.S.B.O.; formal analysis, A.S.B.O.; investigation, C.S.; A.L.O.; M.P.; L.M.F.; P.C.L.A.; R.M.B.; H.N.M.S. and G.M.; resources, C.S.; A.L.O.; M.P.; L.M.F.; P.C.L.A.; R.M.B.; H.N.M.S. and G.M.; data curation, C.S. and A.L.O.; writing—original draft preparation, C.S.; writing—review and editing, C.S. and A.L.O.; visualization, C.S. and A.L.O.; supervision, A.S.B.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board (or Ethics Committee) of Federal University of Sao Paulo, Brazil (protocol code 0288 approved on 31 July 2017).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Conflicts of Interest

None of the authors have any conflict of interest to disclose.

Ethical Publication Statement

We confirm that we have read the Journal’s position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.

References

  1. Burgos, R.; Bretón, I.; Cereda, E.; Desport, J.C.; Dziewas, R.; Genton, L.; Gomes, F.; Jésus, P.; Leischker, A.; Muscaritoli, M.; et al. ESPEN guideline clinical nutrition in neurology. Clin. Nutr. 2018, 37, 354–396. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Worms, P.M. The epidemiology of motor neuron diseases: A review of recent studies. J. Neurol. Sci. 2001, 191, 3–9. [Google Scholar] [CrossRef]
  3. Chio, A.; Logroscino, G.; Hardiman, O.; Swingler, R.; Mitchell, D.; Beghi, E.; Traynor, B.G.; Eurals Consortium. Prognostic factors in ALS: A critical review. Amyotroph. Lateral Scler. 2009, 10, 310–323. [Google Scholar] [CrossRef] [Green Version]
  4. Hardiman, O.; Al-Chalabi, A.; Chio, A.; Corr, E.M.; Logroscino, G.; Robberecht, W.; Shaw, P.J.; Simmons, Z.; Van Den Berg, L.H. Amyotrophic lateral sclerosis. Nat. Rev. Dis. Prim. 2017, 3, 1–9. [Google Scholar] [CrossRef] [PubMed]
  5. Talbott, E.O.; Malek, A.M.; Lacomis, D. The epidemiology of amyotrophic lateral sclerosis. Handb. Clin. Neurol. 2016, 138, 225–238. [Google Scholar]
  6. Desport, J.C.; Preux, P.M.; Truong, T.C.; Vallat, J.M.; Sautereau, D.; Couratier, P. Nutritional status is a prognostic factor for survival in ALS patients. Neurology 1999, 53, 1059. [Google Scholar] [CrossRef]
  7. Marin, B.; Desport, J.-C.; Kajeu, P.; Jésus, P.; Nicolaud, B.; Nicol, M.; Preux, P.-M.; Couratier, P. Alteration of nutritional status at diagnosis is a prognostic factor for survival of amyotrophic lateral sclerosis patients. J. Neurol. Neurosurg. Psychiatry 2010, 82, 628–634. [Google Scholar] [CrossRef] [Green Version]
  8. Shimizu, T.; Nagaoka, U.; Nakayama, Y.; Kawata, A.; Kugimoto, C.; Kuroiwa, Y.; Kawai, M.; Shimohata, T.; Nishizawa, M.; Mihara, B.; et al. Reduction rate of body mass index predicts prognosis for survival in amyotrophic lateral sclerosis: A multicenter study in Japan. Amyotroph. Lateral Scler. 2012, 13, 363–366. [Google Scholar] [CrossRef]
  9. Marin, B.; Arcuti, S.; Jesus, P.; Logroscino, G.; Copetti, M.; Fontana, A.; Nicol, M.; Raymondeau, M.; Desport, J.C.; Preux, P.M.; et al. Population-Based Evidence that Survival in Amyotrophic Lateral Sclerosis Is Related to Weight Loss at Diagnosis. Neurodegener. Dis. 2016, 16, 225–234. [Google Scholar] [CrossRef] [PubMed]
  10. Roubeau, V.; Blasco, H.; Maillot, F.; Corcia, P.; Praline, J. Nutritional assessment of amyotrophic lateral sclerosis in routine practice: Value of weighing and bioelectrical impedance analysis. Muscle Nerve 2015, 51, 479–484. [Google Scholar] [CrossRef]
  11. Kasarskis, E.J.; Berryman, S.; Vanderleest, J.G.; Schneider, A.R.; McClain, C.J. Nutritional status of patients with amyotrophic lateral sclerosis: Relation to the proximity of death. Am. J. Clin. Nutr. 1996, 63, 130–137. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Desport, J.C.; Preux, P.M.; Bouteloup-Demange, C.; Clavelou, P.; Beaufrère, B.; Bonnet, C.; Couratier, P.P. Validation of bioelectrical impedance analysis in patients with amyotrophic lateral sclerosis. Am. J. Clin. Nutr. 2003, 77, 1179–1185. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Ruoppolo, G.; Schettino, I.; Frasca, V.; Giacomelli, E.; Prosperini, L.; Cambieri, C.; Roma, R.; Greco, A.; Mancini, P.; De Vincentiis, M.; et al. Dysphagia in amyotrophic lateral sclerosis: Prevalence and clinical findings. Acta Neurol. Scand. 2013, 128, 397–401. [Google Scholar] [CrossRef] [PubMed]
  14. Desport, J.C.; Preux, P.M.; Magy, L.; Boirie, Y.; Vallat, J.M.; Beaufrère, B.; Couratier, P. Factors correlated with hypermetabolism in patients with amyotrophic lateral sclerosis. Am. J. Clin. Nutr. 2001, 74, 328–334. [Google Scholar] [CrossRef] [Green Version]
  15. Brooks, B.R.; Miller, R.G.; Swash, M.; Munsat, T.L. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. Other Mot. Neuron Disord. 2000, 1, 293–299. [Google Scholar] [CrossRef] [PubMed]
  16. Chumlea, W.C.; Roche, A.F.; Steinbaugh, M.L. Estimating Stature from Knee Height for Persons 60 to 90 Years of Age. J. Am. Geriatr. Soc. 1985, 33, 116–120. [Google Scholar] [CrossRef]
  17. White, J.V.; Dwyer, J.T.; Posner, B.M.; Ham, R.J.; Lipschitz, D.A.; Wellman, N.S. Nutrition screening initiative: Development and implementation of the public awareness checklist and screening tools. J. Am. Diet. Assoc. 1992, 92, 163–167. [Google Scholar]
  18. World Health Organization. Physical Status: The Use and Interpretation of Anthropometry; WHO, Ed.; World Health Organization: Geneve, Swittzerland, 1995; Volume 854, p. 452. [Google Scholar]
  19. Adams, V.; Mathisen, B.; Baines, S.; Lazarus, C.; Callister, R. A Systematic Review and Meta-analysis of Measurements of Tongue and Hand Strength and Endurance Using the Iowa Oral Performance Instrument (IOPI). Dysphagia 2013, 28, 350–369. [Google Scholar] [CrossRef]
  20. Crary, M.A.; Mann, G.D.C.; Groher, M.E. Initial Psychometric Assessment of a Functional Oral Intake Scale for Dysphagia in Stroke Patients. Arch. Phys. Med. Rehabil. 2005, 86, 1516–1520. [Google Scholar] [CrossRef]
  21. American Speech-Language-Hearing Association. National Outcome Measurement System (NOMS). Adult Speech-Language Pathology Training Manual; ASHA: Rockville, MD, USA, 1998. [Google Scholar]
  22. Strand, E.A.; Miller, R.M.; Yorkston, K.M.; Hillel, A.D. Management of oral-pharyngeal dysphagia symptoms in amyotrophic lateral sclerosis. Dysphagia 1996, 11, 129–139. [Google Scholar] [CrossRef]
  23. Cedarbaum, J.M.; Stambler, N.; Malta, E.; Fuller, C.; Hilt, D.; Thurmond, B.; Nakanishi, A. The ALSFRS-R: A revised ALS functional rating scale that incorporates assessments of respiratory function. J. Neurol. Sci. 1999, 169, 13–21. [Google Scholar] [CrossRef]
  24. Bettini, M.; Gargiulo-Monachelli, G.M.; Rodríguez, G.; Rey, R.C.; Peralta, L.M.; Sica, R.E. Epidemiology of amyotrophic lateral sclerosis patients in a centre in Buenos Aires. Arq. Neuro Psiquiatr. 2011, 69, 867–870. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Rooney, J.; Burke, T.; Vajda, A.; Heverin, M.; Hardiman, O. What does the ALSFRS-R really measure? A longitudinal and survival analysis of functional dimension subscores in amyotrophic lateral sclerosis. J. Neurol. Neurosurg. Psychiatry 2016, 88, 381–385. [Google Scholar] [CrossRef] [PubMed]
  26. Salvioni, C.C.D.S.; Stanich, P.; Oliveira, A.S.B.; Orsini, M. Anthropometry of Arm: Nutritional Risk Indicator in Amyotrophic Lateral Sclerosis. Neurol. Int. 2015, 7, 48–53. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Atassi, N.; Berry, J.; Leitner, M.; Shui, A.; Zach, N.; Sherman, A.; Sinani, E.; Walker, J.; Katsovskiy, I.; Schoenfeld, D.; et al. The PRO-ACT database: Design, initial analyses, and predictive features. Neurology 2014, 83, 1719–1725. [Google Scholar] [CrossRef] [Green Version]
  28. Ludolph, A.C.; Dorst, J.; Dreyhaupt, J.; Weishaupt, J.H.; Kassubek, J.; Weiland, U.; Meyer, T.; Petri, S.; Hermann, A.; Emmer, A.; et al. Effect of High-Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis. Ann. Neurol. 2020, 87, 206–216. [Google Scholar] [CrossRef]
  29. Martin, S.; Trevor-Jones, E.; Khan, S.; Shaw, K.; Marchment, D.; Kulka, A.; Ellis, C.E.; Burman, R.; Turner, M.R.; Carroll, L.; et al. The benefit of evolving multidisciplinary care in ALS: A diagnostic cohort survival comparison. Amyotroph. Lateral Scler. Front. Degener. 2017, 18, 569–575. [Google Scholar] [CrossRef]
  30. Paipa, A.J.; Povedano, M.; Corbella, X.; Barcelo, M.A.; Domínguez, R.; Saez, M.; Turon-Sans, J.; Prats, E.; Farrero, E.; Virgili, N.; et al. Survival benefit of multidisciplinary care in amyotrophic lateral sclerosis in Spain: Association with noninvasive mechanical ventilation. J. Multidiscip. Healthc. 2019, 12, 465–470. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Desport, J.C.; Preux, P.M.; Truong, C.T.; Courat, L.; Vallat, J.M.; Couratier, P. Nutritional assessment and survival in ALS patients. Amyotroph. Lateral Scler. Other Mot. Neuron Disord. 2000, 1, 91–96. [Google Scholar]
  32. Stavroulakis, T.; McDermott, C.J. Nutritional Support in Amyotrophic Lateral Sclerosis. In Nutrition in Neurologic Disorders; Springer International Publishing: Sheffield, UK, 2017; pp. 91–104. [Google Scholar]
  33. Bond, L.; Ganguly, P.; Khamankar, N.; Mallet, N.; Bowen, G.; Green, B.; Mitchell, C.S. A comprehensive examination of percutaneous endoscopic gastrostomy and its association with amyotrophic lateral sclerosis patient outcomes. Brain Sci. 2019, 9, 223. [Google Scholar] [CrossRef] [Green Version]
  34. Alves, P.C.; Oda, A.L.; Vecina, A.L.; Neves, J.W.; Borges, R.M.; Sierra, N.M.H.; Orsini, M.; Rocha, M.S.; Oliveira, A.S. Interface Between Dysphagia and Nutritional Implication on Patients with Motor Neuron Disease/Amyotrophic Lateral Sclerosis. J. Sci.Tech. Res. 2018, 4, 3866–3872. [Google Scholar] [CrossRef]
  35. Da Costa Franceschini, A.; Mourão, L.F. Dysarthria and dysphagia in Amyotrophic Lateral Sclerosis with spinal onset: A study of quality of life related to swallowing. NeuroRehabilitation 2015, 36, 127–134. [Google Scholar] [CrossRef] [PubMed]
  36. Börjesson, M.S.; Hartelius, L.; Laakso, K. Communicative participation in people with amyotrophic lateral sclerosis. Folia Phoniatr. Logop. 2021, 73, 101–108. [Google Scholar]
  37. Weikamp, J.G.; Schelhaas, H.J.; Hendriks, J.C.M.; De Swart, B.J.M.; Geurts, A.C.H. Prognostic value of decreased tongue strength on survival time in patients with amyotrophic lateral sclerosis. J. Neurol. 2012, 259, 2360–2365. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. De Freitas Borges, A.L.; Velasco, L.C.; Ramos, H.V.; Imamura, R.; de Castro Roldão, P.M.; Petrillo, M.V.; Costa, C.C. Association between dysphagia and tongue strength in patients with amyotrophic lateral sclerosis. Braz. J. Otorhinolaryngol. 2020. [Google Scholar] [CrossRef]
  39. Mendes, A.E. Indicação da Gastrostomia em Pacientes com Esclerose Lateral Amiotrófica: Critérios Fonoaudiológicos. Master’s Thesis, University of Sao Paulo, Sao Paulo, Brazil, 2015. [Google Scholar]
  40. Oda, A.L. Marcadores Clínicos Fonoaudiológicos Como Modelo Prognóstico nas Funções Orofaringolaringeais em Pacientes com Doença do Neurônio Motor. Ph.D. Thesis, Federal University of São Paulo, Sao Paulo, Brazil, 2016. [Google Scholar]
  41. Piret, S.; Béziers, M.M. A Coordenação Motora—Aspecto Mecânico da Organização Psicomotora do Homem; Editora Summs: São Paulo, Brazil, 1992. [Google Scholar]
  42. Kendall, H.O.; McCreary, E.K.; Provance, P.G.; Rodgers, M.M.; Romani, W.A. Músculos—Provas e Funções; Editora Manole: Barueri, Brazil, 2007. [Google Scholar]
  43. Papadopoulou, S.; Exarchakos, G.; Beris, A.; Ploumis, A. Dysphagia Associated with Cervical Spine and Postural Disorders. Dysphagia 2013, 28, 469–480. [Google Scholar] [CrossRef]
  44. Nakamura, R.; Atsuta, N.; Watanabe, H.; Hirakawa, A.; Watanabe, H.; Ito, M.; Senda, J.; Katsuno, M.; Tanaka, F.; Izumi, Y.; et al. Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients. J. Neurol. Neurosurg. Psychiatry 2013, 84, 1365–1371. [Google Scholar] [CrossRef]
  45. Watanabe, H.; Atsuta, N.; Nakamura, R.; Hirakawa, A.; Watanabe, H.; Ito, M.; Senda, J.; Katsuno, M.; Izumi, Y.; Morita, M.; et al. Factors affecting longitudinal functional decline and survival in amyotrophic lateral sclerosis patients. Amyotroph. Lateral Scler. Front. Degener. 2014, 16, 230–236. [Google Scholar] [CrossRef]
  46. Matsuo, H.; Yoshimura, Y. Calf circumference is associated with dysphagia in acute-care inpatients. Geriatr. Nurs. 2018, 39, 186–190. [Google Scholar] [CrossRef]
  47. Ogawa, N.; Mori, T.; Fujishima, I.; Wakabayashi, H.; Itoda, M.; Kunieda, K.; Shigematsu, T.; Nishioka, S.; Tohara, H.; Yamada, M.; et al. Ultrasonography to Measure Swallowing Muscle Mass and Quality in Older Patients With Sarcopenic Dysphagia. J. Am. Med. Dir. Assoc. 2018, 19, 516–522. [Google Scholar] [CrossRef]
  48. Maeda, K.; Takaki, M.; Akagi, J. Decreased Skeletal Muscle Mass and Risk Factors of Sarcopenic Dysphagia: A Prospective Observational Cohort Study. J. Gerontol. Ser. Boil. Sci. Med Sci. 2016, 72, 1290–1294. [Google Scholar] [CrossRef]
  49. Wakabayashi, H.; Takahashi, R.; Watanabe, N.; Oritsu, H.; Shimizu, Y. Prevalence of sarcopenia and its association with dysphagia in cancer patients who require rehabilitation. J. Rehabil. Med. 2017, 49, 682–685. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Wakabayashi, H.; Takahashi, R.; Watanabe, N.; Oritsu, H.; Shimizu, Y. Prevalence of skeletal muscle mass loss and its association with swallowing function after cardiovascular surgery. Nutrition 2017, 38, 70–73. [Google Scholar] [CrossRef] [PubMed]
  51. Sakai, K.; Nakayama, E.; Tohara, H.; Takahashi, O.; Ohnishi, S.; Tsuzuki, H.; Hayata, M.; Takehisa, T.; Takehisa, Y.; Ueda, K. Diagnostic accuracy of lip force and tongue strength for sarcopenic dysphagia in older inpatients: A cross-sectional observational study. Clin. Nutr. 2019, 38, 303–309. [Google Scholar] [CrossRef]
  52. Alix, J.J.; McDonough, H.E.; Sonbas, B.; French, S.J.; Rao, D.G.; Kadirkamanathan, V.; McDermott, C.; Healey, T.J.; Shaw, P.J. Multi-dimensional electrical impedance myography of the tongue as a potential biomarker for amyotrophic lateral sclerosis. Clin. Neurophysiol. 2020, 131, 799–808. [Google Scholar] [CrossRef] [PubMed]
  53. Perry, B.J.; Stipancic, K.L.; Martino, R.; Plowman, E.K.; Green, J.R. Biomechanical Biomarkers of Tongue Impairment During Swallowing in Persons Diagnosed with Amyotrophic Lateral Sclerosis. Dysphagia 2021, 36, 147–156. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Boxplots of the subscale scores and the total score of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised at each time evaluated, according to the two diagnostic groups. Abbreviations: ALSFRS-R (Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised); SG (Spinal Group); BG (Bulbar Group). Significance determined using the Mann–Whitney test; * p < 0.05.
Figure 1. Boxplots of the subscale scores and the total score of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised at each time evaluated, according to the two diagnostic groups. Abbreviations: ALSFRS-R (Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised); SG (Spinal Group); BG (Bulbar Group). Significance determined using the Mann–Whitney test; * p < 0.05.
Neurolint 13 00032 g001
Figure 2. Averages of the total score of the functionality scale for the diagnostic groups and the whole cohort studied. Abbreviations: ALSFRS-R (Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised); SG (Spinal group); BG (Bulbar group).
Figure 2. Averages of the total score of the functionality scale for the diagnostic groups and the whole cohort studied. Abbreviations: ALSFRS-R (Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised); SG (Spinal group); BG (Bulbar group).
Neurolint 13 00032 g002
Figure 3. Average variation in body weight, skeletal muscle mass, percent body fat and phase angle during follow-up. Abbreviations: T (Follow-up time).
Figure 3. Average variation in body weight, skeletal muscle mass, percent body fat and phase angle during follow-up. Abbreviations: T (Follow-up time).
Neurolint 13 00032 g003
Figure 4. Averages of the comparisons of speech-language assessment measures between the diagnostic groups. Abbreviations: FOIS (Functional Oral Intake Scale); ASHA (Swallowing Rating Scale of the American Speech-Language-Hearing Association); Speech intelligibility by Yorkston); Commissure R (Commissure right); Commissure L (Commissure left); IOPI (Iowa Oral Performance Instrument). Significance determined using the Mann–Whitney test; * p < 0.05.
Figure 4. Averages of the comparisons of speech-language assessment measures between the diagnostic groups. Abbreviations: FOIS (Functional Oral Intake Scale); ASHA (Swallowing Rating Scale of the American Speech-Language-Hearing Association); Speech intelligibility by Yorkston); Commissure R (Commissure right); Commissure L (Commissure left); IOPI (Iowa Oral Performance Instrument). Significance determined using the Mann–Whitney test; * p < 0.05.
Neurolint 13 00032 g004
Table 1. Categorical clinical variables of subjects.
Table 1. Categorical clinical variables of subjects.
Demographic Data N(%)
Diagnosis
Spinal onset
2882.4
Bulbar onset
617.6
Gender
  • Men
1955.9
  • Woman
1544.1
Age (Years)
  • <60
1544.1
  • 60
1955.9
n (T1)n (T1)(%)n (T4)(%)
NIV
  • Yes
12.91132.3
PEG
  • Yes
00617.6
Abbreviations: Y (Years); NIV (Non-Invasive Ventilation); PEG (Percutaneous Endoscopic Gastrostomy); T1 (Baseline); T4; (Final evaluation); N (Number of patients).
Table 2. Classification of the nutritional status, according to the BMI, according to diagnostic groups.
Table 2. Classification of the nutritional status, according to the BMI, according to diagnostic groups.
Spinal GroupBulbar Group
BMIN (T1)% (T1)N (T4)% (T4)N (T1)% (T1)N (T4)% (T4)
Malnutrition13.6414.3116.7116.7
Normal1864.31553.6466.6350.0
Overweight414.3310.7116.7233.3
Obesity517.8621.40000
Abbreviations: BMI (Body Mass Index); T1 (Baseline); T4; (Final evaluation); N (Number of patients).
Table 3. Spearman’s correlation coefficients between body composition and clinical speech therapy assessment, according to diagnostic groups.
Table 3. Spearman’s correlation coefficients between body composition and clinical speech therapy assessment, according to diagnostic groups.
Spinal Group
BWBMIBFM%BFVFAFFMSMMt FFMPA
FOISCorr (r)0.2230.1750.0230.0100.1160.0990.0860.0170.079
p-value0.030 *0.2560.9100.9350.4730.5920.6570.9200.659
ASHACorr (r)0.1700.3290.0330.0760.1530.1680.1570.1270.076
p-value0.2560.0080.8930.6590.3000.2560.2920.4110.659
YorkstonCorr (r)0.0340.288−0.0310.0940.1100.2050.1970.1810.072
p-value0.8930.0500.8960.6570.5920.2530.2560.2890.732
TongueCorr (r)0.0890.4200.242−0.058−0.0090.4510.4340.4420.136
p-value0.6570.0010.025 *0.7690.9350.0010.0010.0010.411
Commissure RCorr (r)0.0730.402−0.180−0.0190.0120.3640.3360.3150.038
p-value0.6930.0010.2560.9200.9350.0040.0080.0140.893
Commissure LCorr (r)0.1370.396−0.1370.0310.0590.3370.3140.3120.041
p-value0.4110.0010.4110.8930.7690.0080.0140.0140.891
Bulbar Group
BWBMIBFM%BFVFAFFMSMMt FFMPA
FOISCorr (r)0.3620.3090.1990.2920.3060.2950.3240.4020.741
p-value0.5090.5090.5430.5090.5090.5090.5090.5090.001
ASHACorr (r)0.3130.2530.1710.2380.2600.2550.2810.3350.777
p-value0.5090.5090.6180.5090.5090.5090.5090.5090.001
YorkstonCorr (r)0.1470.1280.2710.2430.250−0.120−0.103−0.145−0.230
p-value0.6700.6780.5090.5100.5090.6900.7060.6700.515
TongueCorr (r)0.3700.2290.1210.1570.2100.1240.1640.3360.660
p-value0.5090.5500.6970.6700.5950.6970.6700.5090.004
Commissure RCorr (r)−0.284−0.072−0.378−0.265−0.2510.3010.2420.1620.136
p-value0.5090.7770.5090.5090.5150.5090.5150.6700.678
Commissure LCorr (r)−0.346−0.099−0.419−0.295−0.2890.3230.2630.1450.075
p-value0.5090.7230.5090.5090.5090.5090.5090.6780.777
Abbreviations: FOIS (Functional Oral Intake Scale); ASHA (Swallowing Rating Scale of the American Speech-Language-Hearing Association); Yorkston (Speech intelligibility by Yorkston); Commissure R (Commissure right); Commissure L (Commissure left); BW (Body Weight); BMI (Body Mass Index); BFM (Body Fat Mass); %BF (Percent Body Fat); VFA (Visceral Fat Area); FFM (Fat Free Mass); MME (Skeletal Muscle Mass); t FFM (Fat Free Mass of Trunk); PA (Phase Angle); Spearman’s correlation coefficients (Corr (r)). Significance as determined by the Spearman correlation method. * Uncorrected p-values for FDR method.
Table 4. Spearman’s correlation coefficients between speech-language clinical findings and the total score of the ALSFRS-R and its subscale scores for the diagnostic groups.
Table 4. Spearman’s correlation coefficients between speech-language clinical findings and the total score of the ALSFRS-R and its subscale scores for the diagnostic groups.
Spinal Group
ALSFRS-R
BulbarFine MotorGross MotorRespiratoryTotal Score
FOISCorr (r)0.5680.2580.2890.4010.420
p-value0.0000.0130.0060.0000.000
ASHACorr (r)0.5880.2770.2770.4060.427
p-value0.0000.0090.0090.0000.000
YokstonCorr (r)0.6640.4370.2570.2090.465
p-value0.0000.0000.0280.0740.000
TongueCorr (r)0.4110.4910.3100.2840.491
p-value0.0000.0000.0060.0100.000
Commissure RCorr (r)0.4120.4390.3990.2840.502
p-value0.0000.0000.0000.0090.000
Commissure LCorr (r)0.3620.4840.3600.2900.504
p-value0.0010.0000.0010.0090.000
Bulbar Group
ALSFRS-R
BulbarFine motorGross motorRespiratoryTotal score
FOISCorr (r)0.801−0.091−0.3970.5000.178
p-value0.0000.9070.3740.021 *0.801
ASHACorr (r)0.8220.036−0.3080.5460.268
p-value0.0000.9540.4730.013 *0.540
YokstonCorr (r)0.149−0.3250.0210.276−0.040
p-value0.8420.4730.9540.5400.954
TongueCorr (r)0.403−0.024−0.359−0.081−0.136
p-value0.4530.9540.4730.9540.875
Commissure RCorr (r)0.0160.4070.262−0.1260.544 *
p-value0.9540.4530.6520.8750.144
Commissure LCorr (r)−0.0460.1810.183−0.1570.379
p-value0.9540.8370.8370.8420.453
Abbreviations: ALSFRS-R (Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised); MMSS (Membros Superiores); MMII (Membros Inferiores); FOIS (Functional Oral Intake Scale); ASHA (Swallowing Rating Scale of the American Speech-Language-Hearing Association); Yorkston (Speech intelligibility by Yorkston); Commissure R (Commissure right); Commissure L (Commissure left); Spearman’s correlation coefficients (Corr (r)). Significance as determined by the Spearman correlation method. * Uncorrected p-values for FDR method.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Salvioni, C.; Oda, A.L.; Orsini, M.; Pauli, M.; Frabasile, L.M.; Alves, P.C.L.; Borges, R.M.; Sierra, H.N.M.; Menegatti, G.; Pinho, M.O.; et al. Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis. Neurol. Int. 2021, 13, 315-327. https://0-doi-org.brum.beds.ac.uk/10.3390/neurolint13030032

AMA Style

Salvioni C, Oda AL, Orsini M, Pauli M, Frabasile LM, Alves PCL, Borges RM, Sierra HNM, Menegatti G, Pinho MO, et al. Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis. Neurology International. 2021; 13(3):315-327. https://0-doi-org.brum.beds.ac.uk/10.3390/neurolint13030032

Chicago/Turabian Style

Salvioni, Cristina, Adriana Leico Oda, Marco Orsini, Michele Pauli, Luciana M. Frabasile, Percilia C. L. Alves, Rosana M. Borges, Helena N. M. Sierra, Gabriela Menegatti, Márcio Ottoboni Pinho, and et al. 2021. "Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis" Neurology International 13, no. 3: 315-327. https://0-doi-org.brum.beds.ac.uk/10.3390/neurolint13030032

Article Metrics

Back to TopTop