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Effects of home-based inspiratory muscle training on sickle cell disease (SCD) patients

ABSTRACT

Introduction:

Inspiratory muscle training (IMT) has been shown to be an efficient method of improving exercise tolerance and inspiratory and expiratory muscle strength in several diseases. The effects of IMT on patients with sickle cell anemia (SCD) are relatively unknown. Our study aimed to evaluate the effects of IMT on adult SCD patients, regarding respiratory muscle strength (RMS) variables, lung function, exercise tolerance, blood lactation concentration, limitation imposed by dyspnea during daily activities and impact of fatigue on the quality of life.

Methods:

This was a randomized single-blind study, with an IMT design comprising true load (TG) and sham load (SG) groups. Initial assessment included spirometry, volumetric capnography (VCap) and measurement of RMS by maximal inspiratory and expiratory pressure (PImax and PEmax). The Medical Research Council dyspnea scale and modified fatigue impact scale were also applied and blood lactate concentration was measured before and after the 6-minute walk test. After this initial assessment, the patient used the IMT device at home daily, returning every 6 weeks for RMS reassessment. Both groups used the same device and were unaware of which group they were in. After a period totaling 18 weeks, patients underwent the final evaluation, as initially performed.

Results:

Twenty-five patients in total participated until the end of the study (median age 42 years). There were no significant differences between TG and SG based on age, sex, body mass index or severity of genotype. At the end of the training, both groups showed a significant increase in PEmax and PImax, improvement in Vcap and in exercise tolerance and dyspnea reduction while performing daily life activities. The same was observed in patients grouped according to disease severity (HbSS and HbSβ0 vs HbSC and HbSβ+), without differences between groups.

Conclusion:

Home-based inspiratory muscle training benefits outpatients with SCD, including the sham load group.

Trial registration:http://www.ensaiosclinicos.gov.br; registration number: RBR-6g8n92.

Keywords:
Inspiratory muscle training; Sickle cell disease; Volumetric capnography; Exercise tolerance; PImax; PEmax

Introduction

Sickle cell disease (SCD) is an autosomal recessive, clinically heterogeneous disorder affecting millions worldwide, and is characterized by hemolytic anemia, progressive vascular injury, vaso-occlusive crises, end-organ injury and a reduced life expectancy.11 Piel FB, Steinberg MH, Rees DC. Sickle cell disease. N Engl J Med. 2017;376(16):1561-73.,22 Houwing ME, de Pagter PJ, van Beers EJ, Biemond BJ, Rettenbacher E, Rijneveld AW, et al. Sickle cell disease: clinical presentation and management of a global health challenge. Blood Rev. 2019;(37):100580. Pulmonary complications, including acute chest syndrome, pulmonary hypertension, venous thromboembolism, asthma/recurrent wheezing and sleepdisordered breathing are an important cause of morbidity and mortality in SCD.33 Mehari A, Klings ES. Chronic pulmonary complications of sickle cell disease. Chest. 2016;149(5):1313-24.,44 DeBaun MR, Strunk RC. The intersection between asthma and acute chest syndrome in children with sickle-cell anaemia. Lancet. 2016;387(10037):2545-53. Individuals with SCD also tend to have an increased concentration of lactate in the blood ([Lac]) due to the greater use of the anaerobic metabolism.55 Petto J, de Jesus JB, Vasques LMR, Pinheiro RLS, Oliveira AM, Spinola KAB, et al. Resting blood lactate in individuals with sickle cell disease. Rev Bras Hematol Hemoter. 2011;33(1):26-30.

Pulmonary disorders often lead to breathlessness and mild abnormalities in pulmonary function tests (PFT).66 Delclaux C, Zerah-Lancner F, Bachir D, Habibi A, Monin JL, Godeau B, et al. Factors associated with dyspnea in adult patients with sickle cell disease. Chest. 2005;128(5):3336-44. In addition, pulmonary complications, as well as other complications inherent to SCD, such as arterial oxyhemoglobin desaturation, anemia, damage to organs and tissues related to the adaptation to exercise (such as heart or skeletal muscles) may cause exercise intolerance.77 Messonnier LA, Gellen B, Lacroix R, Peyrot S, Rupp T, Mira J, et al. Physiological evaluation for endurance exercise prescription in sickle cell disease. Med Sci Sports Exerc. 2019;51(9):1795-801.,88 Connes P, MacHado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63. Thus, the mechanisms related to exercise intolerance observed in SCD patients are numerous, conferring a multifactorial character to sickle cell disease.99 Adnot S, Maitre B, Yaïci A, Hajji L, Callaghan DS, Clerson P, et al. A hemodynamic study of pulmonary hypertension in sickle cell disease. N Engl J Med. 2011;365(1):44-53.

Inspiratory muscle training (IMT) has been shown to be an efficient method of improving exercise tolerance and inspiratory and expiratory muscle strength in a number of diseases.1010 Cutrim AL, Duarte AA, Silva-Filho AC, Dias CJ, Urtado CB, Ribeiro RM, et al. Inspiratory muscle training improves autonomic modulation and exercise tolerance in chronic obstructive pulmonary disease subjects: a randomized-controlled trial. Respir Physiol Neurobiol. 2019;263:31-7.,1111 Basakci Calik B, Gur Kabul E, Taskın H, Telli Atalay O, Bas Aslan U, Tascı M, et al. The efficiency of inspiratory muscle training in patients with ankylosing spondylitis. Rheumatol Int. 2018;38(9):1713-20. Some studies have shown that IMT even enables increased oxygen uptake in the blood, decreases the perception of dyspnea and delays the onset of premature fatigue.1212 Özdal M. Influence of an eight-week core strength training program on respiratory muscle fatigue following incremental exercise. Isokinet Exerc Sci. 2016;24(3):225-30.,1313 Álvarez-Herms J, Julià-Sánchez S, Corbi F, Odriozola-Martínez A, Burtscher M. Putative role of respiratory muscle training to improve endurance performance in hypoxia: a review. Front Physiol. 2019;9:1970. However, the effects of IMT on patients with sickle cell anemia are relatively unknown. To our knowledge, a single case study evaluated the application of this training, and showed in that patient improvement in exercise tolerance and respiratory muscle strength.1414 Camcıoğlu B, Boşnak-Güçlü M, Karadallı MN, Akı ŞZ, Türköz-Sucak G. The role of inspiratory muscle training in sickle cell anemia related pulmonary damage due to recurrent acute chest syndrome attacks. Case Rep Hematol. 2015;2015:1-6.

The aim of the current study was to investigate the effects of inspiratory muscle training on SCD patients. We hypothesized that eighteen weeks of IMT would enhance respiratory muscle strength and exercise tolerance, improve measurements in the pulmonary function tests and reduce the impact of fatigue on the quality of life.

Methods

Participants

Patients with the diagnosis of sickle cell disease (homozygote HbS, compound heterozygote HbS and HbC or β-thalassemia) were recruited from the Hemoglobinopathy Outpatient Clinic of the Hematology and Transfusion Medicine Center at the School of Medical Sciences, University of Campinas (UNI-CAMP).

Exclusion criteria comprised disorders that could prevent proper assessment or IMT during the study period, such as asthma or neurological disorders. For result analysis, patients who missed the reevaluation more than once or who remained for more than one week without training were also excluded. All patients were instructed to maintain their medical treatments throughout the research period.

Experimental design

This was a randomized study on inspiratory muscle training for SCD patients of true and sham load group (TG and SG respectively) design. All the patients who agreed to participate signed a written informed consent form. The study was approved by the UNICAMP ethics committee (Protocol number: CAAE - 44635415.2.0000.5404) and registered to http://www.ensaiosclinicos.gov.br website (registration number: RBR-6g8n92). Patients were randomized by order of evaluation, being sequentially alternated between SG and TG. The TG performed the IMT with a true load, whereas the SG performed the IMT with a device with no true load.

Both groups used the same equipment model for IMT and were unaware of which group they were in. The study began with an assessment that included spirometry and volumetric capnography (VCap) and assessment of respiratory muscle strength by maximal inspiratory and expiratory pressure, PImax and PEmax, respectively. Two scales, the Medical Research Council (MRC) dyspnea scale and the modified fatigue impact scale (MFIS) were then applied and the [Lac] was subsequently assessed before and after the 6-minute walk test (6MWT). After this initial assessment, the patients were instructed on how to use the IMT device and took it to train at home, returning every 6 weeks for PImax and PEmax assessment and training load adjustment. Each newly included patient received a training device with a true or sham load, according to an alternating list kept by the investigator. After a period totaling 18 weeks, the patients underwent the final evaluation composed of the same tests as the first evaluation (Figure 1).

Figure 1
Patients flow diagram. Vcap, Volumetric capnography; PImax, maximum inspiratory pressure; PEmax, maximum expiratory pressure; MRC, Medical Research Council dyspnea scale; MFIS, Modified Fatigue Impact Scale; [Lac], blood lactate concentration; 6MWT, 6-minute walk test; Borg, modified Borg scale.

The entire study was carried out at Hospital de Clínicas at UNICAMP. All evaluations at baseline and at the end of 18 weeks were performed by the same physiotherapists, according to protocols, and under the same conditions. The evaluations were carried out by three physiotherapists, one being responsible for volumetric capnography (VCap), the other for spirometry and the third, along with the second, for the other evaluations.

Pulmonary Function Tests

The pulmonary Function Tests (PFT) included spirometry and volumetric capnography (VCap) and were always performed in the morning at the Pulmonary Function Laboratory of the Pulmonary Diseases Service at the Hospital de Clinicas da UNICAMP. Spirometry is capable of measuring the inhalation and exhalation of air volumes as a function of time.1515 Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al. Standardisation of spirometry. Eur Respir J. 2005;26(2):319-38. All the patients underwent spirometry before and 20 min after the inhalation of 400 µg of salbutamol, using a spirometer (EasyOne-PC®, NDD Medizintechnik AG, Zurich, Switzerland). The test was performed according to the American Society guidelines1515 Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al. Standardisation of spirometry. Eur Respir J. 2005;26(2):319-38. and the analyzed values were: forced vital capacity (FVC), forced expiratory volume in the first second (FEV1), FEV1/FVC ratio and mean forced expiratory flow between 25-75% of expired vital capacity (FEF25-75%).

To perform the VCap, a CO2SMOS Plus 8100 (Dixtal/Novametrix; Respironics, Murrisville, PA, USA) was used. The VCap assesses the concentration of expired CO2 as a function of expired tidal volume, analyzing the functional components of tidal volume (VC) and dead space; this method enables the determination of the relationship between ventilation and perfusion.1616 Verscheure S, Massion PB, Verschuren F, Damas P, Magder S. Volumetric capnography: lessons from the past and current clinical applications. Crit Care. 2016;20(1):1-9.

17 Veronez L, Pereira MC, Maria S, Da Silva D, Affi Barcaui L, Mello E, et al. Volumetric capnography for the evaluation of chronic airways diseases Background: obstructive lung diseases of different etiologies present with progressive. Int J Chron Obstruct Pulmon Dis. 2014:983-9.
-1818 Modena DAO, Moreira MM, Paschoal IA, Pereira MC, Martins LC, Cazzo E, et al. Respiratory evaluation through volumetric capnography among grade III obese and eutrophic individuals: a comparative study. Sao Paulo Med J. 2019;137(2):177-83.

The Analysis Plus software was used for online recording of respiratory cycles, continuing for five minutes. An off-line sequence of patient respiratory cycles was selected at the end of the data collection to accommodate a variation of less than 15% for the expiratory tidal volume and less than 5% for the end tidal partial pressure of CO2 concentration (PetCO2). In addition, sequences showing phases 2 and 3 slopes equal to zero were eliminated, along with discrepant values.1818 Modena DAO, Moreira MM, Paschoal IA, Pereira MC, Martins LC, Cazzo E, et al. Respiratory evaluation through volumetric capnography among grade III obese and eutrophic individuals: a comparative study. Sao Paulo Med J. 2019;137(2):177-83.

Respiratory muscle strength

The PEmax and PImax were determined using a digital manuvacuometer (MVD30-Globalmed). The patient used a nasal clip and remained seated during these maneuvers. The PImax and PEmax evaluation maneuvers were performed from residual volume (RV) and total lung capacity (TLC), respectively.

For data analysis, the highest value was recorded, each maneuver being performed at least five times, provided that the difference between the highest and the lowest value among three values presented a difference less than 10%.1919 Luiz LC, Marson FAL, Bresciani Almeida CC, Toro AA, Nucci A, Ribeiro JD. Analysis of motor and respiratory function in Duchenne muscular dystrophy patients. Respir Physiol Neurobiol. 2019;262:1-11.,2020 Gayraud J, Ramonatxo M, Rivier F, Humberclaude V, Petrof B, Matecki S. Ventilatory parameters and maximal respiratory pressure changes with age in Duchenne muscular dystrophy patients. Pediatr Pulmonol. 2010;45(6):552-9.

Medical Research Council dyspnea scale (MRC)

The MRC scale consists of only five items, of which the patient chose the item that corresponded to how much dyspnea limited his or her daily living activities (DLA). The patient then reported the degree of dyspnea subjectively, choosing a value between 1 and 5, being: 1 (only suffers from shortness of breath during intense exercise), 2 (suffers from shortness of breath when walking hastily or climbing a ramp), 3 (walking slower than people of the same age due to shortness of breath or having to stop to breathe even when walking slowly), 4 (stops to breathe after walking less than 100 m or after a few minutes) and 5 (feels so short of breath that does not leave the house anymore, or feels short of breath when getting dressed). The higher the score, the greater the limitation of DLA due to dyspnea. When the patient reported no dyspnea status, the classification was 0.66 Delclaux C, Zerah-Lancner F, Bachir D, Habibi A, Monin JL, Godeau B, et al. Factors associated with dyspnea in adult patients with sickle cell disease. Chest. 2005;128(5):3336-44. In Brazil, the MRC scale was validated by Kovelis et al.2121 Kovelis D, Segretti NO, Probst VS, Lareau SC, Brunetto AFPF. Validation of the Modified Pulmonary Functional Status and Dyspnea Questionnaire and the Medical Research Council scale for use in Brazilian patients with chronic obstructive pulmonary disease. J Bras Pneumol. 2008;34(12):1008-18.

Modified fatigue impact scale (MFIS)

The MFIS consists of 21 items distributed in three domains: physical (9 items), cognitive (10 items) and psychosocial (2 items), so that for each item there are 4 possible answers, graded from 0 to 4, in which the highest scores reflect greater impact of fatigue.

For the physical domain, the scores vary from 0 to 36, the cognitive ranges from 0 to 40 and the psychosocial ranges from 0 to 8. Therefore, the total score of the MFIS is given by the sum of the three domains and ranges from 0 to 84 points. Values below 38 are classified as the absence of fatigue. From 38, the higher the score, the greater the degree of patient fatigue.

The MFIS underwent cross-cultural adaptation and was validated for the Portuguese language (in the Brazilian standard), by Pavan et al., in 2007.2222 Pavan K, Schmidt K, Marangoni B, Mendes MF, Tilbery CP, Lianza S. Esclerose múltipla: adaptação transcultural e validação da escala modificada de impacto de fadiga TT - Multiple sclerosis: cross-cultural adaptation and validation of the modified fatigue impact scale. Arq Neuropsiquiatr. 2007;65(3a):669-73.

Blood lactate concentration ([Lac])

The [Lac] was measured preand immediately post-6MWT, using a portable lactate meter (Accutrend plus, Roche, Switzerland), which has a procedure previously validated in the scientific literature.2323 Baldari C, Bonavolontà V, Pietro Emerenziani G, Gallotta MC, Guidetti L, Silva AJ. Accuracy, reliability, linearity of Accutrend and Lactate Pro versus EBIO plus analyzer. Eur J Appl Physiol. 2009;107(1):105-11. Measurements were performed in blood collected from fingertips after the superficial perforation with a disposable lancet. The cleaning of the skin was carried out before and after the perforation with 70% alcohol-soaked cotton.

Six-minute walk test

All the participants performed the six-minute walk test (6MWT) according to the standardized protocol2424 ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories, ATS statement. guidelines for the six-minute walk test. Am J Respir Crit Care Med. 2002;166(1):111-7. before and after the IMT period. A pulse oximeter (Nonin Medical, Inc.; MN, USA) was used to evaluate pulse rate and oxygen saturation. The modified Borg scale (Borg) was used to evaluate dyspnea and perceived exertion rate scores before and after the 6MWT, ranging from 0 to 10 (0 being n¨ othinga¨ nd 10 being m¨ aximal¨).2525 Borg G. Psychophysical bases of perceived exertion. Med Sci Sport Exerc. 1982;14(5):377-81. The patients were gently and periodically encouraged to walk on a level surface 30 m long during the 6-minute test.

Inspiratory muscle training (IMT) procedure

A specific inspiratory training device (POWERbreathe® Wellness, IMT Technologies Ltd., Birmingham, UK) was used for the IMT, with load adjustment based on PImax. Instructions for proper use at home consisted of exclusive diaphragmatic breathing, not using accessory respiratory muscles during training. The training group used an adjusted load of 30% of the PImax during the first two weeks of training, aiming to facilitate the adaptation to the use of the device, with the load being adjusted by 40% of the PImax during the third week, 50% of the PImax during the fifth week and 60% of the PImax during the sixth week of the IMT up to the end of the study. Every 6 weeks of IMT, respiratory muscle strength (PImax and PEmax) was reassessed and, if the PImax was altered, the load was readjusted. The SG group performed the training with the same device, but without the flap valve; however, load adjustments were simulated so that the patients did not realize that they had used a sham load. Patients from both groups were instructed to perform the IMT daily for 10 min per day with a 1-min rest after 5 min, 7 days a week, until completing 18 weeks of training. The number of repetitions was between 13 and 15 breaths per minute during the 10 min of daily training.

All participants received a paper notepad for notes on the date and time of the IMT. If they did not do IMT on a given day, they could also write down the reason that prevented them from doing so. In addition, for greater reliability when performing the IMT at home, patients were also contacted by cell phone (voice or text message) to verify that they were performing the training correctly and daily or to clarify any problems they might have had with the use.

Statistical analysis

Exploratory data analysis was performed through summary measures (median, minimum and maximum). Comparison between groups was performed using the Mann-Whitney, Fisher’s exact or Chi-square tests. The comparison between times and groups was performed with the ANOVA for repeated measures with the transformed responses in ranks. Differences with a p-value < 0.05 were considered significant. All statistical analyses were performed using the Statistical Analysis System (SAS) for Windows, version 9.4 (SAS Institute Inc., Cary, NC, USA).

Results

Thirty patients were initially recruited, however five were excluded. Three patients from the SG group dropped out for personal reasons and two other patients belonging to the TG group were excluded for remaining more than 7 days without training, one due to pneumonia and the other due to a sickle cell crisis. Therefore, 25 patients in total participated until the end of the study. Descriptive characteristics of the participants are shown in Table 1. There were no significant differences between the TG and SG groups as for age, sex, body mass index (BMI), hemoglobin gene mutation (p > 0.05) (Table 1).

Lung function

Regarding spirometry, none of the variables showed a significant change, comparing the preand post-IMT periods in both groups. However, FEV1, FEV1/FVC and FEF 25 - 75% showed a significant increase (p < 0.05) in the preand post-bronchodilator comparison, both in the initial and final evaluations, but not in the comparison between the evaluations (Table 2).

Volumetric capnography (VCap)

The results of volumetric capnography showed no statistically significant change (p > 0.05) in the variables evaluated in the comparison between the two groups (SG and TG), except for the inspiratory time (Ti) variable, which was significantly higher in the SG compared to the TG (p < 0.05, group effect). However, the following variables: inspiratory tidal volume (Vi), peak expiratory flow (PEF), phase 3 slope of the capnography curve (P3Slp), phase 3 slope normalized according to the expired tidal volume (P3Slp/Ve), peak inspiratory flow (PIF) and Tobin Index (RSBI), had a significant change regarding the time effect in both groups (p < 0.05) (Table 3).

Table 1
Characteristics of the study groups.
Table 2
Pulmonary function test pre- and post-bronchodilator.

Respiratory muscle strength (RMS)

In both groups, the PImax and PEmax significantly increased after the IMT (p < 0.05, time effect). For the PEmax, there was a significant increase in the second evaluation, in relation to the first, and in the fourth evaluation, in relation to the third evaluation. Regarding the PImax, there was a significant increase in the second evaluation, compared to the first, and in the third, in relation to the second (Figure 2A and B).

Medical Research Council (MRC) dyspnea Scale and Modified Fatigue Impact Scale (MFIS)

The MRC scale showed a significant reduction in the final evaluation of the values measured (p < 0.05, time effect), the pre-IMT and for both the SG and TG (Figure 2C), with the medians of both groups varying in an identical manner. No significant changes were detected in the MFIS.

Six-minute walk test (6MWT)

In both groups, there was a significant increase in the distance covered after the IMT, compared to the pre-IMT assessment (p < 0.05) (Figure 2D and Table 4).

Blood lactate concentration [Lac]

The [Lac] was significantly increased (p < 0.05), comparing preand post-6MWT, before and after IMT in both groups; however, there were no changes in the comparison between the initial and final evaluations (Table 4).

Modified Borg scale (Borg)

The values reported by the patients on the Borg, used before and after the 6MWT application, showed a significant increase between the preand post-6MWT evaluations in both groups (p < 0.05), but there were no changes in the comparison between the initial and final evaluations (Table 4).

All the data were also analyzed in patients grouped according to the sickle cell disease severity, i.e., HbSS plus HbSβo vs HbSC plus HbSβ+, and revealed no significant difference.

Discussion

This study aimed to evaluate the effects of long-term IMT on sickle cell disease patients. In both groups, control or true load, there was a significant increase in inspiratory and expiratory muscle strength at the end of the training protocol, improvement in volumetric capnography variables, exercise tolerance and reduction of dyspnea in performing daily life activities. Regarding respiratory muscle strength, although the effects of the IMT on patients with sickle cell disease have been poorly studied,1414 Camcıoğlu B, Boşnak-Güçlü M, Karadallı MN, Akı ŞZ, Türköz-Sucak G. The role of inspiratory muscle training in sickle cell anemia related pulmonary damage due to recurrent acute chest syndrome attacks. Case Rep Hematol. 2015;2015:1-6. studies conducted on individuals with chronic obstructive pulmonary disease (COPD),1010 Cutrim AL, Duarte AA, Silva-Filho AC, Dias CJ, Urtado CB, Ribeiro RM, et al. Inspiratory muscle training improves autonomic modulation and exercise tolerance in chronic obstructive pulmonary disease subjects: a randomized-controlled trial. Respir Physiol Neurobiol. 2019;263:31-7. older women2626 Rodrigues GD, Gurgel L, R. Gonçalves T, Soares Silva. Inspiratory muscle training improves physical performance and cardiac autonomic modulation in older women. Eur J Appl Physiol. 2018;118(6):1143-52. or those with ankylosing spondylitis1111 Basakci Calik B, Gur Kabul E, Taskın H, Telli Atalay O, Bas Aslan U, Tascı M, et al. The efficiency of inspiratory muscle training in patients with ankylosing spondylitis. Rheumatol Int. 2018;38(9):1713-20. showed an increase in the PImax and PEmax after the termination of the training protocol. Ciesla2727 Ciesla ND. Chest physical therapy for patients in the intensive care unit. Phys Ther. 1996;76(6):609-25. includes the IMT as one of the types of breathing exercises and points out several benefits in these exercises, as it improves thoracic-cage mobility, increased tidal volume and increased inspiratory capacity. Our study, however, also showed a significant increase in respiratory muscle strength in the control group. We hypothesized that, as the two groups performed 10 min of deep inspiration daily, that is, they actually did breathing exercises, despite the real resistance to the inspiratory flow of home exercises for the TG, the IMT was possibly able to modify the respiratory mechanics in both groups, leading to an increase in the PImax and PEmax, not only for the true load group, but also for the control group.

Table 3
Volumetric capnography.
Table 4
six-minute walk test and related tests.
Figure 2
A: Maximal inspiratory pressure (PImax) in the first, second, third, and last evaluation, PImax1 < PImax2 < PImax3, PImax4. B: Maximal expiratory pressure (PEmax) in the first, second, third, and last evaluation, PEmax1 < PEmax2, PEmax3 < PEmax4. Figure C: Medical Research Council (MRC) scale of dyspnea in the first and last evaluation, MRC1 > MRC2. Figure D: Distance measurements of the 6-minute walking test (6MWT) in the first and last evaluation, 6MWT1 < 6MWT2. The statistical test used was ANOVA on ranks transformation, showing a time effect of the training for both groups (p < 0.05). Statistical analysis showed no interaction or group effect. Values are median.

The spirometry results here obtained showed no significant differences regarding the initial and final evaluations, in either group. Nor were there any changes in these variables reported for older women, COPD or heart failure.2626 Rodrigues GD, Gurgel L, R. Gonçalves T, Soares Silva. Inspiratory muscle training improves physical performance and cardiac autonomic modulation in older women. Eur J Appl Physiol. 2018;118(6):1143-52.,2828 Beckerman M, Magadle R, Weiner M. The effects of 1 year of specific inspiratory muscle training in patients with COPD. Chest. 2005;128(5):3177-82.,2929 Laoutaris I, Dritsas A, Brown MD, Manginas A, Alivizatos PA, Cokkinos DV. Inspiratory muscle training using an incremental endurance test alleviates dyspnea and improves functional status in patients with chronic heart failure. Eur J Prev Cardiol. 2004;11(6):489-96. On the other hand, in our study the volumetric capnography showed significant changes in some variables after the IMT in both groups. Inspired volume (Vi), peak expiratory flow (PEF) and peak inspiratory flow (PIF) increased significantly, while the Tobin index (RSBI) decreased significantly. These changes suggest that daily deeper inspiratory exercises influenced an increase in inspired and exhaled air volume, even in the control group.

Another variable, the phase 3 slope (P3Slp), decreased significantly in both groups in the final assessment, compared to the initial assessment. As phase 3 of the capnogram represents the elimination of pure alveolar gas, the greater the plateau of the curve in this phase, the more homogenous the distribution of ventilation in distal airspaces.3030 da Silva SM, Paschoal IA, de Capitani EM, Moreira MM, Palhares LC, Pereira MC. COPD phenotypes on computed tomography and its correlation with selected lung function variables in severe patients. Int J COPD. 2016;11(1):503-13. The alveolar recruitment is related to a reduced P3Slp.3131 Godet T, Constantin JM, Jaber S, Futier E. How to monitor a recruitment maneuver at the bedside. Curr Opin Crit Care. 2015;21(3):253-8. Therefore, the reduction in the P3Slp observed in this study suggests that there was alveolar recruitment after the IMT. Furthermore, considering that the higher the expired volume (Ve), the lower the P3Slp, this variable was normalized according to the expired tidal volume (P3Slp/Ve),3232 Ribeiro MÂ, Silva MT, Ribeiro JD, Moreira MM, Almeida CC, Almeida-Junior AA, et al. Volumetric capnography as a tool to detect early peripheric lung obstruction in cystic fibrosis patients. J Pediatr. 2012;88(6):509-17. which also decreased after the IMT, confirming the result presented by the P3Slp.

In both groups after the IMT, a significant reduction in dyspnea assessed by the MRC was observed. This scale has been used for many years to classify the limitation imposed by dyspnea on the DLA.2121 Kovelis D, Segretti NO, Probst VS, Lareau SC, Brunetto AFPF. Validation of the Modified Pulmonary Functional Status and Dyspnea Questionnaire and the Medical Research Council scale for use in Brazilian patients with chronic obstructive pulmonary disease. J Bras Pneumol. 2008;34(12):1008-18.,3333 Bestall JC, Paul EA, Garrod R, Garnham R, Ones PW, Wedzicha J. Usefulness of the Medical Research Council (MRC) dyspnoea scale as a measure of disability in patients with chronic obstructive pulmonary disease. Thorax. 1999;54(7):581-6. The scale is a simple application tool, which allows the patient to indicate to what extent their dyspnea affects their mobility. This is a widely used scale for the assessment of dyspnea in patients with COPD; however, this scale has also been used as an instrument for the indirect measurement of dyspnea in a study of patients with sickle cell disease.66 Delclaux C, Zerah-Lancner F, Bachir D, Habibi A, Monin JL, Godeau B, et al. Factors associated with dyspnea in adult patients with sickle cell disease. Chest. 2005;128(5):3336-44. Other studies that evaluated the effects of the IMT on patients with pulmonary arterial hypertension, as well as COPD, showed a reduction in dyspnea after the end of the training protocol in the true load group.3434 Sánchez Riera H, Montemayor Rubio T, Ortega Ruiz F, Cejudo Ramos P, Del Castillo Otero D, Elias Hernandez T. Inspiratory muscle training in patients with COPD: Effect on dyspnea, exercise performance, and quality of life. Chest. 2001;120(3):748-56.,3535 Saglam M, Arikan H, Vardar-Yagli N, Calik-Kutukcu E, Inal-Ince D, Savci S, et al. Inspiratory muscle training in pulmonary arterial hypertension. J Cardiopulm Rehabil Prev. 2015;35(3):198-206. In our study, improvement in dyspnea may have occurred due to increased respiratory muscle strength and increased post-IMT alveolar recruitment in both groups.

The MFIS, which allows for the indirect assessment of the impact of fatigue on the quality of life, did not change significantly at the end of the IMT in both groups. This scale, originally developed by Fisk et al. in 1994,3636 Fisk JD, Ritvo PG, Ross L, Haase DA, Marrie TJ, Schlech WF. Measuring the fatigue impact of fatigue : initial validation measuring the functional impact scale. Clin Infect Dis. 1994;18 Suppl 1:S79-83. though widely used to assess the impact of fatigue on the quality of life in patients with multiple sclerosis, has also been used to assess indirect fatigue in a study on patients with sickle cell disease.66 Delclaux C, Zerah-Lancner F, Bachir D, Habibi A, Monin JL, Godeau B, et al. Factors associated with dyspnea in adult patients with sickle cell disease. Chest. 2005;128(5):3336-44. Both groups however, had a significant increase in the distance covered during the 6MWT, which can be considered a form of direct assessment of fatigue66 Delclaux C, Zerah-Lancner F, Bachir D, Habibi A, Monin JL, Godeau B, et al. Factors associated with dyspnea in adult patients with sickle cell disease. Chest. 2005;128(5):3336-44. and exercise functional capacity. Some studies on patients with COPD and asthma have also reported reduced muscle fatigue and increased exercise functional capacity after the IMT.3434 Sánchez Riera H, Montemayor Rubio T, Ortega Ruiz F, Cejudo Ramos P, Del Castillo Otero D, Elias Hernandez T. Inspiratory muscle training in patients with COPD: Effect on dyspnea, exercise performance, and quality of life. Chest. 2001;120(3):748-56.,3737 Basso-Vanelli RP, Di Lorenzo VA, Labadessa IG, Regueiro EM, Jamami M, Gomes ELCD. Effects of inspiratory muscle training and calisthenics-and-breathing exercises in COPD with and without respiratory muscle weakness. Respir Care. 2016;61:50-60. There is an increase in the level of metabolites in the circulation, such as lactate and hydrogen ions because of the increase in the anaerobic metabolism induced by exercise in hypoxia.1313 Álvarez-Herms J, Julià-Sánchez S, Corbi F, Odriozola-Martínez A, Burtscher M. Putative role of respiratory muscle training to improve endurance performance in hypoxia: a review. Front Physiol. 2019;9:1970. Especially in the respiratory muscles, the IMT improves clearance ability and tolerance to the levels of lactate and hydrogen ions.3838 McConnell AK, Sharpe GR. The effect of inspiratory muscle training upon maximum lactate steady-state and blood lactate concentration. Eur J Appl Physiol. 2005;94(3):277-84.,3939 Brown PI, Sharpe GR, Johnson MA. Inspiratory muscle training abolishes the blood lactate increase associated with volitional hyperpnoea superimposed on exercise and accelerates lactate and oxygen uptake kinetics at the onset of exercise. Eur J Appl Physiol. 2012;112(6):2117-29. Therefore, strengthening of inspiratory muscles probably attenuated the metaboreflex of the inspiratory muscles, which increased blood flow and oxygenation of limb muscles, reducing premature fatigue during exercise in hypoxia.1313 Álvarez-Herms J, Julià-Sánchez S, Corbi F, Odriozola-Martínez A, Burtscher M. Putative role of respiratory muscle training to improve endurance performance in hypoxia: a review. Front Physiol. 2019;9:1970.,4040 Archiza B, Andaku DK, Caruso FC, Bonjorno JC, Oliveira CRD, Ricci PA, et al. Effects of inspiratory muscle training in professional women football players: a randomized sham-controlled trial. J Sports Sci. 2018;36(7):771-80.,4141 Hansen J, Sander M, Hald CF, Victor RG, Thomas GD. Metabolic modulation of sympathetic vasoconstriction in human skeletal muscle: Role of tissue hypoxia. J Physiol. 2000;527(2):387-96. Nevertheless, these results must be viewed with caution, since direct metaboreflex measurements were not performed in the present study.

Regarding the [Lac], normal values in healthy individuals should be between 0.5 and 2.0 mmol/l.4242 Hallisey SD, Greenwood JC. Beyond mean arterial pressure and lactate: perfusion end points for managing the shocked patient. Emerg Med Clin North Am. 2019;37(3):395-408. However, there was a tendency for the [Lac] to be higher in patients evaluated before the 6MWT and therefore at rest, when compared to normal values in healthy individuals. Some of the evaluated patients had pre-TC6 maximum values between 5.2 mmol/l and 8.1 mmol/l, i.e., well above the maximum normal value found in healthy individuals. Some authors attribute the increase in the [Lac] in patients with sickle cell disease to the adaptation to the lower O2 availability to body cells, caused by the change from the basal to the anaerobic metabolic pathway, due to the sickle cell process. Thus, the anaerobic glycolysis increases the participation in the cellular energy metabolism, favoring the production and increase in the [Lac].4343 Petto J, Jesus JBD, Vasques LM, Pinheiro RL, Oliveira AM, Spinola KA, et al. Resting blood lactate in individuals with sickle cell disease. Rev Bras Hematol Hemoter. 2010;33(1):26-30.,4444 Phypers B, Pierce JMT. Lactate physiology in health and disease. Contin Educ Anaesthesia. Crit Care Pain. 2006;6(3):128-32.

The [Lac] showed no significant change in the comparison of the initial and final evaluation results. As expected, there was an increase in the [Lac] after the 6MWT, probably related to the greater participation of the anaerobic metabolism.4545 Faude O, Meyer T, Kindermann W. Lactate threshold concepts how valid are they? (PDF Download Available). Sports Med. 2009;39(6):469-90. The [Lac] tends to increase significantly to levels between 50% and 60% of the maximum oxygen uptake rate (VO2max).4646 Ferguson BS, Rogatzki MJ, Goodwin ML, Kane DA, Rightmire Z, Gladden LB. Lactate metabolism: historical context, prior misinterpretations, and current understanding. Eur J Appl Physiol. 2018;118(4), 691-728691-728. Patients with sickle cell disease may have a reduction in VO2max due to the pathophysiological changes of the disease itself that reduce the half-life of red blood cells, leading to reduced oxygen transport. In addition, intrinsic lung disease also worsens peripheral oxygenation, contributing to the lower oxygen uptake peak in these patients.4343 Petto J, Jesus JBD, Vasques LM, Pinheiro RL, Oliveira AM, Spinola KA, et al. Resting blood lactate in individuals with sickle cell disease. Rev Bras Hematol Hemoter. 2010;33(1):26-30.,4747 Liem RI, Nevin MA, Prestridge A, Young LT, Thompson AA. Functional capacity in children and young adults with sickle cell disease undergoing evaluation for cardiopulmonary disease. Am J Hematol. 2009;84(10):645-9. Thus, these patients tend to have a greater increase in the [Lac] during exertion. Thus, IMT does not appear to have influenced an improvement in these conditions and, therefore, did not contribute to a lower elevation in the [Lac].

Finally, the comparison of patients grouped according to disease severity revealed no differences, suggesting homogeneity of the patients, probably due to the medical intervention in the natural history of the disease.

However, despite the important results found, we believe that other studies with a larger sample size and over a longer period should be made to test our hypothesis.

Conclusion

In this study on SCD, the inspiratory muscle training at home is a strategy that can be easily applied in outpatients, providing benefits, such as increasing respiratory muscle strength, improvement in Vcap and exercise tolerance and reducing dyspnea in activities of daily living. Further studies in a larger sample and over a longer period should be performed to obtain more details on the effects of the IMT on patients with SCD.

Abbreviations:

  • 6MWT  6-minute walk test
  • CO2  carbon dioxide
  • COPD  chronic obstructive pulmonary disease
  • DLA  daily living activities
  • FEF 25 - 75%  mean forced expiratory flow between 25-75% of expired vital capacity
  • FEV1  forced expiratory volume in the first second
  • FEV1/FVC ratio  ratio of forced expiratory volume in 1 second to forced vital capacity
  • FVC  forced vital capacity
  • HbC  hemoglobin C
  • HbS  hemoglobin S
  • HR  heart rate
  • IMT  inspiratory muscle training
  • [Lac]  blood lactate concentration
  • MFIS  modified fatigue impact scale
  • MRC  Medical Research Council dyspnea scale
  • MV alv  alveolar minute volume
  • NIP  negative inspiratory pressure
  • PEF  peak expiratory flow
  • PEmax  maximal expiratory pressure
  • PeCO2  mean end-tidal partial pressure of CO2
  • PetCO2  end-tidal partial pressure of CO2
  • P2Slp  phase 2 slope
  • P3Slp  phase 3 slope
  • P3Slp/Ve  phase 3 slope normalized according to expired tidal volume
  • PIF  peak inspiratory flow
  • PFT  pulmonary function tests
  • PImax  maximal inspiratory pressure
  • RMS  respiratory muscle strength
  • RR  respiratory rate
  • RSBI  Tobin index
  • RV  residual volume
  • SCD  sickle cell disease
  • HbSC  heterozygote composed of hemoglobin S and hemoglobin C
  • SpO2  oxygen saturation
  • HbSS  homozygous for hemoglobin S
  • HbSβ0  sickle cell/β-thalassemia phenotype with higher degree of hematological involvement in comparison to HbSβ+ patients
  • HbSβ+  sickle cell/β-thalassemia phenotype with lower degree of hematological involvement in comparison to HbSβ+ patients
  • SG  sham load group
  • Te  expiratory time
  • TG  true load group
  • Ti  inspiratory time
  • TLC  total lung capacity
  • UNICAMP  University of Campinas
  • VCap  volumetric capnography
  • VCO2  CO2 production
  • VCO2/br  CO2 production per breath
  • VD (aw)  anatomical dead space
  • Ve  expiratory tidal volume
  • Vi  inspiratory tidal volume
  • VO2  maximum oxygen uptake
  • VT  tidal volume.
  • Funding
    This study was funded in part by the grant #2011/51959-0 and 2017/21801-2d, the São Paulo Research Foundation (FAPESP) and the Ministry of Science, Technology, Innovations and Communications (CNPq) grant # 301676/2013-5.

Availability of data and materials

The datasets generated during and/or analyzed during the current study are available upon request to the corresponding author.

Ethics approval and consent to participate

This study complied with the declaration of Helsinki and was approved by the Research Ethics Committee of the University of Campinas (CAAE 44635415.2.0000.5404).

Consent for publication

Not applicable.

Acknowledgments

The authors would like to thank Prof. Alberto Cliquet Jr. for providing a space at the Laboratory of Biomechanics and Locomotive Apparatus Rehabilitation at UNICAMP, Roberto Zulli for the statistical analysis and Raquel S. Foglio for the writing assistance and English revision.

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Publication Dates

  • Publication in this collection
    29 Nov 2021
  • Date of issue
    2021

History

  • Received
    28 Apr 2020
  • Accepted
    23 Aug 2020
  • Published
    14 Sept 2020
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular (ABHH) R. Dr. Diogo de Faria, 775 cj 133, 04037-002, São Paulo / SP - Brasil - São Paulo - SP - Brazil
E-mail: htct@abhh.org.br