Literature DB >> 29075109

Echo intensity of the rectus femoris in stable COPD patients.

Xiong Ye1, Mingjie Wang2, Hui Xiao2.   

Abstract

OBJECTIVE: The aim of this study was to investigate whether echo intensity of the rectus femoris when measured using ultrasound can distinguish muscles affected by COPD compared with healthy non-COPD affected muscles and whether the severity of ultrasonic abnormalities was associated with health-related quality of life (HRQoL).
METHODS: Echo intensity, areas of the rectus femoris, and the thickness of quadriceps muscles were measured using ultrasound in 50 COPD outpatients and 21 age-matched non-COPD controls. The results of the 8-Item Short-Form Health Survey and the functional assessment of chronic illness therapy fatigue scales were used to evaluate HRQoL.
RESULTS: There was a significantly higher echo intensity of the rectus femoris in all stages of COPD patients than in age-matched non-COPD subjects; the quadriceps muscle thickness and cross-sectional area of the rectus femoris significantly decreased in COPD GOLD III-IV only. Furthermore, in our stable COPD patients, echo intensity of the rectus femoris was associated with HRQoL independently.
CONCLUSION: Quantitative ultrasound distinguishes healthy muscles from those affected by COPD grade I-IV, and quality and quantity of muscles are associated with HRQoL and forced expiratory volume in 1 second. Ultrasonic echo intensity of the rectus femoris may be a useful instrument for assessing disease severity and monitoring the changes of skeletal muscle resulting from disease progression or clinical intervention in patients with COPD.

Entities:  

Keywords:  chronic obstructive pulmonary disease; echo intensity; rectus femoris; ultrasound

Mesh:

Year:  2017        PMID: 29075109      PMCID: PMC5648322          DOI: 10.2147/COPD.S143645

Source DB:  PubMed          Journal:  Int J Chron Obstruct Pulmon Dis        ISSN: 1176-9106


Introduction

Skeletal muscle dysfunction contributes to impaired physical capacity, reduced health-related quality of life (HRQoL), increased health care utilization and even mortality in COPD patients,1,2 independent of airflow obstruction.3 Quadriceps weakness is demonstrable in one-third of COPD patients,4 provides powerful prognostic information and is associated with HRQoL in patients in all stages of COPD.5 People with COPD are in a “downward disease spiral,” where progressive dyspnea leads to a sedentary lifestyle with consequent muscle deconditioning and further inactivity.6,7 In addition, systemic factors, such as inflammation, oxidative stress, corticosteroid use, hormonal disturbances and nutritional deficits, are involved in the development of muscle weakness.8,9 Quadriceps weakness together with fatigue is the most prominent disabling symptom in many COPD patients and considerably impacts their HRQoL.10,11 Lower limb strength has been demonstrated to correlate with rectus femoris cross-sectional area (RFcsa) as measured by ultrasound (US) and computed tomography in mild-to-severe COPD patients.12,13 US imaging is a radiation-free, safe and easily accessible method which is suitable for the assessment of the size and echo intensity (EI) of skeletal muscle.14,15 The increasing of EI of skeletal muscles can be recognized early and is a key parameter in the diagnosis of chronic neuromuscular disorders,16 and was related to the decrease of muscle strength in middle-aged and elderly people independent of age or muscle size.17 Whether EI of the rectus femoris quantified by US is increased or not and its relevance to the HRQoL and lung function in COPD patients is unclear. The aim of this study was to investigate the relationship between US of the quadriceps, lung function and HRQoL in subjects with COPD. We hypothesized that differences of the EI levels of the rectus femoris measured by US would be observed in mild-to-severe COPD patients compared with age-matched non-COPD subjects. Furthermore, the EI of the rectus femoris would be associated with HRQoL, as measured by the 8-Item Short-Form Health Survey (SF-8) and the functional assessment of chronic illness therapy fatigue (FACITF) scales.

Materials and methods

Study design

From December 2015 to June 2016, we investigated 50 stable COPD patients and 21 non-COPD controls in the Department of Respiratory Medicine, Shanghai General Hospital, Shanghai, China. All subjects completed structured interview and spirometry and US measurements of the quadriceps muscle. The diagnosis of COPD was performed by lung function tests. Subjects were considered as suffering from COPD if their forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) ratio was less than 0.7, after the administration of a reversibility test with 0.4 mg salbutamol. The severity of COPD was classified according to the American Thoracic Society (ATS) guidelines: grade I FEV1≥80% predicted; grade II FEV1≥50% and <80% predicted; grade III FEV1≥30% and <50% predicted; grade IV FEV1<30% predicted. Patients affected by neuromuscular disease or having a history of knee and hip surgery were excluded. All of the participants were living independently, had been clinically stable for at least 4 weeks before the visit and were able to walk without an assistive device. The study was approved by the ethics committee of Shanghai General Hospital (number 2015ky134), and written informed consent was provided by all participants.

Baseline measurements

Specially trained technician performed the interviews and the lung function tests. The questionnaires were validated in other studies.18–20 They included questions about HRQoL (SF-8 and FACITF version 4), respiratory symptoms, heart diseases, hypertension, diabetes, use of medicines and smoking habits.21 Body mass index (BMI) was calculated from weight and height. For spirometry and the 6-minute walk distance (6MWD) test, the ATS guidelines were followed.22,23

SF-8

We used a Chinese version of the SF-8 that was constructed to provide a shorter alternative to the SF-36 and SF-12 for use in general and specific populations, and scored by using the Smart Measurement® Online scoring service, available at http://www.qualitymetric.com. Two summary measures were obtained: physical component summary (PCS) and mental component summary (MCS). A higher score was a better self-reported HRQoL, based on answers about health in the past 4 weeks.

FACITF

FACITF scale is a 13-item self-completed questionnaire, designed for chronic diseases, which has previously been used for COPD patients.24,25 FACITF is assumed from statements that fit the person’s experience during the last 7 days asking about the intensity of fatigue as well as its impact on everyday life. The subjects respond to each item by choosing one of the following five options: not at all (4 scores); a little bit (3 scores); somewhat (2 scores); quite a bit (1 score); very much (0 score). Items seven and eight have to be reversely scored. Overall scores of the FACITF scale range from 0 to 52, with higher scores signifying less fatigue.26

US measurements

The participants were in the supine position with the lower limbs relaxed completely. US scanning was performed with LOGIQ 5A (GE Healthcare Bio-Sciences Corp., Piscataway, NJ, USA) and a linear transducer (10 MHz). All scans were made through the quadriceps muscle halfway along the line from the anterior–superior iliac spine to the superior aspect of the patella.27 To show the best bone echo the transducer is always perpendicular to the targeted muscle. Small adjustments in the angle of the ultrasonic beam will affect muscle echo texture measurements.28 A minimum pressure was maintained at the transducer to avoid distortion of the skin and subcutaneous tissues, using a generous amount of contact gel.14 The gain (86 dB), compression (70 dB), depth (6 cm), time gain compensation (in the neutral position) and focus were kept constant between subjects. Three consecutive images were produced by the same investigator who was blinded to the results of spirometry and questionnaires. The subcutaneous fat thickness (SFT) of the anterior compartment of the mid-thigh was defined as the distance between the dermis and fascia of the rectus femoris muscle. The inner outline of the rectus femoris was manually traced to calculate RFcsa by a movable cursor on a frozen image, while quadriceps muscle thickness (QMT) was measured as the vertical distance from fascia of the rectus femoris to the underlying femur (Figure 1).
Figure 1

Ultrasonography measurements of the subcutaneous fat thickness (SFT), quadriceps muscle thickness (QMT) and rectus femoris cross-sectional area (RFcsa).

Rectus femoris was used only for the analysis of EI. The region of interest was selected within the outline of the rectus femoris to include as much of the muscle as possible without any surrounding fascia.29 EI was defined as the EI in the muscle by using the standard histogram function of Adobe Photoshop 7.0 (Adobe Systems Incorporated, San Jose, CA, USA), expressed as a value between 0 (black) and 255 (white) (Figure 2). EI was measured in three images, and the mean was taken to reduce variation.
Figure 2

The histogram of the echo intensity (EI) of the rectus femoris.

Notes: A region of interest (ROI) is selected within the borders of the rectus femoris muscle (black line), and the EI is determined using a histogram. Inset is the mean EI value of the ROI.

Statistical analyses

Statistical analyses were performed using SPSS 16.0 software (SPSS Inc., Chicago, IL, USA). All values are shown as mean ± standard deviation. Unpaired t-tests were utilized to compare the differences between the two groups, and the analysis of variance (ANOVA) and Kruskal–Wallis test were used to compare more than three groups according to data characteristics. Unitarian comparisons between COPD and non-COPD were assessed using Chi-square tests and independent sample t-test. Paired t-tests were implemented to analyze left–right differences. Correlations between SFT, QMT, RFcsa, EI, PCS, MCS, FACITF, age, BMI and lung function were calculated using Pearson’s correlation coefficients. Multiple linear regression analysis was conducted to evaluate the independent associations of EI, QMT, and RFcsa with PCS in COPD patients. Partial correlation analysis was carried out to determine the effects of QMT, RFcsa, and EI on PCS, controlling for age, height, weight, and SFT. Due to a low number of subjects in GOLD stage III and IV, they were grouped as GOLD ≥III. Statistical significance was defined as P<0.05.

Results

Table 1 summarizes the basic characteristics of the study population. There were no statistically significant differences in age, BMI and gender between COPD and non-COPD subjects. The US measurements, PCS of the SF-8, FACITF and 6MWD of the non-COPD subjects and COPD patients are shown in Figure 3 and Table S1. There were significant differences in EI between non-COPD and GOLD I/II/III–IV COPD patients, respectively, the difference in COPD stage GOLD I compared to GOLD III–IV was also significant (P=0.004). In QMT and RFcsa of the quadriceps with FACITF, non-COPD with GOLD I compared to GOLD ≥III was statistically significant. In PCS and 6MWD, non-COPD compared to GOLD II and GOLD III–IV had significant differences, and GOLD I compared to GOLD III–IV had significant differences also. The SFT, QMT, RFcsa, EI, MCS and PCS showed statistically significant differences between the two genders, while there were no differences in the FACITF (Table S2).
Table 1

Basic characteristics of the study population

CharacteristicsNon-COPD (n=21)COPD (n=50)P-values
Age, years62.10±7.0165.76±8.070.074
Male/female, n13/827/230.607
BMI, kg/m226.98±4.1226.66±5.400.811
Heart rate, beats/min68.38±9.5171.14±10.950.318
SaO2, %96.52±1.2195.52±1.200.002
Respiratory symptom1 (4.8)25 (50.0)0.000
Heart disease2 (9.5)10 (20.0)0.489
Hypertension6 (28.6)16 (32.0)1.000
Diabetes0 (0.0)4 (8.0)1.000
Never smokers9 (42.9)9 (18.0)0.038
Ex-smokers11 (52.4)31 (62.0)0.578
Current smokers1 (4.8)10 (20.0)0.156
Inhaled steroids9 (18.0)
FEV1, L3.228±0.642.068±0.76<0.0001
FEV1% predicted104.3±10.4373.29±19.31<0.0001
FEV1/FVC76.98±4.9262.58±11.85<0.0001
GOLD A/B/C/D, n21/22/6/1

Note: Values are mean ± SD or number (%).

Abbreviations: BMI, body mass index; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; SaO2, resting peripheral oxygen saturation measured by pulse oximetry.

Figure 3

The results of ultrasound measurements of the right quadriceps (A–C), questionnaires (D, E) and 6MWD (F) in the study population.

Abbreviations: 6MWD, 6-minute walk distance; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; GOLD, Global Initiative for Chronic Obstructive Lung Disease; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area.

Table 2 displays the correlation coefficients between US quadriceps muscle measures with age, BMI, PCS, MCS, FACITF and 6MWD as control variables in 50 (27 males) stable COPD patients. QMT and RFcsa showed a significant negative correlation with age (r =−0.412; r =−0.477). EI showed significant negative correlations with PCS (r =−0.624, P=0.000) and was not related to age (r =−0.202, P=0.161). Multivariate regression analysis showed that the EI was independently associated with PCS (Table 3). Table 4 shows the partial correlation coefficients between EI, QMT, RFcsa and PCS with age, height, weight, and SFT as control variables; EI showed a significant negative correlation with PCS (r =−0.651, P=0.003). QMT was positively correlated with PCS (r =0.364, P=0.014) but not significantly with EI (r =−0.195, P=0.071). RFcsa was significantly associated with QMT, but not correlated with EI and PCS.
Table 2

Correlations of quadriceps muscle measures with age, BMI, PCS, MCS, FACITF and 6MWD in 50 (27 males) stable COPD patients (r values)

AgeBMISFTQMTRFcsaEIPCSMCSFACITF6MWD
Age1
BMI0.0231
SFT−0.1250.3151
QMT−0.4120.367−0.0241
RFcsa−0.4770.286−0.1340.8501
EI0.2020.1040.525−0.265−0.2711
PCS−0.272−0.186−0.1190.3210.270−0.6241
MCS−0.044−0.1180.0930.2080.162−0.2920.3481
FACITF−0.1250.0320.0680.2190.148−0.4830.6830.5861
6MWD−0.297−0.189−0.0170.3360.327−0.3040.4110.1000.1801

Notes:

Correlation is significant at the 0.05 level (two tailed).

Correlation is significant at the 0.01 level (two tailed).

Abbreviations: BMI, body mass index; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness; 6MWD, 6-minute walk distance.

Table 3

Association of EI, QMT and RFcsa with PCS using multiple regression analysis in COPD patients (n=50)

VariablesβP-value
EI−0.3120.028
QMT0.1650.520
RFcsa0.0910.717

Abbreviations: EI, echo intensity; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area.

Table 4

Partial correlation coefficients between QMT, RFcsa, EI and PCS with age, height, weight, BMI and SFT as control variables in COPD patients (n=50)

VariablesQMTRFcsaEIPCS
QMT1r =0.760, p=0.000r =−0.195, p=0.071r =0.364, p=0.014
RFcsa1r =−0.211, p=0.058r =0.230, p=0.128
EI1r =−0.651, p=0.003
PCS1

Abbreviations: BMI, body mass index; EI, echo intensity; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness.

Table 5 shows the correlation coefficients among SFT, QMT, RFcsa and EI of the quadriceps, PCS, MCS, FACITF and 6MWD with lung function in 50 (27 males) stable COPD patients. QMT, RFcsa, FACITF and 6MWD showed a significant positive correlation with FEV1, FEV1%, FVC and FEV1/FVC%. EI showed significant negative correlations with FEV1/FVC% (r =−0.413, P<0.01). Table S3 shows the subjects’ characteristics according to PCS above/below 45. There were no significant differences between right and left thigh in US measurements in the study population.
Table 5

Correlations of quadriceps muscle measures, PCS, MCS and FACITF with lung function in 50 (27 males) stable COPD patients (r values)

VariablesQMTRFcsaEIPCSMCSFACITF6MWD
FEV10.6620.649−0.2750.4300.2550.4110.586
FEV1%0.4490.400−0.2560.4810.2670.5720.524
FVC0.4970.496−0.0520.2690.2420.3160.480
FEV1/FVC%0.4700.419−0.4130.2700.0420.2380.460

Notes:

Correlation is significant at the 0.05 level (two-tailed).

Correlation is significant at the 0.01 level (two-tailed).

Abbreviations: 6MWD, 6-minute walk distance; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area.

Discussion

The present study showed that the EI of the rectus femoris was substantially increased in all GOLD stages of COPD patients. However, the QMT and RFcsa were significantly decreased in GOLD ≥III only. This suggests that changes in the EI of the rectus femoris may occur earlier than reductions in muscle size in COPD patients. EI was not correlated with age, BMI and the degree of airflow obstruction in our patients. Our results extend those of a previous study on peripheral muscle function in COPD patients by showing that their quadriceps strength and size are lower compared to those of normal subjects.30 It is well known that loss of muscle bulk of the quadriceps is a major change in COPD patients with the decreasing of low limb strength, as well as qualitative changes such as increased intramuscular fibrous and adipose tissue.31–33 To our knowledge, this is the first study that focused on the EI of the rectus femoris in COPD patients and observed the relationship with HRQoL and lung function. Quantitative muscle US is a reliable method to detect structural changes and determine the severity of muscle pathology.14 Image-based measurements of quadriceps muscle structure may help to identify patients with specific muscle phenotypes. Muscle atrophy, intramuscular fibrosis and fatty infiltration enhanced EI on ultrasound images of skeletal muscle that associated with muscle strength, independently of age or muscle size in middle-aged and elderly people.34–36 Muscle EI can be used in the diagnostic evaluation of patients with suspected neuromuscular diseases, guiding a muscle biopsy and in follow-up or intervention studies.37,38 Quadriceps muscle phenotype varies widely in patients with COPD, which cannot be determined without a muscle biopsy. The SF-8 survey is a good tool for measuring the HRQoL of participants with chronic illness,39 can be expected to be completed in 2–3 minutes and appears to provide a more practical and efficient method for studies in COPD. Our results are consistent with a previous study that COPD patients have a decline in physical health.40 Using a cutoff of 45 of PCS, the EI of the rectus femoris and FACITF scales could differentiate (P<0.0001) between these two groups (PCS above/below 45) in our patients, and also MCS, QMT and 6MWD showed statistically significant associations/differences (P<0.05); however, RFcsa did not. Some studies indicate that females have poorer HRQoL measurements than males in COPD patients.41,42 Our results showed that the SFT, QMT, RFcsa and EI of the quadriceps between the two genders were significantly different, and there were no differences in the FACITF. Fatigue is a prominent disruptive disabling symptom in COPD patients in daily activities and considerably impacts on their quality of life.43,44 The different level of dyspnea, anxiety, hopelessness and concomitant such as heart disease seems to have a negative impact on both physical and mental health. There are some limitations to our study. First, there is no clear criterion for muscle EI value and the results cannot be readily generalized for different US devices, as EI is influenced by US system hardware and software. Recently, however, a correction equation (EI device 1=1.38× EI device 2+9.14) was reported to convert EI from one ultrasound device to another.29 Second, the first author was the sole investigator who performed the ultrasonic assessment, but there was a high test–retest reliability score (kappa 0.953) in our study. The quantity EI evaluation of muscles showed a higher interobserver agreement (kappa 0.86) in the study of Pillen et al,14 the reproducibility and reliability can be expected to be good.45,46 In future, investigations on intra-observer reliability and reproducibility will still be an issue. The small number of patients, particularly stage GOLD ≥III COPD patients (n=7), is another limitation.

Conclusion

There was significant differences in EI between non-COPD and GOLD I COPD patients, but QMT and RFcas have no differences. This means that the change of EI of the quadriceps occur earlier than the decrease in thickness and area of quadriceps in COPD patients. We believe that US is a low-cost, easily accessible, safe method which is suitable for the assessment of EI as a noninvasive biomarker of quadriceps muscle in COPD patients and may assist in determining patients for trials of interventions targeted at specific muscle phenotypes. Further studies should be pursued to ensure that it can accurately diagnose and track disease progression of the skeletal muscle dysfunction. The results of ultrasonography measurements of the right quadriceps, questionnaires and 6MWD in the study population Notes: Compared with non-COPD. Compared with GOLD I. Data presented as mean ± standard deviation. Abbreviations: 6MWD, 6-minute walk distance; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; GOLD, Global Initiative for Chronic Obstructive Lung Disease; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness. SFT, QMT, RFcas, EI of the quadriceps and MCS, PCS, FACITF in 50 stable COPD patients between males and females Note: Data presented as mean ± standard deviation. Abbreviations: EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness. Patients’ characteristics according to PCS ≤ and >45 Notes: Data presented as mean ± standard deviation. Bold values represent the EI of the rectus femoris, FACITF, MCS, QMT and 6MWD being statistically significant, using a cutoff of 45 of PCS. Abbreviations: 6MWD, 6-minute walk distance; BMI, body mass index; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness.
Table S1

The results of ultrasonography measurements of the right quadriceps, questionnaires and 6MWD in the study population

VariablesNon-COPD (n=21)GOLD I (n=21)GOLD II (n=22)GOLD ≥III (n=7)
SFT, cm11.6±4.0913.52±6.3011.21±4.2510.26±3.88
QMT, cm30.57±7.0729.03±8.4425.09±6.2817.41±5.04a,b
RFcsa, cm27.07±1.786.84±2.675.63±1.733.99±1.16a,b
EI121.40±8.80130.50±14.25a132.40±15.88a144.30±6.50a,b
PCS54.95±4.4151.38±9.8246.45±9.22a38.29±7.74a,b
MCS51.05±10.252.90±6.8951.59±9.3146.43±14.06
FACITF43.76±5.7445.24±6.6139.27±9.2531.57±12.51a,b
6MWD, m628.90±81.77612.10±91.67547.40±98.70a433.50±66.90a,b

Notes:

Compared with non-COPD.

Compared with GOLD I. Data presented as mean ± standard deviation.

Abbreviations: 6MWD, 6-minute walk distance; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; GOLD, Global Initiative for Chronic Obstructive Lung Disease; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness.

Table S2

SFT, QMT, RFcas, EI of the quadriceps and MCS, PCS, FACITF in 50 stable COPD patients between males and females

VariablesMale (n=27)Female (n=23)t-valueP-value
SFT, cm8.53±3.3312.16±5.893.2530.003
QMT, cm21.66±11.0817.29±7.125.169<0.0001
RFcsa, cm25.32±2.564.14±1.735.190<0.0001
EI133.7±14.76142.1±9.693.5130.002
MCS52.22±8.4747.88±12.504.1130.0001
PCS42.18±12.7241.22±11.302.3490.023
FACITF41.96±7.4639.22±11.931.5320.120

Note: Data presented as mean ± standard deviation.

Abbreviations: EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness.

Table S3

Patients’ characteristics according to PCS ≤ and >45

VariablesPCS ≤45 (n=18)PCS >45 (n=32)P-value
Age, years68.61±5.7764.16±8.790.060
BMI, kg/m227.79±2.3226.03±4.790.273
SFT, cm12.09±5.2612.02±5.310.964
QMT, cm22.46±6.7027.48±8.180.032
RFcsa, cm25.26±2.096.27±2.370.137
EI142.20±13.97125.80±10.770.000
MCS47.61±11.6553.56±6.870.027
FACITF33.44±10.8644.78±6.18<0.0001
6MWD, m497.4±83.26582.70±104.800.031

Notes: Data presented as mean ± standard deviation. Bold values represent the EI of the rectus femoris, FACITF, MCS, QMT and 6MWD being statistically significant, using a cutoff of 45 of PCS.

Abbreviations: 6MWD, 6-minute walk distance; BMI, body mass index; EI, echo intensity; FACITF, functional assessment of chronic illness therapy fatigue; MCS, mental component summary; PCS, physical component summary; QMT, quadriceps muscle thickness; RFcsa, rectus femoris cross-sectional area; SFT, subcutaneous fat thickness.

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2.  ATS statement: guidelines for the six-minute walk test.

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Journal:  Am J Respir Crit Care Med       Date:  2002-07-01       Impact factor: 21.405

3.  Skeletal muscle ultrasonography: Visual versus quantitative evaluation.

Authors:  Sigrid Pillen; Mieke van Keimpema; Rutger A J Nievelstein; Aad Verrips; Wilma van Kruijsbergen-Raijmann; Machiel J Zwarts
Journal:  Ultrasound Med Biol       Date:  2006-09       Impact factor: 2.998

4.  Health-related quality of life in individuals with chronic obstructive pulmonary disease.

Authors:  Jie Hu; Paula Meek
Journal:  Heart Lung       Date:  2005 Nov-Dec       Impact factor: 2.210

5.  Attacking the disease spiral in chronic obstructive pulmonary disease: an update.

Authors:  Michael I Polkey; John Moxham
Journal:  Clin Med (Lond)       Date:  2011-10       Impact factor: 2.659

6.  A measure of quality of life for clinical trials in chronic lung disease.

Authors:  G H Guyatt; L B Berman; M Townsend; S O Pugsley; L W Chambers
Journal:  Thorax       Date:  1987-10       Impact factor: 9.139

7.  Tissue depletion and health related quality of life in patients with chronic obstructive pulmonary disease.

Authors:  R Mostert; A Goris; C Weling-Scheepers; E F Wouters; A M Schols
Journal:  Respir Med       Date:  2000-09       Impact factor: 3.415

8.  Peripheral muscle weakness in patients with chronic obstructive pulmonary disease.

Authors:  S Bernard; P LeBlanc; F Whittom; G Carrier; J Jobin; R Belleau; F Maltais
Journal:  Am J Respir Crit Care Med       Date:  1998-08       Impact factor: 21.405

9.  Determinants and impact of fatigue in patients with chronic obstructive pulmonary disease.

Authors:  Ramin Baghai-Ravary; Jennifer K Quint; James J P Goldring; John R Hurst; Gavin C Donaldson; Jadwiga A Wedzicha
Journal:  Respir Med       Date:  2008-11-22       Impact factor: 3.415

Review 10.  Musculoskeletal disorders in chronic obstructive pulmonary disease.

Authors:  Nele Cielen; Karen Maes; Ghislaine Gayan-Ramirez
Journal:  Biomed Res Int       Date:  2014-03-25       Impact factor: 3.411

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Authors:  Peter Wallbridge; Selina M Parry; Sourav Das; Candice Law; Gary Hammerschlag; Louis Irving; Mark Hew; Daniel Steinfort
Journal:  Sci Rep       Date:  2018-10-15       Impact factor: 4.379

2.  Objective physical activity level is associated with rectus femoris muscle echo-intensity in patients with chronic obstructive pulmonary disease.

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Review 3.  The current use of ultrasound to measure skeletal muscle and its ability to predict clinical outcomes: a systematic review.

Authors:  Patrick Casey; Mohamed Alasmar; John McLaughlin; Yeng Ang; Jamie McPhee; Priam Heire; Javed Sultan
Journal:  J Cachexia Sarcopenia Muscle       Date:  2022-07-19       Impact factor: 12.063

4.  The thickness of erector spinae muscles can be easily measured by computed tomography for the assessment of physical activity: An observational study.

Authors:  Masafumi Shimoda; Satoshi Takao; Yasushi Sugajima; Yoshiaki Tanaka; Kozo Morimoto; Naoyuki Yoshida; Kozo Yoshimori; Ken Ohta; Hideaki Senjyu
Journal:  Medicine (Baltimore)       Date:  2022-09-23       Impact factor: 1.817

5.  Diagnostic and clinical values of non-cardiac ultrasound in COPD: A systematic review.

Authors:  Jaber S Alqahtani; Tope Oyelade; Jithin Sreedharan; Abdulelah M Aldhahir; Saeed M Alghamdi; Ahmed M Alrajeh; Abdullah S Alqahtani; Abdullah Alsulayyim; Yousef S Aldabayan; Nowaf Y Alobaidi; Mohammed D AlAhmari
Journal:  BMJ Open Respir Res       Date:  2020-09

6.  Ultrasonic Elastography of the Rectus Femoris, a Potential Tool to Predict Sarcopenia in Patients With Chronic Obstructive Pulmonary Disease.

Authors:  Mingming Deng; Xiaoming Zhou; Yanxia Li; Yan Yin; Chaonan Liang; Qin Zhang; Jingwen Lu; Mengchan Wang; Yu Wang; Yue Sun; Ruixia Li; Liming Yan; Qiuyue Wang; Gang Hou
Journal:  Front Physiol       Date:  2022-01-05       Impact factor: 4.566

7.  Ultrasound assessment of the rectus femoris in patients with chronic obstructive pulmonary disease predicts poor exercise tolerance: an exploratory study.

Authors:  Mingming Deng; Chaonan Liang; Yan Yin; Jun Shu; Xiaoming Zhou; Qiuyue Wang; Gang Hou; Chen Wang
Journal:  BMC Pulm Med       Date:  2021-09-25       Impact factor: 3.317

  7 in total

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