Introduction
Liver transplantation (LTx) is the only definitive treatment for end-stage liver disease. Since 1988, patient survival and liver function after LTx have improved markedly, due to improved technical expertise, better selection of patients, improved post-LTx management of complications, and improved immunosuppressive therapy (Adam et al. 2003). In Europe, LTx has achieved a 1-year survival rate of 82% (Burroughs et al. 2006).
Although studies have reported that quality of life improves after LTx (Gross et al. 1999; van der Plas et al. 2003), limitations in daily function still remain (Gross et al. 1999; van der Plas et al. 2003). Amongst these limitations, liver transplant recipients often experience fatigue (Aadahl et al. 2002; Belle et al. 1997; Leyendecker et al. 1993; van den Berg-Emons et al. 2006). Gross et al. (1999), and Belle et al. (1997) reported that, although the intensity of fatigue was reduced after LTx, fatigue remained the most distressing symptom 1 year after surgery. Leyendecker et al. (1993) found that 9 months after LTx, complaints of fatigue were more severe in the LTx group than in the general population. In a previous study, we found severe fatigue in 44% of patients up to 15 years after LTx, and these complaints did not decrease over time (van den Berg-Emons et al. 2006a).
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Rehabilitation programs might be effective in reducing severity of fatigue after LTx, but, to develop appropriate programs, knowledge on the factors associated with fatigue after LTx is necessary. However, data on these factors are scarce. Aadahl et al. (2002) and van den Berg-Emons et al. (2006a) suggested that the fatigue experienced by liver transplant recipients is primarily physical, rather than psychological. Furthermore, van den Berg-Emons et al. (2006b) found that severe complaints of fatigue in liver transplant recipients are associated with low levels of everyday physical activity. A hypoactive lifestyle may lead to a negative spiral: hypoactivity leading to a reduction in physical fitness and deterioration of complaints of fatigue, leading to further hypoactivity.
Few studies have investigated the physical fitness of liver transplant recipients, but the limited data available suggest a reduced physical fitness after LTx (Beyer et al. 1999; Stephenson et al. 2001; Unnithan et al. 2001). Stephenson et al. (2001) found a 40–60% lower maximal oxygen uptake than predicted in liver transplant recipients. Beyer et al. (1999) reported that, although the cardiovascular and neuromuscular fitness in liver transplant recipients improved after a supervised exercise program during the post-operative year, maximal oxygen uptake and muscle strength remained 10–20% lower compared to healthy gender and age-matched individuals. Also in pediatric liver transplant recipients, deficits in cardiovascular fitness, and abdominal muscle strength have been reported (Unnithan et al. 2001).
It may be hypothesized that deficits in physical fitness in liver transplant recipients are associated with complaints of fatigue. Furthermore, deficits in physical fitness may lead to impaired health-related quality of life (HRQoL). However, to our knowledge, no studies are available on the relationships between these parameters in liver transplant recipients.
Because of the scarcity of studies on physical fitness and related parameters in liver transplant recipients, the present study assessed physical fitness (cardiorespiratory fitness, neuromuscular fitness, and body composition) in liver transplant recipients and explored whether physical fitness is related to severity of fatigue in this group. The relationship between physical fitness and HRQoL was also explored.
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Patients and methods
Patients
To obtain a representative sample of liver transplant recipients with respect to fatigue, we recruited liver transplant recipients with varying severity of fatigue, according to the distribution of severity of fatigue as found in our previous study in 96 liver transplant recipients (van den Berg-Emons et al. 2006a). Severity of fatigue in this previous study ranged from ‘no signs of fatigue’ to ‘most disabling fatigue’, and was assessed with the Fatigue Severity Scale of Krupp et al. (1989) (see below). Inclusion criteria for the present study were: LTx between 1 and 5 years ago, sufficient knowledge of the Dutch language, and age between 18 and 65 years. Exclusion criteria were: multiorgan transplant recipients, severe comorbidity, and contra-indication for a progressive maximal cycle ergometer test. Of the original sample of 96 patients in the previous study (van den Berg-Emons et al. 2006a), 4 patients had died, 1 patient had emigrated, 53 patients were transplanted more than 5 years previously, and 10 patients were not eligible because of contra-indications for a maximal cycle ergometer test. Of the 28 eligible patients, 18 patients (64%) agreed to participate. There were no significant differences in relevant characteristics between the patients who decided to participate and the non-participants. The study was approved by the Medical Ethics Committee of the Erasmus University Medical Center. Written informed consent was obtained from all subjects. Table 1 shows the characteristics of the study group.
Table 1
Characteristics of the study group (n = 18)
Age (years) | 48.0 ± 11.8 |
Gender | |
Male | 11 |
Female | 7 |
Primary disease (n) a
| |
Chronic | 17 |
Acute | 1 |
Time since transplantation (years) | 3.3 ± 1.1 |
Immunosuppressive agentsb
| |
1 | 16 |
2 | 1 |
3 | 1 |
Measurements
Physical fitness: cardiorespiratory
Cardiorespiratory fitness was measured with a progressive maximal aerobic test on a cycle ergometer (ER800, Jaeger Toennies, Breda, The Netherlands). The test was preceded by a 1-min warm-up period (20 W). The test started at 20 W, and resistance was increased every minute by 15 or 20 W, depending on the ability of the patients. Individual protocols were constructed such that the total exercise time ranged from 8 to 12 min. The pedal rate was 60 rpm and strong verbal encouragement was given during the test. The test was terminated when the subject voluntarily stopped due to exhaustion, or when the patient was unable to maintain the initial pedal rate. Gas exchange and heart rate (HR) were measured continuously using a breath-by-breath gas analysis system (K4b2, COSMED, Rome, Italy). Subjective strain was measured immediately after the final stage by the Borg Category Scale for Rating of Perceived Exertion (Borg 1982). Patients were asked to indicate how strenuous they had experienced the test by giving a number from 0 (no effort at all) to 10 (maximal effort). Cardiorespiratory fitness was defined as the mean oxygen uptake during the last 30 s of exercise [VO2peak, in ml kg−1 min−1 and in ml kg fat-free mass−1 min−1 (ml kg
FFM
−1
min−1)]. In addition, the ventilatory anaerobic threshold (VAT, expressed as percentage of predicted VO2peak) was estimated by the ventilatory equivalent method, when V
E/VO2 and PetO2 increased while V
E/VCO2 and PetCO2 remained stable (Reinhard et al. 1979; Wasserman et al. 1999).
Finally, patients performed the submaximal 6-min walk test (6MWT) (Guyatt et al. 1985). Patients were instructed to walk, not run, as far as they could along a 30-m marked tape in a hall during a 6-min period. Standardized encouragement was provided with the following phrases: “You are doing well” and “Keep up the good work”. Patients were allowed to stop and rest during the test, but were instructed to resume walking as soon as they felt able to do so. The 6-min walk distance (6MWD) was registered.
Physical fitness: neuromuscular
Isokinetic muscle strength of the knee extensors was assessed in both legs by a Biodex® dynamometer (Shirley, New York, USA), recording strength as torque in Nm. The patients were seated against a back-rest, firmly strapped at the hip and thigh. The rotational axis was aligned with the lateral femoral epicondyle. After five familiarization repetitions, isokinetic strength was measured at 60°/s with 5 maximal contractions and at 180°/s with 15 maximal contractions. Strong verbal encouragement was given during the test. Peak torque (PT) was defined as the maximum torque generated by the patients throughout one series of repetitions at each velocity.
Physical fitness: body composition
Height and body mass were measured without shoes. Body mass was measured using a Cormier Paribel® weighing chair (FH Balances Cormier, Romainville, France). Body mass index (BMI, kg m−2) was calculated from height and body mass. Waist circumference (cm) was measured mid-way between the lowest rib and the iliac crest while standing. Thickness of four skinfolds (biceps, triceps, subscapular, suprailiaca region) was measured twice at the right side of the body with a Harpenden Skin-Fold Caliper (Burgess Hill, UK). The mean of the two measurements was used as representative for each site. Percentage body fat (BF) was predicted from skinfold thickness according to the method of Durnin and Womersley (1974).
Severity of fatigue
Severity of fatigue was assessed by the Dutch version of the Fatigue Severity Scale (FSS) (Krupp et al. 1989). The FSS is a self-administered questionnaire with answers ranging from 1 (‘strongly disagree’) to 7 (‘strongly agree’). The mean score of the nine inquiries ranges from 1 (‘no signs of fatigue’) to 7 (‘most disabling fatigue’). Internal consistency, reliability, validity, and sensitivity of the FSS have been established in several patient groups (Krupp et al. 1989; Merkies et al. 1999).
In addition to the FSS, severity of fatigue was assessed with a horizontal visual analogue scale (VAS). Patients were asked to mark the 100-mm line according to how intense they had experienced fatigue during the last month (0 denotes ‘no fatigue experienced’ and 100 denotes ‘the most severe fatigue’) (ter Borg et al. 2004). Visual analogue scales have been found to yield reliable and valid data (Huskisson 1982; Scott and Huskisson 1979).
Health-related quality of life
HRQoL was assessed by the validated Dutch version (RAND-36) (van der Zee and Sanderman 1993) of the Medical Outcomes Study Short Form-36 (SF-36) (Ware and Sherbourne 1992). The SF-36 is a validated, self-administered questionnaire used internationally to measure health status with respect to different dimensions: physical functioning, social functioning, role limitations due to physical problems, role limitations due to emotional problems, pain, mental health, vitality, general health perception, and change in perceived health during the last 12 months. All raw scores were converted to a 0–100 scale, with higher scores indicating higher levels of functioning or well-being.
Procedure
On the day of the measurements, patients refrained from caffeine, nicotine, and heavy exercise. The order of the tests was standardized: patients started with the 6MWT, followed by the questionnaires (completed under supervision of the researcher), body composition measurements, strength test, and finally the progressive maximal aerobic test. Exercise tests were performed under supervision of a physician. There were sufficient rest periods between the tests.
Statistics
Statistical analysis was performed using SPSS 10.1 for Windows (SPSS Inc., Chicago, IL, USA). Results are presented as mean ± standard deviation (SD), range or numbers. Results on cardiorespiratory fitness were compared to normative values for sedentary persons and to normative values for people who exercise no more than 1–2 h a week (recreational) (Vos et al. 2001). Results on neuromuscular fitness were compared with the normative values of Akima et al. (2001) and 6MWD was compared with the normative values of Enright and Sherill in healthy adults aged 40–80 years (1998). When patients were younger than 40 years, the normative values of Gibbons et al. (2001) were used. Obesity was defined as a BMI ≥ 30 (World Health Organization 1989), a waist circumference ≥102 cm in men and ≥88 cm in women (Lean et al. 1995) or percentage BF ≥25% in men and ≥32% in women (Lohman 1992).
Differences in physical fitness between patients and normative values were tested with the non-parametric Mann-Whitney U Test. Relationships between physical fitness and severity of fatigue and between physical fitness and quality of life were explored using the non-parametric Spearman correlation coefficient (r
s). A probability value ≤0.05 determined statistical significance. However, because of the relatively small study sample, also results on the α = 0.10 level are presented (indicating a trend).
Results
Physical fitness
Mean score on the Borg Scale was 6.3 ± 2.2, indicating that the patients experienced the maximal ergometer test on average as heavy to very heavy. The mean HRmax was 90 ± 10% of what was predicted (predicted HRmax = 220-age) (Fox et al. 1971).
The individual results of the patients are presented in Table 2. Table 3 shows the cardiorespiratory fitness and neuromuscular fitness of the patients compared with normative values. VO2peak in ml kg−1 min−1 was 15 ± 22% (P = 0.07) and 34 ± 15% (P = 0.00) lower than normative values for, respectively, sedentary persons and those who exercise recreationally. VO2peak in ml kg
FFM
−1
min−1 was 16 ± 19.2% (P = 0.02) and 33 ± 14.8% (P = 0.00) lower than normative values for, respectively, sedentary persons and those who exercise recreationally. 6MWD was 16 ± 14% (P = 0.01) lower than normative values. There was no significant deficit in neuromuscular fitness. Table 4 shows the body composition of the LTx group. According to the cut-off points for obesity based on BMI, waist circumference and percentage BF, respectively 17, 36, and 41% of the patients were classified as obese.
Table 2
Individual results on physical fitness in the 18 liver transplant recipients
Age (year/Gender) | BMI (kg m−2) | Waist (cm)a
| Body fat (%)b
|
VO2peak (ml kg−1 min−1) |
VO2peak (ml kg
FFM
−1
min−1)b
| VAT (% predicted VO2peak sed) | VAT (% predicted VO2peak recr) | 6MWD (m) | PT extension 60°/s (Nm) | PT extension 180°/s (Nm) |
|---|---|---|---|---|---|---|---|---|---|---|
56/M | 28.3 | 111.0 | 29.0 | 36.5 | 51.4 | 54.1 | 42.7 | 652 | 156.3 | 88.2 |
52/M | 29.0 | 32.7 | 16.7 | 24.8 | 49.1 | 38.9 | 428 | 101.8 | 73.1 | |
42/F | 22.8 | 28.9 | 34.5 | 48.5 | 90.5 | 65.8 | 530 | 100.0 | 65.6 | |
60/F | 38.4 | 118.5 | 42.0 | 13.1 | 22.5 | 43.6 | 32.5 | 495 | 101.9 | 78.6 |
64/M | 29.7 | 103.5 | 30.6 | 21.7 | 31.3 | 77.4 | 55.4 | 430 | 99.9 | 62.6 |
24/F | 21.0 | 72.0 | 25.9 | 29.9 | 40.4 | 38.8 | 31.1 | 660 | 159.9 | 111.5 |
46/M | 26.5 | 100.0 | 25.8 | 28.2 | 38.0 | 48.6 | 38.7 | 606 | 151.6 | 88.5 |
63/M | 24.4 | 20.5 | 20.9 | 26.4 | 69.4 | 49.7 | 410 | 74.4 | 44.8 | |
42/M | 34.9 | 132.0 | 22.8 | 30.9 | 25.8 | 513 | 145.9 | 118.3 | ||
53/F | 23.9 | 77.5 | 30.1 | 23.1 | 33.0 | 108.6 | 64.8 | 465 | 40.0 | 35.7 |
53/M | 25.9 | 99.6 | 23.6 | 20.7 | 27.1 | 56.7 | 42.6 | 510 | 149.3 | 96.8 |
39/M | 23.7 | 87.0 | 17.4 | 31.2 | 37.8 | 51.5 | 43.5 | 547 | 169.0 | 111.8 |
33/M | 24.0 | 88.0 | 19.8 | 35.1 | 43.7 | 67.9 | 59.9 | 510 | 155.9 | 116.9 |
63/F | 33.0 | 103.0 | 34.8 | 15.8 | 24.2 | 57.9 | 43.2 | 303 | 67.2 | 39.4 |
45/F | 26.8 | 30.8 | 23.6 | 34.1 | 61.0 | 46.2 | 514 | 120.1 | 61.7 | |
39/F | 18.7 | 75.0 | 22.7 | 30.2 | 38.1 | 56.2 | 46.8 | 600 | 115.9 | 67.9 |
32/M | 22.9 | 91.0 | 20.4 | 25.0 | 31.4 | 43.4 | 38.3 | 576 | 180.4 | 124.6 |
58/M | 25.1 | 99.0 | 25.0 | 18.5 | 24.6 | 48.6 | 37.9 | 495 | 128.6 | 91.9 |
Table 3
Cardiorespiratory fitness and neuromuscular fitness in the liver transplant group
LTx group | Norm valuesa
|
P
| ||
|---|---|---|---|---|
Cardiorespiratory fitness | ||||
VO2peak (ml kg−1 min−1) | 24.8 ± 6.9 | 29.4 ± 7.4 | (sed) | 0.07†
|
37.5 ± 6.7 | (recr) | 0.00* | ||
VO2peak (ml kg
FFM
−1
min−1)b
| 34.0 ± 8.7 | 41.0 ± 7.8 | (sed) | 0.02* |
50.9 ± 5.9 | (recr) | 0.00* | ||
6MWD (m) | 513.6 ± 88.9 | 609.6 ± 97.6 | 0.01* | |
Neuromuscular fitness | ||||
PT extension at 60°/s (Nm) | 123.2 ± 38.7 | 138.5 ± 44.1 | 0.22 | |
PT extension at 180°/s (Nm) | 82.1 ± 27.9 | 86.1 ± 30.1 | 0.59 | |
Table 4
Body composition in the liver transplant group
Body composition | Mean ± SD |
|---|---|
Body weight (kg) | 80.6 ± 18.3 |
Height (m) | 1.74 ± .11 |
Body mass index (kg m−2) | 26.6 ± 5.0 |
Waist circumference (cm)a
| 96.6 ± 16.8 |
Body fat (%)b
| 26.9 ± 6.4 |
Relationships
Table 5 shows the correlation coefficients between the physical fitness parameters and severity of fatigue as assessed with the FSS and VAS. None of the parameters of neuromuscular fitness or body composition were significantly related with severity of fatigue, assessed with either the FSS or the VAS.
Table 5
Spearman correlation coefficients for the relationships between fitness parameters and severity of fatigue as measured with the Fatigue Severity Scale (FSS) and the Visual Analogue Scale (VAS) in 18 liver transplant recipients
Physical fitness | Fatigue | |||
|---|---|---|---|---|
FSS | VAS | |||
Rs |
P
| Rs |
P
| |
Cardiorespiratory fitness | ||||
VO2peak (ml kg−1 min−1) | −0.40 | 0.10 | −0.52 | 0.03* |
% of sedentary norm | −0.17 | 0.50 | −0.42. | 0.08†
|
% of recreational norm | −0.32 | 0.20 | −0.53 | 0.03* |
VO2peak (ml kg
FFM
−1
min−1)a
| −0.43 | 0.08†
| −0.51 | 0.04* |
% of sedentary norma
| −0.35 | 0.17 | −0.50 | 0.04* |
% of recreational norma
| −0.45 | 0.07†
| −0.61 | 0.01* |
VAT (% predicted VO2peak sed) | 0.22 | 0.38 | 0.03 | 0.92 |
VAT (% predicted VO2peak recr) | 0.17 | 0.49 | −0.06 | 0.82 |
6MWD (m) | −0.44 | 0.07†
| −0.53 | 0.03* |
% of norm | −0.25 | 0.32 | −0.52 | 0.03* |
Neuromuscular fitness | ||||
PT extension at 60°/s (Nm) | −0.39 | 0.11 | −0.31 | 0.22 |
% of norm | −0.15 | 0.56 | −0.28 | 0.27 |
PT extension at 180°/s (Nm) | −0.30 | 0.22 | −0.12 | 0.64 |
% of norm | 0.02 | 0.93 | 0.04 | 0.87 |
Body composition | ||||
Body mass index (kg m−2) | 0.03 | 0.91 | 0.06 | 0.82 |
Waist circumference (cm)b
| −0.07 | 0.82 | −0.06 | 0.83 |
Body fat (%)a
| 0.32 | 0.21 | 0.15 | 0.58 |
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VO2peak in ml kg
FFM
−1
min−1 (absolute and expressed as percentage of recreational normative values) and 6MWD (absolute) were related with severity of fatigue as assessed with the FSS at the α = 0.10 level (trend). With respect to the VAS, VO2peak in ml kg−1 min−1 (absolute and expressed as percentage of recreational normative values), VO2peak in ml kg
FFM
−1
min−1 (absolute and expressed as percentage of both sedentary and recreational normative values) and 6MWD (absolute and expressed as percentage of normative values) were significantly (P ≤ 0.05) correlated with severity of fatigue. VO2peak in ml kg−1 min−1 as percentage of sedentary normative values was related with severity of fatigue as assessed with the VAS at the α = 0.10 level (trend). The VAT was not correlated with severity of fatigue, assessed with the FSS or the VAS.
Table 6 shows the correlation coefficients between physical fitness parameters and HRQoL. There were several significant correlations between physical fitness and HRQoL and particularly between cardiorespiratory fitness on the one hand and ‘Physical functioning’, ‘Social functioning’ and ‘Vitality’ on the other hand.
Table 6
Spearman correlations coefficients for the relationships between physical fitness and health-related quality of life as assessed with the RAND−36 in 18 liver transplant recipients
Physical fitness | RAND-36 domain | ||||||||
|---|---|---|---|---|---|---|---|---|---|
PF | SF | Rlp | Rle | MH | VT | BP | GH | CH | |
Cardiorespiratory fitness | |||||||||
VO2peak (ml kg−1 min−1) |
0.55
| – | – | – | – | – | – | – | – |
% of sedentary norm | – | 0.42 | – | – | – |
0.50
| – | – | – |
% of recreational norm |
0.48
| – | – | – | – |
0.51
| – | – | – |
VO2peak (ml kg
FFM
−1
min−1)a
|
0.57
|
0.51
| 0.41 | – | – | – | – | – | – |
% of sedentary norma
| – |
0.56
| – | – | – |
0.59
| – | 0.48 | – |
% of recreational norma
| 0.46 |
0.58
| – | – | – |
0.58
| – | – | – |
VAT (% predicted VO2peak sed) | – | – | – | – | – | – | – | – | – |
VAT (% predicted VO2peak recr) | – | – | – | – | – | – | – | – | – |
6MWD (m) |
0.67
|
0.57
| – | – |
0.53
| – |
0.54
| – | – |
% of norm | – |
0.70
| – | – | – |
0.51
| – | – | 0.44 |
Neuromuscular fitness | |||||||||
PT extension at 60°/s (Nm) | 0.44 | – | – | – | .41 | – | – | – | – |
% of norm | – |
0.68
| – | – | – | – |
0.56
| – | – |
PT extension at 180°/s (Nm) | – | – | – | – | – | – | 0.44 | – | – |
% of norm | – |
0.51
| – |
0.54
| – | – |
0.50
| – | – |
Body composition | |||||||||
Body mass index (kg m−2) | – | – | – | – | – | – | – | – | – |
Waist circumference (cm)b
| – | – | –0.49
| –0.41 | – | – | – | – | – |
Body fat (%)a
| – | – | – | – | – | – | – | ||
Discussion
This is the first study in which relationships between several aspects of physical fitness and severity of fatigue are explored after LTx. The study is an initial step in identifying factors that are associated with fatigue in liver transplant recipients. A limitation of this study may be that the sample was relatively small. However, we believe that this sample is representative for patients after LTx and that the study provides important information for the development of rehabilitation programs for liver transplant recipients.
Physical fitness
We found average deficits in VO2peak of 16–34%, when we compared the results in the liver transplant recipients with normative values for, respectively, sedentary persons and those who exercise no more than 1–2 h a week. We believe that a value in between the sedentary and recreational normative values is representative for healthy Dutch persons of the same age as the liver transplant recipients that participated in our study. 6MWD was 16% lower than normative values. This subnormal level of cardiorespiratory fitness (both VO2peak and 6MWD) is in agreement with findings of previous studies (Beyer et al. 1999; Stephenson et al. 2001; Unnithan et al. 2001). Furthermore, the prevalence of obesity was higher in this study than in the general Dutch population; 17% of the patients had a BMI of more than 30 compared to 10% in the general Dutch population (Gezondheidsraad 2003).
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Impaired cardiorespiratory fitness in liver transplant recipients may be due to the use of immunosuppressive medication, e.g. glucocorticoids and calcineurin inhibitors, which may influence both the cardiovascular system and skeletal muscles (Hokanson et al. 1995; Mercier et al. 1996). Immunosuppressive medication can also induce appetite stimulation and diabetes mellitus; this in association with emotional conditions can cause a change in eating habits (Correia et al. 2003; Hussaini et al. 1998). Furthermore, patients with primary biliary cirrhosis and some patients with other chronic liver disease are hypermetabolic. LTx in these patients may lead to a reduction in resting metabolic rate and can also cause an increase in BF (Hussaini et al. 1998; Richardson et al. 2001). Besides immunosuppressive medication and changes in appetite and metabolism, also deconditioning (both before and after transplantation) may contribute to the impaired cardiorespiratory fitness and body composition (Epstein et al. 1998; Grose et al. 1995). In a previous study we found that severe complaints of fatigue were associated with low levels of everyday physical activity in liver transplant recipients (van den Berg-Emons et al. 2006b).
Because of the immunosuppressive medication and deconditioning, we also expected a deficit in neuromuscular fitness. However, this was not demonstrated in the present study, in contrast to Beyer et al. (1999), who found a 10–20% lower muscle strength in liver transplant recipients compared to age- and sex-matched sedentary individuals. They contributed this deficit to muscle weakness as a side-effect of glucocorticoids.
The discrepancy between the findings of our study and those of Beyer et al. (1999) may be explained by the use of Tacrolimus instead of cyclosporine in the majority of our subjects. Tacrolimus is known to have less side effects than cyclosporine (Maes and Vanrenterghem 2004).
Stephenson et al. (2001) reported an early VAT in liver transplant recipients (<45–50% of the predicted VO2max) compared to 50–60% of the VO2max in healthy persons found by Davis et al. (1997). They contributed this early anaerobic threshold in liver transplant recipients to the cyclosporine-induced decrease in mitochondrial oxygen consumption (2001). However, the European Respiratory Society (ERS Task Force 1997) reported that there is a wide range of normal predicted values (35–70%). Therefore, it is difficult to indicate whether the VAT in our patients was reduced compared to normal (58.6 ± 18.9 and 44.7 ± 11.1% of predicted VO2peak for, respectively, sedentary persons and those who exercise recreationally).
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Physical fitness and severity of fatigue
Although relationships between severity of fatigue (as measured with the FSS and VAS) and physical fitness were not univocal, this study demonstrates a relationship between cardiorespiratory fitness and severity of fatigue after LTx. Patients with more severe complaints of fatigue had larger deficits in cardiorespiratory fitness than patients with less severe complaints of fatigue. Although this cross-sectional study does not allow us to conclude that a reduced cardiorespiratory fitness results in fatigue (or vice versa), there may be an interaction between parameters: complaints of fatigue leading to decreased physical activity (van den Berg-Emons et al. 2006b) and decreased physical fitness, leading to further deterioration of complaints of fatigue. It may then be hypothesized that rehabilitation programs, aimed at enhancing cardiorespiratory fitness, can be effective in breaking through this negative spiral and (partly) reduce complaints of fatigue in this population. However, this hypothesis has to be confirmed in future randomized trials.
In contrast to our expectations, the present study indicates that other aspects of physical fitness, neuromuscular fitness and body composition, do not seem to be related with severity of fatigue after LTx. However, it should be realized that our study sample was relatively small and some of the studied relationships may have failed to show statistical significance.
Physical fitness and HRQoL
Previous studies on healthy persons indicate that physical activity, fitness, and body fatness are associated with HRQoL and mood (Han et al. 1998; Stewart et al. 2003). There are also indications that physical activity is related to HRQoL after LTx (Painter et al. 2001; van den Berg-Emons et al. 2006b). Therefore, we expected to find a relationship between physical fitness and HRQoL in our study group. In agreement with the study of Stewart et al. (2003) in healthy elderly subjects, we found several significant correlations between physical fitness (particularly cardiorespiratory fitness) and HRQoL in our liver transplant recipients. Patients with large deficits in physical fitness experienced worse HRQoL than patients with small deficits in physical fitness. However, in contrast with studies in healthy persons (Han et al. 1998; Stewart et al. 2003), we found only few relationships between body composition and HRQoL.
Our results on the relationships between physical fitness and HRQoL imply that rehabilitation programs aimed at improving physical fitness (particularly cardiorespiratory fitness) may consequently result in improved HRQoL, particularly in improved physical and social functioning, vitality, and bodily pain. However, these implications have to be confirmed in future randomized trials on the effects of such rehabilitation programs in liver transplant recipients.
Conclusion
Cardiorespiratory fitness in the liver transplant recipients was distinctly impaired and the prevalence of obesity was higher than in the general population; there were no indications that neuromuscular fitness is impaired after LTx. Based on the relationships we found between cardiorespiratory fitness and severity of fatigue, a rehabilitation program aimed at enhancing cardiorespiratory fitness may help in reducing complaints of fatigue after LTx. Such rehabilitation programs may also result in improved HRQoL.
Acknowledgments
The authors thank the rehabilitation physicians of the Department of Rehabilitation Medicine (Erasmus MC) and Han van Nieuwenhuizen (Department of Rehabilitation Medicine, Erasmus MC), Elly Nijsen, Lara Elshove, Anneloes Wilschut (Department of Gastroenterology and Hepatology, Erasmus MC) and Tim Takken (Department of Pediatric Physical Therapy and Exercise Physiology, Wilhelmina Children’s Hospital University Medical Center Utrecht) for their contributions to this study.
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