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Article

The Evaluation of Functional Abilities Using the Modified Fullerton Functional Fitness Test Is a Valuable Accessory in Diagnosing Men with Heart Failure

by
Magdalena Migaj
1,*,
Marta Kałużna-Oleksy
2,
Jacek Migaj
2 and
Anna Straburzyńska-Lupa
1
1
Department of Physical Therapy and Sports Recovery, Poznan University of Physical Education, 61-871 Poznań, Poland
2
1st Department of Cardiology, Heliodor Swiecicki Clinical Hospital, Poznan University of Medical Sciences, 61-848 Poznań, Poland
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(15), 9210; https://doi.org/10.3390/ijerph19159210
Submission received: 28 May 2022 / Revised: 24 July 2022 / Accepted: 26 July 2022 / Published: 28 July 2022
(This article belongs to the Special Issue New Advance in Cardiovascular Care)

Abstract

:
The assessment of functional abilities reflects the ability to perform everyday life activities that require specific endurance and physical fitness. The Fullerton functional fitness test (FFFT) seems to be the most appropriate for assessing physical fitness in heart failure (HF) patients. The study group consisted of 30 consecutive patients hospitalized for the routine assessment of HF with a reduced ejection fraction (HFrEF). They formed the study group, and 24 healthy subjects formed the control group. Each patient underwent a cardiopulmonary exercise test (CPET), transthoracic echocardiography and FFFT modified by adding the measurement of the handgrip force of the dominant limb with the digital dynamometer. The HF patients had significantly lower peak oxygen uptake (peakVO2), maximal minute ventilation, and higher ventilatory equivalent (VE/VCO2). The concentrations of B-type natriuretic peptide (BNP) and N-terminal proBNP (NT-proBNP) were significantly higher in the study group. The results of all the FFFT items were significantly worse in the study group. FFFT parameters, together with the assessment of the strength of the handgrip, strongly correlated with the results of standard tests in HF. FFFT is an effective and safe tool for the functional evaluation of patients with HFrEF. Simple muscle strength measurement with a hand-held dynamometer can become a convenient and practical indicator of muscle strength in HF patients.

1. Introduction

Heart failure (HF) is a growing clinical, economic, and epidemiological problem. Despite the progress in the treatment, the prognosis is still poor. It is estimated that during the prevailing SARS-CoV-2 pandemic the number of new HF cases may significantly increase both in Europe and worldwide [1].
Heart failure is a progressive and systemic disease characterized by a reduced ability to perform functional activities. Climbing stairs, walking, moving around, cleaning, and bathing are the most burdensome problems in heart failure patients’ everyday activities [2]. Patients also have problems bending down [3] and lifting heavy objects [4]. The assessment of functional abilities reflects the ability to perform everyday life activities that require specific endurance and physical fitness [5].
The gold standard for assessing heart failure patients is the cardiopulmonary exercise test (CPET) [6]. This is an exercise test with assessment of the parameters of ventilation and gas exchange, which allows for a detailed analysis of the capacity of the cardiovascular, respiratory and motor systems. CPET is primarily used in the diagnostic workup of reduced exercise tolerance, qualification for heart transplantation and in training planning and evaluation in professional athletes. A 6-min walk test (6MWT) plays a similar role in severe heart failure patients who are not able to complete a regular exercise test. Reduced exercise capacity, a consequence of progressive heart failure, causes a gradual deterioration of the patient’s condition, limiting their physical activity and, consequently, physical fitness [7]. The Fullerton functional fitness test (FFFT) reflects exercise capacity and fitness [5]. At the same time, CPET and 6MWT, despite their proven value, do not fully assess the problems associated with the daily activities of heart failure patients.
The natriuretic peptides are used widely in the diagnostic workup of heart failure [6]. They indicate overload of the left ventricle, and high values of B-type natriuretic peptide (BNP) and N-terminal B-type natriuretic pro-peptide (NT-pro BNP) may be associated with the severity of heart failure.
The Fullerton functional fitness test seems to be the most appropriate for assessing physical fitness in heart failure patients. Initially, this test was designed to assess the physical fitness of the elderly, i.e., those aged 60–94 [8]. Over time the test has been started to evaluate the results of rehabilitation in various diseases such as chronic obstructive pulmonary disease (COPD) [9], obesity [10], diabetes [11], Parkinson’s disease [12], Alzheimer’s disease [13] and many others [14,15,16]. The Fullerton functional fitness test assesses the key elements of physical fitness: muscle endurance, aerobic capacity, flexibility, agility, and balance. At the same time, this test does not expose the patient to the risk of injuries [17]. Furthermore, the repeatability of each test and the simplicity of its execution enable the test to be carried out by a physiotherapist in hospital and outpatient settings [7].
We aimed to evaluate the usefulness of FFFT in the functional assessment of physical fitness of heart failure patients. In particular, we aimed to correlate FFFT results with CPET and echocardiography results as well as natriuretic peptide values.

2. Materials and Methods

2.1. Study Population

Fifty-four men were included in the study. The study group consisted of 30 consecutive patients hospitalized for the routine assessment of heart failure with a reduced ejection fraction. The control group consisted of 24 men with no history of heart failure and normal left ventricular ejection fraction (LVEF). The inclusion and exclusion criteria are shown in Table 1.
Each patient underwent CPET and transthoracic echocardiography. NYHA functional class, hemoglobin concentration, B-type natriuretic peptide (BNP) and N-terminal B-type natriuretic pro-peptide (NT-pro BNP) levels were also assessed.
This research was approved by the Bioethics Committee at the Medical University of Karol Marcinkowski in Poznan, number 630/15.

2.2. Fullerton Functional Fitness Test

According to commonly accepted procedures, physical fitness was assessed using FFFT (Table 2) [18]. For the safety of patients, the test in both groups was performed by a physiotherapist in the presence of a cardiologist. Before and after the start of the study, the values of heart rate and blood pressure were measured. To complete the assessment of patients with heart failure, the FFFT was modified by adding the measurement of the handgrip force of the dominant limb with the digital dynamometer CHARDER MG-4800, Taiwan.

2.3. Statistical Analysis

Statistical analysis was performed using the Statistica 13.1 software. According to the results of the Shapiro-Wilk test, the distribution of all examined variables was considered non-parametric. The Mann-Whitney U test was used to analyze independent continuous data, and the sign test was used to analyze dependent continuous variables. Spearman’s correlation coefficients were calculated to evaluate the relationship between pairs of selected parameters in the heart failure group. p < 0.05 was considered significant for all tests.

3. Results

The basic characteristics of the study groups are presented in Table 3. The mean left ventricular ejection fraction (LVEF) in the study group was 23.0 ± 6.2%. Moreover, heart failure patients had a significantly larger left ventricular end-diastolic diameter, right ventricular diameter, and left atrium diameter. The mean peak oxygen uptake in the test group was 18.3 ± 5.6 mL/kg/min, and in the control group, this was 33.5 ± 8.1 mL/kg/min. Heart failure patients had significantly lower VCO2, maximal minute ventilation, peakCO2, and higher ventilatory equivalent VE/VCO2. The concentrations of BNP and NT-proBNP were significantly higher in the study group.
Significant differences were observed in the Fullerton functional fitness test results between the study and the control groups (Table 3). Two heart failure patients could not complete FFFT due to rapidly increasing fatigue, but no pathological symptoms of exercise intolerance were observed. All results were significantly worse in the study group. Moreover, two heart failure patients completed the 6-min walk test after 2.36 min and 4.26 min due to very large fatigue and pain in the lower limbs.
Spearman’s correlation analysis (Table 4) was performed to assess the relationship between FFFT including handgrip strength with left ventricular ejection fraction (LVEF), and peak oxygen consumption (peakVO2). FFFT parameters, together with the assessment of the strength of the handgrip, strongly correlated with the results of standard tests in heart failure.

4. Discussion

Our study is the first analysis of the functional performance assessment of heart failure patients using the Fullerton functional fitness test, in which, the results have been correlated with recognized parameters for assessing poor prognosis in patients with heart failure with reduced ejection fraction, such as LVEF, NT-proBNP, and cardiopulmonary stress test results.
Despite the need to assess the physical fitness of heart failure patients, the available literature is dominated mainly by the assessment of fitness and quality of life [20,21]. Functional abilities are primarily assessed with the help of the 6-min walk test, which does not assess the basic characteristics of physical fitness such as muscle strength, endurance, coordination, and flexibility.
Reduced exercise capacity, which is a consequence of progressive heart failure, causes a gradual deterioration of the patient’s condition, limiting physical activity and, consequently, physical fitness [7]. The Fullerton functional fitness test reflects changes in physical capacity and fitness [5], while a cardiopulmonary stress test and a 6-min walk test, despite their proven value, do not fully assess the problems associated with the daily activities of heart failure patients. Therefore, in our research, the Fullerton functional fitness test was used for the initial assessment of functional fitness, which reflects changes in physical capacity and fitness [5].
Muscular endurance is the ability to perform everyday activities without enormous and rapidly increasing fatigue [22]. Muscle endurance depends largely on the body’s endurance, which in people with heart failure is up to about 50% lower than appropriate [23]. In our research, the patients with heart failure obtained significantly worse results in the endurance-related FFFT items than the controls. There were positive correlations of both the “Chair Stand” and “Arm Curl” tests with LVEF and peakVO2 and a negative correlation with NT-proBNP. This can be interpreted as the decreased muscle endurance of lower and upper limbs with progressing heart failure. Our results are consistent with the results of a similar analysis by Węgrzynowska-Teodorczyk et al. [24].
The heart failure hallmark is exercise intolerance, manifested by shortness of breath and a feeling of quickly becoming fatigued. When the disease is highly advanced, symptoms occur even with minimal physical exertion or at rest [6]. Cardiopulmonary exercise test (CPET) on a treadmill or cyclo-ergometer is the “gold standard” for assessing exercise capacity, but it can be difficult for the patient to perform, and its availability is not common.
A healthy person will not achieve maximum effort during a 6-min walk test, but in severely impaired people who cannot perform significant effort during a cardiopulmonary exercise test, a 6-min walk test may be the maximal test. In our study, heart failure patients obtained significantly worse results in both tests. Worse results of a 6-min walk test are associated with an unfavorable prognosis [25].
Our observations are consistent with previously published studies in which patients with severe heart failure (NYHA III-IV) had a much shorter 6-min walk test distance than the controls (NYHA II) [26]. As expected, significant positive correlations between the 6-min walk test distance, LVEF, and peak oxygen consumption (peakVO2) were observed in heart failure patients. Previously, a linear correlation between the 6-min walk test distance and the measurement of peak oxygen consumption was demonstrated and had a significant prognostic value in heart failure [8]. The consistency of these findings was expected because of the characteristics of heart failure patients. The progression of heart failure is associated with the reduction of cardiac output (evaluated using LVEF and peakVO2) and left ventricular overload (evaluated by BNP and NT-proBNP blood concentrations), which is followed by a reduction in exercise tolerance.
Moreover, like other authors, we observed a significant negative correlation between NT-proBNP levels and the 6-min walk test result [27]. However, other studies also found an increase in physical capacity and a decrease in NT-proBNP levels, which correlated with an improvement in the clinical condition assessed with the NYHA functional class in patients with heart failure participating in physical training [28].
Increased fatigue and muscle weakness in patients with heart failure and the adverse effects of some drugs leading to bradycardia and orthostatic hypotension make patients more prone to falls, especially those over 65 years of age [29,30]. Our study shows that heart failure patients have significantly poorer agility and dynamic balance, contributing to an increased risk of falls. Węgrzynowska-Teodorczyk et al. obtained similar results [31], and worse motor skills of heart failure patients were confirmed using magnetic resonance imaging of the head [32]. The assessment of agility and dynamic balance seems to be important in the initial evaluation of heart failure patients because up to 43% of patients report frequent falls [33].
In our study, the heart failure patients performed worse than controls in the flexibility-related FFFT items. However, a similar assessment of flexibility [24,31] showed contradictory results. Some authors state that flexibility is a morphological, genetically determined trait and is not related to the progression of the disease [34,35]. The difference between the results of the above-mentioned papers and our own may be due to the more significant advancement of the disease determined by LVEF in our study.
Loss of muscle strength and mass may be a consequence of chronic diseases, leading to changes in metabolism and muscle structure [36]. It contributes to the deterioration of the patient’s clinical condition and exercise tolerance [37]. The strength of the knee flexors and extensors in heart failure patients was investigated by Toth et al. [38] who determined that the maximum measurement of the muscle strength of the lower limbs was lower by 15–33% in the group of heart failure patients [38]. Other authors obtained similar results in assessing the muscle strength of the lower extremities [37,39]. It is also assumed that a reduction in the strength of the quadriceps muscle of the thigh may have a prognostic value [37,39] and contribute to a reduction in the quality of life of heart failure patients [40]. The handgrip strength strongly correlates with other measures of muscle strength [37,41]. Our research assessed the strength of the dominant handgrip, which was lower in the group of heart failure patients. Additionally, the analysis of our results showed a significant positive correlation between the handgrip strength and LVEF as well as peakVO2, which is consistent with the results of other authors [42]. The observed loss of muscle strength may confirm one of the hypotheses indicating the role of peripheral (muscle) factors in exercise intolerance, which concerns structural, metabolic, or functional changes in skeletal muscles in the course of heart failure [36,37,43]. We chose to examine the dominant limb, similarly to other authors [42].

Study Limitations

The relatively small size of the study group, and considering only men, may make it difficult to generalize the results to the entire population of heart failure patients. We did not evaluate the possible impact of obesity on the Fullerton fitness test results and on the concentrations of natriuretic peptides. Therefore, it may be necessary to continue the research taking into account obesity indicators (percentage and distribution of adipose tissue in the body).

5. Conclusions

The Fullerton fitness test is an effective and safe tool for the functional evaluation of patients with heart failure with reduced ejection fraction. The Fullerton fitness test results correlate well with the results of standardized testing in heart failure patients (most of the FFFT items show positive correlations with left ventricular ejection fraction and negative correlations with BNP and NT-proBNP values). Simple muscle strength measurement with a hand-held dynamometer can become a convenient and practical indicator of muscle strength in heart failure patients.

Author Contributions

Conceptualization, M.M. and A.S.-L.; Methodology, M.M. and A.S.-L.; Validation, J.M.; Formal Analysis, J.M.; Investigation, M.M., M.K.-O., J.M. and A.S.-L.; Resources, M.M.; Data Curation, M.M. and J.M.; Writing—Original Draft Preparation, M.M., M.K.-O., J.M. and A.S.-L.; Writing—Review & Editing, M.M., M.K.-O., J.M. and A.S.-L.; Visualization, M.M., M.K.-O., J.M. and A.S.-L.; Supervision, A.S.-L.; Project Administration, M.M.; All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board (or Ethics Committee) of Poznan University of Medical Sciences, number 630/15.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors thank JO Medical Solutions for providing medical writing support following Good Publication Practice (GPP3) guidelines (http://www.ismpp.org/gpp3, accessed on 18 April 2022).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Einstein, A.J.; Shaw, L.J.; Hirschfeld, C.; Williams, M.C.; Villines, T.C.; Better, N.; Vitola, J.V.; Cerci, R.; Dorbala, S.; Raggi, P.; et al. International impact of COVID-19 on the diagnosis of heart disease. J. Am. Coll. Cardiol. 2021, 77, 173–185. [Google Scholar] [CrossRef] [PubMed]
  2. Dunlay, S.M.; Manemann, S.M.; Chamberlain, A.M.; Cheville, A.L.; Jiang, R.; Weston, S.A.; Roger, V.L. Activities of daily living and outcomes in heart failure. Circ. Heart Fail. 2015, 8, 261–267. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Baeza-Trinidad, R.; Mosquera-Lozano, J.D. Bendopnea: The next prognostic marker of advanced heart failure? Am. Heart J. 2017, 186, e1. [Google Scholar] [CrossRef] [PubMed]
  4. Walthall, H.; Floegel, T.; Boulton, M.; Jenkinson, C. Patients experience of fatigue in advanced heart failure. Contemp. Nurse 2019, 55, 71–82. [Google Scholar] [CrossRef]
  5. Jones, J.; Rikli, E. Measuring functional fitness of older adults. J. Act. Aging 2002, 1, 24–30. [Google Scholar]
  6. McDonagh, T.A.; Metra, M.; Adamo, M.; ESC Scientific Document Group; Gardner, R.S.; Baumbach, A.; Böhm, M.; Burri, H.; Butler, J.; Čelutkienė, J.; et al. 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur. Heart J. 2021, 42, 3599–3726, Erratum in Eur. Heart J. 2021. PMID: 34447992. [Google Scholar] [CrossRef] [PubMed]
  7. Jankowska-Polańska, B.; Uchmanowicz, I. Wielolekowości, choroby współistniejące i upadki u chorych z przewlekłą niewydolnością serca w wieku podeszłym. Geriatria 2014, 8, 184–195. [Google Scholar]
  8. Rikli, R.; Jones, J. Functional fitness normative scores for community-residing older adults, ages 60–94. J. Aging Phys. Act. 1999, 7, 162–181. [Google Scholar] [CrossRef]
  9. Alexander, J.L.; Phillips, W.T.; Wagner, C.L. The effect of strength training on functional fitness in older patients with chronic lung disease enrolled in pulmonary rehabilitation. Rehabil. Nurs. 2008, 33, 91–97. [Google Scholar] [CrossRef]
  10. Budui, S.; Bigolin, F.; Giordano, F.; Leoni, S.; Berteotti, M.; Sartori, E.; Franceschini, L.; Taddei, M.; Salvetti, S.; Castiglioni, F.; et al. Effects of an Intensive Inpatient Rehabilitation Program in Elderly Patients with Obesity. Obes. Facts 2019, 12, 199–210. [Google Scholar] [CrossRef]
  11. Park, S.Y.; Lee, I.H. Effects on training and detraining on physical function, control of diabetes and anthropometrics in type 2 diabetes; a randomized controlled trial. Physiother. Theory Pract. 2015, 31, 83–88. [Google Scholar] [CrossRef]
  12. Urgacz, K.; Cholewa, J.; Uher, I.; Sahin, B.; Cholewa, J. Senior Fitness Test in assessing the effectiveness of motor rehabilitation in the context of Parkinson’s disease patients’ quality of life. Phys. Act. Rev. 2018, 6, 110–116. [Google Scholar]
  13. Santana-Sosa, E.; Barriopedro, M.I.; López-Mojares, L.M.; Pérez, M.; Lucia, A. Exercise training is beneficial for Alzheimer’s patients. Int. J. Sports Med. 2008, 29, 845–850. [Google Scholar] [CrossRef]
  14. Langhammer, B.; Stanghelle, J.K. Senior fitness test; a useful tool to measure physical fitness in persons with acquired brain injury. Brain Inj. 2019, 33, 183–188. [Google Scholar] [CrossRef]
  15. Soriano-Maldonado, A.; Henriksen, M.; Segura-Jiménez, V.; Aparicio, V.A.; CarbonellBaeza, A.; Delgado-Fernández, M.; Amris, K.; Ruiz, J.R. Association of Physical Fitness with Fibromyalgia Severity in Women: The al-Ándalus Project. Arch. Phys. Med. Rehabil. 2015, 96, 1599–1605. [Google Scholar] [CrossRef]
  16. Kocur, P.; Deskur-Smielecka, E.; Wilk, M.; Dylewicz, P. Effects of Nordic walking training on exercise capacity and fitness in men participating in early, short-term inpatient cardiac rehabilitation after an acute coronary syndrome—A controlled 71 trial. Clin. Rehabil. 2009, 23, 995–1004. [Google Scholar] [CrossRef]
  17. Rikli, R.; Jones, J. Development and validation of a functional fitness test for community-residing older adults. J. Aging Phys. Act. 1999, 7, 129–161. [Google Scholar] [CrossRef]
  18. Różanska-Kirschke, A.; Kocur, P.; Wilk, M.; Dylewicz, P. The Fullerton Fitness Test as 76 an index of fitness in the elderly. Reh Med. 2006, 2, 15–19. [Google Scholar]
  19. Izawa, K.P.; Watanabe, S.; Yokoyama, H.; Hiraki, K.; Morio, Y.; Oka, K.; Osada, N.; Omiya, K. Muscle strength in relation to disease severity in patients with congestive heart failure. Am. J. Phys. Med. Rehabil. 2007, 86, 893–900. [Google Scholar] [CrossRef]
  20. Hendrican, M.C.; McKelvie, R.S.; Smith, T.; McCartney, N.; Pogue, J.; Teo, K.K.; Yusuf, S. Functional capacity in patients with congestive heart failure. J. Card. Fail. 2000, 6, 214–219. [Google Scholar] [CrossRef]
  21. Suman-Horduna, I.; Roy, D.; Frasure-Smith, N.; Talajic, M.; Lespérance, F.; Blondeau, L.; Dorian, P.; Khairy, D.; AF-CHF Trial Investigators. Quality of life and functional capacity in patients with atrial fibrillation and congestive heart failure. J. Am. Coll. Cardiol. 2013, 61, 455–460. [Google Scholar] [CrossRef]
  22. American College of Sports Medicine. ACSM’s Guidelines for Exercise Testing and Prescription, 10th ed.; Lippincott Williams & Wilkins: Philadelphia, PA, USA, 2014; pp. 236–256. [Google Scholar]
  23. Arena, R.; Myers, J.; Guazzi, M. The clinical importance of cardiopulmonary exercise testing and aerobic training in patients with heart failure. Braz. J. Phys. Ther. 2008, 12, 75–87. [Google Scholar] [CrossRef]
  24. Węgrzynowska-Teodorczyk, K.; Rudzińska, E.; Jankowska, E.; Grzesło, A.; Nowakowska, K.; Łazorczyk, M.; Banasiak, W.; Ponikowski, P.; Woźniewski, M. Determinants of physical fitness in males with systolic heart fa. Kardiol. Pol. (Pol. Heart J.) 2010, 68, 146–154. [Google Scholar]
  25. Bittner, V.; Weiner, D.H.; Yusuf, S.; Rogers, W.J.; Mcintyre, K.M.; Bangdiwala, S.I.; Kronberg, M.V.; Kostis, J.B.; Kohn, R.M.; Guillotte, M.; et al. Prediction of mortality and morbidity with a 6-min walk test in patients with left ventricular dysfunction. JAMA 1993, 270, 1702–1707. [Google Scholar] [CrossRef]
  26. Opasich, C.; Pinna, G.D.; Mazza, A.; Febo, O.; Riccardi, R.; Riccardi, P.G.; Capomolla, S.; Forni, G.; Cobelli, F.; Tavazzi, L. Six-minute wal king performance in patients with moderate—To severe heart failure. Eur. Heart J. 2001, 22, 488–496. [Google Scholar] [CrossRef]
  27. Laoutaris, I.D.; Vasiliadis, I.K.; Dritsas, A.; Mavrogeni, S.; Kallistratos, M.S.; Manginas, A.; Chaidaroglou, A.; Degiannis, D.; Demosthenes, B.; Panagiotakos, D.B.; et al. High plasma adiponectin is related to low functional capacity in patients with chronic heart failure. Int. J. Cardiol. 2010, 144, 230–231. [Google Scholar] [CrossRef] [PubMed]
  28. Conraads, V.M.; Beckers, P.; Vaes, J.; Viviane Van Hoof, M.M.; Maeyer, C.D.; Possemiers, N.; Wuyts, F.L.; Vrints, C.J. Combined endurance/resistance training reduces NTporBNP levels In patients with chronic heart failure. Eur. Heart J. 2004, 25, 1797–1805. [Google Scholar] [CrossRef]
  29. Wong, C.Y.; Chaudhry, S.I.; Desai, M.M.; Krumholz, H.M. Trends in comorbidity, disability, and polypharmacy in heart failure. Am. J. Med. 2011, 124, 136–143. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Rich, M.W. Pharmacotherapy of heart failure in the elderly: Adverse events. Heart Fail. Rev. 2012, 17, 589–595. [Google Scholar] [CrossRef] [PubMed]
  31. Węgrzynowska-Teodorczyk, K.; Dąbrowska, E.; Łazorczyk, M.; Nowakowska, K.; Kowalska-Superlak, M.; Jankowska, E.A.; Ponikowski, P.; Banasik, W.; Woźniewski, M. Sprawność fizyczna mężczyzn z niewydolnością serca w porównaniu ze zdrowymi równolatkami. Physiother./Fizjoterapia 2007, 15, 44–53. [Google Scholar]
  32. Woo, M.A.; Palomares, J.A.; Macey, P.M.; Fonarow, G.C.; Harper, R.M.; Kumar, R. Global and regional brain mean diffusivity chan ges in patients with heart failure. J. Neurosci. Res. 2015, 93, 678–685. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Lee, P.G.; Cigolle, C.; Blaum, C. The co-occurrence of chronic diseases and geriatric syndromes: The Health and Retirement Study. J. Am. Geriatr. Soc. 2009, 57, 511–516. [Google Scholar] [CrossRef] [PubMed]
  34. Holland, G.J.; Tanaka, K.; Shigematsu, R.; Nakagaichi, M. Flexibility and physical functions of older adults: A review. J. Aging Phys. Act. 2002, 10, 169–206. [Google Scholar] [CrossRef] [Green Version]
  35. Bouchard, C. Genetics of Fitness and Physical Performance; Human Kinetics: Champaign, IL, USA, 1997. [Google Scholar]
  36. Von Haehling, S.; Ebner, N.; dos Santos, M.R.; Springer, J.; Anker, S.D. Muscle wasting and cachexia in heart failure: Mechanisms and therapies. Nat. Rev. Cardiol. 2017, 14, 323–334. [Google Scholar] [CrossRef] [PubMed]
  37. Fülster, S.; Tacke, M.; Sandek, A.; Ebner, N.; Tschöpe, C.; Doehner, W.; Anker, S.; Von Haehling, S. Muscle wasting in patients with chronic heart failure: Results from the 68 studies investigating co-morbidities aggravating heart failure (SICA-HF). Eur. Heart J. 2012, 34, 512–519. [Google Scholar] [CrossRef] [Green Version]
  38. Toth, M.J.; Shaw, A.O.; Miller, M.S.; VanBuren, P.; LeWinter, M.M.; Maughan, D.W.; Ades, P.A. Reduced knee extensor function in heart failure is not explained by inactivity. Int. J. Cardiol. 2010, 143, 276–282. [Google Scholar] [CrossRef] [Green Version]
  39. Hülsmann, M.; Quittan, M.; Berger, R.; Crevenna, R.; Springer, C.; Nuhr, M.; Moser, P.; Pacher, R. Muscle strength as a predictor of long-term survival in severe congestive heart failure. Eur. J. Heart Fail. 2004, 6, 101–107. [Google Scholar] [CrossRef]
  40. Jankowska, E.A.; Wegrzynowska, K.; Superlak, M.; Nowakowska, K.; Lazorczyk, M.; Biel, B.; Kustrzycka-Kratochwil, D.; Piotrowska, K.; Banasiak, W.; Wozniewski, M.; et al. The 12-week progressive quadriceps resistance training improves muscle strength, exercise capacity and quality of life in patients with stable chronic heart failure. Int. J. Cardiol. 2008, 130, 36–43. [Google Scholar] [CrossRef]
  41. Izawa, K.P.; Watanabe, S.; Osada, N.; Kasahara, Y.; Yokoyama, H.; Hiraki, K.; Morio, Y.; Yoshioka, S.; Oka, K.; Omiya, K. Handgrip strength as a predictor of prognosis in Japanese patients with congestive heart failure. Eur. J. Cardiovasc. Prev. Rehabil. 2009, 16, 21–27. [Google Scholar] [CrossRef]
  42. Mroszczyk-McDonald, A.; Savage, P.D.; Ades, P.A. Handgrip strength in cardiac rehabilitation: Normative values, interaction with physical function, and response to training. J. Cardiopulm. Rehabil. Prev. 2007, 27, 298–302. [Google Scholar] [CrossRef]
  43. Ebner, N.; Sliziuk, V.; Scherbakov, N.; Sandek, A. Muscle wasting in ageing and chronic illness. ESC Heart Fail. 2015, 2, 58–68. [Google Scholar] [CrossRef]
Table 1. Inclusion and exclusion criteria.
Table 1. Inclusion and exclusion criteria.
Inclusion CriteriaExclusion Criteria
Study group
  • Age > 18 years
  • Written consent to inclusion in the study
  • Chronic heart failure classified as New York Heart Association (NYHA) functional class II or III
  • reduced left ventricular ejection fraction (LVEF ≤ 40%)
  • HF exacerbation requiring intravenous diuretics during the 4 weeks before study enrollment
  • Acute coronary syndrome
  • Motor dysfunction preventing completion of the Fullerton fitness test items
  • Uncontrolled blood pressure exceeding 160/100 mmHg at rest
Control group
  • Age > 18 years
  • Written consent to inclusion in the study
  • Chronic or acute heart failure
  • Motor dysfunction preventing completion of the Fullerton fitness test items
  • Acute coronary syndrome
  • Uncontrolled blood pressure exceeding 160/100 mmHg at rest
Table 2. Six motor tasks assessed in the Fullerton functional fitness test.
Table 2. Six motor tasks assessed in the Fullerton functional fitness test.
8 Foot Up&GoThe patient circles the cone in the shortest possible time at a distance of 2.44 m from the sitting starting position and returns to the starting position.
30-Second Chair StandThe patient repeats full stands from the sitting position. Repetitions are performed within 30 s with the arms crossed over the chest.
Arm CurlThe patient flexes the forearm with a 3.5 kg weight in 30 s. The result is the number of repetitions.
Back ScratchThe patient tries to join the hands behind the back, leading one hand from the top, and the other from the bottom. The result given in centimeters indicates the distance between the middle fingers. The value may be negative when the patient reaches further than the fingertips.
Chair Sit&ReachFrom a sitting position on a chair, the patient tries to reach the toes with the leg straight in the knee joint. The result in centimeters shows the distance between the fingers and the toes. The value can be negative when the patient is out of range of motion.
6-Min Walking Test (6MWT)The test result is the number of meters the patient walked along a 30-m corridor in 6 min.
The modification of the Fullerton functional fitness test:
Measuring the strength of the handgripThe examination was performed on the dominant limb, in a sitting position, with the elbow extended and the shoulder joint flexed to 90°. Three measurements were made with a 5-s interval between attempts, and the best measurement was selected for analysis, according to the previously proposed methodology [19].
Table 3. Baseline study population characteristics.
Table 3. Baseline study population characteristics.
HF Group
X(SD)
Control Group
X(SD)
p
N
Age (years)
30
56.2 (12.2)
24
55.4 (10.4)

0.60
BMI (kg/m2)
NYHA
28.5 (4.0)
2.4 (0.5)
25.6 (34)
-
0.004
-
LVEF (%)23.0 (6.2)61.6 (3.6)<0.001
LVED (mm)72.4 (8.2)47.2 (5.9)<0.001
RVD (mm)35.4 (7.2)29.2 (3.5)<0.001
LAD (mm)49.8 (10.4)36.3 (4.3)<0.001
IVS (mm)9.6 (1.6)10.0 (1.0)0.22
LVPW (mm)9.9 (1.1)9.9 (0.9)0.77
peakVO2 (%)55.8 (12.6)100.6 (25.5)<0.001
peakVO2 (mL/kg/min)18.3 (5.6)33.5 (8.1)<0.001
peakVO2 (L/min)1.6 (0.5)2.8 (0.7)<0.001
peakVCO2 (L/min)1.6 (0.5)3.1 (0.8)<0.001
VE Max (L/min)60.7 (15.7)91.1 (22.5)<0.001
peakVCO2 (mL/kg/min)33.7 (6.8)40.8 (4.5)<0.001
RER1.31.1
VE/VCO2 slope32.5 (7.3)24.0 (3.5)<0.001
BNP (pg/mL)384.9 (403)39.3 (58.1)<0.001
NT-proBNP (pg/mL)1823.0 (18301.1)139.9 (261.5)<0.001
HGB (mmol/L)9.0 (0.8)9.0 (0.8)0.84
Fullerton functional fitness test results
6MTW (m)363.6 (125.1)563.8 (69.9)>0.001
Chair Stand (repetitions)12.7 (5.2)18.0 (4.5)>0.001
Arm Curl (repetitions)14.7 (4.4)23.3 (4.9)>0.001
Chair Sit&Reach (cm)−15.7 (12.1)−6.8 (8.4)0.004
Back Scratch (cm)−20.1 (16.4)−6.2 (13.6)0.002
8-foot Up&Go (s)8.7 (2.2)6.0 (1.1)>0.001
Handgrip strength (kg)37.9 (10.7)48.3 (10.7) >0.001
6MWT—6-min walk test; BMI—body mass index; LVEF—left ventricular ejection fraction; HF—heart failure; BNP—natriuretic peptide; HGB—hemoglobin; LVED—left ventricular end-diastolic diameter; RVD—right ventricular diameter; LAD—left atrium diameter; IVS—ventricular septum diameter; LVPW—left ventricular posterior wall diameter; VO2—oxygen consumption during exercise; VCO2—production of carbon dioxide; VEmax—maximum minute ventilation; peakCO2—peak carbon dioxide release; RER—respiratory rate; VE/VCO2—exercise ventilation.
Table 4. The correlation between the Fullerton functional fitness test results including handgrip strength with LVEF, peakVO2 and NT-proBNP values.
Table 4. The correlation between the Fullerton functional fitness test results including handgrip strength with LVEF, peakVO2 and NT-proBNP values.
LVEFpeakVO2NT-proBNP
rprprp
6MTW0.76<0.0010.83<0.001−0.71<0.001
Chair Stand0.63<0.0010.60<0.001−0.49<0.001
Arm Curl0.64<0.0010.76<0.001−0.50<0.001
Chair Sit&Reach0.380.0050.360.008−0.220.72
Back Scratch0.46<0.0010.61<0.001−0.36<0.001
8-foot Up&Go−0.69<0.001−0.77<0.0010.57<0.001
Hand grip strength0.390.0040.45<0.001−0.50<0.001
6MWT—6-min walk test; LVEF—left ventricular ejection fraction; NT-proBNP—N-terminal brain natriuretic pro-peptide; peakVO2—peak oxygen uptake.
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Migaj, M.; Kałużna-Oleksy, M.; Migaj, J.; Straburzyńska-Lupa, A. The Evaluation of Functional Abilities Using the Modified Fullerton Functional Fitness Test Is a Valuable Accessory in Diagnosing Men with Heart Failure. Int. J. Environ. Res. Public Health 2022, 19, 9210. https://doi.org/10.3390/ijerph19159210

AMA Style

Migaj M, Kałużna-Oleksy M, Migaj J, Straburzyńska-Lupa A. The Evaluation of Functional Abilities Using the Modified Fullerton Functional Fitness Test Is a Valuable Accessory in Diagnosing Men with Heart Failure. International Journal of Environmental Research and Public Health. 2022; 19(15):9210. https://doi.org/10.3390/ijerph19159210

Chicago/Turabian Style

Migaj, Magdalena, Marta Kałużna-Oleksy, Jacek Migaj, and Anna Straburzyńska-Lupa. 2022. "The Evaluation of Functional Abilities Using the Modified Fullerton Functional Fitness Test Is a Valuable Accessory in Diagnosing Men with Heart Failure" International Journal of Environmental Research and Public Health 19, no. 15: 9210. https://doi.org/10.3390/ijerph19159210

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