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(Circulation. 2009;119:251-260.)
© 2009 American Heart Association, Inc.
Exercise Physiology |
From Northwestern Universitys Feinberg School of Medicine, Chicago, Ill (P.K.G., K.L., L.T., J.T., M.M.M.); Laboratory of Epidemiology, Demography, and Biometry (J.M.G.) and Laboratory of Clinical Epidemiology (L.F.), National Institute on Aging, Bethesda, Md; and University of California at San Diego, San Diego (M.H.C.). Dr Tian is currently affiliated with Stanford University, Palo Alto, Calif. J. Tan currently works for a private company in California.
Correspondence to Mary M. McDermott, MD, 750 N Lake Shore Dr, 10th Floor, Chicago, IL 60611. E-mail mdm608{at}northwestern.edu
Received May 27, 2008; accepted October 24, 2008.
| Abstract |
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Methods and Results— The study population included 203 peripheral arterial disease participants who underwent vertical accelerometer–measured physical activity continuously over 7 days and were followed up annually for up to 4 years (mean, 33.6 months). Outcomes were average annual changes in 6-minute walk performance, usual-paced and fast-paced 4-m walking velocity, and the short performance physical battery. Analyses were adjusted for age, sex, race, comorbidities, body mass index, ankle brachial index, smoking, and walking exercise frequency. Higher baseline physical activity levels measured by a vertical accelerometer were associated with significantly less average annual decline in 6-minute walk performance (P for trend=0.010), fast-paced 4-m walking velocity (P for trend=0.002), and the short performance physical battery (P for trend=0.001). Compared with the lowest baseline quartile, those in the highest baseline quartile of physical activity had less annual decline in 6-minute walk performance (–50.82 versus –107.0 ft/y; P=0.019), fast-paced 4-m walking speed (–0.0034 versus –0.111 m · s–1 · y–1; P=0.002), and the short performance physical battery (–0.074 versus –0.829; P=0.005).
Conclusions— Higher physical activity levels during daily life are associated with less functional decline among people with peripheral arterial disease. These findings may be particularly important for the large number of peripheral arterial disease persons without access to supervised walking exercise programs.
Key Words: claudication exercise peripheral vascular disease risk factors
| Introduction |
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Clinical Perspective p 260
A relationship between higher levels of physical activity during daily life and lower rates of disability has been demonstrated in non-PAD populations.12–15 However, it is unknown whether, across the lower range of physical activity levels observed in people with PAD, higher physical activity levels during daily life are associated with less functional decline.16
Among persons with PAD, we determined whether higher levels of physical activity during daily life were associated with less functional decline. If higher physical activity levels are protective against functional decline in people with PAD, then interventions to increase daily physical activity in this population may be beneficial.
| Methods |
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Participants were part of the Walking and Leg Circulation Study (WALCS),3,4 a prospective, observational study designed to identify predictors of functional decline in PAD. Participants were identified from among consecutive patients
55 years of age in 3 Chicago-area noninvasive vascular laboratories. Participants had an ankle brachial index (ABI) <0.90 at their baseline visit.
Exclusion Criteria
Exclusion criteria have been reported elsewhere.4 Patients with dementia, recent major surgery, or foot or leg amputations were excluded. Nursing home residents and wheelchair-bound patients were excluded. Non–English-speaking patients were excluded because investigators were not fluent in non-English languages. Participants who underwent lower-extremity revascularization after the baseline visit were excluded from analyses after their revascularization.
ABI Measurement
A handheld Doppler probe (Nicolet Vascular Pocket Dop II, Nicolet Biomedical Inc, Golden, Colo) was used to obtain systolic pressures in the right and left brachial, dorsalis pedis, and posterior tibial arteries.17,18 Each pressure was measured twice. The ABI was calculated by dividing the mean of the dorsalis pedis and posterior tibial pressures in each leg by the mean of the 4 brachial pressures.17 Average brachial pressures in the arm with highest pressure were used when 1 brachial pressure was higher than the opposite brachial pressure in both measurement sets and the 2 brachial pressures differed by
10 mm Hg in at least 1 measurement set because, in such cases, subclavian stenosis was possible.17,18 The lowest leg ABI was used in analyses.
Exertional Leg Symptoms
Participants were categorized into the following leg symptom categories based on previous study3,4,19: asymptomatic (no exertional leg symptoms), classic intermittent claudication symptoms, leg pain on exertion and rest (exertional leg pain that sometimes begins at rest), exertional leg pain/carry on (exertional leg pain that does not cause the patient to stop walking), and atypical exertional leg pain (exertional leg pain that is not consistent with any of the previous).
Depressive Symptoms
Depressive symptoms were measured annually with the Geriatric Depression Scale Short Form, a 15-item questionnaire assessing the number of depressive symptoms.20 The Geriatric Depression Scale Short Form score ranges from 0 to 15, with 0 indicating no depressive symptoms and 15 indicating that all depressive symptoms in the Geriatric Depression Scale Short Form are present.
Functional Measures
Functional performance measures were administered at baseline and annually during follow-up.
Six-Minute Walk
Following a standardized protocol,21,22 participants walked up and down a 100-ft hallway for 6 minutes after instructions to cover as much distance as possible.
Repeated Chair Rises
Participants sat in a straight-backed chair with their arms folded across their chests and stood 5 times consecutively as quickly as possible. The time to complete 5 chair rises was measured.
Standing Balance
Participants were asked to hold 3 increasingly difficult standing positions for 10 seconds each: standing with feet together side by side and parallel (side-by-side stand), standing with feet parallel with the toes of 1 foot adjacent to and touching the heel of the opposite foot (semitandem stand), and standing with 1 foot directly in front of the other with both feet in a straight line (tandem stand).23,24
Four-Meter Walking Velocity
Walking velocity was measured with a 4-m walk performed at "usual" and "fastest" pace. For the usual-paced walk, participants were instructed to walk at their usual pace "as if going down the street to the store." Each walk was performed twice. The faster walk in each pair was used in analyses.23,24
Short Physical Performance Battery
The short physical performance battery combines data from the usual-paced 4-m walking velocity, time to rise from a seated position 5 times, and standing balance. Individuals receive a score of 0 for each task that they are unable to complete. Scores of 1 to 4 are assigned for remaining tasks based on quartiles of performance for >6000 participants in the Established Populations for the Epidemiologic Study of the Elderly.23,24 Scores are summed to obtain the short physical performance battery score, ranging from 0 to 12.
Physical Activity
Accelerometer-Measured Physical Activity
Physical activity levels were measured objectively and continuously over 7 days with a vertical accelerometer (Caltrac, Muscle Dynamics Fitness Network Inc, Rocklin, Calif).6,25–29 After 7 days, participants reported the number of activity units displayed on the accelerometer by telephone to investigators and mailed their accelerometer back to investigators. We programmed the accelerometer identically for all participants, which allowed us to compare physical activity levels between participants regardless of individual variations in age, weight, height, and sex.6,25,27,28 Programmed in this way, the accelerometers measured "activity units."6,25,27,28 This method of measuring physical activity in people with PAD has been validated previously.6,8,25 Because of limited numbers of accelerometers, we distributed them to participants (49%) whenever available.
Patient-Reported Physical Activity Measures
Patient-reported physical activity was measured with a questionnaire derived from the Harvard Alumni Activity Survey that has previously been validated in the Cardiovascular Health Study and the Womens Health and Aging Study.30–32 The physical activity questionnaire asked, "During the last week, how many city blocks or their equivalent did you walk? Let 12 city blocks equal 1 mile." It also asked, "In the last week, about how many flights of stairs did you climb up? A flight is 10 steps."
Other Measures
Height and weight were measured at baseline. Body mass index (BMI) was calculated as weight in kilograms divided by height in meters squared. Education and pack-years of cigarette smoking were determined by patient report. Participants were categorized according to their exercise behavior as follows: no walking for exercise, walking for exercise once or twice per week, or walking for exercise
3 times per week.
Follow-Up
Participants were contacted annually for follow-up visits. Final follow-up visits were completed between November 2002 and September 2004. On the basis of previous study, individuals whose data collection forms indicated that they were unable to complete functional measures at follow-up as a result of wheelchair confinement, exhaustion, or other significant symptoms were classified as too disabled to complete functional measures.4,16 When no information was provided for the reason that a participant refused to complete functional tests, those who met at least 2 of the following criteria were considered too disabled to walk: The participant reported walking <5 blocks during the previous week; the score for repeated chair rises equaled 0 or 1; or the score for the standing balance test equaled 0 or 1. The criteria were defined before data analyses. Individuals who refused functional testing at follow-up and met 2 of these criteria were assigned the minimum value for each test not completed. The minimum value for each test was equivalent to the poorest performance among those who completed testing at the corresponding visit.
Statistical Analyses
Baseline physical activity levels for each physical activity measure were categorized into quartiles. The fourth quartile represented the highest activity level. Baseline characteristics between participants who wore vertical accelerometers and those who did not wear vertical accelerometers were compared with general linear models for continuous variables and
2 tests for categorical variables with adjustment for age and sex.
In comparing change in functioning (eg, 6-minute walk distance) across different patient groups, we carried out a longitudinal or repeated-measures ANCOVA using the mixed-effects linear regression analysis.33 Analyses adjusted for baseline covariates (sex, age, and race) and a time-dependent covariate representing functional performance at the immediately preceding visit were carried out on these successive differences. Similar analyses were repeated with additional adjustment for baseline comorbidities, leg symptoms, education, depressive symptoms, and time-dependent covariates (BMI, ABI, and pack-years of smoking). Associations of accelerometer data with decline in functional performance were analyzed using baseline measures of physical activity. Vertical accelerometer data were not available for most participants at subsequent follow-up visits. In contrast, patient-reported physical activity (stair flights climbed during the past week and blocks walked during the past week) were obtained annually. Therefore, time-dependent analyses were used for analyses of associations of patient-reported physical activity with functional decline. We also performed t test pairwise comparisons for both accelerometer-measured and patient-reported data using participants in the lowest quartile of activity as the reference.
Analyses were repeated among PAD participants who were asymptomatic to determine whether associations were maintained in this subset of PAD participants. To determine whether associations between accelerometer-measured physical activity and functional decline were consistent across levels of functional performance, analyses were repeated after participants were stratified according to tertile for each baseline functional measure.
Mixed-Effects Regression and Handling Missing Data
Associations between physical activity and changes in functional measures were evaluated with mixed-effects models in which a subject-specific random effect is used to account for the potential correlations among successive annual differences in each functional measure of the same participant. Dependent variables in each mixed-effect regression analysis were the successive annual differences in each functional measure. Under this initial mixed-effects regression analysis, statistically valid inference is guaranteed, provided that missing data caused by patient dropout are unrelated to unobserved data (ie, any missing data are missing at random). As a safeguard against violations to this assumption that missing data are missing at random, we repeated the fully adjusted comparisons using a repeated-measures pattern-mixture ANCOVA model.34,35 Because data were analyzed using successive differences, multiple patterns of missing differences were observed in our analyses. The different patterns of missing data were included as 2 binary indicator covariates (centered about their means). By including patterns of missing data in analyses as centered covariates and averaging over these patterns using adjusted least-squares means, one can obtain an unbiased estimate of the marginal means adjusted for covariates.35 Analyses were performed with SAS statistical software (version 9.1, SAS Institute Inc, Cary, NC).
The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.
| Results |
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Table 2 shows characteristics of the study population across quartiles of accelerometer-measured physical activity levels. Higher baseline physical activity was associated with more blocks walked during the past week, higher ABI values, lower Geriatric Depression Scale Short Form scores, and better performance on each measure of lower-extremity functioning at baseline.
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Adjusting for age, sex, race, ABI, BMI, smoking, leg symptoms, comorbidities, missing data patterns, education, and depressive symptoms, we observed significant, graded associations between accelerometer-measured physical activity at baseline and average annual decline in 6-minute walk performance, fast-paced walking velocity, and the short performance physical battery (Figure 1). Compared with participants in the lowest baseline quartile of physical activity, PAD participants in the third quartile of physical activity had less decline in the usual-paced 4-m walking velocity (P=0.017), fast-paced 4-m walking velocity (P=0.001), and short performance physical battery (P<0.001). Compared with participants in the lowest baseline quartile of physical activity, those in the highest (fourth) quartile had less decline in 6-minute walk performance (P=0.019), fast-paced walking speed (P=0.002), and short physical performance battery (P=0.005).
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Among the 39 asymptomatic PAD participants who wore vertical accelerometers at baseline, those who were more physically active had significantly less decline in 6-minute walk performance and in usual- and fast-paced walking velocity (Figure 2).
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We repeated the analyses after stratifying participants according to tertiles of baseline functional performance (Table 3). Within these tertiles, significant associations between accelerometer-measured physical activity and average annual functional decline were observed among participants in either or both of the lowest or middle tertiles of baseline performance for all measures except usual-paced 4-m walking velocity. Thus, higher physical activity during daily life may be of greatest benefit to PAD persons with greatest functional limitation.
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Table 4 shows associations between time-dependent patient-reported physical activity and average annual functional decline. After adjustment for age, sex, race, prior years performance, ABI, BMI, smoking, leg symptoms, comorbidities, missing data patterns, education, and depressive symptoms, more blocks walked during the previous week were associated with less average annual decline in the short performance physical battery (P for trend=0.004). More stair flights climbed during the previous week were associated with less decline in the usual-paced (P for trend=0.010) and fast-paced (P for trend=0.022) 4-m walking velocities.
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| Discussion |
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No medications are approved by the Food and Drug Administration for improving walking performance in persons with asymptomatic PAD,36 despite the previously established finding that persons with PAD who are asymptomatic are at particularly high risk of functional decline.4 Although supervised treadmill exercise programs significantly improve walking performance in people with intermittent claudication,9,37 barriers such as cost and transportation limit access to exercise rehabilitation programs for most people with PAD.10,11 Thus, few persons with PAD participate in supervised exercise programs.11 Identifying modifiable behaviors associated with slower rates of functional decline provides new opportunities that are noninvasive and inexpensive for preserving lower-extremity performance in people with PAD.
Several mechanisms may explain the relative preservation of lower-extremity functional performance in persons with PAD who are more physically active during daily life. First, in persons without PAD, higher levels of physical activity may reduce systemic atherosclerosis by improving risk factors like hypertension, hyperlipidemia, and diabetes.38 If higher rates of physical activity during daily life slow the progression of lower-extremity atherosclerosis, that may explain findings presented here. Second, in persons without PAD, physical activity is associated with improved peripheral arterial endothelial function and increased lower-extremity blood flow.39–43 Third, physical activity may improve metabolic efficiency and improve oxygen extraction within the muscle tissue.44,45 Fourth, increased levels of physical activity could favorably alter gait, resulting in more efficient walking techniques.46,47 Finally, higher physical activity levels are inversely associated with inflammatory markers in persons with PAD.48 These physiological and metabolic changes associated with physical activity may explain the association of higher physical activity with slower functional decline among persons with PAD. However, further study is needed.
Patient-reported measures of physical activity were less strongly associated with rates of functional decline compared with associations of the vertical accelerometer measure with functional decline. Objective measures of physical activity are likely to be more accurate than patient-reported physical activity levels.
This study has limitations. Only 49% of participants wore the vertical accelerometer device because of the limited availability of these monitors for study participants. However, no differences in baseline characteristics were found between participants who wore the accelerometer and those who did not. Second, these data are observational. Associations of lower levels of physical activity with greater functional decline cannot be construed as causal. Although we adjusted for confounders including comorbidities, we cannot rule out the possibility that residual confounding, unidentified characteristics, or greater illness severity among participants with lower physical activity levels contributed to the observed differences in functional decline across physical activity groups. Third, we did not collect data on intensity of physical activity.
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| Acknowledgments |
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None.
| References |
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2. McDermott MM, Kerwin DR, Liu K, Martin GJ, O'Brien E, Kaplan H, Greenland P. Prevalence and significance of unrecognized lower extremity peripheral arterial disease in general medicine practice. J Gen Intern Med. 2001; 16: 384–390.[CrossRef][Medline] [Order article via Infotrieve]
3. McDermott MM, Greenland P, Liu K, Guralnik JM, Criqui MH, Dolan NC, Chan C, Celic L, Pearce WH, Schneider JR, Sharma L, Clark E, Gibson D, Martin GJ. Leg symptoms in peripheral arterial disease: associated clinical characteristics and functional impairment. JAMA. 2001; 286: 1599–1606.
4. McDermott MM, Liu K, Greenland P, Guralnik JM, Criqui MH, Chan C, Pearce WH, Schneider JR, Ferrucci L, Celic L, Taylor LM, Vonesh E, Martin GJ, Clark E. Functional decline in peripheral arterial disease: associations with the ankle brachial index and leg symptoms. JAMA. 2004; 292: 453–461.
5. McDermott MM, Liu K, Guralnik JM, Mehta S, Criqui MH, Martin GJ, Greenland P. The ankle brachial index independently predicts walking velocity and walking endurance in peripheral arterial disease. J Am Geriatr Soc. 1998; 46: 1355–1362.[Medline] [Order article via Infotrieve]
6. McDermott MM, Liu K, O'Brien E, Guralnik JM, Criqui MH, Martin GJ, Greenland P. Measuring physical activity in peripheral arterial disease: a comparison of two physical activity questionnaires with an accelerometer. Angiology. 2000; 12: 91–100.
7. Sieminski DJ, Gardner AW. The relationship between free-living daily physical activity and the severity of peripheral arterial occlusive disease. Vasc Med. 1997; 2: 286–291.[Medline] [Order article via Infotrieve]
8. McDermott MM, Greenland P, Liu K, Guralnik JM, Celic L, Criqui MH, Chan C, Martin GJ, Schneider J, Pearce WH, Taylor LM, Clark E. The ankle brachial index is associated with leg function and physical activity: the Walking and Leg Circulation Study. Ann Intern Med. 2002; 136: 873–883.
9. Gardner AW, Poehlman ET. Exercise rehabilitation programs for the treatment of claudication pain: a meta-analysis. JAMA. 1995; 274: 975–980.
10. Falcone RA, Hirsch AT, Regensteiner JG, Treat-Jacobson D, Williams MA, Hiatt WR, Stewart KJ. Peripheral arterial disease rehabilitation: a review. J Cardiopulm Rehabil. 2003; 23: 170–175.[CrossRef][Medline] [Order article via Infotrieve]
11. Regensteiner JG. Exercise rehabilitation for the patient with intermittent claudication: a highly effective yet underutilized treatment. Curr Drug Targets Cardiovasc Haematol Disord. 2004; 4: 233–239.[CrossRef][Medline] [Order article via Infotrieve]
12. Sandler RB, Burdett R, Zaleskiewicz M, Sprowls-Repcheck C, Harwell M. Muscle strength as an indicator of the habitual level of physical activity. Med Sci Sports Exerc. 1991; 23: 1375–1381.[Medline] [Order article via Infotrieve]
13. Jonsson B, Ringsberg K, Josefsson PO, Johnell O, Birch-Jensen M. Effects of physical activity on bone mineral content and muscle strength in women: a cross-sectional study. Bone. 1992; 13: 191–195.[CrossRef][Medline] [Order article via Infotrieve]
14. Tamai M, Kubota M, Ikeda M, Nagao K, Irikura N, Sugiyama M, Yoshikawa H, Kawamori R, Kamada T. Usefulness of anaerobic threshold for evaluating daily life activity and prescribing exercise to the healthy subjects and patients. J Med Syst. 1993; 17: 219–225.[CrossRef][Medline] [Order article via Infotrieve]
15. Hubert HB, Fries JF. Predictors of physical disability after age 50: six-year longitudinal study in a runners club and a university population. Ann Epidemiol. 1994; 4: 285–294.[Medline] [Order article via Infotrieve]
16. McDermott MM, Liu K, Ferrucci L, Criqui MH, Greenland P, Guralnik JM, Tian L, Schneider JR, Pearce WH, Tan J, Martin GJ. Physical performance in peripheral arterial disease: a slower rate of decline in patients who walk more. Ann Intern Med. 2006; 144: 10–20.
17. McDermott MM, Criqui MH, Liu K, Guralnik JM, Greenland P, Martin GJ, Pearce W. Lower ankle/brachial index, as calculated by averaging the dorsalis pedis and posterior tibial arterial pressures, and association with leg functioning in peripheral arterial disease. J Vasc Surg. 2000; 32: 1164–1171.[CrossRef][Medline] [Order article via Infotrieve]
18. Hiatt WR, Hoag S, Hamman RF. Effect of diagnostic criteria on the prevalence of peripheral arterial disease: the San Luis Valley Diabetes Study. Circulation. 1995; 91: 1472–1479.
19. Criqui MH, Denenberg JO, Bird CE, Fronek A, Klauber MR, Langer RD. The correlation between symptoms and non-invasive test results in patients referred for peripheral arterial disease testing. Vasc Med. 1996; 1: 65–71.[Medline] [Order article via Infotrieve]
20. Lyness JM, Noel TK, Cox C, King DA, Conwell Y, Caine ED. Screening for depression in elderly primary care patients: a comparison of the Center for Epidemiologic Studies–Depression Scale and the Geriatric Depression Scale. Arch Intern Med. 1997; 157: 449–454.
21. Montgomery PS, Gardner AW. The clinical utility of a six-minute walk test in peripheral arterial occlusive disease patients. J Am Geriatr Soc. 1998; 46: 706–711.[Medline] [Order article via Infotrieve]
22. Guyatt GH, Sullivan MJ, Thompson PJ, Fallen EL, Pugsley SO, Taylor DW, Berman LB. The 6-minute walk: a new measure of exercise capacity in patients with chronic heart failure. Can Med Assoc J. 1985; 132: 919–923.[Abstract]
23. Guralnik JM, Ferrucci L, Simonsick EM, Salive ME, Wallace RB. Lower-extremity function in persons over the age of 70 years as a predictor of subsequent disability. N Engl J Med. 1995; 332: 556–561.
24. Guralnik JM, Simonsick EM, Ferrucci L, Glynn RJ, Berkman LF, Blazer DG, Scherr PA, Wallace RB. A short physical performance battery assessing lower extremity function: association with self-reported disability and prediction of mortality and nursing home admission. J Gerontol. 1994; 49: M85–M94.[Abstract]
25. McDermott MM, Ohlmiller SM, Liu K, Guralnik JM, Martin GJ, Pearce WH, Greenland P. Gait alterations associated with walking impairment in people with peripheral arterial disease with and without intermittent claudication. J Am Geriatr Soc. 2001; 49: 747–754.[CrossRef][Medline] [Order article via Infotrieve]
26. Sallis JF, Buono MJ, Roby JJ, Carlson D, Nelson JA. The Caltrac accelerometer as a physical activity monitor for school-age children. Med Sci Sports Exerc. 1990; 22: 698–703.[CrossRef][Medline] [Order article via Infotrieve]
27. Richardson MT, Leon AS, Jacobs DR Jr, Ainsworth BE, Serfass R. Ability of the Caltrac accelerometer to assess daily physical activity levels. J Cardiopulm Rehabil. 1995; 15: 107–113.[Medline] [Order article via Infotrieve]
28. Miller DJ, Freedson PS, Kline GM. Comparison of activity levels using the Caltrac accelerometer and five questionnaires. Med Sci Sports Exerc. 1994; 26: 376–382.[Medline] [Order article via Infotrieve]
29. Swan PD, Byrnes WC, Haymes EM. Energy expenditure estimates of the Caltrac accelerometer for running, race walking, and stepping. Br J Sports Med. 1997; 31: 235–239.
30. Lee IM, Paffenbarger RS, Hsieh CC. Time trends in physical activity among college alumni, 1962–1988. Am J Epidemiol. 1992; 135: 912–925.
31. Simonsick EM, Guralnik JM, Volpato S, Balfour J, Fried LP. Just get out the door! Importance of walking outside the home for maintaining mobility: findings from the Womens Health and Aging Study. J Am Geriatr Soc. 2005; 53: 198–203.[CrossRef][Medline] [Order article via Infotrieve]
32. Diehr P, Williamson J, Burke GL, Psaty BM. The aging and dying processes and the health of older adults. J Clin Epidemiol. 2002; 55: 269–278.[CrossRef][Medline] [Order article via Infotrieve]
33. Laird NM, Ware JH. Random-effects models for longitudinal data. Biometrics. 1982; 38: 963–974.[CrossRef][Medline] [Order article via Infotrieve]
34. Little R. Modeling the drop-out mechanism in repeated-measures studies. J Am Stat Assoc. 1995; 90: 1112–1121.[CrossRef]
35. Fitzmaurice GM, Laird NM, Shneyer L. An alternative parameterization of the general linear mixture model for longitudinal data with non-ignorable drop-outs. Stat Med. 2001; 20: 1009–1021.[CrossRef][Medline] [Order article via Infotrieve]
36. Giri J, McDermott MM, Greenland P, Guralnik JM, Criqui MH, Liu K, Ferrucci L, Green D, Schneider JR, Tian L. Statin use and functional decline in patients with and without peripheral arterial disease. J Am Coll Cardiol. 2006; 47: 998–1004.
37. Leng GC, Fowler B, Ernst E. Exercise for intermittent claudication. Cochrane Database Syst Rev. 2000: CD000990.
38. Gornik HL, Creager MA. Contemporary management of peripheral arterial disease, I: cardiovascular risk-factor modification. Cleve Clin J Med. 2006; 73 (suppl 4): S30–S37.
39. Hambrecht R, Fiehn E, Weigl C, Gielen S, Hamann C, Kaiser R, Yu J, Adams V, Niebauer J, Schuler G. Regular physical exercise corrects endothelial dysfunction and improves exercise capacity in patients with chronic heart failure. Circulation. 1998; 98: 2709–2715.
40. Maiorana A, O'Driscoll G, Cheetham C, Dembo L, Stanton K, Goodman C, Taylor R, Green D. The effect of combined aerobic and resistance exercise training on vascular function in type 2 diabetes. J Am Coll Cardiol. 2001; 38: 860–866.
41. Lavrencic A, Salobir BG, Keber I. Physical training improves flow-mediated dilation in patients with the polymetabolic syndrome. Arterioscler Thromb Vasc Biol. 2000; 20: 551–555.
42. Higashi Y, Sasaki S, Kurisu S, Yoshimizu A, Sasaki N, Matsuura H, Kajiyama G, Oshima T. Regular aerobic exercise augments endothelium-dependent vascular relaxation in normotensive as well as hypertensive subjects: role of endothelium-derived nitric oxide. Circulation. 1999; 100: 1194–1202.
43. Higashi Y, Sasaki S, Sasaki N, Nakagawa K, Ueda T, Yoshimizu A, Kurisu S, Matsuura H, Kajiyama G, Oshima T. Daily aerobic exercise improves reactive hyperemia in patients with essential hypertension. Hypertension. 1999; 33: 591–597.
44. Hiatt WR, Regensteiner JG, Hargarten ME, Wolfel EE, Brass EP. Benefit of exercise conditioning for patients with peripheral arterial disease. Circulation. 1990; 81: 602–609.
45. Gardner AW, Katzel LI, Sorkin JD, Bradham DD, Hochberg MC, Flinn WR, Goldberg AP. Exercise rehabilitation improves functional outcomes and peripheral circulation in patients with intermittent claudication: a randomized controlled trial. J Am Geriatr Soc. 2001; 49: 755–762.[CrossRef][Medline] [Order article via Infotrieve]
46. Hiatt WR, Wolfel EE, Meier RH, Regensteiner JG. Superiority of treadmill walking exercise versus strength training for patients with peripheral arterial disease: implications for the mechanism of the training response. Circulation. 1994; 90: 1866–1874.
47. Womack CJ, Sieminski DJ, Katzel LI, Yataco A, Gardner AW. Improved walking economy in patients with peripheral arterial occlusive disease. Med Sci Sports Exerc. 1997; 29: 1286–1290.[Medline] [Order article via Infotrieve]
48. McDermott MM, Greenland P, Guralnik JM, Ferrucci L, Green D, Liu K, Criqui MH, Schneider JR, Chan C, Ridker P, Pearce WH, Martin G, Clark E, Taylor L. Inflammatory markers, D-dimer, pro-thrombotic factors, and physical activity levels in patients with peripheral arterial disease. Vasc Med. 2004; 9: 107–115.[CrossRef][Medline] [Order article via Infotrieve]
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CLINICAL PERSPECTIVE
Men and women with lower-extremity peripheral arterial disease (PAD) have greater functional limitation and faster rates of functional decline compared with persons without PAD. Few modifiable risk factors have been identified that are associated with slower rates of functional decline in persons with PAD. This study assessed the association of greater physical activity during daily life with the rate of decline in functional performance among patients with PAD. Two hundred three men and women with PAD wore a vertical accelerometer for 7 days at baseline for continuous objective monitoring of physical activity and were followed up annually for up to 4 years. Higher baseline physical activity during daily life was associated with significantly less average annual decline in 6-minute walking distance, fast-paced 4-m walking velocity, and the short performance physical battery after adjustment for confounders. Our findings suggest that greater physical activity during daily life is associated with less decline in functional performance among persons with PAD. These findings suggest that clinicians should advise their patients with PAD to maximize physical activity during daily life. However, additional study with a randomized controlled clinical trial is warranted to determine whether interventions that increase physical activity during daily life are associated with slower rates of functional decline in persons with PAD.
Circulation 2009 119: 201-203.
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