(Circulation. 2006;113:2642-2650.)
© 2006 American Heart Association, Inc.
Contemporary Reviews in Cardiovascular Medicine |
From the Center for Exercise Science, College of Health and Human Performance and the College of Medicine, University of Florida, Gainesville (R.W.B.); and the Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, Md (K.J.S.).
Correspondence to Randy Braith, PhD, PO Box 118206, University of Florida, Gainesville, FL 32611. E-mail rbraith{at}hhp.ufl.edu
Key Words: arteriosclerosis cardiovascular diseases exercise risk factors
| Introduction |
|---|
|
|
|---|
This review will critically evaluate whether RT modifies CV risk factors and improves characteristics of CV structure and function. The topics will be limited to the effects of RT on major and independent risk factors for CV disease including diabetes mellitus, hypertension, dyslipidemia, and advancing age.4 The quantitative relation between these risk factors and CV events has been elucidated by the Framingham Heart Study4 and other studies. The topics will also include 2 predisposing risk factorsobesity and physical inactivitythat are designated as major risk factors by the American Heart Association.1,2,4 To the extent possible, this review will examine the separate and independent effects of RT in studies that did not include a concomitant aerobic exercise component. However, in those instances where the data from RT studies are equivocal, studies that combined RT and aerobic exercise will be acknowledged to help the clinician formulate recommendations for their patients. Additionally, the review will focus mainly on primary prevention, for example, risk reduction in persons without established CV disease. Many low- to moderate-risk patients with established CV disease should be encouraged to incorporate RT into their physical conditioning program, especially those who rely on their upper extremities for work or recreational pursuits. However, the safety and effectiveness of RT in other populations of CV patients (eg, women, older patients with low aerobic fitness, patients with severe left ventricular dysfunction) have not been well studied. Accordingly, these patient subsets may require more careful evaluation and initial monitoring, and RT guidelines and recommendations must be modified accordingly. Moreover, there is only a limited body of literature assessing the independent benefits of RT on CV risk factors in patients with established CV disease. Studies conducted in cooperation with comprehensive cardiac rehabilitation programs typically include the confounding influences of aerobic activity, initiation of vasoactive and lipid-lowering drugs, and nutritional education with subsequent dietary modifications.
| Rationale for Resistance Training |
|---|
|
|
|---|
|
Long-term adaptation to RT lowers cortisol response to acute stress,20 increases total energy expenditure and physical activity in healthy18,21 and frail older adults,22 and relieves anxiety, depression, and insomnia in clinical depression.23 RT has beneficial effects on bone density,18,24 osteoarthritic symptoms,22,25 hypertension,26,27 lipid profiles,28 and exercise tolerance in coronary artery disease.29 Conversely, the loss of skeletal muscle mass and contractile function that accompanies aging, for example, sarcopenia, is linked to peripheral insulin resistance, dyslipidemia, and increased adiposity.30 Sarcopenia is also accelerated in patients with chronic heart failure, a condition characterized by peripheral skeletal muscle abnormalities and muscle wasting. Several studies have shown beneficial effects of RT on muscle mass and strength in patients with chronic heart failure.31,32 However, the relative mitigating effects of RT on primary and secondary CV risk factors remains controversial.
| Resistance Training and Diabetes |
|---|
|
|
|---|
Muscle contraction increases glucose uptake in skeletal muscle,34 thereby forming the basis for recommending RT for individuals with abnormal glucose metabolism. Aerobic exercise uses large muscle groups for extended periods of time, but whole-body RT programs may provide equally high or higher recruitment of muscle mass over a comparable period of time. The American College of Sports Medicine has recommended the use of progressive RT as part of a well-rounded exercise program for individuals with type 2 diabetes.35 Similarly, in the absence of contraindications, the American Diabetes Association also recommends RT for those with type 2 diabetes.11 These recommendations are supported by evidence that RT is an integral component in the therapeutic management of glycemic control in both young and older type 2 diabetics,28,3638 particularly if the RT is performed in a supervised versus home-based program.39
Glucose Tolerance and Insulin Sensitivity
A frequent postulate is that RT and subsequent increases in skeletal muscle mass may improve glucose and insulin responses to a glucose load.6,40 However, there are little data available showing that RT prevents type 2 diabetes. RT does not usually alter glucose tolerance or glycemic control regardless of age,57,16,41,42 unless baseline glucose tolerance is abnormal.36,38,4044 Nevertheless, RT reduces acute insulin responses during an oral glucose tolerance test in healthy young, middle-aged, and older men in most studies.5,6,45 RT also reduces acute insulin responses during glucose tolerance testing in diabetic men36,38 and women36,38,44 and improves insulin sensitivity during hyperglycemic and hyperinsulinemic-euglycemic clamps in diabetic and/or insulin-resistant middle-aged6,46,47 and older men42 and diabetic middle-aged48 and older women.42
Glycemic Control
RT decreases glycosylated hemoglobin (HbA1c) levels in diabetic men28,36,37,43 and women,28,36,37 regardless of age. This effect is observed even in the absence of a lasting effect of RT on fasting glucose or insulin levels.37 Improved glycemic control and decreased HbA1c levels are important for reducing the microvascular and macrovascular complications of diabetes. For example, the UK Prospective Diabetes Study49 reported that each percentage point reduction in HbA1c was associated with a 35% reduction in microvascular complications, whereas the European Prospective Investigation of Cancer and Nutrition (EPIC)Norfolk prospective population study showed that an increase of 1 percentage point in HbA1c was associated with a 28% increase in mortality risk, independent of other CV risk factors.50 RT-induced improvements in glycemic control, however, appear to be intensity-dependent, with beneficial effects occurring when subjects train at 70% to 90% of the 1-repetition maximum strength (1-RM). One-repetition maximum is the maximal weight lifted in 1 attempt during strength testing. In studies where the RT intervention was less than 2 months and/or the exercise intensity was less than 50% of the 1-RM, improvements in HbA1c were modest or undetected.47,51,52
| Resistance Training and Hypertension |
|---|
|
|
|---|
Systemic Blood Pressure
The rationale for RT as an adjunct to aerobic exercise for controlling BP stems from multiple studies. Two meta-analyses of RT and hypertension are noteworthy.26,27 Inclusion criteria, consistent across both reviews, were (1) inclusion of a randomized nonexercise control group; (2) RT as the only intervention; (3) training for a minimum of 4 weeks; and (4) participants who were sedentary normotensive and/or hypertensive adults with no other concomitant disease. Kelley and Kelley27 examined the effects of RT on resting BP in studies published between January 1966 and December 1998. A total of 11 studies met the inclusion criteria and represented initial and final BP assessments in 182 RT subjects and 138 control subjects. Decreases (P
0.05) of approximately 3 mm Hg were found for both systolic and diastolic BP across all BP categories as the result of RT. These changes represented a 2% decrease for resting systolic BP and 4% for resting diastolic BP. No differences were found for changes in resting BP between studies that used conventional RT compared with a circuit RT protocol. A conventional RT protocol generally consists of lifting heavier weights with longer rest periods, whereas a circuit RT protocol consists of lifting lighter weights with shorter rest periods between exercises. By moving quickly between exercises and by using lighter weight with higher repetitions, circuit training introduces an aerobic component to the workout.54
In the more recent meta-analysis, Cornelissen and Fagard26 pooled data from studies published between 1996 and 2003 that included 9 randomized controlled trials involving 341 participants. The overall effect of RT was a decrease of 3.2 mm Hg (P=0.10) in systolic BP and a decrease of 3.5 mm Hg (P
0.05) in diastolic BP. Results from these meta-analyses are consistent with conclusions generated by narrative reviews.17,55,56 Although these reductions seem modest, a systolic BP reduction of 3 mm Hg in average populations has been estimated to reduce cardiac morbidity by 5% to 9%, stroke by 8% to 14%, and all-cause mortality by 4%.57 The lack of data on the effects of RT on ambulatory BP warrants further investigation because this may be more indicative of future CV disease morbidity and mortality.58
Control of BP is even more important in individuals who already have hypertension. Although there is general agreement that endurance training lowers resting BP in patients with mild to severe hypertension,27,57 there is a paucity of data on the effects of RT alone on BP in individuals with hypertension. Only 20% of the outcomes in the 2 meta-analysis reviews were based on a mean initial resting systolic BP >140 mm Hg, whereas only 13% had a mean initial resting diastolic BP >90 mm Hg.26,27 One study that used RT in combination with aerobic exercise in middle-aged hypertensive men for 10 weeks demonstrated reductions of 13 mm Hg for both systolic and diastolic BP.59 Conversely, a similar program for 6 months in older adults with hypertension showed mean decreases in systolic and diastolic BP of 5.3 and 3.7 mm Hg, respectively.60 The change in systolic BP, although significantly lower than study entry, was not different from values in the control group. Although any reduction in BP is desirable, the available studies do not answer the question regarding the independent benefit of RT in persons initially classified as being hypertensive or prehypertensive.
Arterial Stiffness
With aging, hypertension, insulin resistance, and diabetes, there is increased arterial stiffness from degeneration of the arterial media, increased collagen and calcium content, and arterial dilation and hypertrophy. These factors lead to increased systolic BP and an increased risk of cardiac events.61 Several studies have shown that aerobic exercise is associated with reduced arterial stiffness in healthy subjects of all ages,62 competitive aerobic athletes,63 patients with coronary artery disease,64 and hemodialysis patients.65 Moreover, when aerobic exercise is combined with RT, there is no evidence of increased arterial stiffness.66 However, less is known about the independent effects or RT on arterial stiffness. Two cross-sectional studies have suggested that young and middle-aged men who participate in regular RT have greater arterial stiffness than age-matched sedentary control subjects.67,68 However, only 3 interventional studies have examined the effect of RT on arterial function.6971 Miyachi et al70 reported that RT 3 days per week for 4 months decreased carotid arterial compliance by 19% (P<0.05) in young, healthy men who were novice weight trainers. Interestingly, carotid arterial compliance returned to baseline values within 2 months after RT was discontinued. Cortez-Cooper et al69 reported that high intensity RT for 4 days per week for 3 months in young, healthy women who were novice weight trainers (n=23; age 29±1 years, mean±SD) increased carotid augmentation index (a measure of arterial wave reflection and arterial stiffness) from 8±13% to 1±18% (P<0.05), and carotid-femoral pulse-wave velocity increased (P
0.05) from 791±88 to 833±96 cm/s. Paradoxically, neither study reported increases in systolic or diastolic BP secondary to RT.
Contradictory results were recently reported by Rakobowchuk and coworkers.71 By using similar vascular measurement techniques, they found that central arterial compliance was unaltered after 3 months of RT in young men (n=28; age 23±3.9 years, mean± SD). The discrepancy between studies may be explained by differences in the RT protocols. The 2 studies in which central arterial stiffness increased used RT protocols consisting of high-intensity super sets and an extremely high volume (up to 6 sets per exercise),69,70 both of which are not commonly recommended for the majority of the population and are usually performed by competitive athletes.9,10 Conversely, the study in which arterial stiffness was unchanged used a progressive training protocol that increased intensity but not the volume of exercise over 12 weeks.
Mechanisms for Change in Arterial Compliance
Studies reporting adverse effects of RT on the arterial system have only speculated about mechanisms responsible for the changes.6770 The elastic properties of the arterial wall are determined by both structural components (eg, relative composition of elastin and collagen) and functional components (eg, vasoconstrictor tone exerted by the vascular smooth muscle cells). Because 3 to 4 months of RT are unlikely to cause marked structural changes in the arterial wall, changes in the functional components of the arterial wall need to be considered. One potential mechanism is endothelial dysfunction manifested as a reduction in the bioavailability of nitric oxide. Recent evidence, however, indicates that 4 months of RT in healthy young men does not impair endothelium-dependent vasodilation in the brachial artery.72 Another mechanism for functional change in the arterial wall is increased sympathetic tone. There is evidence that RT increases resting humoral norepinephrine levels, a surrogate marker of sympathetic nervous system activity.73 However, increased sympathetic nervous system vasoconstrictor tone is likely to be greater in peripheral muscular arteries than in central elastic arteries. Surprisingly, both studies reporting increases in stiffness of central conduit arteries after RT did not show changes in peripheral muscular arteries.69,70 Results from narrative15,17,55,56 and meta-analytical reviews26,27 do not support the contention the RT increases vascular resistance. Moreover, those findings are compatible with the absence of hypertension observed among isometric and power athletes.74,75
| Resistance Training and Obesity |
|---|
|
|
|---|
Obesity Prevention
Epidemiological evidence supports the use of increased exercise in preventing age-associated weight and fat gains.1 Exercise recommendations to treat or prevent obesity have focused mainly on aerobic activities.1 However, RT is a behaviorally feasible and efficacious alternative to endurance exercise for weight control. For example, resting energy expenditure (REE) decreases with aging, and this decrease is closely correlated to losses in skeletal muscle mass.76 RT increases muscle mass by a minimum of 1 to 2 kg in studies of sufficient duration.77 Theoretically, a gain of 1 kg in muscle mass should result in an REE increase of approximately 21 kcal/kg of new muscle.78 In practice, RT intervention studies report REE increases in the range of 28 to 218 kcal/kg of muscle.7982 RT, when sustained over years or decades, translates into clinically important differences in daily energy expenditure and age-associated fat gains. However, even without a change in REE, maintenance of muscle mass through midlife years may prevent age-associated fat gains by promoting an active lifestyle.15,83,84
Visceral Adipose Tissue
RT can reduce total body fat mass in men84,85 and women,83,8587 independent of dietary caloric restriction. However, regional distribution of fat may be more important to health than the total amount of body fat. Excessive central obesity and especially visceral adipose tissue have been linked with the development of hyperlipidemia, hypertension, insulin resistance and glucose intolerance, diabetes, and heart disease.15,17,88,89 Fat distributed in the arms and legs, however, appears to impose little or no risk.15,88,89 Although there may be a genetic predisposition for visceral adipose tissue, increasing age, high fat diets, and a sedentary lifestyle are also important determinants.
Several studies have demonstrated decreases in visceral adipose tissue after RT programs.84,85,87,90,91 Treuth and coworkers84,87 assessed body composition in older men by using dual-energy x-ray absorptiometry84 and in older women by using computed tomography87 and observed significant decreases in visceral fat after 16 weeks of RT. Ross et al90,91 used magnetic resonance imaging to measure regional fat losses after exercise combined with diet interventions. In their first study,90 both diet plus aerobic exercise and diet plus RT elicited similar losses of visceral fat that were greater than losses of whole-body subcutaneous fat. In a follow-up study,91 they isolated the effects of endurance exercise training and RT by comparing the responses to diet alone and diet combined with each training modality in middle-aged obese men. All 3 groups lost significant amounts of total body fat, and all 3 groups experienced a significantly greater visceral fat loss compared with whole-body subcutaneous fat loss. The changes amounted to a 40% reduction in visceral fat in the RT and diet group, 39% in the endurance training and diet group, and a 32% reduction in the diet-only group.
One study has raised the possibility of gender specificity in visceral fat reduction in response to RT. Hunter et al85 studied older women and men (age, 61 to 77 years) after 25 weeks of supervised RT. Both genders significantly increased muscle mass but men increased muscle more than women (2.8 versus 1.0 kg, respectively). Similar decreases in total body fat mass were found for the men (1.8 kg) and women (1.7 kg). However, women lost a significant amount of visceral adipose tissue (131 to 116 cm2), whereas the men did not (143 to 152 cm2). Similarly, women also lost a significant amount of subcutaneous adipose tissue (254 to 239 cm2), but men did not (165 to 165 cm2). Conversely, in a 6-month study of RT combined with aerobic exercise, men lost more visceral adipose tissue than women, but losses of total and subcutaneous adipose tissue were similar.60 Although more research is needed to clarify these possible gender-specific responses, the overall available body of literature supports the use of RT, with or without aerobic exercise, and with or without diet modification, as an effective intervention that contributes to the reduction of abdominal obesity.
Obesity Reduction
Studies of the efficacy of RT in the context of total body weight loss have had mixed results. Studies that use more severe caloric intake restriction have not shown gains in muscle mass,92,93 whereas RT studies with less severe caloric restriction have shown muscle mass gains with only modest losses in body weight.87,90,91,94 RT studies that attempt to maintain caloric balance during the intervention typically do not observe major changes in body weight in either gender, despite significant reductions in fat mass and percent body fat.15,84,85,87 In essence, body weight does not change much because loss of fat mass is generally offset by the gain in muscle mass. Conversely, endurance traininginduced decreases in fat mass are more likely to be associated with reductions in body weight because there is no offsetting gain in muscle mass.
| Resistance Training and Dyslipidemia |
|---|
|
|
|---|
Most interventional studies have failed to adequately control for normal variations in lipoproteins and lacked proper dietary controls and/or lacked statistical power. When these factors are controlled, most studies show no improvement in lipid profiles after RT in either middle-aged or older adults.40,87,98,99 However, the lack of significant lipoprotein-lipid changes with RT may be due to the fact that total cholesterol values for most study groups has been
200 mg/dL at study entry. Individuals with normal lipoprotein-lipid profiles may require greater exercise stimulus and energy expenditure coupled with significant reductions in body weight to further improve lipid profiles. Alternatively, Shoup and Durstine100 postulated that for changes in blood lipids to occur, lipoprotein lipase levels need to increase or remain elevated postexercise, or associated hepatic lipase must be suppressed to reduce conversion of high-density lipoprotein cholesterol (HDL-C) subfraction HDL2-C to HDL3-C. It is possible that the RT stimulus in most studies does not generate these cellular changes.
| Screening and Precautions |
|---|
|
|
|---|
Selected individuals should consult their healthcare practitioners before beginning a vigorous exercise program. For those at moderate risk or higher, such as men age 45 years and over, women age 55 years and over, those with major risk factors for arteriosclerosis, and those with diabetes at any age, the American College of Sports Medicine recommends a medical history and physical examination including an exercise stress test before initiating a vigorous exercise program.95 Because of the marked rise in BP with RT, those with uncontrolled hypertension (systolic BP
160 mm Hg and/or diastolic BP
100 mm Hg) should be controlled to lower levels before starting an exercise program.102 High-intensity RT should also be avoided by individuals who have active proliferative retinopathy or moderate or worse nonproliferative diabetic retinopathy. To minimize excessive BP responses, individuals should be told to avoid extended breath-holding during their workouts.35,80,103
| Resistance Training Exercise Prescription |
|---|
|
|
|---|
|
|
| Summary |
|---|
|
|
|---|
(1) RT does not appear to alter glucose tolerance or glycemic control regardless of age, unless baseline glucose tolerance is abnormal. Nonetheless, most studies show that RT improves insulin action either through reductions in acute insulin responses during an oral glucose tolerance test or increased glucose uptake during glycemic clamp procedures. Moreover, RT significantly decreases HbA1c in diabetic men and women regardless of age, and this effect is observed even in the absence of a lasting effect of RT on fasting glucose.
(2) In healthy, normotensive persons, RT elicits reductions of approximately 3 mm Hg for both systolic and diastolic BP. Future studies are needed in individuals initially classified as hypertensive or prehypertensive to determine the extent to which RT lowers BP when it is elevated at baseline. Until these studies are performed, an RT program combined with aerobic exercise should be recommended for lowering BP in hypertensive adults.
(3) There is some evidence that RT can increase central arterial stiffness during high-intensity and high-volume training regimens, but an explanation for this effect has not been determined. No studies have found increased BP or peripheral vascular resistance secondary to RT.
(4) There is good evidence that RT reduces total body fat mass in men and women, independent of dietary caloric restriction. There is also good evidence that RT reduces visceral adipose tissue in older men and women.
(5) There is little evidence that RT improves lipoprotein-lipid profiles. However, total cholesterol values for most study groups have been
200 mg/dL at study entry. Individuals with normal lipoprotein-lipid profiles may require greater exercise stimulus and energy expenditure coupled with significant reductions in body weight in order to further improve lipid profiles.
(6) Although RT by itself may have limited beneficial effects on CV disease risk factors, this mode of exercise is beneficial in the prevention and management of musculoskeletal injuries and disorders, osteoporosis, and sarcopenia. RT also reduces susceptibility to falls and prevents or delays impaired physical function in frail and elderly persons.
(7) Although performing RT by itself rather than in combination with aerobic exercise appears to contribute to some aspects of CV disease reduction, the available data do not permit accurate estimation of the magnitude of the risk reduction. Thus, for the individual without existing cardiac disease whose goal is to improve their CV health and prevent disease, there is little evidence herein to challenge existing exercise guidelines that call for moderate-intensity RT to be performed in combination with aerobic exercise.
| Acknowledgments |
|---|
None.
| References |
|---|
|
|
|---|
2. Fletcher GF, Balady G, Blair SN, Blumenthal J, Caspersen C, Chaitman B, Epstein S, Sivarajan Froelicher ES, Froelicher VF, Pina IL, Pollock ML. Statement on exercise: benefits and recommendations for physical activity programs for all Americans: a statement for health professionals by the Committee on Exercise and Cardiac Rehabilitation of the Council on Clinical Cardiology, American Heart Association. Circulation. 1996; 94: 857862.
3. Klein S, Burke LE, Bray GA, Blair S, Allison DB, Pi-Sunyer X, Hong Y, Eckel RH. Clinical implications of obesity with specific focus on cardiovascular disease: a statement for professionals from the American Heart Association Council on Nutrition, Physical Activity, and Metabolism: endorsed by the American College of Cardiology Foundation. Circulation. 2004; 110: 29522967.
4. Wilson PW, DAgostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation. 1998; 97: 18371847.
5. Hurley BF, Hagberg JM, Goldberg AP, Seals DR, Ehsani AA, Brennan RE, Holloszy JO. Resistive training can reduce coronary risk factors without altering VO2max or percent body fat. Med Sci Sports Exerc. 1988; 20: 150154.[Medline] [Order article via Infotrieve]
6. Miller JP, Pratley RE, Goldberg AP, Gordon P, Rubin M, Treuth MS, Ryan AS, Hurley BF. Strength training increases insulin action in healthy 50- to 65-year-old men. J Appl Physiol. 1994; 77: 11221127.
7. Poehlman ET, Dvorak RV, DeNino WF, Brochu M, Ades PA. Effects of resistance training and endurance training on insulin sensitivity in nonobese, young women: a controlled randomized trial. J Clin Endocrinol Metab. 2000; 85: 24632468.
8. Smutok MA, Reece C, Kokkinos PF, Farmer CM, Dawson PK, DeVane J, Patterson J, Goldberg AP, Hurley BF. Effects of exercise training modality on glucose tolerance in men with abnormal glucose regulation. Int J Sports Med. 1994; 15: 283289.[Medline] [Order article via Infotrieve]
9. Pollock ML, Franklin BA, Balady GJ, Chaitman BL, Fleg JL, Fletcher B, Limacher M, Pina IL, Stein RA, Williams M, Bazzarre T. AHA Science Advisory: resistance exercise in individuals with and without cardiovascular disease: benefits, rationale, safety, and prescription: an advisory from the Committee on Exercise, Rehabilitation, and Prevention, Council on Clinical Cardiology, American Heart Association; Position paper endorsed by the American College of Sports Medicine. Circulation. 2000; 101: 828833.
10. Pescatello LS, Franklin BA, Fagard R, Farquhar WB, Kelley GA, Ray CA. American College of Sports Medicine position stand. exercise and hypertension. Med Sci Sports Exerc. 2004; 36: 533553.[CrossRef][Medline] [Order article via Infotrieve]
11. Sigal RJ, Kenny GP, Wasserman DH, Castaneda-Sceppa C. Physical activity/exercise and type 2 diabetes. Diabetes Care. 2004; 27: 25182539.
12. Fitzgerald SJ, Barlow CE, Kampert JB, Morrow JR, Jackson AW, Blair SN. Muscular fitness and all-cause mortality: prospective observations. J Physical Activity Health. 2004; 1: 718.
13. Jurca R, Lamonte MJ, Barlow JB, Kampert JB, Church TS, Blair SN. Association of muscular strength with incidence of metabolic syndrome in men. Med Sci Sports Exerc. 2005; 37: 18491855.[CrossRef][Medline] [Order article via Infotrieve]
14. Jurca R, Lamonte MJ, Church TS, Earnest CP, Fitzgerald SJ, Barlow CE, Jordan AN, Kampert JB, Blair SN. Associations of muscle strength and fitness with metabolic syndrome in men. Med Sci Sports Exerc. 2004; 36: 13011307.[CrossRef][Medline] [Order article via Infotrieve]
15. American College of Sports Medicine Position Stand. The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory and muscular fitness, and flexibility in healthy adults. Med Sci Sports Exerc. 1998; 30: 975991.[Medline] [Order article via Infotrieve]
16. Banz WJ, Maher MA, Thompson WG, Bassett DR, Moore W, Ashraf M, Keefer DJ, Zemel MB. Effects of resistance versus aerobic training on coronary artery disease risk factors. Exp Biol Med (Maywood). 2003; 228: 434440.
17. Hurley BF, Roth SM. Strength training in the elderly: effects on risk factors for age-related diseases. Sports Med. 2000; 30: 249268.[CrossRef][Medline] [Order article via Infotrieve]
18. Nelson ME, Fiatarone MA, Morganti CM, Trice I, Greenberg RA, Evans WJ. Effects of high-intensity strength training on multiple risk factors for osteoporotic fractures: a randomized controlled trial. JAMA. 1994; 272: 19091914.
19. Larsson L. Histochemical characteristics of human skeletal muscle during aging. Acta Physiol Scand. 1983; 117: 469471.[Medline] [Order article via Infotrieve]
20. Fabbri A, Giannini D, Aversa A, De Martino MU, Fabbrini E, Franceschi F, Moretti C, Frajese G, Isidori A. Body-fat distribution and responsiveness of the pituitary-adrenal axis to corticotropin-releasing-hormone stimulation in sedentary and exercising women. J Endocrinol Invest. 1999; 22: 377385.[Medline] [Order article via Infotrieve]
21. Vincent KR, Braith RW, Feldman RA, Kallas HE, Lowenthal DT. Improved cardiorespiratory endurance following 6 months of resistance exercise in elderly men and women. Arch Intern Med. 2002; 162: 673678.
22. Fiatorone M, Singh N. The exercise prescription. In: Fiatorone M, Singh N, eds. Exercise, Nutrition, and the Older Woman. Boca Raton, Fla: CRC Press; 2000: 37104.
23. Singh NA, Clements KM, Fiatarone MA. A randomized controlled trial of progressive resistance training in depressed elders. J Gerontol A Biol Sci Med Sci. 1997; 52: M27M35.[Abstract]
24. Braith RW, Mills RM, Welsch MA, Pollock MH, Keller J. Training reverses steroid induced osteoporosis after heart transplantation. J Am Coll Cardiol. 1996; 28: 14711477.[Abstract]
25. Ettinger WH Jr, Burns R, Messier SP, Applegate W, Rejeski WJ, Morgan T, Shumaker S, Berry MJ, OToole M, Monu J, Craven T. A randomized trial comparing aerobic exercise and resistance exercise with a health education program in older adults with knee osteoarthritis: the Fitness Arthritis and Seniors Trial (FAST). JAMA. 1997; 277: 2531.
26. Cornelissen VA, Fagard RH. Effect of resistance training on resting blood pressure: a meta-analysis of randomized controlled trials. J Hypertens. 2005; 23: 251259.[CrossRef][Medline] [Order article via Infotrieve]
27. Kelley GA, Kelley KS. Progressive resistance exercise and resting blood pressure: a meta-analysis of randomized controlled trials. Hypertension. 2000; 35: 838843.
28. Honkola A, Forsen T, Eriksson J. Resistance training improves the metabolic profile in individuals with type 2 diabetes. Acta Diabetol. 1997; 34: 245248.[CrossRef][Medline] [Order article via Infotrieve]
29. McCartney N. Role of resistance training in heart disease. Med Sci Sports Exerc. 1998; 30: S396S402.[Medline] [Order article via Infotrieve]
30. Baumgartner RN, Koehler KM, Gallagher D, Romero L, Heymsfield SB, Ross RR, Garry PJ, Lindeman RD. Epidemiology of sarcopenia among the elderly in New Mexico. Am J Epidemiol. 1998; 147: 755763.
31. Pu CT, Johnson MT, Forman DE, Hausdorff JM, Roubenoff R, Foldvari M, Fielding RA, Singh MA. Randomized trial of progressive resistance training to counteract the myopathy of chronic heart failure. J Appl Physiol. 2001; 90: 23412350.
32. Selig SE, Carey MF, Menzies DG, Patterson J, Geerling RH, Williams AD, Bamroongsuk V, Toia D, Krum H, Hare DL. Moderate-intensity resistance exercise training in patients with chronic heart failure improves strength, endurance, heart rate variability, and forearm blood flow. J Card Fail. 2004; 10: 2130.[CrossRef][Medline] [Order article via Infotrieve]
33. Harris MI, Flegal KM, Cowie CC, Eberhardt MS, Goldstein DE, Little RR, Wiedmeyer HM, Byrd-Holt DD. Prevalence of diabetes, impaired fasting glucose, and impaired glucose tolerance in US adults: the Third National Health and Nutrition Examination Survey, 19881994. Diabetes Care. 1998; 21: 518524.[Abstract]
34. Holloszy JO, Hansen PA. Regulation of glucose transport into skeletal muscle. Rev Physiol Biochem Pharmacol. 1996; 128: 99193.[Medline] [Order article via Infotrieve]
35. Albright A, Franz M, Hornsby G, Kriska A, Marrero D, Ullrich I, Verity LS. American College of Sports Medicine position stand: exercise and type 2 diabetes. Med Sci Sports Exerc. 2000; 32: 13451360.[Medline] [Order article via Infotrieve]
36. Castaneda C, Layne JE, Munoz-Orians L, Gordon PL, Walsmith J, Foldvari M, Roubenoff R, Tucker KL, Nelson ME. A randomized controlled trial of resistance exercise training to improve glycemic control in older adults with type 2 diabetes. Diabetes Care. 2002; 25: 23352341.
37. Dunstan DW, Daly RM, Owen N, Jolley D, De Courten M, Shaw J, Zimmet P. High-intensity resistance training improves glycemic control in older patients with type 2 diabetes. Diabetes Care. 2002; 25: 17291736.
38. Ibanez J, Izquierdo M, Arguelles I, Forga L, Larrion JL, Garcia-Unciti M, Idoate F, Gorostiaga EM. Twice-weekly progressive resistance training decreases abdominal fat and improves insulin sensitivity in older men with type 2 diabetes. Diabetes Care. 2005; 28: 662667.
39. Dunstan DW, Daly RM, Owen N, Jolley D, Vulikh E, Shaw J, Zimmet P. Home-based resistance training is not sufficient to maintain improved glycemic control following supervised training in older individuals with type 2 diabetes. Diabetes Care. 2005; 28: 39.
40. Smutok MA, Reece C, Kokkinos PF, Farmer C, Dawson P, Shulman R, DeVane-Bell J, Patterson J, Charabogos C, Goldberg AP. Aerobic versus strength training for risk factor intervention in middle-aged men at high risk for coronary heart disease. Metabolism. 1993; 42: 177184.[CrossRef][Medline] [Order article via Infotrieve]
41. Fluckey JD, Hickey MS, Brambrink JK, Hart KK, Alexander K, Craig BW. Effects of resistance exercise on glucose tolerance in normal and glucose-intolerant subjects. J Appl Physiol. 1994; 77: 10871092.
42. Ryan AS, Hurlbut DE, Lott ME, Ivey FM, Fleg J, Hurley BF, Goldberg AP. Insulin action after resistive training in insulin resistant older men and women. J Am Geriatr Soc. 2001; 49: 247253.[CrossRef][Medline] [Order article via Infotrieve]
43. Eriksson J, Taimela S, Eriksson K, Parviainen S, Peltonen J, Kujala U. Resistance training in the treatment of non-insulin-dependent diabetes mellitus. Int J Sports Med. 1997; 18: 242246.[Medline] [Order article via Infotrieve]
44. Fenicchia LM, Kanaley JA, Azevedo JL Jr, Miller CS, Weinstock RS, Carhart RL, Ploutz-Snyder LL. Influence of resistance exercise training on glucose control in women with type 2 diabetes. Metabolism. 2004; 53: 284289.[CrossRef][Medline] [Order article via Infotrieve]
45. Reynolds TH, Supiano MA, Dengel DR. Resistance training enhances insulin-mediated glucose disposal with minimal effect on the tumor necrosis factor-alpha system in older hypertensives. Metabolism. 2004; 53: 397402.[CrossRef][Medline] [Order article via Infotrieve]
46. Eriksson J, Tuominen J, Valle T, Sundberg S, Sovijarvi A, Lindholm H, Tuomilehto J, Koivisto V. Aerobic endurance exercise or circuit-type resistance training for individuals with impaired glucose tolerance? Horm Metab Res. 1998; 30: 3741.[Medline] [Order article via Infotrieve]
47. Ishii T, Yamakita T, Sato T, Tanaka S, Fujii S. Resistance training improves insulin sensitivity in NIDDM subjects without altering maximal oxygen uptake. Diabetes Care. 1998; 21: 13531355.[Abstract]
48. Ryan AS, Pratley RE, Goldberg AP, Elahi D. Resistive training increases insulin action in postmenopausal women. J Gerontol A Biol Sci Med Sci. 1996; 51: M199M205.[Abstract]
49. Manley S. Haemoglobin A1c: a marker for complications of type 2 diabetes: the experience from the UK Prospective Diabetes Study (UKPDS). Clin Chem Lab Med. 2003; 41: 11821190.[CrossRef][Medline] [Order article via Infotrieve]
50. Khaw KT, Wareham N, Luben R, Bingham S, Oakes S, Welch A, Day N. Glycated haemoglobin, diabetes, and mortality in men in Norfolk cohort of European prospective investigation of cancer and nutrition (EPIC-Norfolk). BMJ. 2001; 322: 16.
51. Dunstan DW, Puddey IB, Beilin LJ, Burke V, Morton AR, Stanton KG. Effects of a short-term circuit weight training program on glycaemic control in NIDDM. Diabetes Res Clin Pract. 1998; 40: 5361.[CrossRef][Medline] [Order article via Infotrieve]
52. Maiorana A, ODriscoll G, Goodman C, Taylor R, Green D. Combined aerobic and resistance exercise improves glycemic control and fitness in type 2 diabetes. Diabetes Res Clin Pract. 2002; 56: 115123.[CrossRef][Medline] [Order article via Infotrieve]
53. Whelton PK, He J, Appel LJ, Cutler JA, Havas S, Kotchen TA, Roccella EJ, Stout R, Vallbona C, Winston MC, Karimbakas J. Primary prevention of hypertension: clinical and public health advisory from the National High Blood Pressure Education Program. JAMA. 2002; 288: 18821888.
54. Stewart KJ. Weight training in coronary artery disease and hypertension. Prog Cardiovasc Dis. 1992; 35: 159168.[CrossRef][Medline] [Order article via Infotrieve]
55. Schwartz RS, Hirth VA. The effects of endurance and resistance training on blood pressure. Int J Obes Relat Metab Disord. 1995; 19 (suppl 4): S52S57.
56. Stone MH, Fleck SJ, Triplett NT, Kraemer WJ. Health- and performance-related potential of resistance training. Sports Med. 1991; 11: 210231.[Medline] [Order article via Infotrieve]
57. Whelton SP, Chin A, Xin X, He J. Effect of aerobic exercise on blood pressure: a meta-analysis of randomized, controlled trials. Ann Intern Med. 2002; 136: 493503.
58. Verdecchia P. Prognostic value of ambulatory blood pressure: current evidence and clinical implications. Hypertension. 2000; 35: 844851.
59. Kelemen MH, Effron MB. Exercise training combined with antihypertensive drug therapy. JAMA. 1990; 263: 27662771.
60. Stewart KJ, Bacher AC, Turner KL, Fleg JL, Hees PS, Shapiro EP, Tayback M, Ouyang P. Effect of exercise on blood pressure in older persons: a randomized controlled trial. Arch Intern Med. 2005; 165: 756762.
61. Henry RM, Kostense PJ, Spijkerman AM, Dekker JM, Nijpels G, Heine RJ, Kamp O, Westerhof N, Bouter LM, Stehouwer CD. Arterial stiffness increases with deteriorating glucose tolerance status: the Hoorn Study. Circulation. 2003; 107: 20892095.
62. Tanaka H, DeSouza CA, Seals DR. Absence of age-related increase in central arterial stiffness in physically active women. Arterioscler Thromb Vasc Biol. 1998; 18: 127132.
63. Edwards DG, Lang JT. Augmentation index and systolic load are lower in competitive endurance athletes. Am J Hypertens. 2005; 18: 679683.[CrossRef][Medline] [Order article via Infotrieve]
64. Edwards DG, Schofield RS, Magyari PM, Nichols WW, Braith RW. Effect of exercise training on central aortic pressure wave reflection in coronary artery disease. Am J Hypertens. 2004; 17: 540543.[CrossRef][Medline] [Order article via Infotrieve]
65. Mustata S, Chan C, Lai V, Miller JA. Impact of an exercise program on arterial stiffness and insulin resistance in hemodialysis patients. J Am Soc Nephrol. 2004; 15: 27132718.
66. Hayashi K, Sugawara J, Komine H, Maeda S, Yokoi T. Effects of aerobic exercise training on stiffness of central and peripheral arteries in middle-aged sedentary men. Jpn J Physiol. 2005; 55: 235239.[CrossRef][Medline] [Order article via Infotrieve]
67. Bertovic DA, Waddell TK, Gatzka CD, Cameron JD, Dart AM, Kingwell BA. Muscular strength training is associated with low arterial compliance and high pulse pressure. Hypertension. 1999; 33: 13851391.
68. Miyachi M, Donato AJ, Yamamoto K, Takahashi K, Gates PE, Moreau KL, Tanaka H. Greater age-related reductions in central arterial compliance in resistance-trained men. Hypertension. 2003; 41: 130135.
69. Cortez-Cooper MY, DeVan AE, Anton MM, Farrar RP, Beckwith KA, Todd JS, Tanaka H. Effects of high intensity resistance training on arterial stiffness and wave reflection in women. Am J Hypertens. 2005; 18: 930934.[CrossRef][Medline] [Order article via Infotrieve]
70. Miyachi M, Kawano H, Sugawara J, Takahashi K, Hayashi K, Yamazaki K, Tabata I, Tanaka H. Unfavorable effects of resistance training on central arterial compliance: a randomized intervention study. Circulation. 2004; 110: 28582863.
71. Rakobowchuk M, McGowan CL, de Groot PC, Bruinsma D, Hartman JW, Phillips SM, MacDonald MJ. Effect of whole body resistance training on arterial compliance in young men. Exp Physiol. 2005; 90: 645651.
72. Rakobowchuk M, McGowan CL, de Groot PC, Hartman JW, Phillips SM, MacDonald MJ. Endothelial function of young healthy males following whole body resistance training. J Appl Physiol. 2005; 98: 21852190.
73. Pratley R, Nicklas B, Rubin M, Miller J, Smith A, Smith M, Hurley B, Goldberg A. Strength training increases resting metabolic rate and norepinephrine levels in healthy 50- to 65-year-old men. J Appl Physiol. 1994; 76: 133137.
74. Colliander EB, Tesch PA. Blood pressure in resistance-trained athletes. Can J Sport Sci. 1988; 13: 3134.[Medline] [Order article via Infotrieve]
75. Longhurst JC, Stebbins CL. The isometric athlete. Cardiol Clin. 1992; 10: 281294.[Medline] [Order article via Infotrieve]
76. Vaughan L, Zurlo F, Ravussin E. Aging and energy expenditure. Am J Clin Nutr. 1991; 53: 821825.
77. Fleck SJ, Kraemer WJ. Designing Resistance Training Programs. 2nd ed. Champaign, Ill: Human Kinetics; 1997.
78. Weinsier RL, Schutz Y, Bracco D. Reexamination of the relationship of resting metabolic rate to fat-free mass and to the metabolically active components of fat-free mass in humans. Am J Clin Nutr. 1992; 55: 790794.
79. Broeder CE, Burrhus KA, Svanevik LS, Wilmore JH. The effects of either high-intensity resistance or endurance training on resting metabolic rate. Am J Clin Nutr. 1992; 55: 802810.
80. Campbell WW, Crim MC, Young VR, Evans WJ. Increased energy requirements and changes in body composition with resistance training in older adults. Am J Clin Nutr. 1994; 60: 167175.
81. Ryan AS, Pratley RE, Elahi D, Goldberg AP. Resistive training increases fat-free mass and maintains RMR despite weight loss in postmenopausal women. J Appl Physiol. 1995; 79: 818823.
82. Taaffe DR, Pruitt L, Reim J, Butterfield G, Marcus R. Effect of sustained resistance training on basal metabolic rate in older women. J Am Geriatr Soc. 1995; 43: 465471.[Medline] [Order article via Infotrieve]
83. Schmitz KH, Jensen MD, Kugler KC, Jeffery RW, Leon AS. Strength training for obesity prevention in midlife women. Int J Obes Relat Metab Disord. 2003; 27: 326333.[CrossRef][Medline] [Order article via Infotrieve]
84. Treuth MS, Ryan AS, Pratley RE, Rubin MA, Miller JP, Nicklas BJ, Sorkin J, Harman SM, Goldberg AP, Hurley BF. Effects of strength training on total and regional body composition in older men. J Appl Physiol. 1994; 77: 614620.
85. Hunter GR, Bryan DR, Wetzstein CJ, Zuckerman PA, Bamman MM. Resistance training and intra-abdominal adipose tissue in older men and women. Med Sci Sports Exerc. 2002; 34: 10231028.[Medline] [Order article via Infotrieve]
86. Prabhakaran B, Dowling EA, Branch JD, Swain DP, Leutholtz BC. Effect of 14 weeks of resistance training on lipid profile and body fat percentage in premenopausal women. Br J Sports Med. 1999; 33: 190195.[Abstract]
87. Treuth MS, Hunter GR, Kekes-Szabo T, Weinsier RL, Goran MI, Berland L. Reduction in intra-abdominal adipose tissue after strength training in older women. J Appl Physiol. 1995; 78: 14251431.
88. Hunter GR, Kekes-Szabo T, Snyder SW, Nicholson C, Nyikos I, Berland L. Fat distribution, physical activity, and cardiovascular risk factors. Med Sci Sports Exerc. 1997; 29: 362369.[Medline] [Order article via Infotrieve]
89. Williams MJ, Hunter GR, Kekes-Szabo T, Snyder S, Treuth MS. Regional fat distribution in women and risk of cardiovascular disease. Am J Clin Nutr. 1997; 65: 855860.
90. Ross R, Rissanen J. Mobilization of visceral and subcutaneous adipose tissue in response to energy restriction and exercise. Am J Clin Nutr. 1994; 60: 695703.
91. Ross R, Rissanen J, Pedwell H, Clifford J, Shragge P. Influence of diet and exercise on skeletal muscle and visceral adipose tissue in men. J Appl Physiol. 1996; 81: 24452455.
92. Donnelly JE, Jacobsen DJ, Jakicic JM, Whatley JE. Very low calorie diet with concurrent versus delayed and sequential exercise. Int J Obes Relat Metab Disord. 1994; 18: 469475.[Medline] [Order article via Infotrieve]
93. Wadden TA, Vogt RA, Andersen RE, Bartlett SJ, Foster GD, Kuehnel RH, Wilk J, Weinstock R, Buckenmeyer P, Berkowitz RI, Steen SN. Exercise in the treatment of obesity: effects of four interventions on body composition, resting energy expenditure, appetite, and mood. J Consult Clin Psychol. 1997; 65: 269277.[CrossRef][Medline] [Order article via Infotrieve]
94. Marks BL, Ward A, Morris DH, Castellani J, Rippe JM. Fat-free mass is maintained in women following a moderate diet and exercise program. Med Sci Sports Exerc. 1995; 27: 12431251.[Medline] [Order article via Infotrieve]
95. Franklin BA, ed. American College of Sports Medicine Guidelines for Exercise Testing and Prescription. 7th ed. Baltimore, Md: Lippincott Williams & Wilkins; 2006.
96. Tucker LA, Silvester LJ. Strength training and hypercholesterolemia: an epidemiologic study of 8499 employed men. Am J Health Promot. 1996; 11: 3541.[Medline] [Order article via Infotrieve]
97. Kohl HW III, Gordon NF, Scott CB, Vaandrager H, Blair SN. Musculoskeletal strength and serum lipid levels in men and women. Med Sci Sports Exerc. 1992; 24: 10801087.[Medline] [Order article via Infotrieve]
98. Manning JM, Dooly-Manning CR, White K, Kampa I, Silas S, Kesselhaut M, Ruoff M. Effects of a resistive training program on lipoproteinlipid levels in obese women. Med Sci Sports Exerc. 1991; 23: 12221226.[Medline] [Order article via Infotrieve]
99. Vincent KR, Braith RW, Bottiglieri T, Vincent HK, Lowenthal DT. Homocysteine and lipoprotein levels following resistance training in older adults. Prev Cardiol. 2003; 6: 197203.[CrossRef][Medline] [Order article via Infotrieve]
100. Shoup EE, Durstine JL. Acute circuit weight lifting and its effects on postheparin lipoprotein lipase activity. Med Sci Sports Exerc. 1991; 23: 49.[Medline] [Order article via Infotrieve]
101. McKelvie RS, McCartney N, Tomlinson C, Bauer R, MacDougall JD. Comparison of hemodynamic responses to cycling and resistance exercise in congestive heart failure secondary to ischemic cardiomyopathy. Am J Cardiol. 1995; 76: 977979.[CrossRef][Medline] [Order article via Infotrieve]
102. Miller ER III, Jehn ML. New high blood pressure guidelines create new at-risk classification: changes in blood pressure classification by JNC 7. J Cardiovasc Nurs. 2004; 19: 367373.[Medline] [Order article via Infotrieve]
103. Keul J, Dickhuth HH, Simon G, Lehmann M. Effect of static and dynamic exercise on heart volume, contractility, and left ventricular dimensions. Circ Res. 1981; 48 (supp I): I-162I-170.[Medline] [Order article via Infotrieve]
104. Braith RW, Graves JE, Pollock ML, Leggett SL, Carpenter DM, Colvin AB. Comparison of 2 vs 3 days/week of variable resistance training during 10- and 18-week programs. Int J Sports Med. 1989; 10: 450454.[Medline] [Order article via Infotrieve]
This article has been cited by other articles:
![]() |
K. A. Goodwin, S. A. E. Headley, and L. S. Pescatello Exercise Prescription for the Prevention and Management of Hypertension American Journal of Lifestyle Medicine, November 1, 2009; 3(6): 446 - 449. [Abstract] [PDF] |
||||
![]() |
N. S. Granado, T. C. Smith, G. M. Swanson, R. B. Harris, E. Shahar, B. Smith, E. J. Boyko, T. S. Wells, M. A.K. Ryan, and for the Millennium Cohort Study Team Newly Reported Hypertension After Military Combat Deployment in a Large Population-Based Study Hypertension, November 1, 2009; 54(5): 966 - 973. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Manfredini, A. M. Malagoni, S. Mandini, B. Boari, M. Felisatti, P. Zamboni, and R. Manfredini Sport Therapy for Hypertension: Why, How, and How Much? Angiology, April 1, 2009; 60(2): 207 - 216. [Abstract] [PDF] |
||||
![]() |
R A Winett, D M Williams, and B M Davy Initiating and maintaining resistance training in older adults: a social cognitive theory-based approach Br. J. Sports Med., February 1, 2009; 43(2): 114 - 119. [Abstract] [Full Text] [PDF] |
||||
![]() |
B B Barone, N-Y Wang, A C Bacher, and K J Stewart Decreased exercise blood pressure in older adults after exercise training: contributions of increased fitness and decreased fatness Br. J. Sports Med., January 1, 2009; 43(1): 52 - 56. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-N. Chen, L.-M. Chuang, and Y.-T. Wu Clinical Measures of Physical Fitness Predict Insulin Resistance in People at Risk for Diabetes Physical Therapy, November 1, 2008; 88(11): 1355 - 1364. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. A. Gulve Exercise and Glycemic Control in Diabetes: Benefits, Challenges, and Adjustments to Pharmacotherapy Physical Therapy, November 1, 2008; 88(11): 1297 - 1321. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Lindegaard, T. Hansen, T. Hvid, G. van Hall, P. Plomgaard, S. Ditlevsen, J. Gerstoft, and B. K. Pedersen The Effect of Strength and Endurance Training on Insulin Sensitivity and Fat Distribution in Human Immunodeficiency Virus-Infected Patients with Lipodystrophy J. Clin. Endocrinol. Metab., October 1, 2008; 93(10): 3860 - 3869. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Ligibel, N. Campbell, A. Partridge, W. Y. Chen, T. Salinardi, H. Chen, K. Adloff, A. Keshaviah, and E. P. Winer Impact of a Mixed Strength and Endurance Exercise Intervention on Insulin Levels in Breast Cancer Survivors J. Clin. Oncol., February 20, 2008; 26(6): 907 - 912. [Abstract] [Full Text] [PDF] |
||||
![]() |
S F E Praet, R A M Jonkers, G Schep, C D A Stehouwer, H Kuipers, H A Keizer, and L J van Loon Long-standing, insulin-treated type 2 diabetes patients with complications respond well to short-term resistance and interval exercise training Eur. J. Endocrinol., February 1, 2008; 158(2): 163 - 172. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Igwebuike, B. A. Irving, M. L. Bigelow, K. R. Short, J. P. McConnell, and K. S. Nair Lack of Dehydroepiandrosterone Effect on a Combined Endurance and Resistance Exercise Program in Postmenopausal Women J. Clin. Endocrinol. Metab., February 1, 2008; 93(2): 534 - 538. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. White, T. Guerin, H. Swanson, S. Post, H. Zhu, M. Gong, J. Liu, W. V. Everson, X.-A. Li, G. A. Graf, et al. Diabetic HDL-associated myristic acid inhibits acetylcholine-induced nitric oxide generation by preventing the association of endothelial nitric oxide synthase with calmodulin Am J Physiol Cell Physiol, January 1, 2008; 294(1): C295 - C305. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. J. Cheng, E. W. Gregg, N. De Rekeneire, D. E. Williams, G. Imperatore, C. J. Caspersen, and H. S. Kahn Muscle-Strengthening Activity and Its Association With Insulin Sensitivity Diabetes Care, September 1, 2007; 30(9): 2264 - 2270. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Williams, W. L. Haskell, P. A. Ades, E. A. Amsterdam, V. Bittner, B. A. Franklin, M. Gulanick, S. T. Laing, and K. J. Stewart Resistance Exercise in Individuals With and Without Cardiovascular Disease: 2007 Update: A Scientific Statement From the American Heart Association Council on Clinical Cardiology and Council on Nutrition, Physical Activity, and Metabolism Circulation, July 31, 2007; 116(5): 572 - 584. [Abstract] [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2006 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |