Effect of different doses of aerobic exercise on total white blood cell (WBC) and WBC subfraction number in postmenopausal women: results from DREW

Neil M Johannsen, Damon L Swift, William D Johnson, Vishwa D Dixit, Conrad P Earnest, Steven N Blair, Timothy S Church, Neil M Johannsen, Damon L Swift, William D Johnson, Vishwa D Dixit, Conrad P Earnest, Steven N Blair, Timothy S Church

Abstract

Background: Elevated total white blood cell (WBC) count is associated with an increased risk of coronary heart disease and death. Aerobic exercise is associated with lower total WBC, neutrophil, and monocyte counts. However, no studies have evaluated the effect of the amount of aerobic exercise (dose) on total WBC and WBC subfraction counts.

Purpose: To examine the effects of 3 different doses of aerobic exercise on changes in total WBC and WBC subfraction counts and independent effects of changes in fitness, adiposity, markers of inflammation (IL-6, TNF-α, C-reactive protein), fasting glucose metabolism, and adiponectin.

Methods: Data from 390 sedentary, overweight/obese postmenopausal women from the DREW study were used in these analyses. Women were randomized to a non-exercise control group or one of 3 exercise groups: energy expenditure of 4, 8, or 12 kcal kg(-1)⋅week(-1) (KKW) for 6 months at an intensity of 50% VO2peak.

Results: A dose-dependent decrease in total WBC counts (trend P = 0.002) was observed with a significant decrease in the 12KKW group (-163.1±140.0 cells/µL; mean±95%CI) compared with the control (138.6±144.7 cells/µL). A similar response was seen in the neutrophil subfraction (trend P = 0.001) with a significant decrease in the 12KKW group (-152.6±115.1 cells/µL) compared with both the control and 4KKW groups (96.4±119.0 and 21.9±95.3 cells/µL, respectively) and in the 8KKW group (-102.4±125.0 cells/µL) compared with the control. When divided into high/low baseline WBC categories (median split), a dose-dependent decrease in both total WBCs (P = 0.003) and neutrophils (P<0.001) was observed in women with high baseline WBC counts. The effects of exercise dose on total WBC and neutrophil counts persisted after accounting for significant independent effects of change in waist circumference and IL-6.

Conclusion: Aerobic exercise training reduces total WBC and neutrophil counts, in a dose-dependent manner, in overweight/obese postmenopausal women and is especially beneficial for those with systemic low grade inflammation.

Clinical trials identifier: NCT00011193.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. CONSORT schematic of study participation.
Figure 1. CONSORT schematic of study participation.
Figure 2. Change (Δ) in total WBC…
Figure 2. Change (Δ) in total WBC and neutrophil counts by exercise group (control, 4, 8, and 12 kcal kg−1 min−1; KKW) and high/low baseline WBC counts.
Interaction  =  group x high/low WBC category; trend high and low are from general linear model across intervention groups separately for each high/low baseline WBC category. The participant numbers (n) in the high baseline total WBC groups were 41, 71, 41, and 43 and low baseline total WBC groups were 45, 63, 37, and 49 for Control, 4, 8, and 12 KKW, respectively. The participant numbers (n) in the high baseline neutrophil groups were 40, 71, 42, and 42 and low baseline neutrophil groups were 46, 63, 36, and 50 for Control, 4, 8, and 12 KKW, respectively. * Significantly different between high/low baseline WBC categories within an exercise group.

References

    1. Kannel WB, Anderson K, Wilson PW. White blood cell count and cardiovascular disease. Insights from the Framingham Study. Journal of the American Medical Association. 1992;267:1253–1256.
    1. Gillum RF, Ingram DD, Makuc DM. White blood cell count, coronary heart disease, and death: the NHANES I Epidemiologic Follow-up Study. American Heart Journal. 1993;125:855–863.
    1. Brown DW, Giles WH, Croft JB. White blood cell count: an independent predictor of coronary heart disease mortality among a national cohort. Journal of Clinical Epidemiology. 2001;54:316–322.
    1. Grimm RH, Jr, Neaton JD, Ludwig W. Prognostic importance of the white blood cell count for coronary, cancer, and all-cause mortality. Journal of the American Medical Association. 1985;254:1932–1937.
    1. Gillum RF, Mussolino ME, Madans JH. Counts of neutrophils, lymphocytes, and monocytes, cause-specific mortality and coronary heart disease: the NHANES-I epidemiologic follow-up study. Ann Epidemiol. 2005;15:266–271.
    1. Wheeler JG, Mussolino ME, Gillum RF, Danesh J. Associations between differential leucocyte count and incident coronary heart disease: 1764 incident cases from seven prospective studies of 30,374 individuals. Eur Heart J. 2004;25:1287–1292.
    1. Horne BD, Anderson JL, John JM, Weaver A, Bair TL, et al. Which white blood cell subtypes predict increased cardiovascular risk? J Am Coll Cardiol. 2005;45:1638–1643.
    1. Rana JS, Boekholdt SM, Ridker PM, Jukema JW, Luben R, et al. Differential leucocyte count and the risk of future coronary artery disease in healthy men and women: the EPIC-Norfolk Prospective Population Study. J Intern Med. 2007;262:678–689.
    1. Pratley RE, Wilson C, Bogardus C. Relation of the white blood cell count to obesity and insulin resistance: effect of race and gender. Obes Res. 1995;3:563–571.
    1. Vozarova B, Weyer C, Lindsay RS, Pratley RE, Bogardus C, et al. High white blood cell count is associated with a worsening of insulin sensitivity and predicts the development of type 2 diabetes. Diabetes. 2002;51:455–461.
    1. Dixon JB, O'Brien PE. Obesity and the white blood cell count: changes with sustained weight loss. Obes Surg. 2006;16:251–257.
    1. Margolis KL, Manson JE, Greenland P, Rodabough RJ, Bray PF, et al. Leukocyte count as a predictor of cardiovascular events and mortality in postmenopausal women: the Women's Health Initiative Observational Study. Archives of internal medicine. 2005;165:500–508.
    1. Angeli F, Angeli E, Ambrosio G, Mazzotta G, Reboldi G, et al. Neutrophil count for the identification of postmenopausal hypertensive women at increased cardiovascular risk. Obstetrics and gynecology. 2010;115:695–703.
    1. Johannsen NM, Priest EL, Dixit VD, Earnest CP, Blair SN, et al. Association of white blood cell subfraction concentration with fitness and fatness. Br J Sports Med. 2010;44:588–593.
    1. Church TS, Finley CE, Earnest CP, Kampert JB, Gibbons LW, et al. Relative associations of fitness and fatness to fibrinogen, white blood cell count, uric acid and metabolic syndrome. International Journal of Obesity. 2002;26:805–813.
    1. Kakanis MW, Peake J, Brenu EW, Simmonds M, Gray B, et al. The open window of susceptibility to infection after acute exercise in healthy young male elite athletes. Exercise immunology review. 2010;16:119–137.
    1. Michishita R, Shono N, Inoue T, Tsuruta T, Node K. Effect of exercise therapy on monocyte and neutrophil counts in overweight women. The American journal of the medical sciences. 2010;339:152–156.
    1. de Gonzalo-Calvo D, Fernandez-Garcia B, de Luxan-Delgado B, Rodriguez-Gonzalez S, Garcia-Macia M, et al. Long-term training induces a healthy inflammatory and endocrine emergent biomarker profile in elderly men. Age 2011
    1. Morss GM, Jordan AN, Skinner JS, Dunn AL, Church TS, et al. Dose Response to Exercise in Women aged 45–75 yr (DREW): design and rationale. Med Sci Sports Exerc. 2004;36:336–344.
    1. Church TS, Earnest CP, Skinner JS, Blair SN. Effects of different doses of physical activity on cardiorespiratory fitness among sedentary, overweight or obese postmenopausal women with elevated blood pressure: a randomized controlled trial. JAMA. 2007;297:2081–2091.
    1. Pate RR, Pratt M, Blair SN, Haskell WL, Macera CA, et al. Physical activity and public health. A recommendation from the Centers for Disease Control and Prevention and the American College of Sports Medicine. JAMA : the journal of the American Medical Association. 1995;273:402–407.
    1. JAMA. Physical activity and cardiovascular health. NIH Consensus Development Panel on Physical Activity and Cardiovascular Health. JAMA : the journal of the American Medical Association. 1996;276:241–246.
    1. Services. USDoHaH. Physcial activity and health: a report of the Surgeon General. US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease and Prevention and Health Promotion. 1996:9–208.
    1. Whaley M, editor. Medicine ACoS. ACSM's Guidelines for Exercise Testing And Prescription. Media, PA: Williams & Wilkins; 1995.
    1. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, et al. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28:412–419.
    1. Vandanmagsar B, Youm YH, Ravussin A, Galgani JE, Stadler K, et al. The NLRP3 inflammasome instigates obesity-induced inflammation and insulin resistance. Nature medicine. 2011;17:179–188.
    1. Claycombe K, King LE, Fraker PJ. A role for leptin in sustaining lymphopoiesis and myelopoiesis. Proceedings of the National Academy of Sciences of the United States of America. 2008;105:2017–2021.
    1. Zarkesh-Esfahani H, Pockley AG, Wu Z, Hellewell PG, Weetman AP, et al. Leptin indirectly activates human neutrophils via induction of TNF-alpha. J Immunol. 2004;172:1809–1814.
    1. Dixit VD, Schaffer EM, Pyle RS, Collins GD, Sakthivel SK, et al. Ghrelin inhibits leptin- and activation-induced proinflammatory cytokine expression by human monocytes and T cells. J Clin Invest. 2004;114:57–66.
    1. Arsenault BJ, Cote M, Cartier A, Lemieux I, Despres JP, et al. Effect of exercise training on cardiometabolic risk markers among sedentary, but metabolically healthy overweight or obese post-menopausal women with elevated blood pressure. Atherosclerosis. 2009;207:530–533.

Source: PubMed

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