Korean Circ J.  2007 Dec;37(12):623-629. 10.4070/kcj.2007.37.12.623.

Association between the JNC 7 Classification of the Stages of Systolic Hypertension and Inflammatory Cardiovascular Risk Factors

Affiliations
  • 1Division of Cardiology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. cumckhy@catholic.ac.kr

Abstract

BACKGROUND AND OBJECTIVES: It is well known that the higher the blood pressure, the greater the chance of cardiovascular disease, but the factors that are responsible for this association remain largely unknown. We sought to determine whether blood pressure, in a dose-dependent way, is associated with systemic inflammation, which is a known risk factor for cardiovascular events.
SUBJECTS AND METHODS
We analyzed the data from 5,626 participants, aged 40-65 years, of the Third National Health and Nutrition Examination Survey (NHANES III). We quantified the blood pressure by dividing the participants into the normal, pre-, stage 1 and stage 2 hypertension groups based on the Joint National Committee 7 (JNC) classification. We used multiple linear and logistic regression models to determine the relationship between blood pressure and the levels of inflammatory markers.
RESULTS
After adjustments were made for various co-morbidities, participants with stage 2 systolic hypertension had higher circulating leukocyte levels [840/microliter (95% confidence interval [CI], 374 to 939/microliter)] and fibrinogen levels [24.5 mg/dL (95% CI, 8.9 to 31.9 mg/dL)] than those participants with normal blood pressure. They also showed higher circulating C-reactive protein levels (C-reactive protein>10.0 mg/L: p for trend=0.001). There was a dose-dependent increase for the circulating levels of the risk factors across the different levels of systolic blood pressure, but not for diastolic blood pressure.
CONCLUSION
These findings demonstrate that an elevated systolic blood pressure is an independent risk factor for systemic inflammation and this may explain why systolic hypertension is a risk factor for atherosclerosis and cardiovascular events.

Keyword

Hypertension; Inflammation

MeSH Terms

Atherosclerosis
Blood Pressure
C-Reactive Protein
Cardiovascular Diseases
Classification*
Fibrinogen
Hypertension*
Inflammation
Joints
Leukocytes
Logistic Models
Nutrition Surveys
Risk Factors*
C-Reactive Protein
Fibrinogen

Figure

  • Fig. 1 Dose-response relationship between systolic hypertension and the CRP level. CRP: C-reactive protein.


Reference

1. Lewington S, Clarke R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002. 360:1903–1913.
2. Vasan RS, Larson MG, Leip EP, et al. Impact of high-normal blood pressure on the risk of cardiovascular disease. N Engl J Med. 2001. 345:1291–1297.
3. Ridker PM, Hennekens CH, Buring JE, Rifai N. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N Engl J Med. 2000. 342:836–843.
4. Ridker PM. High-sensitivity C-reactive protein: potential adjunct for global risk assessment in the primary prevention of cardiovascular disease. Circulation. 2001. 103:1813–1818.
5. Koenig W, Sund M, Frohlich M, et al. C-reactive protein, a sensitive marker of inflammation, predicts future risk of coronary heart disease in initially healthy middle-aged men: results from the MONICA (Monitoring Trends and Determinants in Cardiovascular Disease) Augsburg Cohort Study, 1984 to 1992. Circulation. 1999. 99:237–242.
6. Weissberg PL, Bennett MR. Atherosclerosis: an inflammatory disease. N Engl J Med. 1999. 340:1928–1929.
7. Lee S, Kim W, Hwang SH, et al. The relationship of inflammatory reaction with the mortality of type B acute aortic syndrome. Korean Circ J. 2006. 36:387–392.
8. Sesso HD, Buring JE, Rifai N, et al. C-reactive protein and the risk of developing hypertension. JAMA. 2003. 290:2945–2951.
9. Bautista LE, Lopez-Jaramillo P, Vera LM, Casas JP, Otero AP, Guaracao AI. Is C-reactive protein an independent risk factor for essential hypertension? J Hypertens. 2001. 19:857–861.
10. Sung KC, Suh JY, Kim BS, et al. High sensitivity C-reactive protein as an independent risk factor for essential hypertension. Am J Hypertens. 2003. 16:429–433.
11. Bautista LE, Atwood JE, O'Malley PG, Taylor AJ. Association between C-reactive protein and hypertension in healthy middle-aged men and women. Coron Artery Dis. 2004. 15:331–336.
12. National Center for Health Statistics. Publication No.: (PHS) 94-1308. Plan and operation of the Third National Health and Nutrition Examination Survey, 1988-94. 1994. Hyattsville, Md: US Dept of Health and Human Services.
13. Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003. 42:1206–1252.
14. Gunter EW, Lewis BG, Konchikowski SM. Laboratory precedures used for the Third National Health and Nutrition Examination Survey (NHANES III), 1988-94. 1996. Hyattsville, Md: National Center for Health Statistics.
15. Lind L. Circulating markers of inflammation and atherosclerosis. Atherosclerosis. 2003. 169:203–214.
16. Cho DK, Kwon SU, Kim SW, et al. Risk factors and predictors for the progression of carotid atherosclerotic stenosis in Korean adults. Korean Circ J. 2005. 35:834–840.
17. Mora S, Rifai N, Buring JE, Ridker PM. Additive value of immunoassay-measured fibrinogen and high-sensitivity C-reactive protein levels for predicting incident cardiovascular events. Circulation. 2006. 114:381–387.
18. Engstrom G, Janzon L, Berglund G, et al. Blood pressure increase and incidence of hypertension in relation to inflammation-sensitive plasma proteins. Arterioscler Thromb Vasc Biol. 2002. 22:2054–2058.
19. Hwang ST, Kim BS, Hwang SJ, et al. Associations between white blood cell count and features of the metabolic syndrome. Korean Circ J. 2004. 34:280–287.
20. Kannel WB, Anderson K, Wilson PW. White blood cell count and cardiovascular disease: insights from the Framingham Study. JAMA. 1992. 267:1253–1256.
21. Hoffman M, Blum A, Baruch R, Kaplan E, Benjamin M. Leukocytes and coronary heart disease. Atherosclerosis. 2004. 172:1–6.
22. Shankar A, Klein BE, Klein R. Relationship between white cell count and incident hypertension. Am J Hypertens. 2004. 17:233–239.
23. Han SW, Ryu KH, Kwon YB, et al. Serum total homocysteine as a risk factor for patients with coronary artery disease. Korean Circ J. 1998. 28:1953–1963.
24. Davey Smith G, Lawlor DA, Harbord R, et al. Association of C-reactive protein with blood pressure and hypertension: life course confounding and mendelian randomization tests of causality. Arterioscler Thromb Vasc Biol. 2005. 25:1051–1056.
25. Marques-Vidal P, Cambou JP, Bongard V, Ruidavets JB, Ferrieres J. Systolic and diastolic hypertension: no relationship with lipid and inflammatory markers in Haute-Garonne, France. Am J Hypertens. 2003. 16:681–684.
26. Yudkin JS, Stehouwer CD, Emeis JJ, Coppack SW. C-reactive protein in healthy subjects: associations with obesity, insulin resistance, and endothelial dysfunction: a potential role for cytokines originating from adipose tissue? Arterioscler Thromb Vasc Biol. 1999. 19:972–978.
27. Woodward M, Rumley A, Lowe GD, Tunstall-Pedoe H. C-reactive protein: associations with haematological variables, cardiovascular risk factors and prevalent cardiovascular disease. Br J Haematol. 2003. 122:135–141.
28. Nielsen WB, Vestbo J, Jensen GB. Isolated systolic hypertension as a major risk factor for stroke and myocardial infarction and an unexploited source of cardiovascular prevention: a prospective population-based study. J Hum Hypertens. 1995. 9:175–180.
29. Staessen JA, Gasowski J, Wang JG, et al. Risks of untreated and treated isolated systolic hypertension in the elderly: meta-analysis of outcome trials. Lancet. 2000. 355:865–872.
30. Kotis JB, Davis BR, Cutler J, et al. Prevention of heart failure by antihypertensive drug treatment in older persons with isolated systolic hypertension. JAMA. 1997. 278:212–216.
Full Text Links
  • KCJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr