全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Relation of Serum Leptin and Adiponectin Level to Serum C-Reactive Protein: The INTERLIPID Study

DOI: 10.1155/2013/601364

Full-Text   Cite this paper   Add to My Lib

Abstract:

Objective. Despite considerable study, the relevance of leptin and adiponectin for atherosclerosis development is still unsettled. We investigated relations of serum leptin and adiponectin to serum C-reactive protein (CRP), using the INTERLIPID dataset on Japanese emigrants living in Hawaii and Japanese in Japan. Design and Methods. Serum leptin, adiponectin, and CRP were measured by standardized methods in men and women of ages 40 to 59 years from two population samples, one Japanese-American in Hawaii (83 men, 89 women) and the other Japanese in central Japan (111 men, 104 women). Participants with CRP >10?mg/L were excluded. Results. Sex-specific multiple linear regression analyses, with log-transformed leptin and adiponectin (log-leptin, log-adipo), site (Hawaii = 1, Japan = 0), SBP, HbA1c, smoking (cigarettes/day), and physical activity index score of the Framingham Offspring Study as covariates, showed that log-leptin directly related and log-adipo inversely related to log-CRP for both sexes ( s < 0.05 to <0.01). Addition to the model of BMI and interaction terms (BMI × log-leptin, BMI × log-adipo, SITE × log-leptin, SITE × log-adipo) resulted in disappearance of statistical significance except for direct relation of log-leptin to log-CRP in men ( ). Conclusions. Leptin directly related to CRP independent of BMI and other confounding factors in men but not in women. 1. Introduction Recent advances have illuminated the role of inflammation and underlying cellular and molecular mechanisms in atherogenesis [1]. C-reactive protein (CRP), a marker of inflammation, has been recognized as an indicator of atherosclerotic and cardiovascular risk [2]. Leptin and adiponectin, secreted by adipose tissue, represent the most abundant adipokines in human serum [3–7]. Recent studies have implicated leptin as a risk factor for cardiovascular diseases independent of traditional risk factors [5]. Adiponectin, on the other hand, may have anti-inflammatory, antiatherogenic, and antidiabetic properties [8, 9]. Lower serum adiponectin concentrations are reported to be associated with coronary heart disease (CHD) risk [10]. As to the relationship between these adipocytokines and CRP direct association of leptin with CRP, and inverse association of adiponectin with CRP have been reported [11–14]. Adjustment for BMI or other obesity measures was done in these previous studies; interaction terms between adipocytokines and obesity measure were not reported. INTERLIPID, an ancillary study of the International Study of Macro/micronutrients and Blood Pressure (INTERMAP),

References

[1]  M. T. Montero-Vega, “The inflammatory process underlying atherosclerosis,” Critical Reviews in Immunology, vol. 32, pp. 373–462, 2012.
[2]  P. M. Ridker, “Clinical application of C-reactive protein for cardiovascular disease detection and prevention,” Circulation, vol. 107, no. 3, pp. 363–369, 2003.
[3]  Y. Matsusawa, T. Funahashi, and I. Shimomura, “Adiponectin and metabolic syndrome,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 24, pp. 29–33, 2004.
[4]  Y.-H. Yu and H. N. Ginsberg, “Adipocyte signaling and lipid homeostasis: sequelae of insulin-resistant adipose tissue,” Circulation Research, vol. 96, no. 10, pp. 1042–1052, 2005.
[5]  N. Sattar, G. Wannamethee, N. Sarwar et al., “Leptin and coronary heart disease. Prospective study and systematic review,” Journal of the American College of Cardiology, vol. 53, no. 2, pp. 167–175, 2009.
[6]  T. Ronti, G. Lupattelli, and E. Mannarino, “The endocrine function of adipose tissue: an update,” Clinical Endocrinology, vol. 64, no. 4, pp. 355–365, 2006.
[7]  G. M. Dallinga-Thie and R. P. F. Dullaart, “Do genome-wide association scans provide additional information on the variation of plasma adiponectin concentrations?” Atherosclerosis, vol. 208, no. 2, pp. 328–329, 2010.
[8]  J. Spranger, A. Kroke, M. M?hlig et al., “Adiponectin and protection against type 2 diabetes mellitus,” The Lancet, vol. 361, no. 9353, pp. 226–228, 2003.
[9]  N. Kubota, Y. Terauchi, T. Yamauchi et al., “Disruption of adiponectin causes insulin resistance and neointimal formation,” The Journal of Biological Chemistry, vol. 277, no. 29, pp. 25863–25866, 2002.
[10]  N. Sattar, G. Wannamethee, N. Sarwar et al., “Adiponectin and coronary heart disease: a prospective study and meta-analysis,” Circulation, vol. 114, no. 7, pp. 623–629, 2006.
[11]  A. S. M. Shamsuzzaman, M. Winnicki, R. Wolk et al., “Independent association between plasma leptin and C-reactive protein in healthy humans,” Circulation, vol. 109, no. 18, pp. 2181–2185, 2004.
[12]  A. Ble, B. G. Windham, S. Bandinelli et al., “Relation of plasma leptin to C-reactive protein in older adults (from the Invecchiare nel Chianti Study),” The American Journal of Cardiology, vol. 96, no. 7, pp. 991–995, 2005.
[13]  K. Matsushita, H. Yatsuya, K. Tamakoshi et al., “Comparison of circulating adiponectin and proinflammatory markers regarding their association with metabolic syndrome in Japanese men,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 4, pp. 871–876, 2006.
[14]  M. Komatsu, H. Ohfusa, T. Aizawa, and K. Hashizume, “Adiponectin inversely correlates with high sensitive C-reactive protein and triglycerides, but not with insulin sensitivity, in apparently healthy Japanese men,” Endocrine Journal, vol. 54, no. 4, pp. 553–558, 2007.
[15]  H. Ueshima, A. Okayama, S. Saitoh et al., “Differences in cardiovascular disease risk factors between Japanese in Japan and Japanese-Americans in Hawaii: the INTERLIPID study,” Journal of Human Hypertension, vol. 17, no. 9, pp. 631–639, 2003.
[16]  N. Okuda, H. Ueshima, A. Okayama et al., “Relation of long chain n-3 polyunsaturated fatty acid intake to serum high density lipoprotein cholesterol among Japanese men in Japan and Japanese-American men in Hawaii: the INTERLIPID study,” Atherosclerosis, vol. 178, no. 2, pp. 371–379, 2005.
[17]  Y. Nakamura, H. Ueshima, N. Okuda et al., “Relation of dietary and other lifestyle traits to difference in serum adiponectin concentration of Japanese in Japan and Hawaii: the INTERLIPID study,” American Journal of Clinical Nutrition, vol. 88, no. 2, pp. 424–430, 2008.
[18]  J. Stamler, P. Elliott, B. Dennis et al., “INTERMAP: background, aims, design, methods, and descriptive statistics (nondietary),” Journal of Human Hypertension, vol. 17, no. 9, pp. 591–608, 2003.
[19]  B. Dennis, J. Stamler, M. Buzzard et al., “INTERMAP: the dietary data—process and quality control,” Journal of Human Hypertension, vol. 17, no. 9, pp. 609–622, 2003.
[20]  W. B. Kannel and P. Sorlie, “Some health benefits of physical activity. The Framingham study,” Archives of Internal Medicine, vol. 139, no. 8, pp. 857–861, 1979.
[21]  M. Korbonits, P. J. Trainer, J. A. Little et al., “Leptin levels do not change acutely with food administration in normal or obese subjects, but are negatively correlated with pituitary-adrenal activity,” Clinical Endocrinology, vol. 46, no. 6, pp. 751–757, 1997.
[22]  L. Poretsky, M. Lesser, and D. Brillon, “Lack of postprandial leptin peaks in patients with type 2 diabetes mellitus,” Diabetes, Obesity and Metabolism, vol. 3, no. 2, pp. 105–111, 2001.
[23]  P. W. Peake, A. D. Kriketos, G. S. Denyer, L. V. Campbell, and J. A. Charlesworth, “The postprandial response of adiponectin to a high-fat meal in normal and insulin-resistant subjects,” International Journal of Obesity, vol. 27, no. 6, pp. 657–662, 2003.
[24]  T. Pischon, G. S. Hotamisligil, and E. B. Rimm, “Adiponectin: stability in plasma over 36 hours and within-person variation over 1 year,” Clinical Chemistry, vol. 49, no. 4, pp. 650–652, 2003.
[25]  S. M. Abdullah, A. Khera, D. Leonard et al., “Sex differences in the association between leptin and CRP: results from the Dallas Heart study,” Atherosclerosis, vol. 195, no. 2, pp. 404–410, 2007.
[26]  A. Samara, B. Herbeth, R. Aubert et al., “Sex-dependent associations of leptin with metabolic syndrome-related variables: the stanislas study,” Obesity, vol. 18, no. 1, pp. 196–201, 2010.
[27]  B. Thorand, J. Baumert, A. D?ring et al., “Sex differences in the relation of body composition to markers of inflammation,” Atherosclerosis, vol. 184, no. 1, pp. 216–224, 2006.
[28]  I. A. Rossi, M. Bochud, P. Bovet et al., “Sex difference and the role of leptin in the association between high-sensitivity C-reactive protein and adiposity in two different populations,” European Journal of Epidemiology, vol. 27, pp. 379–384, 2012.
[29]  S. A. Lear, M. M. Chen, C. L. Birmingham, and J. J. Frohlich, “The relationship between simple anthropometric indices and C-reactive protein: ethnic and gender differences,” Metabolism, vol. 52, no. 12, pp. 1542–1546, 2003.
[30]  A. Khera, D. K. McGuire, S. A. Murphy et al., “Race and gender differences in C-reactive protein levels,” Journal of the American College of Cardiology, vol. 46, no. 3, pp. 464–469, 2005.
[31]  A. Khera, G. L. Vega, S. R. Das et al., “Sex differences in the relationship between c-reactive protein and body fat,” Journal of Clinical Endocrinology and Metabolism, vol. 94, no. 9, pp. 3251–3258, 2009.
[32]  M. Bochud, F. Marquant, P.-M. Marques-Vidal et al., “Association between C-reactive protein and adiposity in women,” Journal of Clinical Endocrinology and Metabolism, vol. 94, no. 10, pp. 3969–3977, 2009.
[33]  J. V. Castell, M. J. Gomez-Lechon, M. David, R. Fabra, R. Trullenque, and P. C. Heinrich, “Acute-phase response of human hepatocytes: regulation of acute-phase protein synthesis by interleukin-6,” Hepatology, vol. 12, no. 5, pp. 1179–1186, 1990.
[34]  J. Santos-Alvarez, R. Goberna, and V. Sánchez-Margalet, “Human leptin stimulates proliferation and activation of human circulating monocytes,” Cellular Immunology, vol. 194, no. 1, pp. 6–11, 1999.
[35]  H. Baumann, K. K. Morella, D. W. White et al., “The full-length leptin receptor has signaling capabilities of interleukin 6-type cytokine receptors,” Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no. 16, pp. 8374–8378, 1996.
[36]  C. M. Khoo, S. Sairazi, S. Taslim et al., “Ethnicity modifies the relationships of insulin resistance, inflammation, and adiponectin with obesity in a multiethnic Asian population,” Diabetes Care, vol. 34, no. 5, pp. 1120–1126, 2011.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133