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Renal function in patients with cardiovascular disease and obesity

Abstract

THE AIM. To study the renal function and the severity of insulin resistance (IR), followed by evaluation of the combined risk of progression of chronic kidney disease (CKD) and cardiovascular complications in patients with obesity and existing cardiovascular disease (CVD). PATIENTS AND METHODS. The study included 140 patients with CVD between the ages of 45 to 70 years. Patients were divided into four comparable in age, sex, smoking, presence / absence of arterial hypertension (AH) and chronic heart failure (CHF), duration of hypertension, functional class (FC) of CHF, the level of office systolic blood pressure (SBP) and diastolic blood pressure (DBP) groups depending on the body mass index (BMI). We assessed the general condition, the clini- cal measurement of the heart rate (HR), and office BP in both arms according to standard procedure, the definition of CHF FC on 6-minute walk test, anthropometry with BMI calculation, measurement of waist circumference (OT) and hip circumference (ON) and body composition by the bioelectric impedance analysis. We also determined proteinuria (PU), albuminuria (AU), calculated glomerular filtration rate (GFR). We analyzed the combined risk of CKD progression and cardiovascular complications, depending on the GFR and the AU. To assess the current IR we used index HOMA-IR, triglycerides (TG) to high-density lipoprotein cholesterol (HDL-C) ratio and the metabolic index (MI) with the use of carbohydrate and lipid parameters. RESULTS. There was a significant increase in the level of PU among patients group 4 compared to group 1 (560,19 ± 454,59 mg / g vs 330,8 ± 85,0 mg / g) and a statistically significant decrease in GFR in patients 3 and 4 groups compared with patients of group 1 (65,83 ± 13,39 and 64,06 ± 14,52 ml / min / 1.73 m 2, respectively, vs 74,94 ± 13,68 ml / min / 1.73 m2). Reliable average power detected correlation between the severity of visceral obesity and AU (r = 0,452), PU (r = 0,360), and GFR (r = -0,491). Analysis of the combined risk of CKD progression and cardiovascular complications showed a significant increase in very high-risk patients in the comparison group and 4 patients 1, 2 and 3 groups (68,6% vs 25, 39.8 and 40%, respectively). In assessing the indices that characterize the severity of IR, a statistically significant increase in HOMA-IR, TG / HSLPVP, MI with increasing BMI from group 1 to group 4 was established. We noted a high fidelity direct strong correlation between the level of visceral fat in the body, and HOMA-IR (r = 0,821), TG / HSLPVP (r = 0,806), MI (r = 0,812). CONCLUSION. The study showed a statistically significant progressive deterioration of renal function and an increase in the severity of IR as well as the increase in the combined risk of progression of CKD and cardiovascular events in patients with CVD with an increase in obesity during the comparable values of SBP office, DBP office and CHF FC among the studied groups. There were significant correlations between parameters of renal function and visceral obesity.

About the Authors

M. E. Statsenko
Volgograd State Medical University
Russian Federation


M. V. Derevyanchenko
Volgograd State Medical University
Russian Federation


N. N. Shilina
Volgograd State Medical University
Russian Federation


M. N. Titarenko
Volgograd State Medical University
Russian Federation


O. R. Pastukhova
Volgograd State Medical University
Russian Federation


References

1. Tsigosa C, Hainerb V, Basdevantc A et al. for the Obesity Management Task Force of the European Association for the Study of Obesity Management of Obesity in Adults: European Clinical Practice Guidelines. Obesity Facts 2008;1:106-116

2. World Health Organisation. Obesity: preventing and managing the global epidemic. Report of a WHO Consultation. WHO Technical Report Series 894. Geneva: World Health Organization, 2000, 268 p

3. Заболотских ИБ, Лебединский КМ, Горобец ЕС и др. Клинические рекомендации Федерации анестезиологов и реаниматологов по периоперационному ведению больных с сопутствующим ожирением. Красноярск, 2013. 19 с.

4. Hall JE, do Carmo JM, da Silva AA et al. Obesity-induced hypertension: interaction of neurohumoral and renal mechanisms. Circ Res 2015 Mar 13;116(6):991-1006. doi: 10.1161/CIRCRE-SAHA.116.305697

5. Levey AS, Stevens LA, Schmid CH et al. A new equation to estimate glomerular filtration rate. Ann Intern Med 2009; 150: 604-612

6. Рабочая группа Российского кардиологического общества, Научного общества нефрологов России, Российской ассоциации эндокринологов, Российского медицинского общества по артериальной гипертонии, Национального общества по изучению атеросклероза, Российского научного медицинского общества терапевтов. Национальные рекомендации. Сердечно-сосудистый риск и хроническая болезнь почек: стратегии кардио-нефропротекции. Российский кардиологический журнал 2014; 8(112): 7-37

7. Ройтберг ГЕ, Дорош ЖВ, Шархун OO и др. Возможности применения нового метаболического индекса при оценке инсулинорезистентности в клинической практике. РФК 2014;10(3):264-274

8. Стаценко МЕ, Деревянченко МВ, Пастухова ОР. Влияние комбинированной антигипертензивной терапии на суточный профиль артериального давления и показатели метаболизма у больных сахарным диабетом 2 типа Кардиология 2014; 54(11):20-24

9. Стаценко МЕ, Деревянченко МВ. Кардионефропротекция - важнейшая задача антигипертензивной терапии у больных сахарным диабетом 2 типа. Кардиология 2015;55(8):43-48

10. Стаценко МЕ, Деревянченко МВ. Метаболические эффекты комбинированной антигипертензивной терапии у больных сахарным диабетом 2 типа. РФК 2015;11(1):36-39

11. Hall JE, da Silva AA, do Carmo JM et al. Obesity-induced hypertension: role of sympathetic nervous system, leptin, and melanocortins. J Biol Chem 2010;285:17271-17276

12. Van Vliet BN, Hall JE, Mizelle HL et al. Reduced parasympathetic control of heart rate in obese dogs. Am J Physiol 1995;269:H629-H637

13. Lohmeier TE, Iliescu R. The sympathetic nervous system in obesity hypertension. Curr Hypertens Rep 2013;15:409-416

14. Freedman D, Ron E, Ballard-Barbash R. Body mass index and all-cause mortality in a nationwide US cohort. Int J Obes (Lond) 2006; 30: 822-829

15. Guh D, Zhang W, Bansback N. The incidence of comorbidities related to obesity and overweight: a systematic review and meta-analysis. BMC Public Health 2009; 9: 88

16. Lenz M, Richter T, Muhlhauser I. The morbidity and mortality associated with overweight and obesity in adulthood: a systematic review. Dtsch Arztebl Int 2009; 106: 641-648

17. Bellamy M, Struys M. Anaesthesia for the Overweight and Obese Patient. 1. Oxford: Oxford University Press; 2007

18. Bouchi R, Takeuchi T, Akihisa M et al. High visceral fat with low subcutaneous fat accumulation as a determinant of atherosclerosis in patients with type 2 diabetes. Cardiovasc Diabetol (2015) 14:136. DOI 10.1186/s12933-015-0302-4

19. Després JP, Lemieux S, Lamarche B et al. The insulin resistance-dyslipidemic syndrome: contribution of visceral obesity and therapeutic implications. Int J Obes Relat Metab Disord. 1995;19(Suppl 1):S76-86.

20. Fox CS, Massaro JM, Hoffmann U et al. Abdominal visceral and subcutaneous adipose tissue compartments: association with metabolic risk factors in the Framingham Heart Study. Circulation 2007;116:39-48

21. ois NE, Bartels ED, Hunter I et al. Natriuretic peptides in cardiometabolic regulation and disease. Nat Rev Cardiol 2014;11:403-412

22. Hall JE. The kidney, hypertension, and obesity. Hypertension. 2003;41:625-633

23. Hall JE, Crook ED, Jones DW et al. Mechanisms of obesity-associated cardiovascular and renal disease. Am J Med Sci 2002;324:127-137

24. Hall ME, do Carmo JM, da Silva AA et al. Obesity, hypertension, and chronic kidney disease. Int J Nephrol Renovasc Dis 2014;7:75-88

25. Dwyer TM, Bigler SA, Moore NA et al. The altered structure of renal papillary outflow tracts in obesity. Ultrastruct Pathol 2000;24:251-257

26. Dwyer TM, Banks SA, Alonso-Galicia M et al. Distribution of renal medullary hyaluronan in lean and obese rabbits. Kidney Int 2000;58:721-729

27. Alonso-Galicia M, Dwyer TM, Herrera GA, Hall JE. Increased hyaluronic acid in the inner renal medulla of obese dogs. Hypertension 1995;25:888-892

28. Hall JE, Brands MW, Henegar JR. Mechanisms of hypertension and kidney disease in obesity. Ann N Y Acad Sci 1999;892:91-107

29. Davy KP, Hall JE. Obesity and hypertension: two epidemics or one? Am J Physiol Regul Integr Comp Physiol 2004;286:R803-R813

30. Yusuf S, Hawken S, Ounpuu S et al. INTERHEART Study Investiga-tors, et al. Obesity and the risk of myocardial infarction in 27,000 partici-pants from 52 countries: a case-control study. Lancet 2005; 366:1640-1649

31. Britton KA, Massaro JM, Murabito JM et al. Body fat distribution, incident cardiovascular disease, cancer, and all-cause mortality. J Am Coll Cardiol 2013;62:921-925


Review

For citations:


Statsenko M.E., Derevyanchenko M.V., Shilina N.N., Titarenko M.N., Pastukhova O.R. Renal function in patients with cardiovascular disease and obesity. Nephrology (Saint-Petersburg). 2016;20(5):43-49. (In Russ.)

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ISSN 1561-6274 (Print)
ISSN 2541-9439 (Online)