The Metabolic Syndrome and Hypertension—R Kelishadi et al
The Metabolic Syndrome in Hypertensive and Normotensive Subjects: The Isfahan Healthy Heart Programme
R Kelishadi,1MD, R Derakhshan,1MD, B Sabet,1 MD, N Sarraf-Zadegan,1MD, M Kahbazi,1MD, GH Sadri,1PhD,AA Tavasoli,1 MD, S Heidari,1MD, A Khosravi,1MD, A Amani,1MD, HR Tolouei,1MD, A Bahonar,1MD, AA RezaeiAshtiani,1MS, A Moatarian,1MSAbstract Introduction: There are numerous correlations between hypertension and the metabolic syndrome, although this is not always the case. The objective of this study was to compare the prevalence of the metabolic syndrome and its different phenotypes among hypertensive and normotensive subjects. Materials and Methods: This cross-sectional study was performed on a representative sample of adults living in 3 cities in Iran. Among the 12,514 subjects selected by multi-stage random sampling, 1736 (13.9%) were hypertensive. The prevalence of the metabolic syndrome [according to the Adult Treatment Panel (ATP) III criteria] was significantly higher in hypertensive than normotensive subjects (51.6% versus 12.9%, respectively; OR, 7.15; 95% CI, 6.4 to 7.9). The metabolic syndrome was more prevalent in normotensive and hypertensive subjects living in urban areas than those living in rural areas (14.2% and 53.9% versus 9.5% and 45.6%, respectively, P <0.05). The mean age of hypertensive subjects, with or without the metabolic syndrome, was not significantly different (55.7 ± 12 years versus 55.4 ± 15.5 years, P = 0.6). Hypertension with the metabolic syndrome was more prevalent in women than men (72% versus 28% respectively, P <0.000), and in subjects living in urban areas than those in rural areas (75.1% versus 24.9%, respectively, P = 0.002). Conclusion: The findings of this study indicate the need for metabolic screening in all hypertensive patients, and emphasise the importance of promoting primary and secondary prevention of high blood pressure and associated modifiable risk factors in order to counter the upcoming epidemic of non-communi- cable disease in developing countries. Ann Acad Med Singapore 2005;34:243-9 Key words: Gender, Hypertension, Insulin resistance, Obesity, Prevalence Introduction
hormones.9,10As Reaven et al11 concluded in their review,
The metabolic syndrome (MS) is characterised by a
the accumulated findings support the possibility that
clustering of metabolic risk factors and an insulin-resistant
metabolic changes play a part in the regulation of blood
state.1 Its prevalence is high in Western, as well as Asian,
pressure, although some contradictions remain. Some
populations.2-4 There are numerous correlations between
epidemiologic studies have shown a direct association
the MS and hypertension, although this is not always the
between blood pressure and insulin resistance,12-14 but the
case.5 Resistance to insulin-mediated glucose disposal and
findings of other studies do not confirm this.15-17 Some
compensatory hyperinsulinaemia are common in patients
studies have shown that hypertension is associated with the
with hypertension. However, not all hypertensive patients
MS in 50% of patients.11 Different studies have shown
have insulin resistance. Several mechanisms appear to be
ethnic differences in the relationship between hypertension
involved in the link between hypertension and insulin
and insulin resistance syndrome.18-22 Some studies have
resistance, involving the sympathetic nervous system,6,7
found different associations between blood pressure and
renal handling of sodium,8 and vasoconstrictor
insulin in the same ethnic group living in different areas.13,14,23
1 Isfahan Cardiovascular Research Centre, Iran
A WHO Collaborating Centre for Research and Training in Cardiovascular Diseases Control, Prevention, and Rehabilitation for Cardiac Patients in theEastern Mediterranean Region
Address for Reprints: Associate Professor Roya Kelishadi, Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences, P.O. Box 81465-1148, Isfahan, Iran. Email: Kelishadi@med.mui.ac.ir
The Metabolic Syndrome and Hypertension—R Kelishadi et al
This may suggest the role of environmental factors,
was recorded as systolic BP and diastolic BP (SBP and
especially dietary habits, in the relationship between
hypertension and insulin resistance.11,24
Participants stood without their shoes for the measurement
Recent studies revealed that the age-adjusted mortality
of their height, which was rounded off to the nearest 0.5 cm.
due to cardiovascular disease (CVD) has increased by 20%
Measurements were taken with a secured metal ruler, while
to 45% in Iran,25,26 with a high prevalence of hypertension,
weight was measured using calibrated scales, with
one of its major risk factors.27 Considering the effect of
participants wearing light clothing. Waist circumference
genetic and lifestyle factors on the MS, the aim of the
(WC) was measured to the nearest half-centimetre, at a
present study – performed for the first time in urban and
level midway between the lower rib margin and the iliac
rural areas in Iran – was to compare the prevalence of this
crest. Obesity was defined as body mass index >30 kg/m2
syndrome and its different phenotypes in hypertensive and
for all subjects. The cutoff point for abnormal WC was
normotensive subjects in a representative sample of the
>102 cm for men and >88 cm for women.29
Iranian adult population living in 3 cities in central Iran.
Blood samples were drawn by venipuncture from the left
Materials and Methods
antecubital vein after 12 hours of fasting. All blood sampleswere collected in the 3 cities and kept frozen at -20°C until
This cross-sectional study was performed as the baseline
assayed within 72 hours in the central laboratory of Isfahan
survey of a community-based interventional programme in
Cardiovascular Research Centre (a WHO collaborating
3 cities in Iran, called the Isfahan Healthy Heart Programme
centre), which meets the criteria of the national reference
(IHHP), the details of which have been previously
laboratory (a WHO collaborating centre) and is under the
external quality control of St Rafael University, Leuven,
Quota sampling was conducted to stratify study population
Belgium. The results from the laboratories were highly
by their living area (urban versus rural) according to the
regional population distribution as per the national
Serum total cholesterol (TC), triglyceride (TG) and fasting
population census in 1999. This baseline survey of 12,514
blood sugar (FBS) were measured by standard kits (Pars
randomly selected adults aged >19 years old was conducted
Azmoon Co., Iran) using an auto-analyser (Ependorf,
with a 2-stage cluster sampling. Initially, census blocks
Germany). Serum HDL cholesterol (HDL-C) was
were randomly selected from each county and divided into
determined after dextran sulphate-magnesium chloride
clusters, each having approximately 1000 households.
precipitation of non-HDL cholesterol. Serum low-density
Approximately 5 to 10 households within these clusters
lipoprotein cholesterol (LDL-C) was calculated by the
were randomly selected for enumeration. After enumeration,
Friedwald equation in those subjects with TG <400 mg/dL,
1 eligible individual above 19 years of age was randomly
selected per household if he or she was Iranian, mentallycompetent and, in the case of females, not pregnant. The
The MS and its components were defined according to
sample size was calculated and distributed into different
the Third Report of the Expert Panel on Detection,
age groups (19 to 24; 25 to 34; 35 to 44; 45 to 54; 55 to 64
Evaluation, and Treatment of High Blood Cholesterol in
and >65 years) according to the distribution in the
Adults (Adult Treatment Panel III or ATP III).31 Considering
community. The total number was doubled due to the
that the ATP III criteria for hypertension consist of high
cluster method, and after taking the missing rate into
simultaneous systolic and diastolic BP, the definition of the
account, the total number was calculated to be 12,600 for
Seventh Report of the Joint National Committee on
the 3 counties. In this study, data from 12,514 cases that
Prevention, Detection, Evaluation, and Treatment of High
completed the study were reported. The urban/rural ratios
Blood Pressure, which includes isolated high SBP or DBP
were 90/10, 60/40 and 66/34 in Isfahan, Najaf-Abad and
(SBP >140 or DBP >90 mm Hg),32 was also used for
dividing subjects into normotensive and hypertensive groupsfor comparison of the prevalence of the MS components
The selected persons were invited to the survey centres
for a clinical examination and to answer a questionnaireabout their socio-demographic and health-related
The data were collected and stored in a computer database.
characteristics. Informed consent was obtained from
A trained team checked the recorded information for
participants at the clinic. A trained team of physicians
missing values and data entry errors. After tidying up the
performed physical examinations and blood sampling,
data, statistical analyses were performed using the SPSS
using standardised and zero-calibrated instruments. Blood
statistical package version 10 for Windows (SPSS Inc.,
pressure (BP) was measured in duplicate in a seated position;
Chicago, USA) at P <0.05. The data were presented as
the average of 2 measures of first and fifth Krotkoff phase
frequencies, percentages and at 95% confidence intervals.
The Metabolic Syndrome and Hypertension—R Kelishadi et al
The prevalence of different phenotypes of MS was compared
Iran indicate that 51.6% of hypertensive subjects had the
MS. This is significantly higher than the prevalence of12.9% in the normal population. This finding is consistent
with other studies revealing that hypertension tends to
In this cross-sectional study performed among 12,514
cluster with metabolic risk factors, and that about half of
individuals (6391 women and 6123 men), 1736 subjects
hypertensive patients are insulin-resistant.11,33,34 The
(13.9%), of an average age of 55.6 ± 13.9 years, were
coexistence of hypertension with other components of MS
hypertensive. Table 1 shows the baseline characteristics of
in the present study is in line with some population-based
subjects studied. The prevalence of different phenotypes of
MS in hypertensive and normotensive subjects to both
However, in the factor analysis by Choi et al,37 blood
genders is presented in Table 2. The prevalence of the MS
pressure was not closely aggregated with other CVD risk
was significantly higher in hypertensive than normotensive
factors. In the study by Saad and colleagues,38 which
subjects (51.6% versus 12.9%, respectively; OR, 7.15;
examined the relationship between blood pressure and
95% CI, 6.4 to 7.9). Among hypertensive subjects, the
insulin resistance among different ethnic groups, a
phenotypes of the MS consisting of high TG and low HDL-
relationship was found in Caucasians but not among Pima
C, as well as abdominal obesity and low HDL-C, were
more prevalent. The most common phenotype of the MS
In the present study, the prevalence of MS in hypertensive
without the component of hypertension was the coexistence
subjects living in urban areas was higher than those living
of high TG, low HDL-C and abdominal obesity (Table 1).
in rural areas. It is suggested that this finding emphasises
In urban areas, MS was present in 53.9% of hypertensive
the impact of lifestyle on the development of the MS.
and 14.2% of normotensive subjects (OR, 7; 95% CI, 6.2
The cumulative prevalence of 5 components of the MS in
to 8). In rural areas these were 45.6% and 9.5%, respectively
men and women was 2.2% and 2.9%, respectively, in the
(OR, 7.9; 95% CI, 6.4 to 9.4). The prevalence of the
study by Ford and colleagues39 in the US, and 1% and 4%,
phenotypes of the MS with at least 1 and/or all its 5
respectively, in the study by Azizi et al40 in Iran. In the
components, as well as the phenotypes without high BP
present study, the prevalence rates among hypertensive
(based on the JNC 7 criteria), is shown in Table 3, according
and normotensive men and women were 1.7%, 4.6%, 0.1%
and 0%, respectively, with hypertensive women showing
As shown in Table 4, the mean age of hypertensive
the highest prevalence. Overall, hypertension with the MS
subjects with or without the MS was not significantly
was more prevalent among women than in men, which
different; but hypertension with MS was more prevalent
could be attributed in part to their sedentary lifestyle. In
among women than men, and in subjects living in urban
addition, this finding is in line with existing evidence of
gender differences in the relationship between bloodpressure and insulin resistance.41-43
Discussion
In the study of a Chinese population by Chen et al,41
The findings of the present study performed among
hypertension was linked to the MS in women but not in
12,514 individuals aged >19 years old living in 3 cities in
men. They suggested that the role of sympathetic activity in
Table 1. Baseline Characteristics in Hypertensive and Normotensive Individuals
116.3 ± 17.9 114.9 ± 20.3 115.6 ± 19.1
194.6 ± 57.7 202.5 ± 54.8 198.7 ± 56.4
216.5 ± 128.1 173.8 ± 115.7 151.4 ± 93.1 162.6 ± 105.5
DBP: diastolic blood pressure; FBS: fasting blood sugar; HDL-C: high-density lipoprotein cholesterol; LDL-C: low-density lipoprotein cholesterol;SBP: systolic blood pressure; TC: total cholesterol; TG: triglyceride; WC: waist circumference
The Metabolic Syndrome and Hypertension—R Kelishadi et al
Table 2. Comparison of Different Phenotypes of the Metabolic Syndrome in Hypertensive and Normotensive Men and Women
AB: abdominal obesity; BP: blood pressure; CI: confidence interval; FBS: fasting blood sugar; HDL-C: high-density lipoprotein;
The Metabolic Syndrome and Hypertension—R Kelishadi et al
Table 3. Comparison of the Number of Metabolic Syndrome Components in Hypertensive and Normotensive Subjects* According to
* Hypertension is defined according to the JNC7 criteria.32
Comparison of Characteristics Between Hypertensive
in hypertensive subjects, the MS amplifies CVD risk
Individuals With or Without Metabolic Syndrome
associated with high blood pressure, independent of theeffect of several traditional cardiovascular risk factors.
According to the review by Christ and colleagues,47
immediate treatment of the MS is mandatory, and
antihypertensive treatment is more effective than tight
glucose control in reducing cardiovascular events. The
lifetime process of treatment for hypertension32,48,49 and the
need for aggressive lifestyle intervention for the metabolic
syndrome50 highlight the need to identify and treat affected
individuals with a multitargeted approach. Conclusion
The high prevalence of the MS among hypertensive
individuals indicates the need for metabolic screening in allhypertensive patients at the first diagnosis. In addition,
the pathogenesis of hypertension may be different between
considering that lifestyle modification is suggested as the
men and women, and that hypertension in women may be
first-line therapy of MS,50,51 the findings of the present
more dependent on insulin resistance than in men. Contrary
study emphasise the need to implement community-based
to their findings, an experimental study found that insulin
programmes for lifestyle changes with regard to the
resistance was associated with hypertension in male rats
modifiable predisposing factors of high blood pressure and
the importance of controlling high blood pressure and
In the study by Vazquez Vigoa et al,45 62% of hypertensive
subjects were found to have MS, with a significantassociation with vascular damage. However, most available
Acknowledgements
studies do not answer the question regarding the clinical
The Isfahan Healthy Heart Programme (IHHP) is
significance of the MS in hypertension. The recent
supported by a grant (No. 31309304) from the Iranian
prospective study by Schillaci et al46 provides evidence that
Budget and Programming Organization, the Deputy of
the MS may be useful as an integrating index on the overall
Health of the Ministry of Health and Medical Education in
burden imposed by metabolic factors on the cardiovascular
the Islamic Republic of Iran, Isfahan Cardiovascular
system in hypertensive patients. Their findings suggest that
Research Centre and Isfahan Provincial Health Center,
the MS represents a strong, independent risk factor for
both affiliated to the Isfahan University of Medical Sciences.
future CVD in hypertensive patients. They concluded that
We thank the personnel of the Isfahan and Arak Provincial
The Metabolic Syndrome and Hypertension—R Kelishadi et al
Health offices for their cooperation. We would also like to
populations. J Clin Epidemiol 1990;43:1369-78.
thank Dr Asgary, Head of the Basic Science Unit and Dr
17. Muller DC, Elahi D, Pratley RE, Tobin JD, Andres R. An epidemiological
test of the hyperinsulinemia-hypertension hypothesis. J Clin Endocrinol
Naderi, Head of Laboratories of the Isfahan Cardiovascular
Research Centre, Dr Ajami, the laboratory supervisor, and
18. Ferrannini E, Buzzigoli G, Bonadonna R, Giorico MA, Oleggini M,
all members of the Computer Unit and laboratories of the
Graziadei L, et al. Insulin resistance in essential hypertension. N Engl J
Isfahan Cardiovascular Research Centre for their assistance.
19. Shen DC, Shieh SM, Fuh MM, Wu DA, Chen YD, Reaven GM.
WHO has designated this project as a model in the
Resistance to insulin-stimulated-glucose uptake in patients with
region; it is indexed as code No. 86 in the Canadian Heart
hypertension. J Clin Endocrinol Metab 1988;66:580-3.
Health Promotion projects: www.med.mun.ca/g8heart
20. Howard BV, Lee ET, Yeh JL, Go O, Fabsitz RR, Devereux RB, et al.
Hypertension in adult American Indians. The Strong Heart Study. Hypertension 1996;28:256-64.
21. Pollare T, Lithell H, Berne C. Insulin resistance is a characteristic feature
of primary hypertension independent of obesity. Metabolism1990;39:167-74.
22. Edwards KL, Burchfiel CM, Sharp DS, Curb JD, Rodriguez BL, Fujimoto
1. Grundy SM. Hypertriglyceridemia, insulin resistance, and the metabolic
WY, et al. Factors of the insulin resistance syndrome in nondiabetic and
syndrome. Am J Cardiol 1999;83:25F-29F.
diabetic elderly Japanese-American men. Am J Epidemiol 1998;147:
2. Park YW, Zhu S, Palaniappan L, Heshka S, Carnethon MR, Heymsfield
SB. The metabolic syndrome: prevalence and associated risk factor
23. Zimmet PZ, Collins VR, Dowse GK, Alberti KG, Tuomilehto J, Knight
findings in the US population from the Third National Health and
LT, et al. Is hyperinsulinaemia a central characteristic of a chronic
Nutrition Examination Survey, 1988-1994. Arch Intern Med
cardiovascular risk factor clustering syndrome? Mixed findings in Asian
Indian, Creole and Chinese Mauritians. Diabet Med 1994;11:388-96.
3. Lakka HM, Laakssonen DE, Lakka TA, Niskanen LK, Kumpusalo E,
24. Reaven GM. Role of insulin resistance in human disease (syndrome X):
Tuomilehto J, et al. The metabolic syndrome and total and cardiovascular
an expanded definition. Annu Rev Med 1993;44:121-31.
disease mortality in middle-aged men. JAMA 2002;288:2709-16.
25. World Health Organization, Eastern Mediterranean Regional Office,
4. Oh JY, Hong YS, Sung YA, Barrett-Connor E. Prevalence and factor
prevention and control of cardiovascular disease. Alexandria, Egypt
analysis of metabolic syndrome in an urban Korean population. Diabetes
26. Zali M, Kazem M, Masjedi MR. Health and Disease in Iran,
5. Bjorntorp P, Holm G, Rosmond R, Folkow B. Hypertension and the
Tehran: Deputy of Research Ministry of Health, 1993. Bulletin No.1 (in
metabolic syndrome: closely related central origin? Blood Press
27. Sarraf-Zadegan N, Boshtam M, Rafiei M. Risk factors for coronary
6. Anderson EA. Insulin and the sympathetic nervous system. Int J Obes
artery disease in Isfahan, Iran. Eur J Pub Health 1999;9:20-6.
28. Sarraf-Zadegan N, Sadri G, Malek-Afzali H, Baghaei M, Mohammadi
7. Verma S, Bhanot S, McNeill JH. Sympathectomy prevents fructose-
Fard N, Shahrokhi S, et al. Isfahan Healthy Heart Programme: a
induced hyperinsulinemia and hypertension. Eur J Pharmacol
comprehensive integrated community-based programme for
cardiovascular disease prevention and control. Design, methods and
8. De Fronzo RA, Goldberg M, Agus A. The effects of glucose and insulin
initial experience. Acta Cardiol 2003;58:309-20.
on renal electrolyte transport. J Clin Invest 1976;58:83-90.
29. World Health Organization. Obesity: Preventing and Managing the
9. Verma S, Bhanot S, McNeill JH. Decreased vascular reactivity in
Global Epidemic. Report of a WHO Consultation on Obesity. Geneva,
metformin-treated fructose-hypertensive rats. Metabolism 1996;45:
Switzerland: World Health Organization, 1998.
30. Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration
10. Galipeau D, Arikawa E, Sekirov I, McNeill JH. Chronic thromboxane
of low-density lipoprotein cholesterol in plasma without use of the
synthase inhibition prevents fructose induced hypertension. Hypertension
preparative ultracentrifuge. Clin Chem 1972;18:499-502.
31. National Institutes of Health, Third Report of The National Cholesterol
11. Reaven GM, Lithell H, Landsberg L. Hypertension and associated
Education Program Expert Panel on Detection, Evaluation, and Treatment
metabolic abnormalities – the role of insulin resistance and the
of High Blood Cholesterol in Adults (Adult Treatment Panel III),
sympathoadrenal system. N Engl J Med 1996;334:374-81.
National Institutes of Health, Bethesda, MD, 2001, NIH Publication
12. Every NR, Boyko EJ, Keane EM, Marshall JA, Rewers M, Hamman RF.
Blood pressure, insulin, and C-peptide levels in San Luis Valley,
32. Chobanian AV, Bakris GL, Black HR, Cushman WC, Green
Colorado. Diabetes Care 1993;16:1543-50.
LA, Izzo JL Jr, et al; National Heart, Lung, and Blood Institute Joint
13. Manolio TA, Savage PJ, Burke GL, Wagenknecht LE, Sidney S, Jacobs
National Committee on Prevention, Detection, Evaluation,
DR Jr, et al. Association of fasting insulin with blood pressure and lipids
and Treatment of High Blood Pressure; National High Blood
in young adults: the CARDIA Study. Arteriosclerosis 1990;10:430-36.
Pressure Education Program Coordinating Committee. The
14. Chen CH, Tsai ST, Chuang JH, Chang MS, Wang SP, Chou P. Population-
Seventh Report of the Joint National Committee on Prevention, Detection,
based study of insulin, C-peptide and blood pressure in Chinese with
Evaluation, and Treatment of High Blood Pressure: the JNC 7 report.
normal glucose tolerance. Am J Cardiol 1995;76:585-8.
JAMA 2003;289:2560-72. Erratum in: JAMA 2003;290:197.
15. Dowse GK, Collins VR, Alberti KG, Zimmet PZ, Touomilehto J, Chiston
33. Zavaroni I, Mazza S, Dall’Aglio E, Gasparini P, Passeri M, Reaven GM.
P, et al; the Mauritius Non-communicable Disease Study Group. Insulin
Prevalence of hyperisulinaemia in patients with high blood pressure. J
and blood pressure levels are not independently related in Mauritians of
Asian Indian, Creole or Chinese origin. J Hypertens 1993;11:297-307.
34. Lind L, Berne C, Lithell H. Prevalence of insulin resistance in essential
16. Collins VR, Dowse GK, Finch CF, Zimmet PZ. An inconsistent
hypertension. J Hypertens 1995;13:1457-62.
relationship between insulin and blood pressure in three Pacific island
35. Vega GL. Results of expert meetings: obesity and cardiovascular disease.
The Metabolic Syndrome and Hypertension—R Kelishadi et al
Obesity, the metabolic syndrome, and cardiovascular disease. Am Heart
43. Koutis AD, Lionis CD, Isacsson A, Jakobsson A, Fioretos M, Lindholm
36. Onat A, Ceyhan K, Basar O, Erer B, Toprak S, Sansoy V. Metabolic
LH. Characteristic of the “metabolic syndrome X” in a cardiovascular
syndrome: major impact on coronary risk in a population with low
risk population in Crete. Eur Heart J 1992;13:865-71.
cholesterol levels: a prospective and cross-sectional evaluation.
44. Galipeau DM, Yao L, McNeill JH. Relationship among hyperinsulinemia,
insulin resistance, and hypertension is dependent on sex. Am J Physiol
37. Choi KM, Lee J, Kim KB, Kim DR, Kim SK, Shin DH, et al. Factor
analysis of the metabolic syndrome among elderly Koreans the South-
45. Vasquez Vigoa A, Vasquez Cruz A, Calderin RO, Buchaca EF, Cruz
West Seoul Study. Diabetes Med 2003;20:99-104.
Alvarez NM, Jimenez Paneque R, et al. Metabolic syndrome in patients
38. Saad MF, Lillioja S, Nyomba BL, Castillo C, Ferraro R, De Gregorio M,
with essential hypertension (Spanish). Nefrologia 2003;23:423-31.
et al. Racial differences in the relation between blood pressure and
46. Schillaci G, Pirro M, Vaudo G, Gemelli F, Marchesi S, Porcellati C, et
insulin resistance. N Engl J Med 1991;324:733-9.
al. Prognostic value of the metabolic syndrome in essential hypertension.
39. Ford ES, Giles WH, Dietz WH. Prevalence of metabolic syndrome
among US adults: findings from the third National Health and Nutrition
47. Christ M, Klima T, Maisch B. Arterial hypertension and metabolic
Examination Survey. JAMA 2002;287:356-9.
syndrome (German). Herz 2003;28:647-85.
40. Azizi F, Salehi P, Etemadi A, Zahedi-Asl S. Prevalence of metabolic
48. Opie LH, Schall R. Old anti-hypertensives and new diabetes. J Hypertens
syndrome in an urban population: Tehran Lipid and Glucose Study.
Diabetes Res Clin Pract 2003;61:29-37.
49. Scott CL. Diagnosis, prevention, and intervention for the metabolic
41. Chen CH, Lin KC, Tsai ST, Chou P. Different association of hypertension
syndrome. Am J Cardiol 2003;92(suppl):35i-42i.
and insulin-related metabolic syndrome between men and women in
50. Natali A, Ferrannini E. Hypertension, insulin resistance, and the metabolic
8437 nondiabetic Chinese. Am J Hypertens 2000;13:846-53.
syndrome. Endocrinol Metab Clin North Am 2004;33:417-29.
42. Haffner SM, Valdez RA, Hazuda HP, Mitchell BD, Morales PA, Stern
51. Scheen AJ. Management of the metabolic syndrome. Minerva Endocrinol
MP. Prospective analysis of the insulin resistance syndrome (syndrome
Eesti ravimistatistika 2006-2009, lk 30-34 Estonian Statistics on Medicines 2006-2009, pp. 30-34 Diabeediravimite kasutamine Eestis Use of Drugs used in Diabetes Endocrinologist, doctor of medicine, Endocrinology Estonia has not been left untouched by the world-puutumata jäänud ka Eesti. See kajastub wide epidemic of diabetes. It is reflected in the süstitavate ja suukaudset