Submit manuscript...
Journal of
eISSN: 2373-4396

Cardiology & Current Research

Research Article Volume 8 Issue 3

Risk Factors Associated with Acute Coronary Syndrome in Northern Saudi Arabia

Shrafeldin M Alhassan,1 Hussain Gadelkarim Ahmed,1 Bassam Ahmed Almutlaq,1 Abdullah Abdulmohsen Alanqari,1 Rawaby Khalid Alshammari,1 Khalid Turki Alshammari,1 Huwayt Abdualmohseen Alshammari,1 Joharah lssa Almubrad,2 Husain Alturkistani,3 Majed Zannon Turkustani,4 Abdulmalik Hassan Alsabban4

1College of Medicine, University of Hail, Kingdom of Saudi Arabia
2College of Medicine, King Saud University, Kingdom of Saudi Arabia
3Department of Radiology and Medical Imaging, College of Medicine, King Saud University, Kingdom of Saudi Arabia
4Baterjy Medical College, Kingdom of Saudi Arabia

Correspondence: Hussain Gadelkarim Ahmed, College of Medicine, University of Hail, Kingdom of Saudi Arabia

Received: February 06, 2017 | Published: February 27, 2017

Citation: Alhassan SM, Ahmed HG, Almutlaq BA, Alanqari AA, Alshammari RK, et al. (2017) Risk Factors Associated with Acute Coronary Syndrome in Northern Saudi Arabia. In Search of a Perfect Outfit. J Cardiol Curr Res 8(3): 00281. DOI: 10.15406/jccr.2017.08.00281

Download PDF

Abstract

Objective: The aim of this study was to find out the common risk factors associated with Acute Coronary Syndrome (ACS) in Northern Kingdom of Saudi Arabia (KSA).

Methodology: One hundred and fifty six patients with ACS were investigated in intensive care unit (ICU), at cardiac center in King Khalid Hospital, in northern KSA, city of Hail. 

Results: Risk factors for ACS including; Hypertension, Ischemic Heart Disease (IHD), Smoking, Diabetes Miletus (DM), and Dyslipidemia were found in 68.6%, 34.6%, 20.5%, 59% and 83.3% of the patients, respectively.

Conclusion: The most common risk factors for ACS in northern KSA (Hail region) were dyslipidemia and hypertension. These favored the urgent need for intervention and control, which lower the burden of ACS.

Keywords: Acute Coronary Syndrome; Unstable angina; NSTEMI; STEMI

Introduction

ACS is a group of clinical symptoms well-matched with acute myocardial ischemia, representing the most important cause of death worldwide, with a great clinical and financial impact. The clinical types of ACS includes unstable angina and acute myocardial infarction (AMI) with or without ST-segment elevation [1].

The mechanism of ACS includes a complicated interaction among the endothelium, the inflammatory cells, and the thrombogenicity of the blood [2,3]. Angiographically, non-critical coronary lesions (<50% stenosis in the diameter of the vessel) may be accompanied with abrupt progression to severe or complete occlusion and may ultimately account for two-thirds of cases of ACS [4,5]. Factors such as, the severity of the plaque rupture, the lipid and tissue factor content of the plaque, the degree of inflammatory reactions at the site, and the blood flow in the area, are important in monitoring the amount of thrombus formation which defining whether a given plaque rupture will cause ACS [6-8]. Previous studies using intravascular ultrasonography have revealed that at least 80% of patients with ACS display multiple plaque ruptures distinct from the culprit lesion [9].

There are many modifiable risk factors for ACS. Most risk factors that initiate cardiovascular disease have genetic, physiologic, behavioral, and environmental components. Non-modifiable risk factors include age, genetics, and gender. Modifiable risk factors comprise smoking, dyslipidemia, hypertension, and diabetes, with obesity and metabolic syndrome are commonly involved [10-12]. The Saudi Project for assessment of coronary events recruited patients admitted with ACS from 17 hospitals in KSA from 2005 to 2007. A total of 4523 patients with ACS were investigated, of whom 905 (20%) had Congestive Heart Failure (CHF) [13]. With a lack of studies from KSA regarding ACS, Saudi population has diverse racial, socioeconomic, and demographic characteristics which might be risk factors for ACS in different KAS regions. Therefore, the aim of the present study was to assess risk factors associated with Acute Coronary Syndrome in Northern Saudi Arabia.

Materials and Methods

This is a retrospective descriptive study conducted in coronary care unit (CCU) at King Khalid Hospital-cardiac Centre, Hail, KSA. One thousand and nine hundred patients were referred to cardiac Centre during one year time, with suspected cardiac diseases. One hundred and fifty six patients were categorized as having acute coronary syndrome (ACS) and were further included as study subjects (cases). Records regarding patients with ACS were retrieved from patient’s files in CCU. The diagnosis of ACS was based on physical examination, electrocardiography, radiologic tests, cardiac biomarker estimations and patient’s history. On diagnosis ACS, ACS was further categorized into unstable angina (UA), none-ST-segment elevation myocardial infarction (NSTEMI), and ST-segment elevation myocardial infarction (STEMI). Data regarding the underlying risk factors such as a positive family history, diabetes mellitus, smoking, hypertension, dyslipidemia and demographical characteristics, complications and outcome were also revised.

Statistical analysis

Data management was done using Statistical Package for Social Sciences (SPSS version 16). SPSS was used for analysis and to perform Pearson Chi-square test for statistical significant (P value P<0.5). The 95% confidence level and confidence intervals were used.

Ethical consent

The protocol of the present study was approved by the ethical committee at College of Medicine, University of Hail. The informed consent was agreed about by Pulmonary Medicine Department at King Khalid Hospital. All procedures performed this study were in accordance with the ethical standards of the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Results

The current study investigated 156 patients with ACS, their age ranging from 27 to 90 years with a mean age of 59 years old.  Of the 156 patients, 130/156 (83.3%) were males and 26/156(16.7%) were females, giving males' females' ratio of 5.00:1.00. Most of the patients (both males and females) were diagnosed with STEMI followed by NSTEMI and UA, representing 83/156(53.2%), 43/156(27.6%), 30/156(19.2%), in this order. The males and females constituted 69/83(83%) & 14/83(17%), 38/43(88.4%) & 5/43(11.6%) and 25/30(83.3%) & 5/30(16.7%) of STEMI, NSTEMI and AU, respectively. Saudi civilian represent the majority of cases 137/156(87.8%). Of the 137 Saudi patients 74/137(54%), 39/137(28.5%) and 24/137(17.5%), were found with STEMI, NSTEMI and UA, respectively. Non-Saudi patients represented 19/156(12.2%). Among non-Saudi patients, most of the patients were detected with STEMI constituting 9/19(47.4%) followed by UA and NSTEMI, representing 6/19(31.6%) and 4/19(21%), respectively, as indicated in Table 1 and Figure 1.

Variable

Category

UA

NSTEMI

STEMI

Total

Sex

Males

23

38

69

130

Females

7

5

14

26

Total

30

43

83

156

Nationality

Saudi

24

39

74

137

Non-Saudi

6

4

9

19

Age

<45 years

3

8

18

29

46-55

11

9

14

34

56-65

8

13

27

48

66-75

4

11

14

29

76+

4

2

10

16

Table 1: Distribution of ACS by Demographical characteristics.

Figure 1: Description of the ACS by Sex and Nationality.

In regard to the age, most of the cases of ACS were found among age group 56-65 years constituted 48/156(30.8%) followed by 46-55years and (both 66-75 and <45 years), representing 34/156(22%) and 29/156(19%), in this order, as indicated in Table 1 and Figure 2.

Figure 2: Description of the ACS by age.

Table 2, summarizes the relationship between ACS and risk factors (Hypertension, IHD and Smoking). Hypertension was found in 107/156(68.6%) of the patients. Of the 107 patients, 53/107(49.5%), 28/107(26%) and 26/107(24.5%) were identified with STEMI, NSTEMI and UA, respectively. Ischemic Heart Disease (IHD) was found in 54/156(34.6%) of the patients. Of the 54 patients, 19/54(35%), 19/54(35%) and 16/54(30%) were identified with UA, NSTEMI, and STEMI, respectively. Tobacco smoking was identified in 32/156(%) of the patients. Of the 32 patients, 16/32(50%), 11/32(34.4%) and 5/32(15.6%) were identified with STEMI, NSTEMI and UA, respectively, as indicated in Table 2 and Figure 3.

Variable

Category

UA

NSTEMI

STEMI

Total

P value

Hypertension

Yes

26

28

53

107

No

4

15

30

49

0.001

Total

30

43

83

156

IHD

Yes

19

19

16

54

No

11

24

67

102

Smoking

Yes

5

11

16

32

No

25

32

67

124

Table 2: Distribution of ACS by Hypertension, IHD and Smoking.

Figure 3: Description of the ACS by Hypertension, IHD and Smoking.

Table 3 summarizes the distribution of ACS by family history of IHD, DM and Dyslipidemia. Family history of IHD was identified in 10/156(6.4%) patients of whom 5/10(50%) were found with NSTEMI and 5/10(50%) with STEMI. DM was identified in 92/156(59%). Of the 92 diabetic patients with ACS, STEMI, NSTEMI and UA were revealed in 47/92(51%), 27/92(29.4%) and 18/92(19.6%), respectively. Dyslipidemia was specified in 130/156(83.3%) patients of whom, STEMI, NSTEMI and UA were determined in 71/130(54.6%), 37/130(28.4%) and 22/130(17%), in this order as indicated in Table 3 and Figure 4.

Variable

Category

UA

NSTEMI

STEMI

Total

Family History (IHD)

Yes

0

5

5

10

No

30

38

78

146

Total

30

43

83

156

DM

Yes

18

27

47

92

No

12

16

36

64

Dyslipidemia

Yes

22

37

71

130

No

8

6

12

26

Table 3: Distribution of ACS by Family history of IHD, DM and Dyslipidemia.

Figure 4: Description of the ACS by Family history of IHD, DM and Dyslipidemia.

Discussion

In the present study we found high proportions of different risk factors that associated with various categories of ACS.  The most common factors were sex, age hypertension, IHD, smoking, DM, and dyslipidemia. In the current study dyslipidemia scored 83.3% of the patients with ACS and this was the highest percentage among these risk factors. The great majority of patients with ACS in the current study were elderly males. Such relationship (the occurrence of ACS in elderly men) were well established in several studies [14]. In the present study, most of the males were found with STEMI, followed by NSTEMI and unstable angina respectively. On the other hand, most of the females were observed with STEMI but followed by UA. Compared to men, women with high-risk for ACS undergo less coronary angiography, and angioplasty. Further more women do not have higher incidence of cardiovascular death, recurrent MI, or stroke, thus, they undergo a higher rate of refractory ischemia and re-hospitalization [15]. It was documented that about 33% of all ACS episodes happen in patients over 75 years old and account for approximately 60% of total mortality due to ACS [16-18]. The incidence of ACS in the elderly is expected to rise due to improvements in prior ACS treatment in an aging population [18].   

However, the presentation of dyslipidemia among patients with ACS, differ in different studies, which may indicate some sort of demographical factors influence. Moreover, the majority of cases of dyslipidemia were found with STEMI followed by NSTEMI. May studies have shown that dyslipidemia is one the major risk factors which is extensively prevalent in patients with ACS and is more predominant in males than in females [20]. In a study investigated the rate of incidence, clinical and angiographic characteristics, and long-term clinical outcome of ACS in Swiss hospitals. Current smoking (81%) and dyslipidemia (59%) were the most common risk factors [21,22].

Hypertension (68.6%) was one of the prominent risk factors in the present study. Notably, the great majority of patients with hypertension were found with STEMI followed by NSTEMI. In general, the prevalence of hypertension rises progressively with age in both men and women and ac as strong risk factor for ACS [23]. A previous study revealed a 63.4% prevalence of hypertension among ACS patients [24]. However, in patients with acute myocardial infarction (AMI), the prevalence of hypertension varies from 31 to 59% [25]. A recent study from Barazil has reported that the main risk factors were arterial hypertension (68%), smoking (67%), and dyslipidemia (43%) [26].

Our study revealed a 59% prevalence of DM among ACS patients. DM is a major independent risk factor for acute coronary syndrome (ACS). Diabetic patients with ACS suffer from higher mortality compared to their nondiabetic peers [27]. The presence of type 2 DM extends the risks associated with ACS, increasing the risk of recurrent cardiovascular events (CVEs) and doubling the risk of death. Managing cardiovascular risk factors has slight outcome on lowering the mortality risk in patients with type 2 DM [28]. According to proof obtained from large epidemiological studies, an incidence rate of ACS in diabetics is 2-3 times higher than in general population [29].

Our study revealed a 59% prevalence of history of IHD among ACS patients. At definite time periods following ischemic stroke (IS), ACS as IHD represents a higher risk of death than IS. Not all IS patients can undergo specific examination for IHD detection. IS patients are mostly endangered by stroke recurrence in the first 2 years after the onset of IS [30]. After this period, coronary death due to IHD, is the leading cause of the long-term mortality in IS patients, with an incidence of 1.5–5.4% [31]. Consequently, excessive efforts are dedicated to IHD identification and its proper management [32]. The majorities of initial presentations of CVD are neither AMI nor IS, yet most primary prevention studies focus on these presentations. Sex has divergent associations with diverse CVDs, with consequences for risk prediction and management strategies [33].

The present study has shown a 20.5% prevalence of DM among ACS patients. Smokers were more commonly diagnosed with ST-segment elevation MI (46.0%) than former smokers (27.4%) and non-smokers (30.2%) (P<0.001). Smokers were habitually men, were younger and more aggressively treated than ex-smokers and non-smokers through the three acute coronary syndrome groups [34]. Family history of IHD was identified in 6.4% of the patients ACS. Although, there is a debate about the role of positive family history as an independent risk factor for coronary artery disease, it was reported that, positive family history is a major risk factor for coronary artery disease which intensely predisposes to the atherosclerotic development at younger ages; therefore, these patients should be assessed and managed more intensively for other risk factors [35]. Family history of coronary heart disease (CHD) is a well-established risk factor for CHD. Nevertheless, the prognostic association of family history has not been proven evidently in patients with AMI [36].

Conclusion

There is substantial association of conventional CV risk factors, such as, dyslipidemia, hypertension, diabetes and  smoking with ACS, and the high prevalence of these risk factors, mainly in relatively younger individuals, demands rapid consideration, and implementation of prevention programs to reduce the burden of CV morbidity and mortality in Northern Saudi Arabia, Hail Region.

References

  1. Teich V, Piha T, Fahham L, Squiassi HB, Paloni Ede M, et al. (2015) Acute Coronary Syndrome Treatment Costs from the Perspective of the Supplementary Health System. Arq Bras Cardiol 105(4): 339-344.
  2. Naghavi M, Libby P, Falk E, Casscells SW, Litovsky S, et al. (2003) From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: part I. Circulation 108(14): 1664-1672.
  3. Naghavi M, Libby P, Falk E, Casscells SW, Litovsky S, et al. (2003) From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: part II. Circulation 108(15): 1772-1778.
  4. Lüscher TF, Tanner FC, Noll G (1996) Lipids and endothelial function: effects of lipid-lowering and other therapeutic interventions. Curr Opin Lipidol 7(4): 234-240.
  5. Chen L, Chester MR, Crook R, Kaski JC (1996) Differential progression of complex culprit stenoses in patients with stable and unstable angina pectoris. J Am Coll Cardiol 28(3): 597-603.
  6. Moreno PR, Bernardi VH, López-Cuéllar J, Murcia AM, Palacios IF, et al. (1996) Macrophages, smooth muscle cells, and tissue factor in unstable angina: implications for cell-mediated thrombogenicity in acute coronary syndromes. Circulation 94(12): 3090-3097.
  7. Fosang AJ, Smith PJ (2001) Human genetics: to clot or not. Nature 413(6855): 475-476.
  8. König A, Klauss V (2011) Intravascular ultrasound for recognition of atherosclerotic plaques and plaque composition. Current state of the diagnostic value. Herz 36(5): 402-409.
  9. Rioufol G, Finet G, Ginon I, André-Fouët X, Rossi R, et al. (2002) Multiple atherosclerotic plaque rupture in acute coronary syndrome: a three-vessel intravascular ultrasound study. Circulation 106(7): 804-808.
  10. Thompson A, Gao P, Orfei L, Watson S, Di Angelantonio E, et al. (2010) Lipoprotein-associated phospholipase A(2) and risk of coronary disease, stroke, and mortality: collaborative analysis of 32 prospective studies. Lancet 375(9725): 1536-1544.
  11. Richard Kones (2011) Primary prevention of coronary heart disease: integration of new data, evolving views, revised goals, and role of rosuvastatin in management. A comprehensive survey. Drug Des Devel Ther 5: 325-380.
  12. Cziraky MJ, Reddy VS, Luthra R, Xu Y, Wilhelm K, et al. (2015) Clinical outcomes and medication adherence in acute coronary syndrome patients with and without type 2 diabetes mellitus: a longitudinal analysis 2006-2011. J Manag Care Spec Pharm 21(6): 470-477.
  13. Albackr HB, Alhabib KF, Ullah A, Alfaleh H, Hersi A, et al. (2013) Prevalence and prognosis of congestive heart failure in Saudi patients admitted with acute coronary syndrome (from SPACE registry). Coron Artery Dis 24(7): 596-601.
  14. Bentley-Lewis R, Aguilar D, Riddle MC, Claggett B, Diaz R, et al. (2015) Rationale, design, and baseline characteristics in Evaluation of LIXisenatide in Acute Coronary Syndrome, a long-term cardiovascular end point trial of lixisenatide versus placebo. Am Heart J 169(5): 631-638.e7.
  15. Anand SS, Xie CC, Mehta S, Franzosi MG, Joyner C, et al. (2005) Differences in the management and prognosis of women and men who suffer from acute coronary syndromes. J Am Coll Cardiol 46(10): 1845-1851.
  16. Goldberg RJ, McCormick D, Gurwitz JH, Yarzebski J, Lessard D, et al. (1998) Age-related trends in short- and long-term survival after acute myocardial infarction: a 20-year population-based perspective (1975–1995). Am J Cardiol 82(11): 1311-1317.
  17. Roger VL, Jacobsen SJ, Weston SA, Goraya TY, Killian J, et al. (2002) Trends in the incidence and survival of patients with hospitalized myocardial infarction, Olmsted County, Minnesota, 1979 to 1994. Ann Intern Med 136(5): 341-348.
  18. Alexander KP, Roe MT, Chen AY, Lytle BL, Pollack CV, et al. (2005) CRUSADE Investigators. Evolution in cardiovascular care for elderly patients with non-ST–segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative. J Am Coll Cardiol 46(8): 1479-1487.
  19. CDC Public health and aging: trends in aging: United States and worldwide (2003). MMWR 52(6): 101-106.
  20. Mohamed Fawzy, Addulla Abdelaziz (2014) Prevalence and Pattern of Dyslipidemia in Acute Coronary Syndrome Patients Admitted to Medical Intensive Care Unit in Zagazig University Hospital, Egypt. World Journal of Medical Research 20(3).
  21. Yusuf S, Hawken S, Ounpuu S, Dans T, Avezum A, et al. (2004) Effect of potentially modifiable risk factors associated with MI in 52 countries (the INTERHEART study): case-control study. Lancet 364(9438): 937-952.
  22. Puricel S, Lehner C, Oberhänsli M, Rutz T, Togni M, et al. (2013) Acute coronary syndrome in patients younger than 30 years--aetiologies, baseline characteristics and long-term clinical outcome. Swiss Med Wkly 143: w13816.
  23.  Picariello C, Lazzeri C, Attanà P, Chiostri M, Gensini GF, et al. (2011) The Impact of Hypertension on Patients with Acute Coronary Syndromes. Int J Hypertens 2011: 563657.
  24. Maria Dorobantu, Oana-Florentina Tautu, Ana Fruntelata, Lucian Calmac, Gabriel Tatu-Chitoiu, et al. (2014) Hypertension and acute coronary syndromes in Romania: data from the ISACS-TC registry. European Heart Journal Supplements 16(Suppl A), A20-A27.
  25. Willich SN, Müller-Nordhorn J, Kulig M, Binting S, Gohlke H, et al. (2001) PIN Study Group. Cardiac risk factors, medication, and recurrent clinical events after acute coronary disease; a prospective cohort study. Eur Heart J 22(4): 307-313.
  26. Soeiro Ade M, Fernandes FL, Soeiro MC, Serrano Jr CV, Oliveira Jr MT (2015) Clinical characteristics and long-term progression of young patients with acute coronary syndrome in Brazil. Einstein (Sao Paulo) 13(3): 370-375.
  27. Sethi SS, Akl EG, Farkouh ME (2012) Diabetes mellitus and acute coronary syndrome: lessons from randomized clinical trials. Curr Diab Rep 12(3): 294-304.
  28. Cziraky MJ, Reddy VS, Luthra R, Xu Y, Wilhelm K, et al. (2015) Clinical outcomes and medication adherence in acute coronary syndrome patients with and without type 2 diabetes mellitus: a longitudinal analysis 2006-2011. J Manag Care Spec Pharm 21(6): 470-477.
  29. Ametov AS, P'ianykh OP, Aslandziia EN (2011) Acute coronary syndrome in patients with type 2 diabetes mellitus. Ter Arkh 83(9): 66-70.
  30. Kovacik M, Madarasz S, Bartko D, Pesta M, Herzig R, et al. (2010) Cievna mozgova prihoda a ischemicka choroba srdca. Cesk Slov Neurol N 73: 497-502.
  31. Diener HC, Cunha L, Forbes C, Sivenius J, Smets P, et al. (1996) European stroke prevention study 2, dipyridamole and acetylsalicylic acid in the secondary prevention of stroke. J Neurol Sci 143(1-2): 1-13.
  32. Griva M, Naplava R, Spendlikova M, Jarkovsky J, Hlinomaz O, et al. (2010) Potential role of selected biomarkers for predicting the presence and extent of coronary artery disease. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 154(3): 219-225.
  33. George J, Rapsomaniki E, Pujades-Rodriguez M, Shah AD, Denaxas S, et al. (2015) How Does Cardiovascular Disease First Present in Women and Men? Incidence of 12 Cardiovascular Diseases in a Contemporary Cohort of 1,937,360 People. Circulation 132(14): 1320-138.
  34. Himbert D, Klutman M, Steg G, White K, Gulba DC (2005) Cigarette smoking and acute coronary syndromes: a multinational observational study. Int J Cardiol 100(1): 109-117.
  35. Hoseini K, Sadeghian S, Mahmoudian M, Hamidian R, Abbasi A (2008) Family history of cardiovascular disease as a risk factor for coronary artery disease in adult offspring. Monaldi Arch Chest Dis 70(2): 84-87.
  36. Prabhakaran D, Jeemon P (2012) Should your family history of coronary heart disease scare you? Mt Sinai J Med 79(6): 721-732.
Creative Commons Attribution License

©2017 Alhassan, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.