Background: - Globally, cardiovascular diseases (CVD) are the primary cause of death. According to estimates, ischemic heart disease and cerebrovascular illnesses were responsible for 85% of 18 million CVD-related fatalities that occurred globally in 2017. One of the main causative risk factors for atherosclerotic cardiovascular disease is elevated low-density lipoprotein cholesterol (LDL-C). LDL particles can migrate from plasma into the subendothelial region of the artery, where they induce inflammation and lead to the development of atherosclerotic plaques. Thus, LDL-C lowering should be tailored to reach the target objective suggested by guidelines to reduce cardiovascular disease risk. Objective: -Assessment of low-density lipoprotein cholesterol target attainment and associated factors among patients with established coronary heart disease at the cardiology clinic, Tikur Anbessa Specialized Hospital. Methods: - Institutional-based retrospective cross-sectional study design was conducted from August 2023 to October 2023. In this study, among 240 planned participants, 221 participants were extracted, making a chart retrieval rate of 91.7%. Data analysis was done by using SPSS version 26. Multiple regression was applied to identify associated factors. Result: - In this study, about two-thirds of the participants were male, and more than one-third were between the ages of sixty-one and seventy. The level of LDL-C target attainment was 41%. The factors significantly associated with the LDL-C target attainment were male sex (AOR=1.8, 95%CI=1.44, 3.42), hypertension (AOR=0.57, 95%CI=0.31, 0.91), and taking SGLT2 inhibitors (AOR=1.5, 95%CI=1.37, 4.85). Conclusion: The level of LDL-C target attainment was low. Male sex and taking sodium-glucose transporter 2 (SGL2) inhibitors were favorable factors, but hypertension was associated with a low level of LDL target attainment.
Cardiovascular diseases (CVD) are the leading cause of death globally. According to estimates, ischemic heart disease and cerebrovascular illnesses accounted for 85% of the estimated 18 million CVD-related deaths worldwide in 2017 1. About one-third of mortality has decreased as a result of the adoption of healthy lifestyles and pharmaceutical therapies 2, 3. CVD remains the most common cardiac condition seen by cardiologists, affecting roughly half of all heart disease patients 4.
Elevated LDL-C is a significant risk factor for atherosclerotic cardiovascular disease (ASCVD) because LDL particles can form atherosclerotic plaques, which can rupture and lead to ischemia 5, 6. In China, patients with established ASCVD are regarded as extremely high risk, with an LDL-C treatment target of below 70 mg/dL 7. Lowering LDL-C is crucial for reducing ASCVD risk in adults. However, the recent European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS) guidelines advocate for even more aggressive goals: less than 70 mg/dL for high-risk ASCVD patients, less than 55 mg/dL for very high-risk or those with established ASCVD; and less than 40 mg/dL for very high-risk patients who have had a second vascular event within two years 8.
Despite progress in lowering LDL-C and advancing preventive measures, a significant gap remains between treatment goals and achieving LDL-C targets. 9, 10, 11. In Europe, ASCVD accounts for nearly half of all deaths 12. While managing ASCVD benefits from a long-term, team-based approach, many patients still struggle to reach their LDL-C goals 13. This highlights the need for improvement in LDL-C management.
Global studies showed a substantial gap between LDL-cholesterol treatment goals and target achievement. The Dyslipidemia International Study (DYSIS) found that only 21.7% of 44,015 very high-risk patients in 30 countries met their LDL-C target of less than 70 mg/d 14. Similarly, an African study reported that 71% of patients did not reach their target LDL-C levels 15.
There is a lack of data on how Ethiopian patients with established coronary heart disease achieve LDL-C goals according to recent guidelines, particularly for high-risk patients. Therefore, this study aimed to evaluate LDL-C target achievement and related factors in patients with established coronary heart disease at the cardiology clinic of Tikur Anbessa Specialized Hospital.
Study design
An institutional-based cross-sectional study was conducted at the cardiology clinic of Tikur Anbessa Specialized Hospital (TASH), Addis Ababa, Ethiopia, from August 01, 2023–to October 31, 2023, to assess LDL-C target attainment and associated factors among patients with established coronary heart disease. All patients with established coronary heart disease who had cardiac clinic follow-up at TASH during the study period fulfilled the inclusion criteria included in the study. Patients on Lipid-lowering drugs for less than three months and incomplete data were excluded from the study.
Sampling Determination and Sampling Procedures
All patients who fulfilled the eligibility criteria were included in the study, and there was no need for sample size calculation sampling procedures.
Operational definitions
• CHD: ACS and CCS
• ACS: STEMI, NSTEMI), or unstable angina
• CCS: Clinical diagnosis by treating cardiologist (cardiology fellow or cardiologist)
• LDL Target Attainment: We will consider patients to have achieved their LDL target if their LDL level is below 70 mg/dL after three months of statin treatment.
• Statin Therapy Intensity: Statin medications are categorized based on their expected LDL-C reduction:
Low-intensity: This includes daily treatment with Simvastatin 10mg, which is expected to reduce LDL-C by less than 30%.
Moderate-intensity: This includes daily treatment with Simvastatin 20-40mg, Atorvastatin 10-20mg, or Rosuvastatin 5-10mg, and is expected to reduce LDL-C by 30 to 50%.
High-intensity: This includes daily treatment with Atorvastatin 40-80mg or Rosuvastatin 20-40mg and is expected to reduce LDL-C by 50% or more.
• Smoker: history of cigarette smoking (ever smoking)
Study Procedures
The questionnaire was developed by compiling several questions from similar study materials and reviewing relevant literature and articles that could address the study's objective. A questionnaire pre-test was carried out, and modification was done based on feedback from the pre-test. The questionnaire generally included information about sociodemographic characteristics, comorbidity, concomitant drugs, and laboratory results. Data was collected from electronic medical records.
Statistical Analysis
Data was checked and cleaned for completeness and consistency, then coded, entered, and analyzed using SPSS version 26. Simple descriptive analysis was used to show the frequencies and percentages of variables. Bivariate logistic regression examined the association between independent and dependent variables. Those with a p-value less than 0.25 were transferred to multivariate logistic regression. Variables with a p-value <0.05 were declared as having statistical significance.
Socio-demographic characteristics of the study participants
In this study, among 240 planned participants, 221 participants were extracted, making a chart retrieval rate of 91.7%. Most study participants were 61-70 years old, with a mean and SD of 59.64±10.86 years. The majority (63.3%) of the study participants were male, and only 1.3% had a smoking history, as shown in Table 1.
characteristics of coronary heart disease
In this study, 78.3% of the study participants had chronic coronary syndrome at diagnosis, 73.3% of the participants had 1-5 years duration of coronary heart disease, and 11.3% of the CHD patients had primary coronary intervention procedures, as shown in Table 2.
characteristics of comorbid disease
Most (88.7%) of the study participants had comorbid disease. Of those who had the comorbid disease, 63.8% of them had hypertension, 49% of them had diabetes mellitus, 15.8% of them had CKD, and 12.8% had heart failure, as shown in Table 3.
In this study, 93.2% of the study participants took antiplatelets, and of those taking antiplatelets, 87.8% were receiving aspirin. Almost ninety-three percent of the participants received beta-blockers. Of those taking beta blockers, 76.6% used metoprolol, 93.7% of the study participants took ACEI, and 47.5% took spironolactone. Almost thirty-nine percent of the study participants took SGL2 inhibitors, 18.6% received Calcium channel blockers, and 33.5% took oral glucose-lowering agents.
Characteristics of lipid-lowering drugs
All the study participants took lipid-lowering drugs, all lipid-lowering drugs were statin, and 97.3% took atorvastatin. Ninety-two percent of the participants take a high-intensity statin, and 73.8% of the participants were taking a statin for 1-5 years (Table 4).
Level of LDL C target attainment after statin treatment
In this study, a lipid profile was done after 24 months of treatment for 60.2% of participants; 6.2% had ≥200 total cholesterol, and 21.3% had ≥150 triglycerides, as shown in Table 5 and Figure Overall, only 41% of patients achieved LDL-C target.
Factors associated with low-density lipoprotein target attainment.
As shown in Table 6 below, the study participant’s sex, hypertension, and taking SGL2 inhibitors were associated with LDL-C target attainment on bivariate logistic regression. The multivariate logistic regression revealed that being male was associated with a1.6 1.6-fold increase in LDL-C target attainment compared to females (AOR=1.6, 95%CI=1.24, 3.42). Hypertension was associated with a 43% less likelihood of LDL-C target attainment (AOR=0.57, 95%CI=0.31, 0.91). Study participants who took SGLT2iinhibitor had a 1.5-fold increase in LDL-C target attainment compared to those not taking (AOR=1.5, 95% CI=1.37, 4.85).
This study found that the level of LDL-C target attainment was 41%. The factors significantly associated with the LDL-C target attainment were male sex (AOR=1.8, 95%CI=1.44, 3.42), hypertension (AOR=0.57, 95%CI=0.31, 0.91), and taking SGLT2 inhibitors (AOR=1.5, 95%CI=1.37, 4.85).
Hypertension, diabetes mellitus, and CKD were the most common co-morbidities in our study, similar to studies done in Kenya where hypertension, dyslipidemia, and diabetes mellitus were the most prevalent diseases among patients with coronary heart disease 16. The difference in dyslipidemia may be because our study participants had a missing baseline lipid profile.
The finding of this study revealed that 41% of the study participants had good LDL-C target attainment. This finding was higher than the study done in the European Society of Cardiology (36.9%) 17, Thailand (27%) 18, South Africa 19 % 19, Kenya 17.1 % 16, but this is lower than the studies done in Sweden and Canada 52 % 20, Spain 56.7 % 21 and Korea 22 ,and a study done by Groenhaf et al. 23. These differences in LDL-C target attainment rate could be due to different factors related to the study population, such as age, sex, ethnicity, and overall cardiac condition. These factors can all influence how well someone responds to treatment.
Male study participants had a 1.8-fold increase in LDL-C target attainment compared to females (AOR=1.8, 95%CI=1.44, 3.42). This finding was similar to a study done by Groenhaf et al. and a study done in China 23, 24. This may be due to the observation that LDL-C target attainment may differ between males and females in some cases and could be influenced by various factors, especially hormonal influence 25. In other studies, statins are less effective in females than in males and are associated with more side effects and poor adherence due to the pronounced side effects. The other explanation for this unfavorable target attainment for females is that female patients have additional comorbidities than males 26.
In our study, participants with hypertension had 43% LDL-C off target compared to those patients without hypertension (AOR=0.57, 95%CI=0.31, 0.91). This finding is comparable with previous studies 19, 27. This may be due to patients with hypertension who may have metabolic syndrome with dyslipidemia. In many previous studies, hypertension and other metabolic disorders are associated with increased failure to achieve target LDL 22. Patients with metabolic syndrome and hypertension had more difficulty achieving the target LDL levels 19. It is more difficult to achieve target cholesterol levels, especially in patients with obesity and hypertension 28.
Our study showed that patients who took SGLT 2 inhibitors had a lower probability of achieving target LDL with an AOR of 1.5 (95% CI: 1.37, 4.85). Dapagliflozin suppresses potent atherogenic LDL-C and increases HDL-C, a favorable cardiometabolic marker. Although LDL-C levels are increased after using dapagliflozin, this was because of increased concentrations of the less atherogenic lb LDL-C. So, these failures to achieve the target number of LDL could be due to elevated 1b LDL-C 29. SGLT2 inhibitors are effective antihyperglycemic agents by inhibiting glucose reabsorption in the kidney's proximal tubule. Besides improving glycemic control in patients with type 2 diabetes, they also have additional favorable effects, such as lowering body weight and fat 30. Even though the exact mechanisms are unknown, recent studies suggest that SGLT-2 inhibitors could provide extra-glycemic benefits in lipid metabolism. It may pronounce lipolysis, normalizing the lipid metabolism and preventing or improving dyslipidemia 31.
Some studies showed that the achievement of target LDL could be affected by different factors such as statin dose and type, patient-related factors, provider-related factors 29. Treating physicians and concomitant drug use while treating may affect the achievement of target LDL. In contrast, our study found that the intensity of statin was not associated with LDL target attainment.
Managing comorbidities and achieving target levels of LDL-C are crucial to managing cardiovascular health. In our study, most (88.7%) participants had comorbid disease. Of those having comorbid disease, 63.8% of them had hypertension, 49% of them had diabetes mallets, 15.8% of them had CKD, and 12.8% had heart failure; the target levels of LDL can vary based on an individual's risk factors and existing health conditions. Medical guidelines, such as those from organizations like the American College of Cardiology (ACC) and the American Heart Association (AHA), provide recommendations for LDL-C target levels based on risk categories. These guidelines are regularly updated to reflect the latest research findings. Accordingly, in these guidelines, LDL-C <70 was used for target attainment 32.
Strength and limitation
It is the first study to explore secondary LDL-C target attainment in Ethiopia. However, the retrospective nature of the study design presents a limitation. Additionally, lacking baseline LDL-C levels for most patients might inflate the target attainment rate. Finally, while the study considered LDL-C values updated within the past six months, it did not account for the specific duration of statin treatment each participant received. This lack of information could influence the interpretation of target achievement.
In this study, the level of LDL-C target attainment was 41%, which is better than the studies done in Kenya and South Africa but lower than those done in Sweden, Canada, and Spain. Factors significantly associated with LDL-C target attainment were being male (AOR=1.8, 95%CI=1.44, 3.42), and Hypertension (AOR=0.57, 95%CI=0.31, 0.91) and taking SGLT2 Inhibitors (AOR=1.5, 95%CI=1.37, 4.85).
ACEI -angiotensin-converting enzyme inhibitor
ACS -acute coronary syndrome
AF -atrial fibrillation
AOR -adjusted odds ratio
ASCVD -atherosclerotic cardiovascular disease
BPH -benign prostatic hyperplasia
CCS-chronic coronary syndrome
CHD -coronary heart disease
CI -confidence interval
CKD -chronic kidney disease
COR -crude odds ratio
CVD -cardiovascular diseases
DM -diabetes mellitus
DVHD -degenerative valvular heart disease
DYSIS -Dyslipidemia International Study
EAS -European Atherosclerosis Society
ESC -European Society of Cardiology
HDL-C -high-density lipoprotein cholesterol
HIV -human immunodeficiency virus
LDL-C -low-density lipoprotein cholesterol
LV -left ventricle
NAFLD -nonalcoholic fatty liver disease
NSTEMI -non-ST-segment elevation myocardial infarction
PAD -peripheral arterial disease
PTE-pulmonary thromboembolism
SD- standard deviation
SGLT2 inhibitor -sodium-glucose cotransporter-2 inhibitor
STEMI -ST-segment elevation myocardial infarction
TASH -Tikur Anbessa Specialized Hospital
Author Contributions: conceptualization, Methodology, Investigation, Analysis, and Writing of the manuscript- Desalegn Aychiluhm Abate, Senbeta Guteta Abdissa, Zekarias Seifu Ayalew.
Methodology, Data curation, Drafting, Interpretation, and Supervision and edition of the manuscript- Gebeyehu Tessema Azibte, Zelalem Belay Ayele.
All authors revised the manuscript and have approved the final version of the manuscript.
Funding: This research received no external funding.
Institutional Review Board Statement: The study was conducted by the Declaration of Helsinki and approved by the Institutional Review Board of Addis Ababa University, College of Health Sciences.
Informed Consent Statement: Informed consent was obtained from all subjects involved in the study.
Data Availability Statement: The authors confirm that the data supporting the findings of this study are available within the article.
Acknowledgments: Not applicable.
Conflicts of Interest: The authors declare no conflicts of interest.
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Published with license by Science and Education Publishing, Copyright © 2024 Desalegn Aychiluhm Abate, Senbeta Guteta Abdissa, Zekarias Seifu Ayalew, Gebeyehu Tessema Azibte and Zelalem Belay Ayele
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit
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[1] | Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018; 392(10159): 1736-88. | ||
In article | |||
[2] | Hartley A, Marshall DC, Salciccioli JD, Sikkel MB, Maruthappu M, Shalhoub J. Trends in Mortality From Ischemic Heart Disease and Cerebrovascular Disease in Europe: 1980 to 2009. Circulation. 2016; 133(20): 1916-26. | ||
In article | View Article PubMed | ||
[3] | Cordero A, Bertomeu-Martínez V, Mazón P, Fácila L, Cosín J, Bertomeu-González V, et al. Patients with cardiac disease: Changes observed through last decade in out-patient clinics. World J Cardiol. 2013; 5(8): 288-94. | ||
In article | View Article PubMed | ||
[4] | Yusuf S, Joseph P, Rangarajan S, Islam S, Mente A, Hystad P, et al. Modifiable risk factors, cardiovascular disease, and mortality in 155 722 individuals from 21 high-income, middle-income, and low-income countries (PURE): a prospective cohort study. Lancet. 2020; 395(10226): 795-808. | ||
In article | View Article PubMed | ||
[5] | Bentzon JF, Otsuka F, Virmani R, Falk E. Mechanisms of plaque formation and rupture. Circ Res. 2014; 114(12): 1852-66. | ||
In article | View Article PubMed | ||
[6] | Danchin N, Almahmeed W, Al-Rasadi K, Azuri J, Berrah A, Cuneo CA, et al. Achievement of low-density lipoprotein cholesterol goals in 18 countries outside Western Europe: The International ChoLesterol management Practice Study (ICLPS). Eur J Prev Cardiol. 2018; 25(10): 1087-94. | ||
In article | View Article PubMed | ||
[7] | [2016 Chinese guideline for the management of dyslipidemia in adults]. Zhonghua Xin Xue Guan Bing Za Zhi. 2016; 44(10): 833-53. | ||
In article | |||
[8] | Mach F, Baigent C, Catapano AL, Koskinas KC, Casula M, Badimon L, et al. 2019 ESC/EAS guidelines for the management of dyslipidaemias: Lipid modification to reduce cardiovascular risk. Atherosclerosis. 2019; 290: 140-205. | ||
In article | View Article PubMed | ||
[9] | Barrios V, Soronen J, Carter AM, Anastassopoulou A. Lipid management across Europe in the real-world setting: a rapid evidence review. Curr Med Res Opin. 2021; 37(12): 2049-59. | ||
In article | View Article PubMed | ||
[10] | Mensah GA, Wei GS, Sorlie PD, Fine LJ, Rosenberg Y, Kaufmann PG, et al. Decline in Cardiovascular Mortality: Possible Causes and Implications. Circ Res. 2017; 120(2): 366-80. | ||
In article | View Article PubMed | ||
[11] | Moran AE, Forouzanfar MH, Roth GA, Mensah GA, Ezzati M, Murray CJ, et al. Temporal trends in ischemic heart disease mortality in 21 world regions, 1980 to 2010: the Global Burden of Disease 2010 study. Circulation. 2014; 129(14): 1483-92. | ||
In article | View Article PubMed | ||
[12] | Townsend N, Nichols M, Scarborough P, Rayner M. Cardiovascular disease in Europe--epidemiological update 2015. Eur Heart J. 2015; 36(40): 2696-705. | ||
In article | View Article PubMed | ||
[13] | Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C, Catapano AL, et al. 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Eur Heart J. 2016; 37(29): 2315-81. | ||
In article | View Article PubMed | ||
[14] | Gitt AK, Lautsch D, Ferrieres J, Kastelein J, Drexel H, Horack M, et al. Low-density lipoprotein cholesterol in a global cohort of 57,885 statin-treated patients. Atherosclerosis. 2016; 255: 200-9. | ||
In article | View Article PubMed | ||
[15] | Ramjeeth A, Butkow N, Raal FJ, Maholwana-Mokgatlhe M. The evaluation of low-density lipoprotein cholesterol goals achieved in patients with established cardiovascular disease and/or hyperlipidaemia receiving lipid-lowering therapy: the South African Not at Goal study (SA-NAG). Cardiovasc J Afr. 2008; 19(2): 88-94. | ||
In article | |||
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