Literature DB >> 35481326

Prevalence of Self-Reported Muscle Pain Among Statin Users From National Guard Hospital, Riyadh.

Ihab Suliman1, Abdulaziz Batarfi2, Hassan Almohammadi2, Hisham Aljeraisi2, Hassan Alnaserallah2, Ali Alghamdi2.   

Abstract

Background Statin, a hydroxymethylglutaryl-coenzyme A reductase inhibitor, is one of the commonly used lipid-lowering drugs that is used for lowering lipid levels in the body. Muscle pain is a commonly reported adverse effect of statins, yet little is known about the prevalence of muscle pain and statin use in the general population. Methods The cross-sectional study was conducted in National Guard Hospital, Riyadh, Saudi Arabia. All study subjects were adult statin users aged 18 years old or above. A total of 313 patients were included in the study. The study was conducted based on a questionnaire distributed among patients according to inclusion and exclusion criteria. Results Among 313 statin users, patients underwent cardiac catheterization (39, 12.5%), stress test (62; 19.8%), percutaneous coronary intervention (three; 1.0%), and coronary artery bypass graft (six, 1.9%), while 203 patients didn't have any intervention (64.9%). Most of the study subjects were on atorvastatin (139; 44.4%). The prevalence of muscle pain was 73.5%; 95% CI = (68.4% - 78.1%). The most common sites of pain were lower limb pain (160; 51.1%), upper limb pain (145; 46.3%), and trunk pain (96; 30.7%). The common types of pain were joint pain (52; 16.6%), muscle weakness (51; 16.3%), muscle aches (43; 13.7%), and muscle cramps (41; 13.1%); and patients who reported that they stopped statin at some point because of muscle pain were 92 (29.4%). Conclusion Statins are important for managing and preventing ischemic heart diseases. Our study found that muscle pain is highly associated with statin use with a prevalence of 73.5%, which causes many patients to tend to stop taking their medication. Therefore, preventing the side effects by adjusting the proper dose or switching to another type of statin for high-risk patients will help them to continue using the drug. Also, it is important to rule out secondary causes of myopathy such as physical activity, fracture, thyroid dysfunction, or infection.
Copyright © 2022, Suliman et al.

Entities:  

Keywords:  cardiac intervention; ischemic heart disease; muscle pain; rhabdomyolysis; statin

Year:  2022        PMID: 35481326      PMCID: PMC9034880          DOI: 10.7759/cureus.23463

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


Introduction

Ischemic heart disease (IHD) is a common and important disease that must be controlled. Ischemia is defined as a "restriction of blood flow and thus oxygen in a part of the body due to narrowing of the blood vessel." [1]. Coronary artery disease (CAD) narrowing can be caused by a blood clot, constriction of the blood vessel, or as in most cases, caused by a buildup of plaque. When there is a complete obstruction of the blood flow to the cardiac myocytes, the heart muscle cells die, which can result in a heart attack or myocardial infarction (MI) [1]. Most people with slight narrowing of the vessels do not experience symptoms of ischemic heart disease. However, as narrowing progresses, especially if it is untreated, symptoms may occur. They are most likely to occur during exercise or secondary to emotional stress when there is an increase in body demand for oxygen [1]. Nowadays statin is considered standard practice for management after acute coronary syndrome, regardless of lipid levels [2]. Statin, a hydroxymethylglutaryl-coenzyme A (HMG-COA) reductase inhibitor, is one of the antihyperlipidemic drugs used for lowering lipid levels in the body [2]. These drugs appear to inhibit the synthesis or promote the breakdown of cholesterol. They are used to treat hyperlipidemia when non-pharmacological treatment failed to reduce cholesterol levels, and they are used in the prevention and treatment of cardiovascular disease [3, 4]. However, they can be associated with many side effects, such as myalgia, myopathy, rhabdomyolysis, and diabetes mellitus. Therefore, many patients frequently stop statin therapy without medical consultation secondary to the side effects, and therefore they are at higher risk for cardiovascular events [5-7]. Myopathic effect with muscles weakness can occur with a normal or minor increase in creatine kinase (CK). Activity in plasma is observed in some patients receiving statins, frequently associated with heavy physical activity. Rarely, the patient may have a marked elevation in CK activity, often accompanied by generalized discomfort or weakness in skeletal muscles. If the drug is not discontinued, myoglobinuria can occur, leading to serious injury [8-10]. Common factors that will lead to the development of muscle pain include age more than 75 years old, gender, alcohol abuse, renal and hepatic dysfunction, and the use of drugs inhibiting the metabolism of statins such as erythromycin [3]. Moreover, genetic variation in anion-transporting polypeptides 1B1 (OATP1B1) is associated with severe myopathy and rhabdomyolysis induced by statins [11-14]. Globally, there are few studies exploring this problem [15, 16]. For example, a study reported the prevalence of muscle pain to be 27.9% in patients taking statins; as a result, clinicians had to adjust the dose or use alternative statins to minimize the side effects [15]. Another cross-sectional study at the Punjab Institute of Cardiology, Pakistan, reported that 51% of patients had myalgia, that it was more common in patients aged 40-50, and that the female to male ratio was 57:47, showing higher susceptibility in females compared to males [16]. Also, it appears that the prevalence of myalgia and an increase in creatine phosphokinase (CK) levels were dose-related. In other words, an increase in the doses would lead to an increase in muscle-related problems. Also, it has been shown that myalgia is associated with the duration of statin use [16]. There are many details required to be covered in the future, including identifying the dosage of statins that triggers muscles pain. Moreover, there are many subtypes of statin, so we must discover which subtype causes more serious muscle pain than others, and also whether muscle pain is associated with other comorbidities unrelated to statin use or not. These points may be used for the initiation of new studies in the future. Because there is a lack of research in Saudi Arabia about this problem, we are conducting this research to determine the prevalence of self-reported muscle pain among statin users attending National Guard Hospital, Riyadh. Moreover, we will assess the compliance of statin due to self-reported muscle pain, and we will determine which musculoskeletal regions are affected by statin muscle pain.

Materials and methods

Study design and area and settings This is a cross-sectional study to measure the prevalence of self-reported side effects of statins amongst the selected population, conducted in National Guard Hospital, Riyadh, Saudi Arabia. Identification of study participants The study about the prevalence of self-reported muscle pain included 313 patients who were using statins. It included patients on statins who were above 18 years of age with or without cardiac intervention such as cardiac catheterization, coronary artery bypass grafting (CABG), or percutaneous coronary intervention (PCI). We used the non-probability convenient sampling method as we had chosen our study population according to certain characteristics. Data collection process The data was collected using a self-administered questionnaire to patients who are using statins and attending the National Guard Hospital. The questionnaire contained different types of questions to determine the prevalence of a specific side effect of a drug, which region of the body is more susceptible, which drug is being used, and how many patients have stopped using the drug due to this side effect. The questionnaire contained 14 questions, and they were translated into Arabic by group members. The questionnaire was reviewed by experts in the cardiac clinic to test for its content validity and reliability. Also, we used in our questionnaire some questions from Statin Experience Approved Questionnaire [17]. After the translation, the questionnaire was given to 10 people who were not part of the study to check for difficulties in understanding questions and the average time it takes to finish the questionnaire. The awareness was measured quantitatively by the number of questions answered correctly. Finally, the grouping variables chosen were gender, age, and educational level. Data analysis Data was entered and analyzed using SPSS Statistics v. 24.0 (IBM Corp., Armonk, NY). The descriptive statistics were presented as frequency and percentage for the categorical variables e.g. (Gender, education level) and the mean ± SD for numerical variables. Chi-square was used for the association between body pain and patients’ characteristics. A test was significant if p-value < 0.05.

Results

The questionnaire responders were N=313; 163 (52.1%) were males and 150 (47.9%) were females (Table 1). The overall mean age was 55.1±11.5. Among 313 statin users, 39 (12.5%) patients underwent cardiac catheterization, 62 (19.8%) stress echo, three (1.9%) percutaneous coronary intervention, and six (1.9%) coronary artery bypass graft (Table 2), while patients who didn’t have any interventions were 203 (64.9%). Atorvastatin, with 139 (44.4%) users, was the most used drug, followed by rosuvastatin (44; 14.1%), and simvastatin (22; 7%). Additionally, 101 (32.3%) patients used other statins and seven (2.2%) didn’t know the name of the drug (Table 3).
Table 1

Presence of muscle pain with respect to demographic characteristics

Demographic CharacteristicsBody pain 
 NoYes 
GenderN%N%P-value
  Male4829.411570.60.221
  Female3523.311576.7 
Age group     
  < = 401025.62974.4<0.001
  41 - 502646.43053.6 
  51 - 601916.19983.9 
  61+28287272 
Educational level      
  Non-educated715.93784.10.007
  Elementary school1538.52461.5 
  Middle school210.51789.5 
  High school2044.42555.6 
  Higher diploma423.51376.5 
  Bachelors2420.99179.1 
  Master or doctorate degree1132.42367.6 
Table 2

Demographic characteristic of study subjects

 Demographic characteristicsN%
Age group< = 403912.5
 41 - 505617.9
51 - 6011837.7
61+10031.9
Educational levelNon-educated4414.1
 Elementary school3912.5
Middle school196.1
High school4514.4
Higher diploma175.4
Bachelors11536.7
Master or doctorate degree3410.9
Diagnostic testStress test6219.8
 Percutaneous coronary intervention (PCI)31.0
Coronary artery bypass grafting (CABG)61.9
Cardiac catheterization3912.5
None20364.9
DrugAtorvastatin (Lipitor)13944.4
 Rosuvastatin (Crestor)4414.1
Simvastatin (Zocor)227
Others10132.3
Don’t know72.2
Table 3

Severity and type of pain with respect to the type of statin used

  Atorvastatin (Lipitor)Rosuvastatin (Crestor)Simvastatin (Zocor)OthersDon’t know
Type of painSeverityN%N%N%N%N%
Severity of muscle aches (muscles feeling sore, strained, or stiff).None4129.5920.5731.83231.7114.3
Mild2417.3920.51045.52019.8342.9
Moderate5338.12454.5313.63332.7114.3
Severe2115.124.529.11615.8228.6
Severity of muscle cramps.None5539.61329.5940.94847.500
Mild32231636.4940.91817.8342.9
Moderate3021.61329.529.12019.8457.1
Severe2215.824.529.11514.900
Severity of muscle weakness (feeling of heaviness or tiredness in the muscle)None4330.91329.5627.33837.600
Mild3525.2613.61045.51615.800
Moderate3928.12352.3418.22221.87100
Severe2215.824.529.12524.800
Severity of joint painNone3424.51227.3418.23130.700
Mild3122.3818.2627.32221.800
Moderate50362147.71045.52928.7342.9
Severe2417.336.829.11918.8457.1
The prevalence of muscle pain was 73.5%; 95% CI = (68.4% - 78.1%). The most common sites of pain were lower limb pain (160; 51.1%), upper limb pain (145; 46.3%), and trunk pain (96; 30.7%) (Figure 1). Common types of pain were joint pain (52; 16.6%), muscle weakness (51; 16.3%), muscle aches (43; 13.7%), and muscle cramps (41; 13.1%). The number of patients who reported that they stopped statin at some point because of muscle pain was 92 (29.4%) while 221 (70.6%) patients reported that they will most likely continue using statin despite having muscle pain.
Figure 1

The distribution of the site of pain in statin users

Discussion

Statin-induced myopathy is a commonly reported adverse effect. In this study, we found that the prevalence of muscle pain was 73.5%; 95%CI = (68.4% - 78.1%). Around 76.7% of female statin users and 70.6% of male statin users reported pain. This means that statin-induced myopathy is slightly more prevalent in females. In comparison to our study, there is another cross-sectional study done in 2018 which studied the prevalence of statin-induced myopathy at Punjab Institute of Cardiology, Lahore, Pakistan. The results showed that 51% of patients were myalgic [16]. In addition to that, muscle pain was more common in patients aged between 40-50, with females 57% and males 47%, so it is concluded that females were more prone to have muscle pain compared to males [16]. Furthermore, a prospective cohort study conducted at the National Center for Diabetes, Endocrinology, and Genetics (NCDEG) in Jordan showed that the overall incidence of myopathy statin users was 27.8%. Also, the incidence of statin-induced myopathy was highest with simvastatin 40 mg (50%) and lowest with fluvastatin XL 80 mg (8%) and rosuvastatin 10 mg (10.8%) [15]. On the other hand, in our study, we found that muscle pain was prevalent in 79.5% of rosuvastatin users, 70.5% of atorvastatin users, and 68.2% of simvastatin users. Nowadays statin is considered standard practice for management after acute coronary syndrome regardless of lipid level [2]. Statin is one of the antihyperlipidemic drugs used to lower lipid levels in the body [2]. It acts as an inhibitor for HMG-COA reductase. Along with this drug’s beneficial outcomes, it also has risks, and most found is myopathy [18]. Myopathy ranges from myalgia (muscle symptoms with normal creatinine kinase levels) to myositis (muscle symptoms with elevated creatinine kinase levels). In rare situations, it can worsen to life-threatening rhabdomyolysis (muscle symptoms with markedly elevated creatinine kinase levels and myoglobinuria) [6]. This present study shows that patients on statins have muscle pain in various body parts, manifesting most commonly in the lower limbs, upper limbs, trunk, and back. The symptoms vary in severity from mild to moderate to severe muscle pain. Other symptoms reported are muscle cramps, muscle weakness, and joint pain. Among statin users, we included patients that had one or more of these interventions, namely cardiac catheterization, stress test, percutaneous coronary intervention, coronary artery bypass graft, or those who didn’t have any intervention. A minority of patients reported that they stopped statin at some point because of muscle pain; this may affect their adherence to the medications, consequently leading to abnormalities in their cholesterol levels.

Conclusions

Statin is important for managing and preventing ischemic heart diseases. Muscle pain is highly associated with statin use with a prevalence of 73.5%. As a result, patients tend to stop taking their prescribed medications. Therefore, preventing the side effects by adjusting the proper dose or switching to another type of statin for patients at high risk will help them to continue using the drug. Also, it is important to rule out secondary causes of myopathy such as physical activity, fracture, thyroid dysfunction, or infection.
  13 in total

1.  Prevalence of statin induced myopathy in Lahore, Pakistan.

Authors:  Saleha Sadeeqa; Mariam Maqsood; Maqsood Ahmad
Journal:  Pak J Pharm Sci       Date:  2018-03       Impact factor: 0.684

Review 2.  Statin-induced myopathy: a review and update.

Authors:  Thura T Abd; Terry A Jacobson
Journal:  Expert Opin Drug Saf       Date:  2011-02-23       Impact factor: 4.250

3.  Statin-induced rhabdomyolysis: a comprehensive review of case reports.

Authors:  Polyana Mendes; Priscila Games Robles; Sunita Mathur
Journal:  Physiother Can       Date:  2014       Impact factor: 1.037

Review 4.  Individualized risk for statin-induced myopathy: current knowledge, emerging challenges and potential solutions.

Authors:  QiPing Feng; Russell A Wilke; Tesfaye M Baye
Journal:  Pharmacogenomics       Date:  2012-04       Impact factor: 2.533

5.  Does statin therapy initiation increase the risk for myopathy? An observational study of 32,225 diabetic and nondiabetic patients.

Authors:  Gregory A Nichols; Carol E Koro
Journal:  Clin Ther       Date:  2007-08       Impact factor: 3.393

Review 6.  The genetics of statin-induced myopathy.

Authors:  Abhijit Ghatak; Osman Faheem; Paul D Thompson
Journal:  Atherosclerosis       Date:  2009-11-27       Impact factor: 5.162

7.  SLCO1B1 variants and statin-induced myopathy--a genomewide study.

Authors:  E Link; S Parish; J Armitage; L Bowman; S Heath; F Matsuda; I Gut; M Lathrop; R Collins
Journal:  N Engl J Med       Date:  2008-07-23       Impact factor: 91.245

Review 8.  Statin adverse effects : a review of the literature and evidence for a mitochondrial mechanism.

Authors:  Beatrice A Golomb; Marcella A Evans
Journal:  Am J Cardiovasc Drugs       Date:  2008       Impact factor: 3.571

9.  Development and Content Validity of the Statin Experience Assessment Questionnaire (SEAQ)©.

Authors:  Terry A Jacobson; Steven V Edelman; Nina Galipeau; Alan L Shields; Usha G Mallya; Andrew Koren; Michael H Davidson
Journal:  Patient       Date:  2017-06       Impact factor: 3.883

Review 10.  Management of Statin Intolerance in 2018: Still More Questions Than Answers.

Authors:  Peter P Toth; Angelo Maria Patti; Rosaria Vincenza Giglio; Dragana Nikolic; Giuseppa Castellino; Manfredi Rizzo; Maciej Banach
Journal:  Am J Cardiovasc Drugs       Date:  2018-06       Impact factor: 3.571

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