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ORIGINAL RESEARCH article

Front. Cardiovasc. Med., 14 April 2022
Sec. Cardiovascular Epidemiology and Prevention

Comparison of Mortality Outcomes in Acute Myocardial Infarction Patients With or Without Standard Modifiable Cardiovascular Risk Factors

\nChing-Hui Sia,&#x;Ching-Hui Sia1,2Junsuk Ko&#x;Junsuk Ko3Huili ZhengHuili Zheng4Andrew Fu-Wah Ho,,Andrew Fu-Wah Ho5,6,7David FooDavid Foo8Ling-Li FooLing-Li Foo4Patrick Zhan-Yun LimPatrick Zhan-Yun Lim9Boon Wah LiewBoon Wah Liew10Ping Chai,Ping Chai1,2Tiong-Cheng Yeo,Tiong-Cheng Yeo1,2James W. L. Yip,James W. L. Yip1,2Terrance ChuaTerrance Chua11Mark Yan-Yee Chan,Mark Yan-Yee Chan1,2Jack Wei Chieh TanJack Wei Chieh Tan11Gemma FigtreeGemma Figtree12Heerajnarain Bulluck&#x;Heerajnarain Bulluck13Derek J. Hausenloy,,,,
&#x;Derek J. Hausenloy2,6,14,15,16*
  • 1Department of Cardiology, National University Heart Centre Singapore, Singapore, Singapore
  • 2Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
  • 3MD Program, Duke-NUS Medical School, Singapore, Singapore
  • 4Health Promotion Board, National Registry of Diseases Office, Singapore, Singapore
  • 5SingHealth Duke-NUS Emergency Medicine Academic Clinical Programme, Singapore, Singapore
  • 6National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore
  • 7Pre-hospital and Emergency Care Research Centre, Health Services and Systems Research, Duke-NUS Medical School, Singapore, Singapore
  • 8Tan Tock Seng Hospital, Singapore, Singapore
  • 9Khoo Teck Puat Hospital, Singapore, Singapore
  • 10Changi General Hospital, Singapore, Singapore
  • 11Department of Cardiology, National Heart Centre Singapore, Singapore, Singapore
  • 12Sydney Medical School (Northern), University of Sydney, Sydney, NSW, Australia
  • 13Leeds Teaching Hospital NHS trust, Leeds, United Kingdom
  • 14Cardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, Singapore, Singapore
  • 15The Hatter Cardiovascular Institute, University College London, London, United Kingdom
  • 16Cardiovascular Research Center, College of Medical and Health Sciences, Asia University, Taichung City, Taiwan

Background: Acute myocardial infarction (AMI) cases have decreased in part due to the advent of targeted therapies for standard modifiable cardiovascular disease risk factors (SMuRF). Recent studies have reported that ST-elevation myocardial infarction (STEMI) patients without SMuRF (termed “SMuRF-less”) may be increasing in prevalence and have worse outcomes than “SMuRF-positive” patients. As these studies have been limited to STEMI and comprised mainly Caucasian cohorts, we investigated the changes in the prevalence and mortality of both SMuRF-less STEMI and non-STEMI (NSTEMI) patients in a multiethnic Asian population.

Methods: We evaluated 23,922 STEMI and 62,631 NSTEMI patients from a national multiethnic registry. Short-term cardiovascular and all-cause mortalities in SMuRF-less patients were compared to SMuRF-positive patients.

Results: The proportions of SMuRF-less STEMI but not of NSTEMI have increased over the years. In hospitals, all-cause and cardiovascular mortality and 1-year cardiovascular mortality were significantly higher in SMuRF-less STEMI after adjustment for age, creatinine, and hemoglobin. However, this difference did not remain after adjusting for anterior infarction, cardiopulmonary resuscitation (CPR), and Killip class. There were no differences in mortality in SMuRF-less NSTEMI. In contrast to Chinese and Malay patients, SMuRF-less patients of South Asian descent had a two-fold higher risk of in-hospital all-cause mortality even after adjusting for features of increased disease severity.

Conclusion: SMuRF-less patients had an increased risk of mortality with STEMI, suggesting that there may be unidentified nonstandard risk factors predisposing SMuRF-less patients to a worse prognosis. This group of patients may benefit from more intensive secondary prevention strategies to improve clinical outcomes.

Introduction

Cardiovascular disease (CVD) is one of the leading causes of death and disability worldwide (1, 2). The incidence of acute myocardial infarction (AMI) has been reported to be about 300 per 100,000 people or greater, depending on the country or ethnicity (3). Cases of hospitalization due to AMI have decreased over the past few decades presumably due to the advent of targeted therapies for specific risk factors. The reduction in AMI morbidity and mortality has been achieved in part through secondary prevention of CVD along with other non-pharmacological interventions and measures, such as lifestyle modification and the adoption of community screening (4, 5). Hypertension, hyperlipidemia, diabetes, obesity, and cigarette smoking are well-recognized standard modifiable cardiovascular risk factors (SMuRF) that are commonly associated with CVD and are therefore used to evaluate the risk of AMI in patients (6).

Interestingly, recent studies have suggested that the number of AMI patients without apparent SMuRF (termed “SMuRF-less”) has increased over the years (7, 8). In an initial retrospective study from a single center in Australia, the prevalence of SMuRF-less ST-elevation myocardial infarction (STEMI) patients increased from 11 to 27% over 8 years (8), a finding that was also observed in a large study cohort from the Australian national registry, where the proportion of SMuRF-less STEMI patients increased from 14 to 23% over a period of 18 years (7). In contrast, a recent study based on the Swedish national registry displayed no evidence of increasing numbers of SMuRF-less STEMI patients, suggesting that the emergence of the SMuRF-less population may be ethnicity- or cohort-dependent and should be validated in other settings (9). Nonetheless, these studies have consistently reported that SMuRF-less STEMI patients have poorer clinical outcomes when compared to SMuRF-positive STEMI patients, such as in-hospital all-cause mortality, suggesting that the care for this population is suboptimal, presumably due to the lack of understanding of the mechanisms contributing to the worse outcomes in this group of patients (7, 9, 10).

Therefore, these studies have raised the awareness of a traditionally neglected group of STEMI patients without any apparent modifiable CVD risk factors. However, the following questions remain unanswered: (1) whether the proportion of SMuRF-less patients for AMI is increasing in different ethnic groups and (2) whether SMuRF-less status is associated with worse mortality outcomes in STEMI and non-STEMI (NSTEMI) patients, compared to the SMuRF-positive patients. As such, to address these issues, we analyzed data from a national population-based multiethnic Asian AMI registry in Singapore.

Methods

Data Sources

Data from the Singapore Myocardial Infarction Registry (SMIR) from January 2008 to June 2018 were utilized for this study. The SMIR is a national, government-funded registry, maintained by the National Registry of Diseases Office (NRDO) in Singapore (11). This study received an exemption review (SingHealth CIRB Reference No. 2016/2480) with a waiver for informed consent from patients as the study was based on de-identified data. The study was performed in accordance with the Declaration of Helsinki. The statistician was the only person who had access to the anonymized individual-level data, while the rest of the coauthors had access to the analyzed and aggregated data.

The SMIR database contains demographic, clinical, and outcome data of all AMI patients from the public and private hospitals in Singapore. Notification of AMI by healthcare professionals to the registry is mandated by law (12). The notification sources include medical claims listings, patient discharge summaries, and laboratory results, based on the International Classification of Diseases 9th Revision (ICD-9) Clinical Modification code 410 prior to 2012 and the ICD-10 Australian Modification codes I21 and I22 from 2012 onward. The registry coordinators collected detailed individual-level data from the medical records after ascertaining that the notified cases were, in fact, AMI. The quality of SMIR data was maintained through annual audits for accuracy and inter-rater reliability and review for outliers and illogical data. The SMIR data were subsequently merged with the death data from the Registry of Births and Deaths to obtain mortality outcomes. It is mandatory to report all deaths in Singapore.

Data Definitions and Exclusion Criteria

The classification of the type of myocardial infarction was based on documentation in the medical records. STEMI was defined by (1) typical chest pain of 20 min, (2) significant ST-segment elevation (0.1 or 0.2 mV on 2 adjacent limb or precordial leads, respectively, or new left bundle-branch block), and (3) confirmed later by a raise in biomarkers. NSTEMI was defined by (1) typical chest pain, (2) new horizontal or downsloping ST-depression (0.05 mV in 2 contiguous leads and/or T inversion >0.1 mV in two contiguous leads with prominent R wave or R/S ratio >1), and (3) confirmed by a raise in biomarkers (8). Troponin (T or I) was defined as abnormal if the value was >99th percentile of the reference range for each hospital's laboratory (11). Smoking included ex- and current smokers, regardless of when the ex-smokers stopped smoking and regardless of the type, frequency, and number of cigarettes smoked for current smokers. Data on smoking were self-reported during the admission for AMI. Obesity referred to a body mass index of ≥27.5 kg/m2, the cutoff value for Asian populations (13). Data on body mass index was based on the weight measured during the admission for AMI and the latest measured height documented in the medical records. We did not assess abdominal obesity as waist circumference data were not captured by the registry. Medical histories of hypertension, diabetes, and hyperlipidemia were based on past diagnoses and treatments given. Newly diagnosed hypertension was based on systolic blood pressure >130 bpm or diastolic blood pressure >85 bpm in the admission for AMI. Newly diagnosed diabetes was based on fasting blood glucose ≥7.0 mmol/L or random glucose ≥11.1 mmol/L in the admission for AMI. Newly diagnosed hyperlipidemia was based on total cholesterol >6.2 mmol/L, low-density lipoprotein (LDL) cholesterol >4.1 mmol/L, or triglyceride >1.7 mmol/L in the admission for AMI. We used two different definitions of SMuRF status as follows: (1) hypertension, diabetes, hyperlipidemia, smoking, and obesity; and (2) the same SMuRF but excluding obesity to reflect previously published analyses more closely in other ethnic groups. Some preceding studies did not include obesity as one of the SMuRF, but obesity was included in this study as it is one of the important risk factors in this study population (14).

In this study, only AMI patients who underwent percutaneous coronary intervention (PCI) were included. AMI patients who were treated medically without PCI were excluded as this population was heterogeneous and the majority of the patients had type 2 MI. Patients who had at least one risk factor with unknown status due to the nonavailability of data were excluded. Patients with a known history of AMI, PCI, or coronary artery bypass graft surgery were excluded. For patients with recurrent AMI, their first AMI was included, but subsequent AMIs were excluded.

The mortality outcomes in this study were in-hospital all-cause mortality, in-hospital cardiovascular mortality, 1-year (from the onset of AMI) all-cause mortality, and 1-year cardiovascular mortality. Cardiovascular mortality included the following ICD-9 and ICD-10 codes for the identification of cardiovascular death: AMI (410 for ICD-9 and I21 for ICD-10), unstable angina (411.1 and 411.8 for ICD-9 and I20.0 for ICD-10), heart failure (428.0, 428.1, 428.9, and 402.9 for ICD-9 and I50 for ICD-10), acute ischemic stroke (433, 434, and 436 for ICD-9 and I63 for ICD-10), and transient ischemic attack (435 for ICD-9 and G45.9 for ICD-10).

Statistical Analysis

Categorical variables were expressed as the frequency with percentages, while continuous variables were expressed as median with interquartile range. The chi-square test was used to compare the categorical variables between the SMuRF-less and SMuRF-positive patients, while the Wilcoxon rank-sum test was used to compare the continuous variables between the two groups. Missing data were excluded from analyses through case deletion without imputation in order to maintain data in its original form.

Cox regression was performed to determine the hazard ratios (HR) of mortality for SMuRF-less patients compared to SMuRF-positive patients. Age, creatinine on admission, and hemoglobin on admission were included in the multivariable Cox regression model 1. Age, Killip class on admission, CPR on admission, creatinine on admission, and hemoglobin on admission were included in the multivariable Cox regression model 2. Additionally, the type of myocardial infarction and anterior infarct was included in the models for all AMI and STEMI patients, respectively. These variables were selected based on stepwise backward elimination, starting with all variables captured by the SMIR. All analyses were stratified into STEMI and NSTEMI and replicated for the SMuRF that included and excluded obesity. Subgroup analyses by gender, ethnicity, and age group were undertaken to see if the effect of SMuRF differed across the various subsets of patients.

Linear regression with the logarithmic annual proportion of SMuRF-less patients as outcome and calendar year as a covariate was performed to analyze the trend of SMuRF-less prevalence over the years.

Statistical analysis was performed using Stata (StataCorp. 2013. Stata Statistical Software: Release 13. College Station, TX: StataCorp LP). All statistical tests were 2-tailed, and results were deemed to be statistically significant if p < 0.05.

Results

Study Population

When obesity was included as a SMuRF, 11,821 (95.3%) STEMI patients had at least one risk factor, while 578 (4.7%) STEMI patients did not have any of the five risk factors (Figure 1), only 4.7% of the STEMI population were SMuRF-less. Similarly, 7,854 (97.1%) and 233 (2.9%) NSTEMI patients were SMuRF-positive and SMuRF-less, respectively. For STEMI, smoking was the most common risk factor, followed by hyperlipidemia, hypertension, diabetes, and obesity (Table 1), whereas for NSTEMI, hyperlipidemia was the most common risk factor, followed by hypertension, smoking, diabetes, and obesity. Compared to SMuRF-less patients, SMuRF-positive STEMI patients tended to be younger, while SMuRF-positive NSTEMI patients tended to be older. The proportions of men and non-Chinese were higher in both STEMI and NSTEMI SMuRF-positive patients. SMuRF-positive STEMI patients had a lower proportion of Killip class 4 on admission, while SMuRF-positive NSTEMI patients had a lower proportion of Killip class 1 on admission. SMuRF was associated with increased serum creatinine and a less favorable lipid profile in both STEMI and NSTEMI, and increased hemoglobin in STEMI. The proportions of SMuRF-positive STEMI patients who received aspirin, angiotensin-receptor converting enzyme inhibitor/angiotensin receptor blocker (ACEI/ARB), a lipid-lowering drug, and P2Y12 inhibitor during their hospitalization were higher than SMuRF-less. Similarly, the proportions of SMuRF-positive NSTEMI patients who received beta-blockers and ACEI/ARB during hospitalization were higher than SMuRF-less.

FIGURE 1
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Figure 1. Flowchart of data inclusion. The following criteria for exclusion were applied in this selection: (1) undocumented diagnosis, (2) no percutaneous intervention (PCI) performed, (3) past MI/PCI/coronary arterial bypass surgery (CABG), (4) recurrent MI in this study period, and (5) any risk factor missing. For both STEMI and NSTEMI, obesity was included or excluded to evaluate the impact of obesity as a risk factor in AMI.

TABLE 1
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Table 1. Baseline characteristics of STEMI and NSTEMI patients with respect to SMuRF (including obesity) (n = 20,476).

When obesity was excluded from the SMuRF, 12,747 (94.3%) STEMI patients had at least one risk factor, while 776 (5.7%) STEMI patients did not have any of the four risk factors (Figure 1). Similarly, 8,314 (96.3%) and 323 (3.7%) patients were SMuRF and SMuRF-less, respectively. The profile of risk factors was similar to the results where obesity was included as a SMuRF (Table 2).

TABLE 2
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Table 2. Baseline characteristics of STEMI and NSTEMI patients with respect to SMuRF (excluding obesity) (n = 22,160).

Regardless of whether obesity was included as a SMuRF, SMuRF-less AMI patients were found to have a higher prevalence of increased disease severity compared to SMuRF-positive AMI patients, where a higher proportion of SMuRF-less patients had a higher Killip class, anterior infarction, and received CPR (Tables 1, 2).

There was a general upward trend in the proportion of SMuRF-less STEMI patients over the past 10 years regardless of including obesity as one of the SMuRF (Figure 2). However, the magnitude of this increase was modest with a 3.3% and 3.7% increase over the period, respectively. The proportion of SMuRF-less NSTEMI patients only started rising from 2015 onward.

FIGURE 2
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Figure 2. General trends of STEMI and NSTEMI patients without SMuRF from 2008 to 2018. Percentages of STEMI and NSTEMI patients with one or more of SMuRF were traced from 2008 to 2018. Obesity was included as one of the SMuRF (top) or excluded (bottom). The P-values represent the statistical significance for the overall trend of STEMI and NSTEMI.

Mortality Outcomes

With the inclusion of obesity as one of the SMuRF, the unadjusted HR for in-hospital all-cause mortality was 53% higher for SMuRF-less STEMI patients (HR 1.53, 95% CI 1.12–2.10) compared to SMuRF-positive STEMI patients (Table 3). After adjusting for age, creatinine, and hemoglobin, the HR for in-hospital all-cause mortality remained statistically significant for STEMI patients with no SMuRF (HR 1.54, 95% CI 1.12–2.11 for model 1). However, when Killip class, CPR, and anterior infarct were included for adjustment, the HR for in-hospital all-cause mortality was no longer statistically significant for STEMI patients with no SMuRF (HR 1.31, 95% CI 0.95–1.81 for model 2). For in-hospital cardiovascular mortality and 1-year all-cause mortality, a similar pattern was observed among the STEMI patients, where the HRs of the SMuRF-less attenuated substantially after adjustment, though the HRs were not significant. Similarly, the unadjusted HR for 1-year cardiovascular mortality was 54% higher for STEMI patients with no SMuRF (HR 1.54, 95% CI 1.08–2.19). However, with adjustment, the statistical significance was lost (HR 1.39, 95% CI 0.97–1.99 for model 1; HR 1.16, 95% CI 0.80–1.67 for model 2). The nonsignificantly higher mortality hazards for NSTEMI SMuRF-less patients all dropped after Killip class, CPR, and anterior infarct were included in the models.

TABLE 3
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Table 3. Risk of death among SMuRF-less AMI patients compared to those with at least one SMuRF (reference).

Similarly, with the exclusion of obesity as one of the SMuRF, the unadjusted HR for in-hospital all-cause mortality was 45% higher for STEMI patients without SMuRF (HR 1.45, 95% CI 1.11–1.90) compared to the SMuRF (Table 3). After adjusting for age, creatinine, and hemoglobin, the HR for in-hospital all-cause mortality remained statistically significant for STEMI patients without SMuRF (HR 1.48, 95% CI 1.13–1.93 for model 1). However, when Killip class, CPR, and anterior infarct were included for adjustment, the HR for in-hospital all-cause mortality was no longer statistically significant for STEMI patients without SMuRF (HR 1.20, 95% CI 0.92–1.58 for model 2). Similarly, the unadjusted HRs for in-hospital cardiovascular mortality and 1-year cardiovascular mortality were 43% and 45% higher for STEMI patients without SMuRF (HR 1.43, 95% CI 1.06–1.93 and HR 1.45, 95% CI 1.08–1.94, respectively). These increased HRs remained statistically significant after adjustment only in the adjusted model 1 (in-hospital cardiovascular mortality HR 1.44, 95% CI 1.06–1.95 for model 1; HR 1.12, 95% CI 0.80–1.56 for model 2) and model 2 (1-year cardiovascular mortality HR 1.39, 95% CI 1.03–1.87 for model 1; HR 1.11, 95% CI 0.82–1.52 for model 2). No significant difference in 1-year all-cause mortality was observed between the SMuRF-less and SMuRF-positive STEMI patients. There was also no significant difference in HRs between those with SMuRF and the SMuRF-less for all mortality outcomes among NSTEMI patients.

Subgroup analysis revealed that there was an increased adjusted HR for in-hospital all-cause mortality within the South Asian SMuRF-less group regardless of the inclusion of obesity as a SMuRF (HR 3.13, 95% CI 1.57–6.23 if obesity was included; HR 2.58, 95% CI 1.41–4.72 if obesity was excluded) (Table 4 and Figure 3).

TABLE 4
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Table 4. Risk of death among SMuRF-less AMI patients compared to those with at least one SMuRF (reference) within subgroups.

FIGURE 3
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Figure 3. Forest plot for an adjusted hazard ratio of mortality within subgroups. Adjusted hazard ratios of mortalities within subgroups (men, women, Chinese, Malay, South Asian, and age) were calculated and plotted in forest plots for patients with myocardial infarction (MI) with 95% confidence intervals (CI). Obesity was included (A) or excluded (B) as a SMuRF for the analysis.

Discussion

In this national registry-based retrospective study with a multiethnic cohort of both STEMI and NSTEMI patients, we demonstrated that SMuRF-less STEMI patients had a worse in-hospital all-cause mortality and 1-year cardiovascular mortality, regardless of the inclusion of obesity as a risk factor. The proportion of SMuRF-less STEMI patients has increased over time, although this trend was modest. These findings suggest that being SMuRF-less is associated with an increased risk of mortality in STEMI but not NSTEMI patients when compared to SMuRF-positive.

One of the first studies reporting an association between the SMuRF and prognosis of AMI patients was published in 2011 by Canto et al., who showed that the number of CVD risk factors was inversely correlated with in-hospital all-cause mortality in AMI patients in the US cohort (15). Given the pathogenesis of AMI and the roles of these risk factors for the formation of coronary atherosclerosis, this result appeared counterintuitive and was controversial at the time (1619). Subsequently, the clinical importance and the awareness of SMuRF-less patients were highlighted by two retrospective studies based on an Australian cohort, which reported that the proportion of SMuRF-less among AMI patients had substantially increased over time and was associated with a worse prognosis (79). The authors proposed that these studies provided indirect evidence for the existence of other clinically critical but unidentified risk factors in this patient group. Our study, in part, supports this hypothesis. In our multiethnic southeast Asian study, we observed worse mortality outcomes in SMuRF-less compared to SMuRF-positive STEMI patients after adjustment for baseline characteristics (adjusted model 1). However, this finding was no longer significant after adjusting for the significantly higher rates of anterior infarction, cardiopulmonary resuscitation (CPR), and Killip class observed in SMuRF-less (adjusted model 2). These results suggest that although being SMuRF-less is not an independent predictor of clinical outcomes, SMuRF-less patients do have worse mortality outcomes following STEMI. In addition to this finding, our subgroup analysis revealed that the South Asian subgroup had a higher risk of in-hospital death even after adjusting for the significantly higher rates of anterior infarction, CPR, and Killip class observed in SMuRF-less, suggesting the presence of so far unidentified CVD risk factors that can be determinants of worse outcomes in SMuRF-less, such as lipoprotein A (2022). In support of this, SMuRF-less AMI patients had more favorable lipid profiles (lower LDL and triglyceride levels and higher high-density lipoprotein (HDL) levels) compared to SMuRF-positive patients supporting the presence of unknown CVD risk factors in SMuRF-less patients. Interestingly, although being SMuRF-less was associated with worse mortality outcomes in STEMI, there was no difference with NSTEMI, the reasons for which are not clear but may relate to the differing pathophysiology and risk factor profiles of STEMI vs. NSTEMI.

As explained above, unknown CVD risk factors, such as lipoprotein A, could be a cause of the worse clinical outcomes in SMuRF-less STEMI patients. Another alternative explanation for the worse prognosis is the involvement of the genetic factors predisposing the patients to worse outcomes. In addition to the genetic predisposition or unidentified risk factors, there could be other alternative explanations for the worse prognosis in SMuRF-less STEMI patients. As shown in Table 2, SMuRF-less patients were less likely to receive evidence-based treatment as compared to SMuRF patients. This undertreatment may have contributed to the worse mortalities noted in previous studies (79). Furthermore, the presence of coronary collaterals in patients with silent myocardial ischemia, which is often observed in patients with CVD risk factors, could lead to lower mortality in SMuRF patients (23, 24).

Obesity is associated with the incidence of AMI (2530) and is associated with the premature occurrence of AMI in young patients (3133). Despite the association between obesity and the incidence of AMI, whether obesity increases the risk of mortalities following AMI events has been controversial. Obesity significantly decreased the risk of mortality outcomes after AMI, and this phenomenon has been termed the “obesity paradox in AMI” (3440). However, other follow-up studies have demonstrated no difference in mortality outcomes between obese and nonobese patients after STEMI (41, 42) and AMI (33) or even worse prognosis in obese patients following AMI (43). Presumably, due to this controversy, obesity has been excluded as a risk factor in previous SMuRF studies. Our study included two independent datasets with and without obesity as a SMuRF to assess whether the SMuRF-less status performs better as a predictor of clinical outcomes. Regardless of the inclusion of obesity as a risk factor, being SMuRF-less was associated with worse mortality outcomes, although being SMuRF-less was not an independent predictor of mortality.

One potential critique for studies examining the role of SMuRF on outcomes is that accurate identification of risk factors is challenging as this is often based on (1) the patient's self-reported history, (2) medical records, or (3) current medications. To minimize the risk of under-identifying SMuRF, we included not only the three criteria mentioned above but also risk factors confirmed through laboratory tests. For this reason, our study further extends knowledge in the field by strictly defining the SMuRF based on medical records and laboratory values during hospitalization. Moreover, only never smokers were included as nonsmokers, as compared to previous analyses where ex-smokers were considered nonsmokers due to the persistent negative impact of smoking on cardiovascular mortalities even after cessation (79, 4446). Interestingly, although the proportions of SMuRF-less were 25% (8), 19% (7), and 15% (9) for STEMI patients in the previous studies, our study revealed <6% for STEMI and NSTEMI patients without SMuRF, which may, in part, be explained by the detection of SMuRF in our study. An alternative explanation could be that the CVD risk factor burden is greater in our multiethnic AMI population when compared to the Australian and Swedish AMI cohorts.

Currently, it is unclear whether the proportion of AMI patients without any standard CVD risk factors is changing over time worldwide. The only studies that have reported this increasing trend are two investigations in Australia; the proportion of SMuRF-less patients increased from 11% in 2006 to 27% in 2014 in one study and from 14% in 1999 to 23% in 2017 in another study (7, 8). These findings may be clinically important as they may suggest the increasing importance of a traditionally misidentified group with unknown CVD risk factors. However, this trend was not reported in a collaborative follow-up study performed by the original authors using the Swedish national registry, suggesting that this increasing trend in the proportion of the SMuRF-less patients among AMI patients might have been ethnicity-specific (9). This hypothesis is strengthened by the following evidence: in the Japan AMI registry, the proportion of AMI patients with the traditional CVD risk factors, such as hypertension, diabetes mellitus, and hypercholesterolemia, has increased over time (47). Similarly, the mean number of SMuRF increased from 1.76-fold in 1997 to 2.26-fold in 2017 among male AMI patients and from 1.83-fold to 2.24-fold among female AMI patients in the Swiss National AMI Registry (48). Moreover, given the fact that the profile of the SMuRF was significantly different among the aforementioned studies, careful interpretation and application of these findings are warranted (4954). In our multiethnic AMI cohort, we observed a modest increase in the prevalence of SMuRF-less STEMI patients but no difference with NSTEMI patients.

Strengths and Limitations

Our study significantly contributes to the field for the following reasons. It is controversial whether the proportion of the SMuRF-less STEMI patients has been increasing as previous studies reported conflicting results. Using a national multiethnic AMI registry, we demonstrated that the incidence of SMuRF-less STEMI has been increasing in this study. Prior studies have focused only on clinical outcomes in SMuRF-less STEMI patients, whereas in our study we included both STEMI and NSTEMI patients. To the best of our knowledge, this is the first time that it has been reported that short-term mortalities were higher in SMuRF-less STEMI patients but not in NSTEMI patients. Taken together, these data suggest that STEMI SMuRF-less patients may require more aggressive medical interventions and attention and the absence of SMuRF should not lead to undertreatment in this group of patients. Additionally, the strength of this study is that the registry of AMI patients ensures near-complete case coverage at the national level with its mandatory notification. Due to the nature of the database and study design, there was minimal risk of selection bias. Furthermore, our study strictly defined patients' risk factors using not only the patient's self-reported history, previous medical records, and current medications but also the results obtained during hospitalization for AMI. Nevertheless, we acknowledge several limitations of this study. Only AMI patients who underwent PCI were included in this study as they were a homogenous group of patients. Therefore, the results of our study are only applicable to patients who received PCI but not other patient populations, such as those who did not receive revascularization (but received medical therapy alone or thrombolysis). While the subgroup analysis revealed that there was an increased adjusted HR for in-hospital all-cause mortality within the South Asian SMuRF-less group, the low prevalence of SMURF-less and low rate of mortality among the patients might lead to statistical bias in the risk estimates. We attempted to keep the multivariable models parsimonious by including only statistically significant predictors of mortality and ensuring there were at least 15 outcomes per predictor in all models by subgroup. Moreover, as data on coronary angiogram was not available in the registry, we could not analyze which coronary artery would likely be the culprit for the worse prognosis in SMuRF-less patients. Additionally, as we attempted to include as many eligible patients as possible while ensuring the patients had a complete follow-up with the available death data, we could only evaluate short-term clinical outcomes (with the longest follow-up of 1-year mortality) among SMuRF-less patients in this study. Therefore, future studies not limited to patients with PCI, of bigger sample size, with data on coronary angiograms and longer-term outcomes will be useful to ascertain and build on our findings.

Summary and Conclusion

The proportion of the SMuRF-less has been increasing in STEMI patients. In-hospital mortalities and 1-year cardiovascular mortality were significantly higher in SMuRF-less STEMI patients. However, this difference did not remain after adjusting for the significantly higher rates of anterior infarction, CPR, and Killip class observed in SMuRF-less. In contrast to Chinese and Malay patients, SMuRF-less patients of South Asian descent had a two-fold higher risk of in-hospital all-cause mortality even after adjusting for features of increased disease severity (higher Killip class, more CPR, and anterior infarction), suggesting the presence of so far unidentified CVD risk factors in this population that could provide an opportunity for intensifying secondary prevention in order to improve health outcomes in this high-risk patient group. Future studies need to be done to investigate potential unidentified AMI risk factors in STEMI patients.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved this study received an exemption review (SingHealth CIRB Reference No: 2016/2480) with a waiver for informed consent from patients as the study was based on de-identified data. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

C-HS, JK, HB, and DH designed this study. HZ contributed to this study by obtaining and analyzing the data from SMIR. C-HS, JK, and DH contributed to interpreting the data. C-HS, JK, and HZ wrote the manuscripts. AH, DF, L-LF, PL, BL, PC, T-CY, JY, TC, MC, JT, and GF contributed to this study by providing constructive comments and insights. DH and HB supervised and provided a critical review of the manuscript. All authors contributed to the article and approved the submitted version.

Funding

C-HS was supported by the National University of Singapore Yong Loo Lin School of Medicine's Junior Academic Faculty Scheme. JK was supported by the SingHealth Medical Student Talent Development Award (SMSTDA). AH was supported by Khoo Clinical Scholars Programme, Khoo Pilot Award (KP/2019/0034), Duke-NUS Medical School, and the National Medical Research Council (NMRC/CS_Seedfd/012/2018). DH was supported by the British Heart Foundation (CS/14/3/31002), the National Institute for Health Research, University College London Hospitals Biomedical Research Centre, Duke-National University of Singapore Medical School, and Singapore Ministry of Health's National Medical Research Council under its Clinician Scientist-Senior Investigator scheme (NMRC/CSA-SI/0011/2017), Centre Grant scheme (CG21APR1006), and the Collaborative Centre Grant scheme (NMRC/CG21APRC006). This study is based upon work from COST Action EU-CARDIOPROTECTION CA16225, supported by COST (European Cooperation in Science and Technology).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

We convey our sincere thanks to the registry coordinators of the SMIR for their help and contribution to maintaining the national registry.

References

1. Ojha N, Dhamoon AS. Myocardial Infarction. StatPearls. (2021) Available at: https://www.ncbi.nlm.nih.gov/books/NBK537076/ (accessed August 17, 2021)

Google Scholar

2. Roth GA, Mensah GA, Johnson CO, Addolorato G, Ammirati E, Baddour LM, et al. Global burden of cardiovascular diseases and risk factors, 1990–2019: update from the GBD 2019 study. J Am Coll Cardiol. (2020) 76:2982–3021. doi: 10.1016/j.jacc.2020.11.010

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Kaifoszova Z, Widimsky P. Increasing the penetration of primary angioplasty in Europe. Eur Cardiol. (2012) 8:60–2. doi: 10.15420/ecr.2012.8.1.60

CrossRef Full Text | Google Scholar

4. Krumholz HM, Normand S-LT, Wang Y. Twenty-year trends in outcomes for older adults with acute myocardial infarction in the United States. JAMA Netw Open. (2019) 2:e191938. doi: 10.1001/jamanetworkopen.2019.1938

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Chen J, Normand S-LT, Wang Y, Drye EE, Schreiner GC, Krumholz HM. Recent declines in hospitalizations for acute myocardial infarction for medicare fee-for-service beneficiaries. Circulation. (2010) 121:1322–8. doi: 10.1161/CIRCULATIONAHA.109.862094

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Flora GD, Nayak MK, A. Brief review of cardiovascular diseases, associated risk factors and current treatment regimes. Curr Pharm Des. (2019) 25:4063–84. doi: 10.2174/1381612825666190925163827

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Vernon ST, Coffey S, D'Souza M, Chow CK, Kilian J, Hyun K, et al. ST-Segment-Elevation Myocardial Infarction (STEMI) patients without standard modifiable cardiovascular risk factors-how common are they, and what are their outcomes? J Am Heart Assoc. (2019) 8:e013296 doi: 10.1161/JAHA.119.013296

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Vernon ST, Coffey S, Bhindi R, Soo Hoo SY, Nelson GI, Ward MR, et al. Increasing proportion of ST elevation myocardial infarction patients with coronary atherosclerosis poorly explained by standard modifiable risk factors. Eur J Prev Cardiol. (2017) 24:1824–30. doi: 10.1177/2047487317720287

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Figtree GA, Vernon ST, Hadziosmanovic N, Sundström J, Alfredsson J, Arnott C, et al. Mortality in STEMI patients without standard modifiable risk factors: a sex-disaggregated analysis of SWEDEHEART registry data. Lancet. (2021) 397:1085–94. doi: 10.1016/S0140-6736(21)00272-5

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Gonzalez MI, Hoyo D, Peiro Ibanez OM, Vaquez-Nunez K, Dominguez Benito F, Ferrero M, et al. The absence of standard modifiable cardiovascular risk factors does not predict better outcomes in patients with acute coronary syndrome. Eur Heart J. (2020) 41:ehaa946–1341. doi: 10.1093/ehjci/ehaa946.1341

CrossRef Full Text | Google Scholar

11. Thygesen K, Alpert JS, Jaffe AS, Chaitman BR, Bax JJ, Morrow DA, et al. Fourth universal definition of myocardial infarction. J Am Coll Cardiol. (2018) 72:2231–64. doi: 10.1016/j.jacc.2018.08.1038

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Office NR of D. Singapore Myocardial Infarction Registry Annual Report 2018. Heal Promot Board (2020)

13. Nishida C, Barba C, Cavalli-Sforza T, Cutter J, Deurenberg P, Darnton-Hill I, et al. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. (2004) 363:157–63. doi: 10.1016/S0140-6736(03)15268-3

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Wong CP, Loh SY, Loh KK, Ong PJ, Foo D, Ho HH. Acute myocardial infarction: Clinical features and outcomes in young adults in Singapore. World J Cardiol. (2012) 4:206. doi: 10.4330/wjc.v4.i6.206

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Canto JG, Kiefe CI, Rogers WJ, Peterson ED, Frederick PD, French WJ, et al. Number of coronary heart disease risk factors and mortality in patients with first myocardial infarction. JAMA. (2011) 306:2120. doi: 10.1001/jama.2011.1654

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Landesberg G. The pathophysiology of perioperative myocardial infarction: facts and perspectives. J Cardiothorac Vasc Anesth. (2003) 17:90–100. doi: 10.1053/jcan.2003.18

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Burke AP, Virmani R. Pathophysiology of acute myocardial infarction. Med Clin North Am. (2007) 91:553–72. doi: 10.1016/j.mcna.2007.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Saleh M, Ambrose JA. Understanding myocardial infarction. F1000Research. (2018) 7. doi: 10.12688/f1000research.15096.1

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Heusch G, Gersh BJ. The pathophysiology of acute myocardial infarction and strategies of protection beyond reperfusion: a continual challenge. Eur Heart J. (2017) 38:774–84. doi: 10.1093/eurheartj/ehw224

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Paré G, Çaku A, McQueen M, Anand SS, Enas E, Clarke R, et al. Lipoprotein(a) levels and the risk of myocardial infarction among 7 ethnic groups. Circulation. (2019) 139:1472–82. doi: 10.1161/CIRCULATIONAHA.118.034311

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Cai G, Huang Z, Zhang B, Yu L, Li L. Elevated lipoprotein (a) levels are associated with the acute myocardial infarction in patients with normal low-density lipoprotein cholesterol levels. Biosci Rep. (2019) 39:BSR20182096. doi: 10.1042/BSR20182096

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Kamstrup PR, Benn M, Tybjærg-Hansen A, Nordestgaard BG. Extreme lipoprotein(a) levels and risk of myocardial infarction in the general population: The Copenhagen City Heart Study. Circulation. (2008) 117:176–84. doi: 10.1161/CIRCULATIONAHA.107.715698

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Xing Z, Pei J, Tang L, Hu X. Traditional cardiovascular risk factors and coronary collateral circulation: Protocol for a systematic review and meta-analysis of case-control studies. Medicine (Baltimore). (2018) 97:e0417. doi: 10.1097/MD.0000000000010417

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Pei J, Wang X, Xing Z. Traditional cardiovascular risk factors and coronary collateral circulation: a meta-analysis. Front Cardiovasc Med. (2021) 0:1442. doi: 10.3389/fcvm.2021.743234

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Zhu J, Su X, Li G, Chen J, Tang B, Yang Y. Systematic review/meta-analysis the incidence of acute myocardial infarction in relation to overweight and obesity: a meta-analysis. Arch Med Sci. (2014) 10:855–62. doi: 10.5114/aoms.2014.46206

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Tavani A, Bertuzzi M, Gallus S, Negri E, La Vecchia C. Risk factors for non-fatal acute myocardial infarction in Italian women. Prev Med (Baltim). (2004) 39:128–34. doi: 10.1016/j.ypmed.2004.01.010

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Marín A, Medrano MJ, González J, Pintado H, Compaired V, Bárcena M, et al. Risk of ischaemic heart disease and acute myocardial infarction in a Spanish population: observational prospective study in a primary-care setting. BMC Public Health. (2006) 6: doi: 10.1186/1471-2458-6-38

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Schargrodsky H, Rozlosnik J, Ciruzzi M, Ruffa R, Paterno C, Ardariz M, et al. Body weight and nonfatal myocardial infarction in a case-control study from Argentina. Soz Praventivmed. (1994) 39:126–33. doi: 10.1007/BF01299656

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Oliveira A, Ramos E, Lopes C, Barros H. Self-reporting weight and height: misclassification effect on the risk estimates for acute myocardial infarction. Eur J Public Health. (2009) 19:548–53. doi: 10.1093/eurpub/ckp022

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Yusuf S, Hawken S, Ôunpuu S, Bautista L, Franzosi MG, Commerford P, et al. Obesity and the risk of myocardial infarction in 27,000 participants from 52 countries: a case-control study. Lancet (London, England). (2005) 366:1640–9. doi: 10.1016/S0140-6736(05)67663-5

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Basoor A, Cotant JF, Randhawa G, Janjua M, Badshah A, DeGregorio M, et al. High prevalence of obesity in young patients with ST elevation myocardial infarction. Am Heart Hosp J. (2011) 9:37–40. doi: 10.15420/ahhj.2011.9.1.37

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Al Suwaidi J, Scott Wright R, Grill JP, Hensrud DD, Murphy JG, Squires RW, et al. Obesity is associated with premature occurrence of acute myocardial infarction. Clin Cardiol. (2001) 24:542–7. doi: 10.1002/clc.4960240804

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Wells B, Gentry M, Ruiz-Arango A, Dias J, Landolfo CK. Relation between body mass index and clinical outcome in acute myocardial infarction. Am J Cardiol. (2006) 98:474–7. doi: 10.1016/j.amjcard.2006.02.053

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Kim HT, Jung SY, Nam JH, Lee JH, Lee CH, Son JW, et al. Clinical implication of ‘obesity paradox' in elderly patients with acute myocardial infarction. Hear Lung Circ. (2021) 30:481–8. doi: 10.1016/j.hlc.2020.08.013

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Kragelund C, Hassager C, Hildebrandt P, Torp-Pedersen C, Køber L. Impact of obesity on long-term prognosis following acute myocardial infarction. Int J Cardiol. (2005) 98:123–31. doi: 10.1016/j.ijcard.2004.03.042

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Elbaz-Greener G, Rozen G, Carasso S, Kusniec F, Marai I, Sud M, et al. The relationship between body mass index and in-hospital mortality in the contemporary era of an acute myocardial infarction management. Vasc Health Risk Manag. (2021) 17:551–9. doi: 10.2147/VHRM.S315248

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Park SJ, Ha KH, Kim DJ. Body mass index and cardiovascular outcomes in patients with acute coronary syndrome by diabetes status: the obesity paradox in a Korean national cohort study. Cardiovasc Diabetol. (2020) 19:1–8. doi: 10.1186/s12933-020-01170-w

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Wang L, Liu W, He X, Chen Y, Lu J, Liu K, et al. Association of overweight and obesity with patient mortality after acute myocardial infarction: a meta-analysis of prospective studies. Int J Obes 2016 402. (2015) 40:220–8. doi: 10.1038/ijo.2015.176

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Bucholz EM, Rathore SS, Reid KJ, Jones PG, Chan PS, Rich MW, et al. Body mass index and mortality in acute myocardial infarction patients. J Med. (2012) 125:796–803. doi: 10.1016/j.amjmed.2012.01.018

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Kim DW, Her SH, Park HW, Park MW, Chang K, Chung WS, et al. Association between body mass index and 1-year outcome after acute myocardial infarction. PLoS ONE. (2019) 14:e0217525. doi: 10.1371/journal.pone.0217525

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Jamaly S, Redfors B, Omerovic E, Carlsson L, Karason K. Prognostic significance of BMI after PCI treatment in ST-elevation myocardial infarction: a cohort study from the Swedish Coronary Angiography and Angioplasty Registry. Open Hear. (2021) 8:e001479. doi: 10.1136/openhrt-2020-001479

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Champagne-Langabeer T, Kim J, Bower JK, Gardner A, Fowler R, Langabeer JR. Obesity, treatment times, and cardiovascular outcomes after st-elevation myocardial infarction: findings from mission: lifeline North Texas. J Am Heart Assoc. (2017) 6:e005827. doi: 10.1161/JAHA.117.005827

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Thomsen M, Nordestgaard BG. Myocardial infarction and ischemic heart disease in overweight and obesity with and without metabolic syndrome. JAMA Intern Med. (2014) 174:15–22. doi: 10.1001/jamainternmed.2013.10522

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Choi W, Kim SH, Kang SH, Park JJ, Yoon CH, Youn TJ, et al. Differential impact of smoking on cardiac or non-cardiac death according to age. PLoS ONE. (2019) 14:e0224486. doi: 10.1371/journal.pone.0224486

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Duncan MS, Freiberg MS, Greevy RA, Kundu S, Vasan RS, Tindle HA. Association of smoking cessation with subsequent risk of cardiovascular disease. JAMA. (2019) 322:642–50. doi: 10.1001/jama.2019.10298

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Wang JY, Goodman SG, Saltzman I, Wong GC, Huynh T, Dery JP, et al. Cardiovascular risk factors and in-hospital mortality in acute coronary syndromes: insights from the canadian global registry of acute coronary events. Can J Cardiol. (2015) 31:1455–61. doi: 10.1016/j.cjca.2015.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Nishiyama S, Watanabe T, Arimoto T, Takahashi H, Shishido T, Miyashita T, et al. Trends in coronary risk factors among patients with acute myocardial infarction over the last decade: the Yamagata AMI registry. J Atheroscler Thromb. (2010) 17:989–998. doi: 10.5551/jat.4671

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Gale CP, Cattle BA, Woolston A, Baxter PD, West TH, Simms AD, et al. Resolving inequalities in care? Reduced mortality in the elderly after acute coronary syndromes. The Myocardial Ischaemia National Audit Project 2003-2010. Eur Heart J. (2012) 33:630–9. doi: 10.1093/eurheartj/ehr381

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Gupta M, Doobay AV, Singh N, Anand SS, Raja F, Mawji F, et al. Risk factors, hospital management and outcomes after acute myocardial infarction in South Asian Canadians and matched control subjects. C Can Med Assoc J. (2002) 166:717. Available at: /pmc/articles/PMC99450/ (accessed August 20, 2021).

Google Scholar

50. Selak V, Poppe K, Grey C, Mehta S, Winter-Smith J, Jackson R, et al. Ethnic differences in cardiovascular risk profiles among 475,241 adults in primary care in Aotearoa, New Zealand. N Z Med J. (2020) 133:14–27. Available at: https://www.nzma.org.nz/journal-articles/ethnic-differences-in-cardiovascular-risk-profiles-among-475-241-adults-in-primary-care-in-aotearoa-new-zealand (accessed August 20, 2021).

Google Scholar

51. Chiu M, Austin PC, Manuel DG, Tu J V. Comparison of cardiovascular risk profiles among ethnic groups using population health surveys between 1996 and 2007. CMAJ. (2010) 182:E301–10. doi: 10.1503/cmaj.091676

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Lu HT, Nordin R Bin. Ethnic differences in the occurrence of acute coronary syndrome: results of the Malaysian National Cardiovascular Disease (NCVD) Database Registry (March 2006–February 2010). BMC Cardiovasc Disord. (2013) 13:1–14. doi: 10.1186/1471-2261-13-97

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Gijsberts CM, Seneviratna A, Carvalho LP de, Ruijter HM den, Vidanapthirana P, Sorokin V, et al. Ethnicity modifies associations between cardiovascular risk factors and disease severity in parallel Dutch and Singapore coronary cohorts. PLoS ONE. (2015) 10:e0132278. doi: 10.1371/journal.pone.0132278

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Abdelnoor M, Eritsland J, Brunborg C, Halvorsen S. Ethnicity and acute myocardial infarction: risk profile at presentation, access to hospital management, and outcome in Norway. Vasc Health Risk Manag. (2012) 8:505. doi: 10.2147/VHRM.S33627

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: acute myocardial infarction, standard modifiable cardiovascular disease risk factors, STEMI, NSTEMI, mortality, SMuRF

Citation: Sia C-H, Ko J, Zheng H, Ho AF-W, Foo D, Foo L-L, Lim PZ-Y, Liew BW, Chai P, Yeo T-C, Yip JWL, Chua T, Chan MY-Y, Tan JWC, Figtree G, Bulluck H and Hausenloy DJ (2022) Comparison of Mortality Outcomes in Acute Myocardial Infarction Patients With or Without Standard Modifiable Cardiovascular Risk Factors. Front. Cardiovasc. Med. 9:876465. doi: 10.3389/fcvm.2022.876465

Received: 15 February 2022; Accepted: 16 March 2022;
Published: 14 April 2022.

Edited by:

Rajeev Gupta, Medicilinic, United Arab Emirates

Reviewed by:

Vito Maurizio Parato, Marche Polytechnic University, Italy
Rajeev Gupta, Rajasthan University of Health Sciences, India
Pierre Sabouret, Sorbonne University, France

Copyright © 2022 Sia, Ko, Zheng, Ho, Foo, Foo, Lim, Liew, Chai, Yeo, Yip, Chua, Chan, Tan, Figtree, Bulluck and Hausenloy. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Derek J. Hausenloy, derek.hausenloy@duke-nus.edu.sg

These authors have contributed equally to this work and share first authorship

These authors have contributed equally to this work and share last authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.