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Association of air pollution and 1-year clinical outcomes of patients with acute myocardial infarction [1]

['Se Yeon Choi', 'Cardiovascular Research Institution', 'Korea University College Of Medicine', 'Seoul', 'Seung-Woon Rha', 'Cardiovascular Center', 'Korea University Guro Hospital', 'Jinah Cha', 'Graduate Program', 'Department Of Biomedical Sciences']

Date: 2022-08 

Abstract Background Exposure to air pollution (AP) is an important environmental risk factor for increased risk of cardiovascular morbidity and triggering acute myocardial infarction (AMI). However, there are limited data regarding the clinical impact of AP on long-term major clinical outcomes of AMI patients. This study aimed to evaluate the clinical effects of ambient AP concentration on short-term and 1-year clinical outcomes of AMI patients. Methods A total of 46,263 eligible patients were enrolled in the Korea Acute Myocardial Infarction (KAMIR) and KAMIR-National Institutes of Health (NIH) registry from January 2006 to December 2015. We performed Cox proportional hazard regression to assess the risk of all-cause death and any-revascularization according to the annual average concentration of AP during one-year follow-up period. Results The assessment of the annual average of air pollutants before symptom date and all-cause death up to 30 days showed the hazard ratio (HR) of SO 2 per 1 part per billion (ppb) increase was 1.084 (95% confidence interval [CI]: 1.016–1.157), and particulate matter with diameter of 10 microns or less (PM 10 ) per 1 μg/m3 increase was 1.011 (95% CI: 1.002–1.021). The results of the 30-day and one-year all-cause death showed a similar trend. For SO 2 , the HR per 1 ppb increase was 1.084 (95% CI: 1.003–1.172), and the HR of PM 10 was 1.021 (95% CI: 1.009–1.033) per 1 μg/m3 increase. We observed that SO 2 , CO, and PM 10 were associated with an increased risk of incidence for any-revascularization up to one-year. Conclusion In some air pollutants, a higher AP concentration was an environmental risk factor for poor prognosis in AMI patients up to 1 year. AMI patients and high-risk individuals need a strategy to reduce or prevent exposure to high AP concentrations.

Citation: Choi SY, Rha S-W, Cha J, Byun JK, Choi BG, Jeong Mh, et al. (2022) Association of air pollution and 1-year clinical outcomes of patients with acute myocardial infarction. PLoS ONE 17(8): e0272328. https://doi.org/10.1371/journal.pone.0272328 Editor: R. Jay Widmer, Baylor Scott and White, Texas A&M College of Medicine, UNITED STATES Received: February 10, 2022; Accepted: July 18, 2022; Published: August 1, 2022 Copyright: © 2022 Choi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability: Data cannot be shared publicly because of the KAMIR group policy. Data are available from the Chonnam National University Hospital Institutional Data Access / Ethics Committee (contact via research manager) for researchers who meet the criteria for access to confidential data. Contact information: Research manager: Kyung Hoon Cho, E-mail: zarazoro@hanmail.net, Telephone: +82 62-220-5272. Funding: SWR: This research was supported by a grant (2020ER630800) from the Research of Korea Centers for Disease Control and Prevention (https://www.kdca.go.kr/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing interests: The authors have declared that no competing interests exist.

Introduction Exposure to ambient air pollution (AP) is an inevitable circumstance for the population, and it is an important environmental risk factor for adverse health effects. AP concentrations in most Asian countries exceed the air quality guidelines of the World Health Organization, and concentrations in low- and middle-income countries are relatively high and increasing [1]. The population living in these countries is estimated to have a large burden of adverse health effects due to exposure to AP, and is expected to gradually increase depending on AP concentration. The impact of AP on human health is known to cause 4.2 million premature deaths worldwide per year, and is related to not only respiratory diseases but many acute and chronic diseases [2–5]. In addition, short- and long-term exposure to AP is associated with cardiovascular diseases such as the increased risk of cardiovascular morbidity, triggering acute myocardial infarction (AMI), and even increased cardiovascular death via pulmonary and systemic inflammation [6–11]. The majority of AP-related studies that have been conducted focused on the onset and relevance of disease based on the concentration of exposure to AP in the general population. There are limited data on the clinical aspects of patients with specific diseases. Our previous study investigated the association between short-term clinical outcomes and AP exposure in AMI patients. We found that AP exposure within 24 h before AMI admission was associated with mortality and cardiovascular events [12]. This study was conducted via an extended period of clinical follow-up and AP concentration data as a serial study followed by our previous study and aimed to evaluate the clinical effects of ambient AP concentration in AMI patients using nationwide prospective multicenter registry data.

Materials and methods Study population The data was collected from the Korea Acute Myocardial Infarction (KAMIR) and KAMIR-National Institutes of Health (KAMIR-NIH). The KAMIR study design has been introduced in previous studies [12, 13]. KAMIR and KAMIR-NIH are a nationwide prospective multicenter registration study series that aims to establish treatment guidelines and derive risk factors through various clinical characteristics and follow-up of Korean AMI patients from October 2005. A flowchart of the study is shown in Fig 1. A total of 50,130 AMI patients were enrolled in the KAMIR and the KAMIR-NIH from January 2006 to December 2015. Exclusion criteria were (1) symptom data before the year 2006 or missing year, (2) input error for symptom date, (3) healing MI or healed MI, and (4) missing important demographic factors such as age and sex. A total of, 46,263 eligible patients were included in the study. The study protocol was approved by the Korea University Guro Hospital Institutional Review Board (#2011GR0481J). All patients received information of participation in this study and provided written informed consent. PPT PowerPoint slide

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TIFF original image Download: Fig 1. Flow chart of study population. https://doi.org/10.1371/journal.pone.0272328.g001 AP measurement Air pollutant measurement data, which are available on the Air Korea website (http://www.airkorea.or.kr) operated by the Korean Ministry of Environment has been provided. The monitoring station measured PM 2.5 by mass concentration, PM 10 by the β-ray absorption method, CO by the non-dispersive infrared method, SO 2 by pulse ultraviolet fluorescence method, NO 2 by chemiluminescence method, and O 3 by ultraviolet photometric method. The measurement of PM 2.5 , began in January 2015, while the other pollutants began in 2001. We collected hourly concentrations of AP data from 329 monitoring stations nationwide and then transformed them into the daily average value. An individual’s exposure concentration to air pollutants was measured by matching each monitoring station with 68 hospitals registered in KAMIR in the order of the closest straight line. Since addresses of patients were unavailable from the multicenter registry, the monitoring station was selected based on the admitted hospital. Because AMI is an emergent event, patients would have been admitted to the nearest hospital, which was the closest to their residency or workplace at the time of disease onset. When a missing value occurred owing to problems such as breakdown and connection error with the monitoring station, the value of the next nearest monitoring station was inputted. The reference date was based on the onset of the symptom date defined the first time of MI related symptoms such as chest pain or dyspnea, and the annual average value of air pollutants before and after the symptom day was calculated. Study definitions and study endpoints AMI were defined as the presence of clinical symptoms, changes in electrocardiogram (EKG) indicating new ischemic signs, and elevation of cardiac enzymes by at least one value above the upper limit of the reference range until 7 days after symptom onset. Individual cardiovascular risk factors such as hypertension, dyslipidemia, diabetes mellitus (DM), prior cardiovascular disease, heart failure (HF), prior cerebrovascular disease, and smoking history were based on patient self-reports. The study endpoints were the cumulative incidence of all-cause death and any-revascularization during a one-year clinical follow-up period. All-cause death was defined as the incidence of death from cardiac or non-cardiac origin. Any-revascularization was defined as revascularization of the target vessel or non-target vessel revascularization. Statistical analysis All statistical analyses were conducted in R version 4.0.2 (R Core Team, 2020; R: Language and Environment for Statistical Computing; R Foundation for Statistical Computing, Vienna, Austria. URL: https://www.R-project.org/). Continuous variables were described as mean ± standard deviation, and categorical data were expressed as percentages. We performed Cox proportional hazard regression and stratified the hospitals to assess the hazard ratio (HR) of each air pollutant with a 95% confidence interval (CI) in terms of the clinical outcomes, and to account for the hospital and regional effects such as accessibility and treatment plans. Using a multivariable model, we adjusted all available variables that could be potentially relevant factors: age, sex, body mass index, smoking status, ST-segment elevation MI (STEMI), hypertension, DM, dyslipidemia, stroke, HF, previous ischemic heart disease, percutaneous coronary intervention (PCI), multi-vessel disease, left main disease, cardiopulmonary resuscitation (CPR), left ventricular ejection fraction (LVEF), and symptom date. Statistical significance was defined as a p-value of < 0.05.

Discussion The present study provides strong evidence of an association between ambient AP exposure and 1-year major clinical outcomes in patients with AMI. The results imply that the risk of mortality and recurrent cardiovascular disease may be affected by high AP concentration during the periods not only after but also before hospitalization. The strength of this study was that it focused on the clinical aspects more than prior studies had and measured the effect of AP exposure over a certain time period on each individual. Several studies have reported that short- and long-term exposure to AP is associated with mortality in cardiovascular disease patients [11, 12, 14–18]. Long-term exposure to PM 10 from the year of death or end of the follow-up to 3 years prior was associated with an increase in the HR to 1.3 (95% CI: 1.2–1.5) per 10 μg/m3 in MI patients [16]. Another cohort study in acute coronary syndrome patients reported that increase in NO 2 , NO x , PM 10 , and PM 2.5 during follow-up periods were associated with increased all-cause mortality in the adjusted model, including demographic and clinical factors; however, the mutually adjusted model with added pollutant and income, showed that only PM 2.5 was related to increased mortality [17]. In our previous study using the same registry, short-term exposure to NO 2 , SO 2 , and CO was related to increased mortality during the 30-day follow-up period [12]. This study was an extended analysis of exposure and follow-up duration, and the results demonstrated that SO 2 and PM 10 were associated with an increased risk of all-cause death. The results of this study suggest that changes in the concentrations of air pollutants may affect clinical outcomes. There seems to be no association with mortality during the entire follow-up period for one year. This result showed that most of the all-cause death occurred before 30 days, it may not reflect the annual average concentration of AP after AMI. Therefore, it will be necessary to estimate the association according to different time periods. In the case of all-cause death, we assessed the effect of the short-term outcome based on the concentration of AP of the symptom date and the effect of the long-term outcome based after the symptom date. It may explain more properly the association between all-cause death and AP according to time periods. As a result, the short-term results showed an association with SO 2 and PM 10 before AMI onset. The results of extended periods of exposure after the 30-day follow-up showed an association between mortality and AP concentrations during the follow-up periods. Therefore, even if the AP concentration before the onset of AMI was high, a decrease in the concentration after onset was expected to lead to a reduced risk of all-cause death. Another finding of the study was that a high concentration of SO 2 , CO, and PM 10 after the onset of AMI was closely related to a higher incidence of hospitalization due to revascularization. In particular, PM 10 , compared with the first quintile, showed that a difference appeared in the low quintile, and HR gradually increased as the quintile increased. Previously published cohort studies in AMI survivors reported that long-term exposure to PM 10 was associated with an increased risk of heart failure and second MI [16]. In a cohort study of five European cities, the risk of hospital re-admissions due to cardiac causes was increased by daily concentrations of PM 10 , particle number concentrations (PNC), NO 2 , CO, and O 3 in the MI population [19]. Many suggestive evidence have demonstrated that AP exposure is positively associated with cardiovascular disease incidence even in the general population [3, 6, 7, 20–25]. The results of this study was similar to other studies, wherein AP was associated with adverse health effects; however, there was a difference in pollutants that increased the risk. Particularly in the case of PM 2.5 , the data collection period was short; therefore, a relatively small number of subjects and short study periods were insufficient to determine an association with the clinical outcomes. Further research with sufficient study periods and number of subjects is needed to evaluate the association between PM 2.5 and clinical outcomes. Moreover, in AP studies, characteristics according to exposure period, study population, location, and concentration were different for each study; therefore, it is difficult to obtain consistent results for every single pollutant [3, 26]. To reduce the risk of AP exposure, it is necessary not only to implement a government policy to reduce AP emissions but also to respond to individual exposure to high concentrations of AP. Wearing a face mask was shown to be an effective protection method to reduce the inhalation of PM, alleviate symptoms of cardiovascular disease, reduce blood pressure, and increase heart rate variability in patients with cardiovascular disease [27]. In addition, in a recent study, moderate to vigorous physical activity more than 5 times per week reduced the risk of cardiovascular disease and stroke even high PM 10 concentration [28]. Education such as continuous reduction or prevention of AP exposure and encouraging indoor exercise when AP concentration is high, should be recommended for AMI patients and high-risk individuals. This study had several limitations. First, it was likely that misclassification of patients to their exposure levels occurred because the addresses of patients were not available; thus patients who visited near or transferred hospitals could be misclassified. This study was conducted based on the concentration of ambient AP. The concentrations of exposure to each air pollutant at home or in the workplace were unavailable. Second, we were unable to detect significant adverse health associations with PM 2.5 , but this was likely due to the very limited sampling data available for this air pollution metric, which was monitored only in the last year of the study. Additional data and studies are needed to determine the association between PM 2.5 and clinical events. Third, although the clinical factors influencing the prognosis were adjusted, factors such as socioeconomic status could not be adjusted due to the limitations of the study design. Fourth, all clinical results were confirmed by the data coordinators and researchers at each hospital. Although the main research center performed rigorous data management and training, input errors and misclassification of clinical events were possible because the sample size was large and many hospitals participated. Finally, the one-year follow-up period was relatively short to clarify the association with long-term AP exposure. Since the long-term prognosis is continuously poor in AMI patients compared with the general population, it is necessary to establish an association through studies with longer follow-up durations.

Conclusion In AMI patients, a higher concentration of SO 2 and PM 10 , not only after but also before hospitalization, was associated with an increased risk of all-cause death. During the follow-up period, a higher concentration of SO 2 , CO, and PM 10 was associated with an increased risk of any-revascularization up to 1-year using a nationwide prospective multicenter registry. We suggest that AMI patients and high-risk individuals establish a strategy to reduce or prevent exposure to high concentrations of AP.

Acknowledgments The KAMIR registry was performed with the support of the Korean Circulation Society (KCS) to commemorate the 50th anniversary of the KCS. The KAMIR study group of the KCS was as follows: Myung Ho Jeong (Principal investigator, E-mail: myungho@chollian.net), Chonnam National University Hospital, Gwangju; Yong Hoon Kim, Kangwon National University School of Medicine, Chuncheon; Young Jo Kim, Yeungnam University Hospital, Daegu; Chong Jin Kim, East West Neo Medical Center, Seoul; Myeong Chan Cho, Chungbuk National University Hospital, Chungju; Youngkeun Ahn, Chonnam National University Hospital, Gwangju; Jong Hyun Kim, Hanseo Hospital, Busan; Shung Chull Chae, Kyungbook National University Hospital, Daegu; Seung Ho Hur, Keimyung University Dongsan Medical Center, Daegu; In Whan Seong, Chungnam National University Hospital, Daejeon; Taek Jong Hong, Pusan National University Hospital, Busan; Dong Hoon Choi, Yonsei Cardiovascular center, Seoul; Jei Keon Chae, Chonbuk National University Hospital, Jeonju; Jae Young Rhew, Presbyterian Medical Center, Jeonju; Doo Il Kim, Inje University Busan Paik Hospital, Busan; In Ho Chae, Seoul National University Bundang Hospital, Seoul; Jung Han Yoon, Wonju Severance Christian Hospital, Wonju; Bon Kwon Koo, Seoul National University Hospital, Seoul; Byung Ok Kim, Inje University Sanggye Paik Hospital, Seoul; Myoung Yong Lee, Dankook University Hospital, Cheonan; Kee Sik Kim, Daegu Catholic University Medical Center, Daegu; Jin Yong Hwang, Gyeongsang National University Hospital, Jinju; Seok Kyu Oh, Wonkwang University Hospital, Iksan; Nae Hee Lee, Soon Chun Hyang University Hospital, Bucheon; Kyoung Tae Jeong, Eulji University Hospital, Daejeon; Seung Jea Tahk, Ajou University Hospital, Suwon; Jang Ho Bae, Konyang University Hospital, Daejeon; Seung-Woon Rha, Cheol Ung Choi, Ji Bak Kim, Dong Oh Kang, Soohyung Park, Korea University Guro Hospital, Seoul; Keum Soo Park, Inha University Hospital, Incheon; Kyoo Rok Han, Hallym University Kangdong Medical Center, Seoul; Tae Hoon Ahn, Gachon University Gil Medical Center, Incheon; Moo Hyun Kim, Dong- A University Hospital, Busan; Joo Young Yang, National Health Insurance Service Ilsan Hospital, Goyang; Chong Yun Rhim, Hallym University Medical Center, Seoul; Hyeon Cheol Gwon, Samsung Medical Center, Seoul; Seong Wook Park, Asan Medical Center, Seoul; Young Youp Koh, Chosun University Hospital, Gwangju; Seung Jae Joo, Jeju National University Hospital, Jeju; Soo Joong Kim, Kyunghee University Medical Center, Seoul; Dong Kyu Jin, Soon Chun Hyang University Hospital, Cheonan; Jin Man Cho, Kyunghee University Hospital, Seoul; Wook Sung Chung, Catholic University Hospital, Seoul; Yang Soo Jang, Yonsei Cardiovascular Center, Seoul; Jeong Gwan Cho, Chonnam National University Hospital, Gwangju; Ki Bae Seung, Catholic University Hospital, Seoul; and Seung Jung Park, Asan Medical Center, Seoul.

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