Effect of Statins on the Risk of Poststroke Pneumonia: National Population-Based Cohort Study.

PURPOSE: Statins are widely prescribed medications for treatment of dyslipidemia and prevention of cardiovascular disease. Beyond their lipid-lowering property, statins exhibit multiple pleiotropic and antimicrobial effects. We aimed to investigate the effect of statins on the long-term risk of pneumonia after acute ischemic stroke.
METHODS: This retrospective observational research was performed using South Korean National Health Insurance Service claim data, which consist of population-based random sampling. We included patients discharged with acute ischemic stroke (I63 in the ICD10) and no prior history of pneumonia. The primary outcome measure was the occurrence of pneumonia determined based on ICD10 code J09-J18. Treatment with statins during follow-up was collected as a time-dependent variable based on prescription records.
RESULTS: A total of 7,001 subjects with acute ischemic stroke and no prior history of pneumonia were included. During the mean 3.96-year follow-up, pneumonia occurred in 1,715 subjects (24.5%). On multivariate time-dependent Cox proportional hazard-regression analyses, significant preventive benefit of treatment with statins against pneumonia was noted (adjusted HR 0.86, 95% CI 0.77-0.97). Compared to no use of statin, adjusted HRs (95% CIs) for current use of low-intermediate high-intensity statins were 0.88 (0.78-0.99) and 0.49 (0.27-0.87), respectively.
CONCLUSION: Our retrospective national cohort study found reduced risk of poststroke pneumonia with statin therapy after acute ischemic stroke. Our study suggests that treatment with statins may have a preventive effect against the common complication of poststroke pneumonia.

Introduction

Stroke victims are at particularly increased risk of acquiring pneumonia, a critical cause of death after stroke.1 Stroke victims frequently experience dysphagia leading to aspiration of food and development of pneumonia. Additionally, not only older age but also malnutrition and limited physical activity due to stroke are well-known risk factors for developing pneumonia.2,3 Because poststroke pneumonia is fatal and a marker of worse prognosis,4 identification of risk factors and development of preventive strategies for poststroke pneumonia are clinically important in stroke victims.5,6

Statins are widely prescribed medications for treatment of dyslipidemia and prevention of cardiovascular disease. Beyond their lipid-lowering property, statins exhibit multiple pleiotropic and antimicrobial effects. Statins can affect a variety of immuno responses, including immune-cell activation, migration, cytokine production, stimulation of antigen-presenting cells, and immune-cell metabolism and survival, which are related to protection against infection or inflammation.7 Owing to statins’ immunomodulating effects, prior studies have suggested that treatment with them may lower the risk of pneumonia.8,9 There have been studies on whether treatment with statins before admission or during the acute phase of stroke might reduce the development of pneumonia.10,11 However, the findings were inconsistent and unclear, and so failed to establish a definitive relationship between long-term risk of pneumonia and exposure to statins beyond the acute phase of stroke.11 In clinical practice, the use of drugs is dynamic and may be frequently changed. The influence of statin intensity on the risk of developing pneumonia is not well known. Therefore, the current retrospective study was conducted using a Korean national sample cohort data, which include longitudinal data regarding the occurrence of pneumonia and records of prescription, to evaluate the effects of treatment with statins on the long-term risk of poststroke pneumonia.

Methods

Data Sources

This was a retrospective study based on the random-sampling dataset of the South Korean National Health Insurance Service claim database.12 This dataset is composed of 1,025,340 subjects randomly sampled and stratified by age, sex, and earning level. Because the National Health Insurance Service in South Korea is a single-payer system, overall health claims comprising demographics, hospitals visits, receipt of surgery or procedures, prescriptions, diagnosis, and mortality information of the participants included were available. Diagnostic codes at each hospital visit were recorded based on the ICD10. The National Health Insurance database is fully anonymized and does not contain any personal identification information. The Institutional Review Board of Bundang CHA Medical Center (IRB CHAMC 2017–12-043) approved the study and waived the requirement for informed consent.

Study Subjects

Patients ≥20 years of age who had been hospitalized (visited emergency medical center or admitted to hospital) between July 2002 and December 2013 with a main diagnosis of ischemic stroke (I63 in ICD10) were included. In order to enroll subjects with acute ischemic stroke, participants who had undergone brain magnetic resonance imaging or computed tomography during hospital admission were selected, considering that subjects with acute ischemic stroke would have had brain imaging performed.13 Patients who had ICD10 code of J09–J18 (pneumonia) prior to discharge date of the index stroke were excluded. In South Korea’s health-claim system, the previously registered diagnostic code may be automatically registered in the latter visit. Therefore, once the pneumonia ICD10 code has been assigned to a patient, it is not possible to determine clearly whether the pneumonia has been cured or remains in the NHIS-NSC data set. When a patient revisits the same hospital, it is ambiguous whether the revisit is due to recurrence of pneumonia or another medical problem. Therefore, to exclude the potency of false positives due to prior diagnosis, we included only patients who had not had a prior diagnosis of pneumonia (excluding patients with a history of pneumonia). Because inclusion of prevalent statin users in the observational study may introduce selection bias, patients who had exposure to statins within 6 months before the admission of acute ischemic stroke were excluded.14,15 To detect only patients who newly developed pneumonia after stroke as outcome, patients who had less than a month of follow-up after discharge were also excluded.16 Flowchart of the inclusion and exclusion criteria of patients is shown in Figure 1.

Figure 1

Flowchart of patients included.

Abbreviation: NHIS-NSC, National Health Insurance Service national sample cohort.

Outcome and Follow-Up

The primary outcome measure was the time of occurrence of pneumonia, which was considered from hospital-visit records with diagnostic codes J09–J18.17,18 Detection of pneumonia from ICD10 codes has been reported to be reliable and widely used in research data.19,20 All subjects were followed up until the occurrence of pneumonia, death, loss of eligibility for the South Korean National Health Insurance Service, or 31 December, 2013, whichever occurred first.

Drug-Exposure Assessment

On each day of follow-up after discharge from the index stroke, data on treatment with statins was accessed using the prescription records of each patient, which were collected as time-dependent variables. To evaluate the dose–response relationship, statin intensity was grouped into low– intermediate intensity (atorvastatin <20 mg, rosuvastatin <10 mg, pravastatin ≤80 mg, lovastatin ≤40 mg, simvastatin ≤40 mg, fluvastatin ≤80 mg, pitavastatin ≤4 mg) and high intensity (atorvastatin ≥40 mg, rosuvastatin ≥20 mg) according to the type and daily dose of the statins in accordance with the low-density lipoprotein–lowering potency of each agent.21

Other Covariates

Other covariates were age, sex, earning level, and comorbidities: hypertension, diabetes mellitus, atrial fibrillation, myocardial infarction, and chronic obstructive pulmonary disease. In the NHIS-NSC dataset, age is recorded at 5-year intervals for privacy protection. Earning level is stratified into tertile groups. Use of thrombolysis (653,500,660, 653,500,670, E04260071, E04260161 for intravenous and M6631, M6632, M6633 for intra-arterial) for acute ischemic stroke was determined by the procedure codes in the NHIS-NSC. The presence of hypertension (I10–I15), diabetes mellitus (E08–E11, E13–E14), atrial fibrillation (I48), myocardial infarction (I21), and chronic obstructive pulmonary disease (J42, J43 [not J43.0], J44) were defined by diagnostic and procedure codes before or during hospitalization for the index stroke.13,22 Hypertension and diabetes mellitus were recognized as relevant only if subjects had received antihypertensive or antidiabetic medications at the time of diagnosis.23 Stroke severity was considered a possible marker of prognosis; however, data were unavailable in the NHIS-NSC, with limitations in health insurance–claim data. Instead, length of hospital stay following index stroke was considered an alternative marker, which has proven to be reliably associated with baseline stroke severity and stroke-related disability.24 Participants were divided into two groups (≤16 days, >16 days) based on median length of hospital stay following index stroke. Based on the health-care resources of the hospital at index stroke, classification was “general hospital”, which referred to large-scale hospitals, and “clinic or hospital”.

Statistical Analyses

Age recorded at 5-year intervals was treated as a continuous variable in the statistical analysis and expressed as medians and IQRs. Comparison of characteristics between the two groups was performed using χ2 tests for categorical variables and Mann–Whitney U tests for continuous variables (age-groups). The use of statins on each day of follow-up was considered the time-dependent variable (unit of time is day). Plots for estimated pneumonia-free probability according to treatment with statins were done considering the nature of the time-dependent variable.25 HRs and 95% CI were calculated by time-dependent Cox proportional hazard–regression models. During follow-up, patients who died without pneumonia were treated as censoring events. To investigate associative factors for occurrence of pneumonia, adjustments were performed for age, sex, earning level, history of hypertension, diabetes mellitus, atrial fibrillation, myocardial infarction, chronic obstructive pulmonary disease, use of thrombolysis, and type of hospital at index stroke. Linear trends in statin intensity and clinical outcome were estimated by regarding the statin-intensity groups as a continuous variable (no statins 0, low–intermediate intensity statins 1, and high-intensity statins 2). The proportional-hazard assumption for the model was tested by calculating Schoenfeld residuals and found to be satisfactory. Data management and statistical analyses were undertaken with R version 3.4.4 (R Foundation for Statistical Computing, Vienna, Austria; ) and PostgreSQL version 10.6 (PostgreSQL Global Development Group; ). Two-sided p<0.05 was considered statistically significant.

Results

Characteristics

The current study included 7,001 subjects discharged after acute ischemic stroke without a history of pneumonia (Figure 1). The median age was 65–69 years (IQR 55–59 to 75–79 years), and 55.7% were men (Table 1). Figure 2 shows the proportions of participants with current use of statins during the follow-up period after stroke. In the figure, the proportion of subjects with current use of statins was relatively consistent (about 30%) throughout the poststroke period. At 1 year after discharge from index stroke, 5,640 subjects were at risk of developing pneumonia (patients remained and had no pneumonia until the time point). Among the 5,640 subjects at 1 year postdischarge, 1,386 (24.6%) were current users of statins. To identify the difference in characteristics of subjects who received statins with those who did not, clinical characteristics were compared between the groups (Table 2). Subjects with current use of statins were more likely to be male, younger, have hypertension and/or diabetes mellitus, have received thrombolysis and been hospitalized in a general hospital with longer length of stay in hospital for index stroke.

Table 1

Baseline Characteristics of Patients with Acute Ischemic Stroke

	n=7,001
Sex, male	3,902 (55.7)
Age, years	65–69 (55–59 to 75–79)
Hypertension	5,083 (72.6)
Diabetes mellitus	1,862 (26.6)
Myocardial infarction	473 (6.8)
Atrial fibrillation	688 (9.8)
Chronic obstructive pulmonary disease	1,383 (19.8)
Thrombolysis	230 (3.3)
Household income
Low	2,314 (33.1)
Middle	2,551 (36.4)
High	2,136 (30.5)
Hospital type at index stroke
General hospital	5,844 (83.5)
Hospital or clinic	1,157 (16.5)
Duration of hospital stay following index stroke
≤16 days	3,690 (52.7)
>16 days	3,311 (47.3)

Note: Data presented as n (%) or medians (IQRs).

Figure 2

Proportion of patients with current of statin use throughout the poststroke period. The proportion was calculated by dividing the number of patients with current statin use by the number of patients still at risk of pneumonia at each time point.

Table 2

Comparison of Characteristics Between Patients with Current Use of Statin and Those Without at 1-Year After Acute Ischemic Stroke

	No use of statins (n=4,254)	Current use of statins (n=1,386)	p-value
Sex, male	2323 (54.6)	817 (58.9)	0.005
Age, years	65–69 (55–59 to 75–79)	65–69 (55–59 to 70–74)	<0.001
Hypertension	2,965 (69.7)	1,046 (75.5)	<0.001
Diabetes mellitus	982 (23.1)	435 (31.4)	<0.001
Myocardial infarction	268 (6.3)	94 (6.8)	0.567
Atrial fibrillation	369 (8.7)	129 (9.3)	0.505
Chronic obstructive pulmonary disease	784 (18.4)	236 (17.0)	0.255
Thrombolysis	114 (2.7)	61 (4.4)	0.002
Household income			0.152
Low	1,409 (33.1)	421 (30.4)
Middle	1,540 (36.2)	515 (37.2)
High	1,305 (30.7)	450 (32.5)
Hospital type at index stroke			<0.001
General hospital	3,468 (81.5)	1,264 (91.2)
Hospital or clinic	786 (18.5)	122 (8.8)
Duration of hospital stay following index stroke			<0.001
≤16 days	2,389 (56.2)	624 (45.0)
>16 days	1,865 (43.8)	762 (55.0)

Note: Data presented as n (%) or medians (IQRs).

Risk of Pneumonia

During 3.96±2.99 years of follow-up after discharge from index stroke, there were 1,715 subjects that developed pneumonia (24.5%). Censored patients without pneumonia numbered 5,286 (1,218 who had died, 152 with loss of eligibility for national health insurance, and 4,068 subjects who had survived without pneumonia until the study end date). Figure 3 demonstrates the estimated pneumonia-free survival curves according to current treatment with statins during the follow-up period. In the plot, subjects who received statins had lower risk of pneumonia compared to those who did not (unadjusted HR 0.81, 95% CI 0.73–0.91; p<0.001; Figure 3A). When subdivision was based on statin intensity (low– intermediate and “high”), use of both low– intermediate (unadjusted HR (0.83, (95% CI 0.74–0.94; p=0.002) and high (unadjusted HR (0.45, (95% CI 0.25–0.81; p=0.008)–intensity statins was significantly associated with lower risk of pneumonia than no use of statins (Figure 3B). In the multivariate time-dependent Cox proportional hazard–regression model, there was significantly lower risk of developing pneumonia with current use of statins (adjusted HR 0.86, 95% CI 0.77–0.97; p=0.013) than no use of statins (Table 3). Other significant risk factors for poststroke pneumonia were male sex, old age, diabetes mellitus, chronic obstructive pulmonary disease, and admission to a hospital or clinic at index stroke.

Figure 3

Estimated pneumonia-free probability according to treatment with statins (A) and according to intensity of statins (B) during follow-up. HRs for pneumonia and 95% CIs were derived from the univariate time-dependent Cox proportional hazard–regression model.

Table 3

Effects of Treatment with Statins on Risk of Poststroke Pneumonia

	Unadjusted HR (95% CI)	Adjusted HR (95% CI)
Sex, male	0.95 (0.86–1.04)	1.18 (1.07–1.31)
Age, per 5-year interval	1.22 (1.19–1.24)	1.21 (1.18–1.23)
Hypertension	1.41 (1.26–1.58)	1.12 (1.00–1.25)
Diabetes mellitus	1.28 (1.15–1.42)	1.23 (1.11–1.37)
Myocardial infarction	1.17 (0.97–1.41)	1.09 (0.91–1.32)
Atrial fibrillation	1.40 (1.20–1.63)	1.17 (1.00–1.37)
Chronic obstructive pulmonary disease	1.63 (1.45–1.82)	1.29 (1.15–1.45)
Thrombolysis	1.02 (0.76–1.37)	1.10 (0.81–1.48)
Household income
Low	1 (ref)	1 (ref)
Middle	0.95 (0.84–1.06)	0.96 (0.86–1.08)
High	1.09 (0.97–1.22)	0.95 (0.84–1.07)
Hospital type at index stroke
General hospital	1 (ref)	1 (ref)
Hospital or clinic	1.41 (1.25–1.59)	1.20 (1.06–1.35)
Duration of hospital stay following index stroke
≤16 days	1 (ref)	1 (ref)
>16 days	0.95 (0.87–1.05)	0.92 (0.84–1.01)
Time-dependent variables
No use of statins	1 (ref)	1 (ref)
Current use of statins	0.81 (0.73–0.91)	0.86 (0.77–0.97)

Note: Data derived from Cox proportional hazard–regression model for the development of poststroke pneumonia.

Risk of Pneumonia According to Statin Intensity

In the multivariate model considering statin intensity (Table 4), both statin-intensity groups were significantly associated with lower risk of poststroke pneumonia. Compared with no statin, the risk of pneumonia (adjusted HR [95% CI]) with low- to intermediate-intensity statins and high-intensity statins was 0.88 (0.78–0.99) and 0.49 (0.27–0.87), respectively. There was a significant dose–response relationship between statin intensity and risk of poststroke pneumonia (p for trend=0.004).

Table 4

Risk of Poststroke Pneumonia According to Statin Intensity

Statin therapy	Adjusted HR (95% CI)	p-value	p-value for trend
No use of statins	1 (ref)	—	0.004
Current use of low- to intermediate-intensity statins	0.88 (0.78–0.99)	0.038
Current use of high-intensity statins	0.49 (0.27–0.87)	0.015

Note: Data derived from multivariate time-dependent Cox proportional hazard–regression model adjusted for the variables listed in Table 3.

Discussion

Using the national sample cohort based on health insurance–claim data in South Korea, we investigated the risk of occurrence of pneumonia according to treatment with statins throughout the long-term follow-up period after acute ischemic stroke. Poststroke pneumonia was common in the current study during the mean follow-up of 3.96 years, wherein 24.5% of patients suffered it. The chief finding of this study was that treatment with statins was significantly associated with lower risk of poststroke pneumonia. The amplitude of risk reduction with statins (adjusted HR 0.86) was comparable with data from prior epidemiological studies suggesting a preventive role of statins against pneumonia.26 In this real-world study on acute ischemic stroke, the proportion of patients who received statin therapy was suboptimal. Suboptimal use of statins in the real world, even after major cardiovascular disease, has been consistently reported and remains a major challenge in clinical practice.13 As poststroke pneumonia is common and associated with short-term and long-term disability, attempts should be made to prevent development of the condition.10 Data from the current study suggest that enhancement of guideline-recommended statin therapy after ischemic stroke may further reduce the risk of poststroke pneumonia beyond the established cardiovascular risk reduction.13

The exact mechanism of action of statins on pneumonia remains uncertain. Multiple antimicrobial and immunomodulating mechanisms of statins have been suggested.27 Experimental and animal studies have indicated that treatment with statins results in a protective immunoresponse against pathogens and attenuation of tissue injury by proinflammatory pathways, independently of lipid-lowering properties.28 There are cellular and molecular protective mechanisms of statins in cytokine synthesis, adhesive molecules, Toll-like receptors, B lymphocytes, and helper and regulatory T lymphocytes.29,30 In acute inflammatory states induced by exotoxin, pretreatment with simvastatin significantly attenuates expression of P-selectin in endothelia, leukocyte rolling, adherence, and transmigration of leukocytes.31 The statin-mediated interaction between leukocytes and endothelial cells may be involved in both inflammatory pathways and tissue injury in infectious diseases. In lipopolysaccharide (LPS) stimulation, the protein secretion and mRNA expression of IL6 and IL8 are significantly inhibited by treatment with pitavastatin and pravastatin.32 Atorvastatin attenuates TNFα expression and production in LPS-stimulated macrophages.33 Administration of atorvastatin reduces levels of serum IFNγ and IL4 in Candida albicans–infected mice.34 Proliferation and activation of T lymphocytes is inhibited by multiple statin-mediated mechanisms.35,36 There is evidence of CD4:CD8 ratio and shift from type 1 to type 2 helper T cells with simvastatin.37 These altered immuno responses from statins are predominantly anti-inflammatory and immunosuppressive, which might be predisposing factors in infection.38 However, numerous studies have shown that statins also can induce strong proinflammatory responses when costimulatory signals are provided.39 In addition, there are experimental data that statins can enhance and modulate innate immunity.40,41 In macrophages, statins promote autophagy pathways by inducing endosome maturation and fusion of autophagosomes with lysosomes, resulting in degradation of sequestered bacteria.42 Statins have been shown to increase plasma high-density lipoprotein, which can act as an antioxidative and anti-inflammatory molecule that impedes monocyte chemotaxis.43 Lipoproteins play an important role in immunoresponse.44 Furthermore, statins may exhibit antibacterial activity that interrupts bacterial cell functions via binding and disruption of cell-wall structures such as teichoic acids, lipoteichoic acids, LPSs, and surface proteins.45 Modulation of gene expression in immune cells and cell-adhesion molecules by statins may reduce replication of viruses, including influenza.46 By promotion of the host-defense mechanism and inhibition of pathological inflammation, statins may play a beneficial protective role against infectious diseases.27 Along with the theoretical background, many epidemiological studies have reported that therapy with statins may reduce the risk of pneumonia, infection, and mortality in the general population and various disease groups, including stroke.8,10,26,47,48 As supporting data for the antibacterial and immunoprotective effects of statins, treatment with statins confers a survival advantage to patients with a diagnosis of pneumonia.49 Among thrombolyzed stroke patients, continued treatment with statins is negatively associated with pneumonia after stroke.10 In cohort studies using Taiwan’s National Health Insurance Research Database, statin use exhibited lower risk of hospitalization and vital-organ failure in COPD patients.50,51

Despite the promising reports from animal and observational studies, there are conflicting data from clinical trials on the relationship between statin therapy and risk of pneumonia. A meta-analysis that included eleven randomized trials on use of statins found no significant preventive effect of the drug on the risk of infection.52 Similarly, a recent meta-analysis that included five clinical trials with 8,791 stroke or transient ischemic–attack patients did not report a significant effect of statins on reduction in risk of infection.53 Based on these negative findings, there is a concern for potential bias in observational studies suggesting the preventive effect of statins in pneumonia.54,55 Treatment with statins may reflect the willingness of the patient to follow treatment and better functional status (healthy-user effects), rather than the true biological preventive effect of the drug.10 However, caution must be exercised in interpretation of the negative findings of the clinical trials, because none of the trials set pneumonia as the primary outcome measure. The randomized, double-blind, placebo-controlled JUPITER trialdocumented that the rosuvastatin group had a lower risk of pneumonia than the placebo group.26

In the present study, the preventive effect of statins remained unchanged after additional adjustment for treatment with antihypertensive medications. This finding suggested that the preventive effect of treatment with statins was not completely explained by compliance with medical treatment. The conflicting data among studies might be related to heterogeneous regimens, timing of treatment with statins, variability in definition of pneumonia, and study duration.56 Patients with acute ischemic stroke in the present study, who were particularly at great risk for pneumonia, may be more likely to benefit from treatment with statins than the general population. To date, no large randomized clinical study has been conducted evaluating the effect of statins on the development of pneumonia as the primary outcome measure. Further evidence based on well-designed prospective randomized trials is needed to address the key question of the beneficial role of statins in pneumonia.8

In accordance with the initial expectation, we found a dose-dependent relationship between risk of pneumonia and intensity of statins. Along with lipid-lowering potency, the beneficial pleiotropic effects of statins, such as the antibacterial and immunomodulatory properties, may act in a dose-dependent fashion.57 To maximize the potential benefits of statins, further experimental and clinical investigations are warranted to elucidate the underlying biological mechanism of action of statins in pneumonia.

The main strength of the current study is the use of information from the population-based random-sampling database, which enabled inclusion of >7,000 subjects with acute ischemic stroke. Based on the national database, longitudinal follow-up of the participants to assess the occurrence of pneumonia was possible. Unlike prior studies, which have focused mainly on exposure to statins before or during the early phase of admission following a stroke, data on treatment with statins throughout follow-up after discharge from hospital were collected in the current study, reflecting dynamic changes in medications in clinical practice. The potential limitations of this study should also be acknowledged. Clinical data regarding stroke severity, functional disability, dysphagia, smoking, and lipid levels were not obtained, owing to unavailability of such information from the health-insurance database. Due to the retrospective observational design of the study, causality between statin use and risk of pneumonia could not be established. Data on statin use was obtained from the prescription records of each subject. There may be a gap between prescribed medication and actual medicine-taking behaviors of subjects. Previous research has shown a good association between values calculated from prescription records and real intake of medications.58 In the current study, detection of pneumonia outcome was based on ICD10 codes, which may be associated with loss of subjects with pneumonia by error of registration in clinical practice or by them missing hospital visits. Moreover, the ICD10 codes J09–J18 can overestimate pneumonia diagnosis, since suspected diagnoses can also be labeledICD10 J09–J18 in real-world practice. The current study was performed using data of Asian subjects with acute ischemic stroke. Further studies must be conducted to evaluate the general applicability of the results in different ethnicities and disease populations.

Conclusion

Using a national health-insurance database, the current study found reduced risk of poststroke pneumonia with statin therapy after acute ischemic stroke. The preventive effect of statins on pneumonia did not differ based on statin intensity. Encouragement of statin treatment after ischemic stroke, the guideline-recommended treatment, may reduce poststroke pneumonia, which is a common and critical illness in stroke subjects.