The impact of aspirin on Klebsiella pneumoniae liver abscess in diabetic patients

In this study, we aimed to investigate the impact of aspirin on the risk of pyogenic liver abscess caused by Klebsiella pneumoniae (KP-PLA) and invasive KP-PLA syndrome (IKPS) in diabetic patients. Diabetic patients who were propensity-score matched were retrospectively included from hospital-based database. Kaplan–Meier approach with a log-rank test was used to compare the cumulative incidences of KP-PLA including IKPS between aspirin users and non-users. Totally, 63,500 patients were analyzed after propensity-score matching (1:1). Compared with that of non-users, the incidence of KP-PLA was significantly reduced in aspirin users (0.31% vs. 0.50%, p < 0.01), but not for that of IKPS (0.02% vs. 0.03%, p = 0.29). Patients taking aspirin for ≥ 90 days had a significantly lower risk for KP-PLA (hazard ratio, 0.67; 95%CI, 0.50–0.90). Females, taking clopidogrel or metformin for ≥ 90 days, and taking H2-blockers or proton pump inhibitors (PPIs) for ≥ 5 days were also associated with a lower risk of KP-PLA. However, cholangitis and a glycated hemoglobin ≥ 8.5% were associated with an increased risk of KP-PLA.


Scientific Reports
| (2020) 10:21329 | https://doi.org/10.1038/s41598-020-78442-8 www.nature.com/scientificreports/ previously been performed to investigate the association between KP-PLA, including invasive KP-PLA syndrome, and aspirin use. The primary aim of the current study was to determine the role of aspirin use in diabetic patients and its association with the risk of KP-PLA and invasive KP-PLA syndrome.

Results
Clinical characteristics of diabetic patients with and without aspirin use. A total of 95,627 patients diagnosed with diabetes between 2001 and 2018 fulfilled the study criteria (Fig. 1). The mean age was 62.04 ± 12.65 years, 48% of the included patients were female, 1.6% had cholangitis, 67.4% took metformin, and the mean value of glycated hemoglobin was 8.42 ± 2.25%. Table 1 shows their clinical characteristics before and after PSM.
In the PSM cohort, the baseline comorbid conditions and prior medications were not significantly different between the aspirin users and non-users. The mean follow-up time was 5.69 years (Supplementary Table S1-1). Among aspirin users, 14.2% and 35.8% were exposed to aspirin for 1-90 days and > 90 days during the followup, respectively (Supplementary Table S1-2). Table 2 presents the concomitant medications used during the Patients who received aspirin were propensity matched in a 1:1 ratio with those who were not taking aspirin and were alive at the time of the first dispensed prescription to their matched counterpart. 2. Comorbidities: cirrhosis, injury to the liver, hepatobiliary malignancy, gastric cancer, colon cancer, cholangitis, bile duct stones/cholelithiasis, viral hepatitis, hepatitis B, hepatitis C, renal disease, hepatocellular carcinoma, metastatic cancers, other malignancies, ischemic heart disease and myocardial infarction, ischemic stroke, arrhythmia, all cardiovascular or cerebrovascular accident events, and atherosclerosis. 3. Medication: centrally acting anti-adrenergic agents, ą-blockers, thiazide-type diuretics, ß-blockers, calcium channel blockers, angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists, anti-diabetic therapies (metformin, sulfonylureas, acarbose, TZD, DPP4, GLP1, SGLT2, meglitinides, and insulin). Table 1. Baseline characteristics before and after propensity score matching. DPP4, dipeptidyl peptidase 4 inhibitors; GLP1, glucagon-like peptide-1 analogues; HbA1c, glycated hemoglobin; SGLT2, sodium-glucose co-transporter 2 inhibitors; SMD, standardized mean differences. *an SMD < 0.1 was considered well balance. There was a small number of patients with unspecified liver injury (n = 28), other viral hepatitis (n = 97), or taking centrally acting anti-adrenergic agents (n = 332) and they were not considered in further analyses.
KP liver abscess and in-hospital mortality. The cumulative incidence of KP-PLA was 0.35% in the primary cohort and 0.41% in the PSM cohort over the 15 years of follow-up. In the primary cohort, the incidence of KP-PLA was significantly higher in the non-user group compared with the aspirin user group (0.57% vs. 0.29%, p < 0.01) ( Table 3). This significant difference in the incidence of KP-PLA remained between the two groups after matching (0.50% in the non-users vs. 0.31% in the aspirin users; log-rank test, p < 0.01) (Fig. 2). The incidence of invasive KP-PLA syndrome was low (n = 18 in the primary cohort and n = 14 in the PSM cohort) and was not significantly different between the aspirin user and non-user groups in both primary and PSM cohorts (Table 3). In-hospital mortality was 9.3% in the primary cohort and 8.2% in the PSM cohort over the study period. Although the all-cause mortality rate was slightly higher in the aspirin user group compared with the non-user group (8.83% vs.7.64%, p < 0.01) in the PSM cohort, it was not significantly different over the study period (log-rank test, p = 0.24) (Fig. 3).
Duration of aspirin exposure was significantly associated with the risk of KP-PLA, after controlling for baseline characteristics and concomitant medications during the follow-up ( Table 4). The risk of KP-PLA was significantly lower among patients with > 90 days of aspirin exposure (aHR, 0.67; 95%CI, 0.50-0.90; p = 0.01) compared with non-users; however, there was no significant difference between those with < 90 days of aspirin exposure (aHR, 0.87; 95%CI, 0.56-1.34; p = 0.52) and non-users.

Discussion
The current study demonstrates that use of aspirin for > 90 days was associated with a lower risk of KP-PLA in diabetic patients without an increase in mortality. Although the risk of KP-PLA decreased with aspirin use, that of invasive KP-PLA syndrome did not. This was probably due to the low prevalence of metastatic infection in both aspirin users and non-users. Aspirin has been reported to inhibit the production of KP CPS, which is important to its virulence because of its anti-phagocytic effect against macrophages and neutrophils 12,21 . Plateletmonocyte aggregation is also involved in the pathogenesis of KP-PLA in diabetic patients, which was shown to be decreased by aspirin 22 . www.nature.com/scientificreports/ In addition to aspirin use, our study revealed that taking clopidogrel reduced the risk of KP-PLA. Chao et al. found that taking aspirin and clopidogrel for 1-12 months could change the intestinal flora; the number of Lactobacillales and Lactobacillaceae within the flora increased at the order level and family level, respectively 23 . The development of KP-PLA is associated with changes in the gut microbiota, especially a reduction in the Lactobacillales and Lactobacillaceae flora 24 . Some species of Lactobacillus have been proved to inhibit KP in vitro 25 . On the other hand, ticagrelor and other anti-platelet agents, such as dipyridamole, tirofiban, or cilostazol, were not demonstrated to change the gut microbiota. Our study also did not find that these agents were associated with a reduced risk of KP-PLA.
Our study demonstrates that using H 2 receptor antagonists or proton pump inhibitors for a minimum of 5 days was associated with a lower risk of KP-PLA. Previous studies had shown that treatment with proton pump inhibitors increased Lactobacillales not only in animal models but also in healthy individuals 26,27 . There was no direct evidence for changes in the gut microbiota after using H 2 receptor antagonists, yet it seemed that the microflora Table 3. Comparisons of incidences of K. pneumoniae liver abscess, invasive K. pneumoniae liver abscess syndrome and mortality between aspirin users and non-users in unmatched cohort and propensity-score matched (PSM) cohort. www.nature.com/scientificreports/ was still affected by those medications 28,29 . In contrast to our findings, Wang et al. used the National Health Insurance Research Database (NHIRD) in Taiwan and discovered that using proton pump inhibitors for > 5 cumulative defined daily doses increased the risk of PLA 30 . Our study, using the CGRD, could accurately identify diabetic patients with KP-PLA, and this information cannot be gathered from the NHIRD. After propensity-score matching of the glycated hemoglobin value, we found that using metformin for > 90 days could considerably reduce the risk of KP-PLA. Individuals taking metformin for 2 months were shown to have changes in their gut microbiota, especially in the growth of Bifidobacterium, of which some strains seemed to have antibacterial activity against enteropathogenic bacteria 31,32 . Other studies revealed increased amount of Lactobacillus with metformin treatment 33,34 . These results indicate that metformin could alter the human gut microbiota; however, how it affects KP colonization in the human gut warrants more investigations. Compared to male patients, female patients had a lower incidence of PLA, not only in our study but also in previous studies using the Taiwan NHIRD 6,18 . Biliary tract disease was reported to be associated with PLA and was much more likely to be associated with polymicrobial infections, including Escherichia coli, Enterococcus and Klebsiella species 6,35 . Our study supported the finding that diabetic patients who previously had cholangitis were at greater risk of KP-PLA. Patients with a glycated hemoglobin level > 7% were associated with impaired phagocytosis of KP serotypes K1 and K2 and a higher incidence of PLA 17,36 . Our findings support the theory that poor glycemic control, defined as a glycated hemoglobin level more than 8.5%, was associated with a significantly increased risk of KP-PLA.
A strength of the current study was that it was performed using the CGRD, a database gathered from two medical centers and five local hospitals, with high overall coverage of individuals seeking care reimbursed by the National Health Insurance in Taiwan 37 . It could provide detailed information on the patients' diagnosis, medications, laboratory and examination data. However, there were still some limitations. Previous studies demonstrated that patients in the CGRD had more severe comorbidities than the general population 37 . Therefore, we used propensity-score matching to minimize the differences in comorbidities. In addition, patients might return to their primary care facilities, not the Chang Gung Memorial Hospitals, for their long-term follow-up after their disease stabilized. This might cause bias in the event rate and mortality. To eliminate the bias of loss to follow-up, we excluded patients who didn't have any medical records for one year prior to their diagnosis of diabetes. The incidence of invasive KP-PLA syndrome was previously reported to be 15% in Taiwan 12 ; however, it was about 4.2% (18/422) and 5.4% (14/257) in unmatched cohort and PSM cohort, respectively in our study. The prevalence of invasive KP-PLA syndrome might be under-estimated in our study because it was not a routine to screen for any metastatic infection in each patient with KP-PLA in clinical practice. Finally, it was a retrospective study and there might be some confounding factors that were not measured in the analysis despite adjustment by propensity-score matching.  www.nature.com/scientificreports/ In conclusion, we found that females, taking clopidogrel or metformin for ≥ 90 days, and taking H2-blockers or proton pump inhibitors for ≥ 5 days, and taking aspirin > 90 days were associated a reduced risk of KP-PLA in diabetic patients without increasing mortality. In contrast, aspirin had no effect on invasive KP-PLA syndrome in these patients. Further randomized controlled trial might be required to establish the role of aspirin in prevention of KP-PLA in diabetic patients.

Methods
Data source. The present retrospective cohort study was performed using the Chang Gung Research Database (CGRD), which is an electronic health records dataset from a large healthcare delivery system at Chang Gung Memorial Hospital in Taiwan, which includes two medical centers and five local hospitals 38 . The CGRD covers approximately 10% of all health services within the Taiwan National Health Insurance program, which is a single-payer nationwide health insurance program that covers over 99% of Taiwan's population 39 . The CGRD contains detailed diagnostic, prescription, and laboratory test result information from the emergency department, inpatient, and outpatient settings. The current study was approved by the Institutional Review Board of Chang Gung Medical Foundation, Taipei, Taiwan (201900920B0). All personal identifiable information was anonymized, and, therefore, the need for informed consent was waived. All methods were carried out in accordance with relevant guidelines and regulations. Study cohort. We identified patients from the CGRD who had DM and were being newly treated with antidiabetic therapy (ADT) (i.e., insulin, GLP-1 agonists or oral hypoglycemic agents) between January 1st 2001 and December 31st 2018. The information of the diabetic patients prescribed ADT was retrieved from the CGRD via their Anatomical Therapeutic Chemical (ATC) codes in the outpatient setting (Supplementary Table S2). The date the patients were first prescribed ADT was defined as the date they received the diagnosis of DM. Patients were excluded if they were aged < 20 years at the date of their diagnosis of DM; or were diagnosed with amebic liver abscess and PLA in the same hospitalization; had a prior hospitalization for PLA; had a history of aspirin use; or had no hospital admission or visit within a one-year prior to their diagnosis (Fig. 1). In addition, for outcome measurements, only diabetic patients who had at least one hospitalization during the follow-up were included in the study cohort.
Included patients were classified into aspirin users and non-users. Aspirin users were defined as those who started taking aspirin following the date of their diabetes diagnosis, and the date of their first aspirin prescription was defined as the study index date. Propensity-score matching (PSM) with a 1:1 ratio was employed to balance the distribution of baseline characteristics between aspirin users and non-users who were alive at the time aspirin was first prescribed to their matched users. The details of the PSM approach are described in the following statistical analysis section.
Outcomes. The primary outcome of interest was KP-PLA, as defined by an International Classification of Disease, 9th and 10th Clinical Modification (ICD-9/10-CM) code for liver abscess at the time of hospital discharge (Supplementary Table S3). KP infection was defined as having a blood, pus or abscess culture that yielded the growth of KP during the hospital stay. The secondary outcome was invasive KP-PLA syndrome, which was a subgroup of KP-PLA, defined as KP-PLA with a metastatic infection, such as endophthalmitis, brain abscess, intra-spinal abscess, extradural and subdural abscess, bacterial meningitis, lung abscess, osteomyelitis, or an abscess of the prostate (Supplementary Table S3) 12 . Any cause of in-hospital mortality was assessed in the analysis. Every patient was followed from the study index date until an event of interest occurred, loss to follow-up, or the last date of the dataset (December 31st, 2018), whichever occurred first.
Covariates. Baseline infection risk, age, sex, co-morbidities including liver cirrhosis, unspecified liver injury, hepatobiliary malignancy, gastric cancer, colon cancer, hepatocellular carcinoma, metastatic cancers, other malignancies, cholangitis, cholelithiasis, hepatitis B, hepatitis C, other viral hepatitis, chronic kidney disease, ischemic heart disease and myocardial infarction, ischemic stroke, arrythmia, any cardiovascular or cerebrovascular disease, or atherosclerosis were identified using the ICD-9/10-CM codes from outpatient visits or hospital discharges within 1 year prior to the study index date (Supplementary Table S3).
Prior medical use of centrally acting anti-adrenergic agents, alpha-and beta-blockers, thiazide-type diuretics, calcium channel blockers, angiotensin-converting enzyme inhibitors, and angiotensin II receptor antagonists within 1 year prior to the index date was identified by ATC codes (Supplementary Table S2). In addition,  www.nature.com/scientificreports/ anti-platelet agents (clopidogrel, ticagrelor and others), H2 receptor antagonists (H2-blockers), or proton pump inhibitors prescribed during the study follow-up were considered as concomitant medications (Supplementary  Table S2).

Statistical analysis.
Continuous variables were reported as the mean and standard deviation (SD) and categorical variables were reported as the number and percentage. The individual's propensity-score was calculated using multivariate logistic regression, including class of ADT (n = 9), baseline comorbid conditions, prior medications, glycated hemoglobin, and interval between diabetes diagnosis and first aspirin prescription (39 variables in total). To minimize the possible effect of immortal time bias, the length of time from diabetes diagnosis to the index date (aspirin initiation) was ascertained and randomly selected non-users who were followed during the same period. The balance between aspirin user and non-user groups was assessed using the absolute standardized mean differences of individual covariates at baseline before and after matching, using a threshold of < 0.1 to indicate balance. The cumulative incidence of an event of interest between the two groups was analyzed using the Kaplan-Meier approach with a log-rank test. Death-censored Cox proportional hazards regression was used to estimate the adjusted hazard ratio (aHR) with 95% confidence intervals (CIs) for KP-PLA or invasive KP-PLA syndrome in the PSM cohort. The level of significance was set as 5% (p < 0.05) for two-sided tests. Statistical analyses and data management were performed using SAS software version 9.4 (SAS Institute Inc. Cary, NC, USA).

Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.