Abstract
Background/Aims
Inflammatory bowel disease (IBD) is associated with the occurrence of venous thromboembolism (VTE). However, to date, there have been few studies on the risk of VTE in Asian IBD patients. We aimed to estimate the incidence of VTE in Asian IBD patients and to determine if IBD is related to increased VTE risk.
Methods
We performed a population-based cohort study between 2004 and 2015 using Korean National Health Insurance data. IBD and VTE were defined by ICD-10 codes. Incidence rates of VTE were calculated among patients with IBD and among age- and sex-matched controls. Hazard ratios were estimated using Cox regression with adjustment for multiple variables. We performed additional analyses stratifying by age, sex, Charlson comorbidity index (CCI) score, and disease type.
Results
Among the 45,037 patients with IBD (IBD cohort) and 133,019 matched controls (non-IBD cohort) included in our analysis, 411 IBD patients and 641 controls developed VTE. The IBD cohort had a higher incidence rate ratio and risk of VTE than the non-IBD cohort (incidence rate ratio 1.92 and hazard ratio 1.93). Older age, female sex, higher CCI scores, cardiovascular disease, chronic kidney disease, use of steroids, and hospitalization were significant risk factors for VTE in patients with IBD.
Conclusions
The IBD patients in this study were approximately two times more likely to develop VTE than the non-IBD individuals. Our findings support the need for thromboprophylaxis in Asian IBD patients with various factors that further increase the risk of VTE.
Keywords: Inflammatory bowel disease, Venous thromboembolism, Prophylaxis, Population, Cohort studies
INTRODUCTION
Inflammatory bowel disease (IBD), which comprises Crohn’s disease (CD) and ulcerative colitis (UC), is a chronic inflammatory disease that affects the gastrointestinal tract.1 Venous thromboembolism (VTE) is a well-studied extraintestinal manifestation of IBD, causing increased morbidity and mortality in IBD patients.2-5 Considering the increasing overall incidence and prevalence of IBD around the world, VTE related to IBD is also becoming a progressively more important issue.6,7 Several studies have demonstrated that IBD is associated with a 2- to 3-fold higher risk of VTE.3,4,8,9 Although IBD patients are at increased risk of VTE, the risk of VTE is not higher in other chronic inflammatory diseases such as rheumatoid arthritis.10 This means that VTE is a characteristic feature only in IBD patients, and eventually, the tendency of thrombosis is increased in this group of patients. Despite this clear connection, the pathogenesis of VTE in IBD is multifaceted and remains imperfectly understood.11
Several guidelines and consensus statements recommend antithrombotic prophylaxis for all hospitalized patients with IBD or in patients with acute severe IBD.12-14 Many studies in the past have supported the basis for these guidelines. However, due to the nature of VTE disease (low incidence and high mortality), most studies are small and retrospective. To overcome this point, several population-based nationwide cohort studies have been conducted and published over the past decade.3,4,9,15-19 Nevertheless, most of the previous studies have several limitations, such as a relatively small number of patients,3,9,17 a short follow-up period,15,16,18 or targeting only patients in specific situations (hospitalization, pediatrics, or use of steroids/biologics).9,15,16,18,19 Moreover, most studies of VTE have been focused on Western IBD patients, and only one study on Asian IBD patients has been published.17 The incidence of IBD is gradually increasing in Asia, and it can no longer be regarded as a disease that occurs primarily in the West.20-23 Even more worrisome, only a handful of clinicians in Asian countries are reported to implement appropriate VTE prophylaxis for inpatients with IBD.24 VTE is comparatively rare in the Asian population compared to Western populations,25,26 and the exact incidence and risk factors of VTE in Asian IBD patients are not known. Also, there have been no previous studies conducted at the population level. Therefore, we aimed to evaluate the incidence and risk factors of VTE in Asian IBD patients in a population-based nationwide cohort setting.
MATERIALS AND METHODS
1. Data source
This study used a nationwide, population-based database from the Korean National Health Insurance System (NHIS). The NHIS is single public health insurance service and has collected health care information from 97% of the Korean population.27,28 The database includes information about patient demographics, prescriptions, disease diagnoses, procedures, and hospitalization records. All IBD patients are asked to ensure that their diagnosis is confirmed by qualified doctors through systematized diagnostic criteria distributed by the NHIS. These procedures are managed and supervised by medical institutions and the NHIS. In addition, various studies have been conducted on IBD patients using NHIS and a lot of data have already been accumulated in making an operational definition for IBD patients in Korea.28-30 Thus, codes registered as IBD in Korea are very reliable. All patient information was de-identified before data processing to comply with the regulations of the Health Insurance Portability and Accountability Act and informed consent was waived. This study was approved by the Institutional Review Board of Wonju Severance Christian Hospital, Wonju, Korea (IRB number: CR312044).
2. Study population
This nationwide cohort study was performed using the NHIS database from 2004 to 2015. The platform and details of the data profile in the NHIS database have been reported in previous studies.31,32 Patients with IBD were identified using International Classification of Diseases 10th revision (ICD-10) codes accompanied by at least one claim for IBD-specific medications.29 According to the recently published nationwide validation study of IBD, our method demonstrated the highest sensitivity and specificity for operational definition of IBD.30 The ICD-10 codes for CD and UC are K50 and K51, respectively. Medications for IBD include 5-aminosalicylic acid, immune modulators (azathioprine, methotrexate, or 6-mercaptopurine), and anti-tumor necrosis factor-α agents (infliximab or adalimumab). Patients with a history of IBD during a washout period from January 2004 to December 2005 were excluded, along with patients with a history of VTE from 2004 to the time of first diagnosis of IBD (index date). Patients newly diagnosed with IBD between 2006 and 2015 were defined as the IBD cohort. For the control group, data were randomly extracted from the general population (people with no history of IBD) and matched by age and sex at a 1:3 ratio for the same index date. Randomization for control selection was conducted using a program in SAS version 9.4 (SAS Institute Inc, Cary, NC, USA). The matched control group was considered the non-IBD cohort.
3. Study variables and end points
We collected demographic data from the study population (age, sex, living area, income, and Charlson comorbidity index [CCI] score), along with data on any history of abdominal surgery, emergency room visits or hospitalization history, comorbidities, and medications. We used ICD-10 codes for all comorbidities that could be extracted from the NHIS (hypertension, diabetes mellitus, malignancy, cardiovascular disease, atrial fibrillation, heart failure, cerebrovascular disease, and chronic kidney disease). We also collected information on medications including 5-aminosalicylic acid, steroids, thiopurines, anti-tumor necrosis factor-α agents, aspirin, clopidogrel, warfarin, and new oral anticoagulants.
The end point of this study was newly diagnosed VTE during the follow-up period in the IBD and non-IBD cohorts, defined as a medical code related to the diagnosis of deep vein thrombosis (I80 or I82) or pulmonary embolism (I26) between 2006 and 2015. We analyzed the information available from the NHIS including data regarding each subject’s VTE diagnosis and the date of diagnosis. Subjects diagnosed with VTE before the follow-up period (or before IBD diagnosis) were excluded from the final analysis. Subjects in both cohorts were followed from the index date to December 2015. During follow-up, the number of subjects without newly developed VTE were counted on the last day of follow-up or the death date.
4. Statistical analysis
The categorical baseline characteristics of the participants are expressed as numbers (%). The incidence rates (IRs) of VTE were calculated as the number of incident cases divided by the follow-up period and presented as incident cases per 1,000 person-years. IRs were also stratified by disease type (CD or UC), age group (0–19, 20–39, 40–59, and >59 years), sex, living area, income, and CCI score. Using the IRs of both cohorts, we calculated IR ratios (IRRs) with 95% confidence intervals (CIs). hazard ratios (HRs) for the risk of VTE based on the presence of IBD were calculated after adjusting for covariates using Cox proportional hazard regression analysis. All statistical tests were two-tailed, and a p-value <0.05 was considered to denote statistical significance. Analyses were performed in SAS version 9.4 (SAS Institute Inc.).
RESULTS
Between January 2006 and December 2015, we identified 45,402 patients who were diagnosed with IBD for the first time. Of these subjects, 131 were excluded due to inadequate follow-up data and 234 due to a history of VTE before the diagnosis of IBD. The remaining 45,037 IBD patients (13,850 CD and 31,187 UC patients) were included in the study. To create age- and sex-matched non-IBD controls, 133,019 subjects (41,073 CD and 91,946 UC) were randomly selected from the general population enrolled in the NHIS (Fig. 1). Detailed demographic characteristics of the study population are summarized in Table 1.
Fig. 1.
Flowchart of this study.
NHIS, National Health Insurance System; IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; VTE, venous thromboembolism.
Table 1.
Demographic Data of the IBD Cohort and the Matched Non-IBD Cohort between 2006 and 2015
| Variable | IBD cohort (n=45,037) |
CD (n=13,850) |
UC (n=31,187) |
Non-IBD cohort (n=133,019) |
|---|---|---|---|---|
| Age, yr | ||||
| 0–19 | 6,251 (13.9) | 4,230 (30.5) | 2,021 (6.5) | 18,743 (14.1) |
| 20–39 | 18,199 (40.4) | 6,503 (47.0) | 11,696 (37.5) | 53,988 (40.6) |
| 40–59 | 14,429 (32.0) | 2,312 (16.7) | 12,117 (38.9) | 42,696 (32.1) |
| ≥60 | 6,158 (13.7) | 805 (5.8) | 5,353 (17.1) | 17,592 (13.2) |
| Sex | ||||
| Male | 28,046 (62.3) | 9,807 (70.8) | 18,239 (58.5) | 82,629 (62.1) |
| Female | 16,991 (37.7) | 4,043 (29.2) | 12,948 (41.5) | 50,390 (37.9) |
| Residence | ||||
| Urban | 41,633 (92.4) | 12,955 (93.5) | 28,678 (92.0) | 119,317 (89.7) |
| Rural | 3,404 (7.6) | 895 (6.5) | 2,509 (8.0) | 13,702 (10.3) |
| Socioeconomic status* | ||||
| Quintile 1 | 10,652 (23.7) | 3,299 (23.8) | 7,353 (23.6) | 33,731 (25.4) |
| Quintile 2 | 13,241 (29.4) | 4,152 (30.0) | 9,089 (29.1) | 48,029 (36.1) |
| Quintile 3 | 21,144 (46.9) | 6,399 (46.2) | 14,745 (47.3) | 51,259 (38.5) |
| CCI score | ||||
| 0 | 13,767 (30.6) | 5,065 (36.6) | 8,702 (27.9) | 50,371 (37.8) |
| 1 | 14,708 (32.6) | 4,859 (35.1) | 9,849 (31.6) | 42,301 (31.8) |
| 2 | 8,098 (18.0) | 2,151 (15.5) | 5,947 (19.1) | 20,166 (15.2) |
| ≥3 | 8,464 (18.8) | 1,775 (12.8) | 6,689 (21.4) | 20,181 (15.2) |
| Comorbidities | ||||
| Hypertension | 10,820 (24.0) | 1,860 (13.4) | 8,960 (28.7) | 31,578 (23.7) |
| Diabetes mellitus | 10,513 (23.3) | 2,411 (17.4) | 8,102 (26.0) | 25,736 (19.3) |
| Cardiovascular disease | 634 (1.4) | 108 (0.8) | 526 (1.7) | 1,188 (0.9) |
| Atrial fibrillation | 513 (1.1) | 117 (0.8) | 396 (1.3) | 1,038 (0.8) |
| Heart failure | 110 (0.2) | 19 (0.1) | 91 (0.3) | 169 (0.1) |
| Cerebrovascular disease | 619 (1.4) | 103 (0.7) | 516 (1.7) | 1,244 (0.9) |
| Chronic kidney disease | 72 (0.2) | 21 (0.2) | 51 (0.2) | 53 (<0.1) |
| Cancer | 1,946 (4.3) | 369 (2.7) | 1,577 (5.1) | 4,828 (3.6) |
| Medications | ||||
| Steroids | 21,757 (48.3) | 7,290 (52.6) | 14,467 (46.4) | 7,760 (5.8) |
| 5-ASA | 44,340 (98.5) | 13,418 (96.9) | 30,922 (99.2) | 26 (<0.1) |
| Thiopurines | 14,866 (33.0) | 9,230 (66.6) | 5,636 (18.1) | 883 (0.7) |
| Anti-TNF-α agents | 5,019 (11.1) | 3,438 (24.8) | 1,581 (5.1) | 32 (<0.1) |
| Aspirin | 6,970 (15.5) | 1,429 (10.3) | 5,541 (17.8) | 19,626 (14.8) |
| Clopidogrel | 2,118 (4.7) | 354 (2.6) | 1,764 (5.7) | 5,656 (4.3) |
| Warfarin | 377 (0.8) | 83 (0.6) | 294 (0.9) | 757 (0.6) |
| NOAC | 150 (0.3) | 25 (0.2) | 125 (0.4) | 435 (0.3) |
| Abdominal surgery history | 7,354 (16.3) | 5,760 (41.6) | 1,594 (5.1) | 2,340 (1.8) |
| Hospitalization | 34,869 (77.4) | 12,450 (89.9) | 22,419 (71.9) | 67,598 (50.8) |
| Follow-up period, yr | 5.03±2.94 | 4.75±2.88 | 5.16±2.95 | 5.13±2.94 |
Data are presented as the number (%) or mean±SD.
IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; CCI, Charlson comorbidity index; 5-ASA, 5-aminosalicylic acid; TNF, tumor necrosis factor; NOAC, new oral anticoagulant.
*Socioeconomic status was calculated based on health insurance premium (from quintile 1 [low] to quintile 3 [high]).
Table 2 shows the number of cases and the IRs of VTE in the IBD and non-IBD cohorts. During the follow-up period, VTE was diagnosed in 411 of 45,037 subjects in the IBD cohort (0.9%) and 641 of 133,019 subjects in the non-IBD cohort (0.5%). Among the VTE cases from the IBD cohort, 106 patients had previously been diagnosed with CD and 305 with UC. The IRs for VTE were 18.0 in the IBD cohort and 9.4 in the non-IBD cohort (IRR, 1.92; 95% CI, 1.69 to 2.18). Subjects younger than 40 years of age were associated with the greatest IRR (age 0–19: IRR, 2.64; 95% CI, 1.45 to 4.79 and age 20–39: IRR, 2.80; 95% CI, 2.15 to 3.64). When subjects were stratified by type of IBD, the IRs for VTE were 16.1 in the CD group and 6.6 in the CD control group (IRR, 2.45; 95% CI, 1.89 to 3.18). The IRs for the UC group and UC control group were 19.0 and 10.5, respectively (IRR, 1.80; 95% CI, 1.56 to 2.08).
Table 2.
Number of Incident Cases and Incidence Rates per 10,000 Person-Years of Venous Thromboembolism in the IBD and Non-IBD Cohorts
| Variable | IBD cohort (n=45,037) | Non-IBD cohort (n=133,019) | IRR (95% CI) | |||
|---|---|---|---|---|---|---|
| Incident cases | Incidence rates | Incident cases | Incidence rates | |||
| Overall | 411 | 18.0 | 641 | 9.4 | 1.92 (1.69–2.18) | |
| Age, yr | ||||||
| 0–19 | 21 | 7.5 | 24 | 2.8 | 2.64 (1.45–4.79) | |
| 20–39 | 111 | 11.9 | 119 | 4.3 | 2.80 (2.15–3.64) | |
| 40–59 | 140 | 18.6 | 244 | 10.8 | 1.73 (1.40–2.13) | |
| ≥60 | 139 | 46.4 | 254 | 27.5 | 1.69 (1.37–2.08) | |
| Sex | ||||||
| Male | 209 | 15.1 | 356 | 8.5 | 1.76 (1.48–2.10) | |
| Female | 202 | 23.0 | 285 | 10.7 | 2.15 (1.79–2.58) | |
| Residence | ||||||
| Urban | 373 | 17.8 | 536 | 8.9 | 2.00 (1.75–2.29) | |
| Rural | 38 | 21.8 | 103 | 14.3 | 1.52 (1.04–2.22) | |
| Socioeconomic status | ||||||
| Quintile 1 | 117 | 22.2 | 195 | 11.2 | 1.99 (1.57–2.51) | |
| Quintile 2 | 112 | 16.9 | 227 | 9.3 | 1.81 (1.44–2.28) | |
| Quintile 3 | 182 | 16.9 | 219 | 8.3 | 2.05 (1.68–2.50) | |
| CCI score | ||||||
| 0 | 59 | 9.0 | 78 | 3.2 | 2.83 (2.00–3.99) | |
| 1 | 98 | 13.5 | 148 | 6.9 | 1.95 (1.50–2.53) | |
| 2 | 88 | 20.9 | 126 | 11.5 | 1.83 (1.38–2.41) | |
| ≥3 | 166 | 35.8 | 289 | 25.3 | 1.42 (1.17–1.72) | |
| Crohn’s disease (n=13,850) | Control group (n=41,073) | IRR (95% CI) | ||||
| Incident cases | Incidence rates | Incident cases | Incidence rates | |||
| Overall | 106 | 16.1 | 131 | 6.6 | 2.45 (1.89–3.18) | |
| Age, yr | ||||||
| 0–19 | 9 | 4.9 | 19 | 3.4 | 1.43 (0.63–3.20) | |
| 20–39 | 38 | 11.9 | 42 | 4.4 | 2.72 (1.74–4.26) | |
| 40–59 | 35 | 30.0 | 36 | 10.1 | 2.98 (1.86–4.79) | |
| ≥60 | 24 | 65.3 | 34 | 29.5 | 2.21 (1.30–3.77) | |
| Sex | ||||||
| Male | 60 | 13.0 | 80 | 5.7 | 2.26 (1.61–3.19) | |
| Female | 46 | 23.5 | 51 | 8.6 | 2.74 (1.83–4.12) | |
| Residence | ||||||
| Urban | 98 | 15.9 | 108 | 6.2 | 2.56 (1.94–3.39) | |
| Rural | 8 | 18.7 | 21 | 10.4 | 1.80 (0.78–4.13) | |
| Socioeconomic status | ||||||
| Quintile 1 | 30 | 19.7 | 44 | 8.3 | 2.37 (1.47–3.80) | |
| Quintile 2 | 38 | 19.0 | 50 | 7.0 | 2.73 (1.78–4.20) | |
| Quintile 3 | 38 | 12.4 | 37 | 5.0 | 2.50 (1.57–3.96) | |
| CCI score | ||||||
| 0 | 18 | 7.6 | 32 | 3.5 | 2.17 (1.21–3.92) | |
| 1 | 28 | 12.5 | 34 | 5.3 | 2.34 (1.41–3.90) | |
| 2 | 24 | 22.9 | 22 | 8.8 | 2.61 (1.45–4.71) | |
| ≥3 | 36 | 38.8 | 43 | 22.7 | 1.71 (1.09–2.68) | |
| Ulcerative colitis (n=31,187) | Control group (n=91,946) | IRR (95% CI) | ||||
| Incident cases | Incidence rates | Incident cases | Incidence rates | |||
| Overall | 305 | 19.0 | 510 | 10.5 | 1.80 (1.56–2.08) | |
| Age, yr | ||||||
| 0–19 | 12 | 12.5 | 5 | 1.7 | 7.25 (2.50–21.02) | |
| 20–39 | 73 | 11.9 | 77 | 4.2 | 2.84 (2.05–3.93) | |
| 40–59 | 105 | 16.5 | 208 | 10.9 | 1.51 (1.19–1.92) | |
| ≥60 | 115 | 43.7 | 220 | 27.2 | 1.61 (1.28–2.02) | |
| Sex | ||||||
| Male | 149 | 16.1 | 276 | 10.0 | 1.62 (1.32–1.98) | |
| Female | 156 | 22.9 | 234 | 11.3 | 2.02 (1.64–2.48) | |
| Residence | ||||||
| Urban | 275 | 18.6 | 428 | 10.0 | 1.86 (1.59–2.17) | |
| Rural | 30 | 22.8 | 82 | 15.9 | 1.44 (0.94–2.20) | |
| Socioeconomic status | ||||||
| Quintile 1 | 87 | 23.3 | 151 | 12.4 | 1.87 (1.43–2.45) | |
| Quintile 2 | 74 | 16.0 | 177 | 10.3 | 1.55 (1.17–2.04) | |
| Quintile 3 | 144 | 18.7 | 182 | 9.5 | 1.96 (1.57–2.45) | |
| CCI score | ||||||
| 0 | 41 | 9.8 | 46 | 3.0 | 3.26 (2.12–5.01) | |
| 1 | 70 | 14.0 | 114 | 7.6 | 1.83 (1.35–2.49) | |
| 2 | 64 | 20.3 | 104 | 12.2 | 1.66 (1.21–2.28) | |
| ≥3 | 130 | 35.0 | 246 | 25.8 | 1.36 (1.09–1.69) | |
IBD, inflammatory bowel disease; IRR, incidence rate ratio; CI, confidence interval; CCI, Charlson comorbidity index.
The risk of VTE was higher in the IBD cohort than in the non-IBD cohort (HR [crude], 1.93; 95% CI, 1.71 to 2.19; p<0.001; adjusted HR [model 1], 1.84; 95% CI, 1.62 to 2.08; p<0.001; adjusted HR [model 2], 1.89; 95% CI, 1.66 to 2.14; p<0.001) (Table 3). Compared to the non-IBD cohort, the HR associated with VTE in IBD patients tended to increase with a younger age or lower CCI score. The HR associated with VTE was especially high in young UC patients (age 0–19 years). We also stratified IRs and HRs by age at diagnosis of IBD (Fig. 2). Table 4 shows the multivariate analysis of the risk factors associated with VTE in the IBD cohort. Age remained associated with an increased risk for VTE in IBD patients; particularly, patients aged >59 years had a higher adjusted HR of 4.10 (CD: 9.00, 95% CI, 3.54 to 22.88; p<0.001 and UC: 2.26, 95% CI, 1.17 to 4.34; p=0.015). In addition, female sex, an increased CCI score, the presence of cardiovascular or chronic kidney disease, use of steroids, and hospitalization were significant risk factors for VTE in patients with IBD.
Table 3.
Comparison of the Risk of Venous Thromboembolic Events between the IBD and Non-IBD Cohorts
| Variable | Crude | Model 1* | Model 2† | |||||
|---|---|---|---|---|---|---|---|---|
| HR (95% CI) | p-value | Adjusted HR (95% CI) | p-value | Adjusted HR (95% CI) | p-value | |||
| IBD vs non-IBD | ||||||||
| Non-IBD | Reference | Reference | Reference | |||||
| IBD | 1.93 (1.71–2.19) | <0.001 | 1.84 (1.62–2.08) | <0.001 | 1.89 (1.66–2.14) | <0.001 | ||
| Age, yr | ||||||||
| 0–19 | 2.64 (1.47–4.74) | 0.001 | 2.43 (1.33–4.43) | 0.004 | 2.61 (1.41–4.83) | 0.002 | ||
| 20–39 | 2.79 (2.16–3.62) | <0.001 | 2.63 (2.02–3.42) | <0.001 | 2.73 (2.10–3.56) | <0.001 | ||
| 40–59 | 1.73 (1.40–2.13) | <0.001 | 1.64 (1.33–2.02) | <0.001 | 1.66 (1.35–2.05) | <0.001 | ||
| ≥60 | 1.68 (1.37–2.07) | <0.001 | 1.62 (1.31–1.99) | <0.001 | 1.62 (1.32–2.00) | <0.001 | ||
| Sex | ||||||||
| Male | 1.76 (1.48–2.09) | <0.001 | 1.66 (1.40–1.98) | <0.001 | 1.70 (1.42–2.02) | <0.001 | ||
| Female | 2.15 (1.80–2.57) | <0.001 | 2.08 (1.74–2.49) | <0.001 | 2.12 (1.77–2.55) | <0.001 | ||
| CCI score | ||||||||
| 0 | 2.17 (1.22–3.87) | 0.008 | 2.49 (1.38–4.50) | 0.002 | 2.44 (1.33–4.49) | 0.004 | ||
| 1 | 2.34 (1.42–3.86) | 0.001 | 2.57 (1.55–4.28) | <0.001 | 2.66 (1.59–4.44) | <0.001 | ||
| 2 | 2.65 (1.48–4.72) | 0.001 | 2.95 (1.65–5.28) | <0.001 | 3.01 (1.67–5.43) | <0.001 | ||
| ≥3 | 1.72 (1.10–2.67) | 0.017 | 1.87 (1.20–2.91) | 0.006 | 1.92 (1.23–3.02) | 0.004 | ||
| Hospitalization | 1.84 (1.36–2.49) | <0.001 | 2.27 (1.67–3.09) | <0.001 | 2.29 (1.68–3.13) | <0.001 | ||
| CD vs control | ||||||||
| Control | Reference | Reference | Reference | |||||
| CD | 2.45 (1.90–3.17) | <0.001 | 2.34 (1.80–3.03) | <0.001 | 2.43 (1.87–3.16) | <0.001 | ||
| Age, yr | ||||||||
| 0–19 | 1.43 (0.65–3.15) | 0.380 | 1.34 (0.60–3.02) | 0.474 | 1.42 (0.62–3.25) | 0.407 | ||
| 20–39 | 2.72 (1.75–4.22) | <0.001 | 2.60 (1.66–4.08) | <0.001 | 2.81 (1.78–4.42) | <0.001 | ||
| 40–59 | 2.98 (1.87–4.75) | <0.001 | 2.87 (1.79–4.59) | <0.001 | 2.85 (1.77–4.58) | <0.001 | ||
| ≥60 | 2.24 (1.33–3.78) | 0.003 | 2.12 (1.24–3.62) | 0.006 | 2.29 (1.33–3.94) | 0.003 | ||
| Sex | ||||||||
| Male | 2.27 (1.62–3.17) | <0.001 | 2.15 (1.53–3.03) | <0.001 | 2.22 (1.57–3.13) | <0.001 | ||
| Female | 2.75 (1.84–4.09) | <0.001 | 2.70 (1.80–4.04) | <0.001 | 2.74 (1.82–4.13) | <0.001 | ||
| CCI score | ||||||||
| 0 | 2.17 (1.22–3.87) | 0.008 | 2.49 (1.38–4.50) | 0.002 | 2.44 (1.33–4.49) | 0.004 | ||
| 1 | 2.34 (1.42–3.86) | 0.001 | 2.57 (1.55–4.28) | <0.001 | 2.66 (1.59–4.44) | <0.001 | ||
| 2 | 2.65 (1.48–4.72) | 0.001 | 2.95 (1.65–5.28) | <0.001 | 3.01 (1.67–5.43) | <0.001 | ||
| ≥3 | 1.72 (1.10–2.67) | 0.017 | 1.87 (1.20–2.91) | 0.006 | 1.92 (1.23–3.02) | 0.004 | ||
| Hospitalization | 1.84 (1.36–2.49) | <0.001 | 2.27 (1.67–3.09) | <0.001 | 2.29 (1.68–3.13) | <0.001 | ||
| UC vs control | ||||||||
| Control | Reference | Reference | Reference | |||||
| UC | 1.80 (1.56–2.07) | <0.001 | 1.71 (1.49–1.98) | <0.001 | 1.76 (1.52–2.03) | <0.001 | ||
| Age, yr | ||||||||
| 0–19 | 7.25 (2.55–20.56) | <0.001 | 6.49 (2.24–18.82) | 0.001 | 6.79 (2.31–19.99) | 0.001 | ||
| 20–39 | 2.83 (2.06–3.90) | <0.001 | 2.63 (1.90–3.63) | <0.001 | 2.69 (1.94–3.73) | <0.001 | ||
| 40–59 | 1.51 (1.20–1.91) | 0.001 | 1.44 (1.14–1.82) | 0.003 | 1.48 (1.16–1.87) | 0.001 | ||
| ≥60 | 1.60 (1.28–2.01) | <0.001 | 1.55 (1.24–1.94) | <0.001 | 1.56 (1.24–1.96) | <0.001 | ||
| Sex | ||||||||
| Male | 1.61 (1.32–1.97) | <0.001 | 1.53 (1.25–1.87) | <0.001 | 1.55 (1.27–1.90) | <0.001 | ||
| Female | 2.02 (1.65–2.47) | <0.001 | 1.96 (1.60–2.40) | <0.001 | 2.00 (1.63–2.45) | <0.001 | ||
| CCI score | ||||||||
| 0 | 3.25 (2.13–4.95) | <0.001 | 3.21 (2.10–4.90) | <0.001 | 3.29 (2.15–5.05) | <0.001 | ||
| 1 | 1.83 (1.36–2.47) | <0.001 | 1.93 (1.43–2.60) | <0.001 | 2.03 (1.51–2.75) | <0.001 | ||
| 2 | 1.66 (1.21–2.26) | 0.002 | 1.73 (1.27–2.37) | 0.001 | 1.75 (1.28–2.39) | 0.001 | ||
| ≥3 | 1.35 (1.09–1.67) | 0.005 | 1.40 (1.13–1.74) | 0.002 | 1.39 (1.12–1.72) | 0.003 | ||
| Hospitalization | 1.79 (1.52–2.12) | <0.001 | 1.92 (1.62–2.27) | <0.001 | 1.94 (1.64–2.30) | <0.001 | ||
IBD, inflammatory bowel disease; HR, hazard ratio; CI, confidence interval; CCI, Charlson comorbidity index; CD, Crohn’s disease; UC, ulcerative colitis.
*Multivariable-adjusted model 1: adjustments for age, sex, CCI score, socioeconomic status, and residence; †Multivariable-adjusted model 2: adjustments for model 1 covariates and comorbidities.
Fig. 2.
Incidence rates and adjusted hazard ratios (model 2) of venous thromboembolism in patients with inflammatory bowel disease (IBD) compared with non-IBD controls by age group.
Table 4.
Multivariate Analysis of Risk Factors for Venous Thromboembolism in an the IBD Cohort
| Factor | IBD | CD | UC | |||||
|---|---|---|---|---|---|---|---|---|
| Adjusted HR (95% CI) | p-value | Adjusted HR (95% CI) | p-value | Adjusted HR (95% CI) | p-value | |||
| Disease type | ||||||||
| CD | Reference | |||||||
| UC | 0.77 (0.60–0.99) | 0.043 | ||||||
| Age, yr | ||||||||
| 0–19 | Reference | Reference | Reference | |||||
| 20–39 | 1.64 (1.01–2.64) | 0.044 | 2.16 (1.03–4.51) | 0.042 | 1.04 (0.56–1.93) | 0.895 | ||
| 40–59 | 2.25 (1.36–3.70) | 0.002 | 4.63 (2.06–10.40) | <0.001 | 1.22 (0.66–2.27) | 0.527 | ||
| ≥60 | 4.10 (2.40–7.02) | <0.001 | 9.00 (3.54–22.88) | <0.001 | 2.26 (1.17–4.34) | 0.015 | ||
| Sex | ||||||||
| Male | Reference | Reference | Reference | |||||
| Female | 1.28 (1.05–1.56) | 0.014 | 1.18 (0.79–1.76) | 0.415 | 1.30 (1.03–1.63) | 0.025 | ||
| Residence | ||||||||
| Urban | Reference | Reference | Reference | |||||
| Rural | 0.92 (0.65–1.28) | 0.608 | 0.87 (0.42–1.81) | 0.708 | 0.92 (0.63–1.35) | 0.662 | ||
| CCI score | ||||||||
| 0 | Reference | Reference | Reference | |||||
| 1 | 1.36 (0.98–1.88) | 0.065 | 1.41 (0.78–2.55) | 0.259 | 1.34 (0.91–1.97) | 0.143 | ||
| 2 | 1.84 (1.30–2.59) | 0.001 | 1.84 (0.97–3.50) | 0.100 | 1.80 (1.20–2.71) | 0.005 | ||
| ≥3 | 2.34 (1.64–3.35) | <0.001 | 2.05 (1.02–4.12) | <0.001 | 2.39 (1.57–3.64) | <0.001 | ||
| Comorbidities | ||||||||
| Hypertension | 1.23 (0.96–1.59) | 0.105 | 0.87 (0.51–1.48) | 0.598 | 1.37 (1.03–1.83) | 0.034 | ||
| Diabetes mellitus | 0.82 (0.65–1.04) | 0.107 | 0.80 (0.49–1.31) | 0.385 | 0.82 (0.62–1.08) | 0.157 | ||
| CAOD | 1.81 (1.14–2.85) | 0.011 | 0.46 (0.06–3.38) | 0.444 | 2.14 (1.34–3.44) | 0.002 | ||
| Atrial fibrillation | 1.54 (0.90–2.64) | 0.117 | 0.89 (0.20–3.93) | 0.879 | 1.76 (0.99–3.14) | 0.054 | ||
| Heart failure | 0.30 (0.04–2.12) | 0.225 | 0.01 (0.01–0.03) | 0.983 | 0.31 (0.04–2.24) | 0.246 | ||
| CVD | 0.79 (0.45–1.41) | 0.425 | 0.30 (0.04–2.28) | 0.244 | 0.92 (0.51–1.69) | 0.794 | ||
| CKD | 3.36 (1.24–9.14) | 0.018 | 4.36 (0.55–34.53) | 0.163 | 3.38 (1.06–10.72) | 0.039 | ||
| Cancer | 1.11 (0.78–1.58) | 0.564 | 1.42 (0.69–2.92) | 0.336 | 1.05 (0.70–1.57) | 0.832 | ||
| IBD medications | ||||||||
| Steroids | 1.88 (1.51–2.33) | <0.001 | 2.09 (1.36–3.21) | 0.001 | 1.79 (1.39–2.30) | <0.001 | ||
| 5-ASA | 0.15 (0.09–0.25) | <0.001 | 0.15 (0.07–0.31) | <0.001 | 0.15 (0.08–0.30) | <0.001 | ||
| Thiopurines | 0.53 (0.39–0.71) | <0.001 | 0.47 (0.29–0.77) | 0.002 | 0.59 (0.41–0.85) | 0.004 | ||
| Anti-TNF-α agents | 0.80 (0.52–1.22) | 0.304 | 0.80 (0.44–1.44) | 0.451 | 0.87 (0.48–1.59) | 0.654 | ||
| Abdominal surgery history | 0.94 (0.68–1.31) | 0.720 | 1.01 (0.64–1.58) | 0.980 | 0.97 (0.59–1.57) | 0.887 | ||
| Hospitalization | 1.56 (1.22–1.98) | <0.001 | 1.39 (0.85–2.27) | 0.187 | 1.60 (1.21–2.12) | 0.001 | ||
Adjustments were made for all variables listed in the table.
IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; HR, hazard ratio; CI, confidence interval; CCI, Charlson comorbidity index; CAOD, cardiovascular disease; CVD, cerebrovascular disease; CKD, chronic kidney disease; 5-ASA, 5-aminosalicylic acid; TNF, tumor necrosis factor.
DISCUSSION
In this population-based nationwide study, we demonstrated that IBD patients exhibited a higher IRR (1.92; 95% CI, 1.69 to 2.18) and a 1.93-fold greater risk (HR, 1.93; 95% CI, 1.71 to 2.19; p<0.001) of developing deep vein thrombosis than did the general population. HRs were especially high in the young IBD cohort compared to the non-IBD cohort, though the absolute risks increased with age. In particular, this trend was more pronounced in patients with UC than in those with CD. We also showed that IBD is a powerful independent risk factor of VTE, because after adjusting for common VTE risk factors (diabetes mellitus, cardiovascular disease, atrial fibrillation, cerebral vascular disease, chronic kidney disease, and malignancy), patients with IBD had an approximately 90% higher risk of developing VTE than did controls. Another key finding in this study was the significant effect of IBD patient age on VTE occurrence. In IBD patients aged 60 years or older, the adjusted HR associated with VTE was much higher than that associated with people 19 years of age or younger.
Compared with previous studies on the occurrence of VTE in IBD patients, this study has the following strengths. First, this is the second nationwide study to evaluate the risk of deep vein thrombosis among IBD patients in an Asian population, with a different result from the first study.17 This study targeted four times more IBD patients than did the previous study, and the follow-up duration was longer. Therefore, the reliability and accuracy of the results of this study are expected to be higher. Second, although past studies have focused on the occurrence of VTE in specific situations and derived their results accordingly,9,15,16,18,19 this study examines the general occurrence of VTE in the wider population. Therefore, the association between IBD and VTE could be evaluated at the level of the entire population. Third, this study selected newly diagnosed IBD patients as an inception cohort. Whereas the ability to determine a clear relationship between early exposure factors and long-term outcomes is limited in a non-inception cohort, the inception cohort was free from these disadvantages and provided additional enhancement in data quality.33 The fourth strength of this study is that it included a large number of subjects by using data from the NHIS. Research using the NHIS database is advantageous in that it is easy to derive research results for a large number of people at the national level, thus providing real-world evidence with relatively little effort and time.
In general, IBD was associated with an increased risk of VTE, and our findings concur with those of previous population-based cohort studies.3,4,34 A previous Western study, however, found that the risk of VTE was 2- to 3-fold higher or even greater in an IBD population compared to the control. In the present study, we found a relatively lower HR increase (1.93) compared to the non-IBD cohort. Similar to our results, in a Taiwanese population-based study, the adjusted HR increased relatively slightly to 1.98.17 The differences in VTE risk for IBD patients in Asia and Western countries may be associated with racial differences and dietary habits.35,36 However, it is clear that IBD patients face an increased risk of VTE regardless of ethnicity or region. Therefore, there is some consensus that thromboprophylaxis should be considered for IBD patients who are indicated for prophylaxis.12,13 Nevertheless, some studies have shown that there is still a large gap in the use of VTE prophylaxis by gastroenterologists in clinical practice.24,37 There are several reasons for low compliance in terms of thromboprophylaxis by doctors. First, they may have concerns about the safety of thromboprophylaxis when active IBD patients are hospitalized;38,39 however, previous studies have reported that pharmacological thromboprophylaxis of VTE does not increase the risk of bleeding.38,40 Second, gastroenterologists may not be aware of the increased risk of VTE in IBD patients, and thus do not follow the guidelines recommending prophylactic anticoagulant therapy in hospitalized IBD patients.37 The failure to adhere to these guidelines is more prevalent in Asia.24 The consequences of VTE can be fatal, and its incidence is clearly higher in IBD patients than in the general population, so correct VTE prophylaxis must be performed based on the guidelines.
This study revealed several interesting findings regarding the development of VTE according to age in IBD patients. The IRR and HR associated with VTE in patients with IBD versus the non-IBD cohort was approximately two to three times higher in the younger age group (<40 years) than in the elderly. In particular, this trend was more apparent in those with UC than in those with CD. Previous studies have also demonstrated that younger IBD patients (including children and adolescents) had a higher risk of developing VTE compared to age-matched non-IBD controls.4,19,41 Considering these results alone, the VTE risk of young IBD patients appears to be very high, but in fact, among all IBD patients, the absolute incidence of VTE is very low at a young age versus an older age. In fact, the IR for VTE in elderly IBD patients (aged 60 years or older) was 46.4, whereas the IRs for ages 0–19 and 20–39 were only 7.5 and 11.9, respectively. Moreover, elderly patients had increased risk for VTE in the IBD cohort. Therefore, since VTE hardly occurred in young subjects belonging to the non-IBD cohort, it is thought that the IRR and HR of the VTE were noticeable higher in the young IBD patients compared with the non-IBD cohort. The current guidelines do not recommend thromboprophylaxis for young IBD patients (younger than 18 years of age) who have no previous history of VTE.12
The other important point we found was the different pattern of VTE development in CD and UC. The incidence of VTE according to age was generally similar between patients with CD and UC. However, the age-related risk of VTE was more pronounced in CD cases (the adjusted HR for CD patients over 60 years of age was 9.00) than in UC cases (the adjusted HR for patients over 60 years of age was 2.26). The reason for this phenomenon is not clear, but it may have to do with two characteristics of Korean UC patients as seen in a recent epidemiology study.20 The first is that the number of elderly UC patients has increased significantly, and the other is that the proportion of patients with proctitis is high. Considering the higher risk of VTE in cases with widespread bowel involvement (e.g., pancolitis),3,4,10 we can speculate that the increase in the number of elderly patients with mild UC may be the major reason for this phenomenon.
VTE in IBD patients is a multifactorial event caused not only by inherited risk but also by acquired factors.40,42-44 Several risk factors are more common in IBD patients than in the general population, including hyperhomocysteinemia, dehydration, infection, prolonged immobilization, and active intestinal disease.40,42,45 In addition, the risk of VTE in IBD patients may increase when it is accompanied by other diseases known to be risk factors for VTE. This hypothesis is supported by the fact that the HR value for VTE gradually increased with CCI score in this study. Of note, chronic kidney disease was associated with a significant risk of VTE (adjusted HR, 3.36; 95% CI, 1.24 to 9.14; p=0.018). This is the first report indicating that chronic kidney disease may be a risk factor for VTE in IBD patients, although one small study previously reported an increased use of VTE prophylaxis in IBD patients with chronic kidney disease.46 Also, patients with chronic kidney disease have a higher risk of developing VTE than those with normal kidney function in the non-IBD group.47 Therefore, if chronic kidney disease is present in IBD patients, it is important to keep in mind that the likelihood of developing VTE will be high, and proactive prophylaxis should be considered.
Due to the nature of IBD, most patients have to take lifelong medication to control the disease. However, little research has been done on whether these medications increase the risk of VTE. We found that prior use of steroids increases the risk of VTE (adjusted HR, 1.88; 95% CI, 1.51 to 2.33; p<0.001), similar to previous studies.48,49 According to a recent meta-analysis, steroid usage was associated with a significantly higher rate of VTE complication in IBD patients (odds ratio, 2.202; 95% CI, 1.698 to 2.856; p<0.001).48 Corticosteroids may elevate thrombogenic risks via mechanisms associated with inflammatory processes, such as excessive production of procoagulant factors and impaired fibrinolytic capacity.11,50 Therefore, caution is particularly needed when using steroids in elderly IBD patients because of the potential high risk of VTE.51
Although our results can be generalized in Korea because of the use of the NHIS database, our study has several limitations mainly related to the features of the claims data, which is an innate limitation. First, we were not able to evaluate the disease severity (clinical or endoscopic) and disease extent of IBD, which may be linked to VTE development. Also, the severity of VTE (fatal VTE, VTE induced permanent damage, etc.) was not evaluated. Second, there was no information on possible confounding factors, such as smoking status, obesity, major trauma, oral contraceptive therapy, or pregnancy, which are essential variables that may modify VTE risk.
In conclusion, IBD is a definite independent risk factor for VTE at the population level. This study also showed that Asian IBD patients had a higher risk of VTE than did a non-IBD cohort. In addition, we found multiple risk factors to be associated with the occurrence of VTE in IBD patients, including an older age, female sex, a high CCI score, cardiovascular disease, chronic kidney disease, use of steroids, and hospitalization. Based on these findings, a prospective study to clarify the indications of thromboprophylaxis and therapeutic outcomes based on patient characteristics is warranted.
ACKNOWLEDGEMENTS
This work was supported by grants from the National Research Foundation of Korea (2019R1A2C1007859), Ministry of Science and ICT, the National R&D Program for Cancer Control (HA17C0046) and the Korean National Health Clinical Research (NHCR) project (HC16C2320), Ministry of Health & Welfare, Republic of Korea. This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (grant number: 2020R1I1A306686511).
Footnotes
CONFLICTS OF INTEREST
No potential conflict of interest relevant to this article was reported.
AUTHOR CONTRIBUTIONS
Concept and design: S.Y.K., Y.S.C., H.S.K. Acquisition and analysis of data: J.K.L., D.R.K. Interpretation of data: S.Y.K., Y.S.C., H.S.K., H.M.K., H.J.P., H.K., J.K. Statistical analysis: J.K.L., D.R.K. Obtained funding: S.Y.K., H.S.K. Administrative, technical, or material support: H.M.K., H.J.P., H.K., J.K. Supervision: S.Y.K., H.S.K. Drafting of the manuscript: S.Y.K., Y.S.C., J.K.L., D.R.K. Critical revision of the manuscript for important intellectual content: S.Y.K., Y.S.C., H.S.K.
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