DOI: https://doi.org/10.21203/rs.3.rs-22705/v1
Most women with systemic lupus erythematosus (SLE) are diagnosed with the disease in their reproductive years, but the incidence and prevalence of SLE among women of childbearing age have not been studied. The objective of this study was to estimate the incidence and prevalence of SLE among the Korean women of childbearing age.
Women aged 20 to 44 years with SLE were identified from National Health Insurance Service – National Health Information Database (2009–2016), which contain health information of approximately 97% of the Korean population. SLE was defined by International Classification of Diseases, 10th revision code, M32. Incidence and prevalence were calculated per 100,000 person-years and stratified by year and age.
A total of 12,756 women with SLE were identified. The incidence of SLE from 2011 to 2016 among women in childbearing years was 8.18/100,000 person-years (95% CI 7.94–8.43), with the highest incidence in 2016 (8.56/100,000 person-years, 95% CI 7.95–9.17) and the lowest incidence in 2012 (7.85/100,000 person-years, 95% CI 7.28–8.42). The prevalence of SLE from 2009 to 2016 among women in childbearing years was 77.07/100,000 person-years (95% CI 75.76–78.39), with the highest prevalence in 2014 (79.47/100,000 person-years, 95% CI 77.64–81.30) and the lowest in 2010 (74.19/100,000 person-years, 95% CI 72.45–75.93). The peak age for SLE incidence was between 25–39 years, and lower incidence was seen in the early (20–24 years) and late (40–44 years) childbearing age periods. There was an increasing trend in prevalence according to age in women of childbearing age, with the highest prevalence occurring in the 40–44 age group.
The risk and burden of SLE are high among women during their childbearing years. This calls for special attention to this particular population group when allocating health resources.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that may affect various organ systems [1]. Despite the improvement in medical care, SLE still carries a higher risk of death compared to the general population with a reported 5-year survival of 95% [2]. Since SLE is a chronic disease with no definite cure, patients have to deal with the complications of the disease and its treatments throughout their lifetime [3].
The worldwide incidence and prevalence of SLE vary greatly according to region and ethnicity, with an incidence range of 0.3 to 23.2 per 100,000 person-years and a prevalence range of 0 to 241 per 100,000 people [4–9]. Despite the high regional and ethnic variation, one common feature of SLE epidemiology is that the disease predominantly affects women during their childbearing years. SLE occurs more often in women, with a female to male ratio of 9:1, and this ratio is higher (up to 15:1) during the reproductive years [10, 11]. The peak incidence age for SLE in women is between the third and the fifth decades, during the peak reproductive years, whereas peak incidence for men is later (fifth to seventh decades) [7, 9]. SLE is the second most common autoimmune disease following thyroid disease in women of childbearing age [12]. Furthermore, high rates of maternal and fetal complications have been reported among women with SLE. Maternal complications such as lupus flare, hypertension, nephritis, pre-eclampsia, and eclampsia and fetal complications such as fetal loss, stillbirths, preterm birth, and intrauterine growth retardation were more frequent during pregnancy in women with SLE compared with healthy women [13–15]. The disease also had a significant psychosocial impact on family life in that many SLE women make choices to limit family size due to concerns about the health of a child and their care [16–18]. Thus, women of childbearing age with SLE are among the most vulnerable population needing special attention, since a high disease burden is imposed upon this particular population group.
To date, no studies have specifically examined the incidence and prevalence of SLE among women during their childbearing years. Determining the nationwide incidence and prevalence rates of SLE in a specific age group of women of childbearing age may yield important insights into the underlying biology and can provide valuable information for the planning and allocation of health care resources. Therefore, this study aimed to estimate the incidence and prevalence of SLE, including temporal trends and age group variations, among Korean women of childbearing age using the nationwide population database.
We conducted a nationwide retrospective study using the Korean National Health Insurance Service – National Health Information Database (NHIS-NHID) from 2009 to 2016. The Korean NHIS was founded in 2000, and is a single insurer that provides coverage for almost the entire Korean population, as 97% of the population is enrolled in the NHIS program and the remaining 3% (with low incomes) are covered by the Medical Aid Program [19]. As of December 2014, the NHIS-NHID included all inpatient and outpatient claims data as well as information on health care utilization for approximately 50 million Korean people [20]. The target population in this study was women of childbearing age (defined as women between the ages of 20–44 years) during the period from January 1, 2009 to December 31, 2016. This study was approved by the Institutional Review Board of the National Health Insurance Service Ilsan hospital (Institutional review board Number: NHIMC 2020-02-010), and it was conducted according to the principles of the Declaration of Helsinki. Since the database used in this study contains anonymized data for research purposes, informed consent was not required.
In 2009, the government of the Republic of Korea subsidized medical expenses for patients with rare and intractable diseases through a co-payment assistance policy which is called the Individual Copayment Beneficiaries Program (ICBP) [21], and SLE was designated as one of the rare diseases to be covered by this program. Under this ICBP system, the NHIS has established a registration program which includes codes for the targeted disease classified per the Korean Standard Classification of Diseases (KCD)-7 (based on the International Classification of Diseases (ICD)-10), date of definite diagnosis, and tests performed for the confirmation of the diagnosis. In case of SLE, patients who satisfied 1997 American College of Rheumatology (ACR) classification criteria for SLE or 2009 Systemic Lupus International Collaborating Clinics (SLICC) criteria were registered. For an accurate identification of cases, we used data from January 1, 2009 to December 31, 2016 with the assumption that all SLE patients have been accurately coded since 2009. We identified SLE cases using the diagnostic code M32 based on International Classification of Diseases, 10th revision, during this period.
For incidence, the year-specific numerator was the number of subjects who were incident cases in the specific calendar year, and the denominator was the total mid-year population at risk. When calculating incidence, data from January 1, 2011 to December 31, 2016 were used since prior data from a period of at least one-year prior is required and a washout period of at least one year is needed to minimize prevalent cases identified as incident cases. For annual prevalence, the year-specific numerator was the number of prevalent cases in the specific calendar year, and the denominator was the total mid-year population from the Korean National Statistical Office for that specific year. Prevalence rates were identified from 2009 to 2016. Crude rates, age-specific rates, standardized rates adjusted for age and 95% confidence intervals (CIs) were calculated. All statistical analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC, USA).
Of total 9,139,933, 4,487 women were newly diagnosed with SLE between 2011 and 2016. The average incidence was 8.18/100,000 person-years (95% CI 7.94–8.43).
Temporal trend
Table 1 shows the trend in incidence by year. Incidence of SLE was relatively constant throughout the years analyzed, with the highest incidence in 2016 (8.56/100,000 person-years, 95% CI 7.95–9.17) and the lowest incidence in 2012 (7.85/100,000 person-years, 95% CI 7.28–8.42).
| Years | Total female population | Number of cases | Incidence per 105 PYs | 95% CI |
|---|---|---|---|---|
| 2011 | 9361241 | 771 | 8.24 | (7.65–8.82) |
| 2012 | 9290139 | 729 | 7.85 | (7.28–8.42) |
| 2013 | 9207754 | 742 | 8.06 | (7.48–8.64) |
| 2014 | 9106227 | 771 | 8.47 | (7.87–9.06) |
| 2015 | 8994585 | 714 | 7.94 | (7.36–8.52) |
| 2016 | 8879651 | 760 | 8.56 | (7.95–9.17) |
| SLE systemic lupus erythematosus, CI confidence interval, PYs person-years | ||||
Age
To analyze the trends in incidence according to ages, we calculated the age-specific incidence rate for 2013. The peak age of SLE incidence in women of childbearing age was between 25–39 years, with bimodal peaks at 25–29 years and 35–39 years. The incidence of SLE was lower among women in the early (20–24 years) and late (40–44 years) childbearing age periods (Fig. 1A).
From 2009–2016, 12,756 women between the age of 20 to 44 years were diagnosed with SLE. The average prevalence of SLE in women in childbearing years was 77.07/100,000 person-years (95% CI 75.76–78.39).
Temporal trend
Table 2 shows the trend in prevalence by year. The prevalence of SLE in women during their childbearing years showed minimal year to year variation with the highest prevalence in 2014 (79.47/100,000 person-years, 95% CI 77.64–81.30) and the lowest prevalence in 2010 (74.19/100,000 person-years, 95% CI 72.45–75.93).
| Years | Total female | Number of cases | Prevalence per 105 PYs | 95% CI |
|---|---|---|---|---|
| population | ||||
| 2009 | 9490033 | 7371 | 77.67 | (75.90–79.44) |
| 2010 | 9407485 | 6979 | 74.19 | (72.45–75.93) |
| 2011 | 9361241 | 7118 | 76.04 | (74.27–77.80) |
| 2012 | 9290139 | 7177 | 77.25 | (75.47–79.04) |
| 2013 | 9207754 | 7202 | 78.22 | (76.41–80.02) |
| 2014 | 9106227 | 7237 | 79.47 | (77.64–81.30) |
| 2015 | 8994585 | 6950 | 77.27 | (75.45–79.09) |
| 2016 | 8879651 | 6791 | 76.48 | (74.66–78.30) |
| SLE systemic lupus erythematosus, CI confidence interval, PYs person-years | ||||
Age
The age-specific prevalence rate in 2013 was calculated to define prevalence in different age groups of the women in childbearing years (Fig. 1B). An increase in prevalence with advancement in age was noted among women during their childbearing years, with the highest prevalence in the 40–44 age group. A steep increase in prevalence was observed between the age-groups of 20–24 and 25–29 years, followed by a near plateau in the 30–34 age group, with a gradual increase thereafter.
This is the first nationwide population-based, epidemiologic study of SLE among women of childbearing age in South Korea using NHIS-NHID that includes health information from nearly the entire Korean population. Our study found high incidence and prevalence rates of SLE in women during childbearing years, reflecting a high burden of disease in this particular population.
An average of 8.12 per 100,000 Korean women of childbearing age per year were at risk for developing SLE in this study. This average incidence was higher than the incidence reported previously in the total Korean population (3.72/100,000 person-years) and in Korean women of all ages (6.52/100,000 person-years), according to a study using information from the same database from the years 2005 to 2015 [7]. This suggests that women of childbearing age are a high-risk population for developing SLE. The incidence of SLE among Korean women of childbearing age was also higher compared with the overall incidence of SLE in the United States (US), Europe, and Asia. A recent epidemiologic review reported overall SLE incidences 5.2–7.2/100,000 person-years in the US [22–24], 1.0-4.9 in Europe [4, 5, 25], and 2.8–8.1 in Asia [21, 26–28].
A previous study reported a decrease in the incidence of SLE between 2005 and 2010 and then a slight annual increase until 2015 in Korea [7], but we observed a relatively constant rate of SLE incidence among Korean women of childbearing age. This suggests that the risk of developing SLE for the total population in a given year is affected by extrinsic factors including differences in environmental exposures such as an influenza epidemic, whereas the risk of developing SLE for the specific sociodemographic group of women of childbearing age is mainly affected by intrinsic factors such as age, gender, and female sex hormones [29, 30].
Although there was a slight bimodal pattern in incidence by age, the peak age of incidence in this study was between 25–39 years, with a lower incidence rate in the early (20–24 years) and late (40–44 years) childbearing age periods, suggesting that women are at risk of developing SLE during the period of time when they are most likely to have children (25–39 years). These results are consistent with previous Koreans studies that have reported a peak age of incidence in the 30–39 year age ranges [7, 21]. The peak age of incidence for SLE in other countries varies: Taiwan and Spain have peak incidence at the age of 20–29, and in Norway, the peak incidence age is 16–29 [11, 31, 32]. However, the incidence of SLE increases steadily with age in the US, peaking in women over fifty [33]. This might be related to an increased frequency of late-onset SLE in the Caucasian population [34].
The average prevalence of SLE in women during their childbearing years was 77.07/100,000 person-years (95% CI 75.76–78.39). The prevalence of SLE in women of childbearing age was 3.6-fold higher than the prevalence in total Korean population (28.02/100,000 person-years), which was reported using the same database from 2005–2015, and 1.5-fold higher than the prevalence in Korean women of all ages (51.00/100,000 person-years) [7]. Most studies report higher prevalence rates in women than in the overall population. Although there is no prevalence data for women of childbearing age, the prevalence in women was much higher in the US (159.8/100,000) and Taiwan (179.4/100,000) compared to Korea [26, 35]. Higher prevalence rates of SLE in women of childbearing age may reflect higher incidences of SLE in this specific age group compared to their lifetime risk as shown in this study.
Although we found a year to year variation of SLE prevalence in the total Korean population with a maximum of 14.2/100,000 person-years [7], there was less variation in the prevalence among women of childbearing age, suggesting that childbearing age itself imposes a significant burden on women with SLE.
The prevalence of SLE increased with age in women during their childbearing years, with a peak prevalence in the 40–44 year of age ranges. This finding is consistent with other studies in the total population [7]. This age-specific prevalence trend in SLE reflects the fact that SLE is a chronic autoimmune disease that requires lifelong management [3]. A steep increase in prevalence that plateaus in the 30–34 age group appeared to be related to a higher incidence between the ages of 25–39 years compared to the incidence in the 20–24 and 40–44 age groups. The plateau in prevalence of the 30–34 age group also coincides with the peak age for childbirth in Korea [36]. This suggests that Korean women of childbearing years have to face the burden of SLE through their pregnancies and childbirth.
Despite these important findings, this study has some limitations. First, since the NHIS-NHID are collected for insurance claim purposes only, the diagnostic codes may be inaccurate. To minimize this problem, we only included NHIS data starting from 2009, since all SLE patients were registered with an accurate diagnostic code to receive benefits from the government on a newly launched individual co-payment program for rare and intractable diseases which started in the second half of the year of 2008. Second, as NHIS data is limited to information on patients who visited health institutions, the prevalence and incidence rates might be underestimated. However, such an underestimation may have only slightly impacted our results, since the NHIS covers the entire population of Korea. Nevertheless, this is the first study defining incidence and prevalence rates for SLE among women of childbearing age, a unique population group with a high disease burden.
In conclusion, the risk of SLE is high in women during their childbearing years and this population bears a significant disease burden. With advancements in disease management and improved survival rates, SLE is no longer a rare disease in women of childbearing age. Therefore, special attention should be paid to this particular population group when allocating health resources. Further research assessing the functional burden of SLE such as disability-adjusted life years (DALY) and economic burden are needed to further understand the overall burden of the disease for this age group.
ACR: American College of Rheumatology; CIs: confidence intervals; DALY: disability-adjusted life years; ICBP: Individual Copayment Beneficiaries Program; KCD: Korean Standard Classification of Diseases; NHIS-NHID: National Health Insurance Service – National Health Information Database; SLE: systemic lupus erythematosus; SLICC: Systemic Lupus International Collaborating Clinics; US: United States
Acknowledgements
This work was supported by the National Health Insurance Ilsan Hospital grant (2018-20-002). This study used NHIS- National Health Information Database, made by NHIS. The authors alone are responsible for the content and writing of the paper.
Author’s contributions
CMK, LHS, PJS contributed to an acquisition of data and analysis. LJ and LCH contributed to the conception and study design and edited the manuscript. All authors were involved in analysis and interpretation of the data, drafting the article, and revising it critically for important intellectual contents, and approving the final version of the article.
Availability of data and materials
The data used during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This study was approved by the Institutional Review of Board of the National Health Insurance Service Ilsan hospital (Institutional review board number: NHIMC 2020-02-010), and it was conducted according to the principles of the Declaration of Helsinki. Since the database used in this study contains anonymized data for research purposes, informed consent was not required.
Funding Not applicable.
Consent for publication Not applicable.
Competing interests
The authors declare that they have no competing interests.
Author details
1Division of Rheumatology, Department of Internal Medicine, Ewha Womans University School of Medicine, Seoul, Korea
2Division of Rheumatology, Department of Internal Medicine, National Health Insurance Service Ilsan Hospital, Goyang, Korea
3Research and Analysis Team, National Health Insurance Service Ilsal Hospital, Goyang-si, Korea