Journal List > J Korean Med Sci > v.37(1) > 1148789

Yoo, Kim, Kang, Kim, Yun, and Lee: Prevalence and Premature Mortality Statistics of Autism Spectrum Disorder Among Children in Korea: A Nationwide Population-Based Birth Cohort Study

Abstract

Background

The aim of this study was to estimate the 8-year prevalence and mortality statistics of autism spectrum disorder (ASD) according to birth year (2002–2012).

Methods

We used the National Health Insurance Service database with 4,989,351 children born from 2002 to 2012 including 35,529 children diagnosed with ASD until 8 years of age. The 8-year cumulative prevalence of ASD was calculated annually (2010–2020) with 8 years of follow-up. The 8-year mortality was estimated using Cox models adjusted for sex, household income, area of residence, and year of birth.

Results

Of the 473,494 children born in 2002, 2,467 (5.2 per 1,000 births) were diagnosed with ASD until 2010. The ASD prevalence was 2.6 times higher among boys (1,839; 7.4 per 1,000 boy births) than girls (628; 2.8 per 1,000 girl births). Of the 467,360 children born in 2012, 4,378 (9.4 per 1,000 births) were diagnosed with ASD until 2020. The ASD prevalence was 2.7 times higher among boys (3,246; 13.5 per 1,000 boy births) than girls (1,132; 5.0 per 1,000 girl births). The risk of all-cause mortality was higher among children with ASD than those without (hazard ratio [HR], 2.340; 95% confidence interval [CI], 2.063–2.654), which is substantially higher among girls (HR, 4.223; 95% CI, 3.472–5.135) than boys (HR, 1.774; 95% CI, 1.505–2.090).

Conclusion

The present study demonstrated that national-level prevalence and mortality statistics of ASD can be estimated effectively using claims data comprising newborns born each year and followed up for to the age of interest. Because this information is essential to establish evidence-based policies, health authorities need to consider producing epidemiological information of ASD continuously using the same methodology.

Graphical Abstract

jkms-37-e1-abf001.jpg

INTRODUCTION

The fundamental step in establishing and implementing national policies for individuals with autism spectrum disorder (ASD) is to identify the current prevalence and mortality of ASD.12345 The information on the prevalence and mortality of ASD among children enables policymakers to estimate the socioeconomic burden of the disease. In addition, this information is also useful for international comparisons.
The prevalence rate of ASD has been consistently increasing around the world. For example, in the United States, 1 in 54 children aged 8 years had a diagnosis of ASD in 2016, a statistic which is 2.03 times (1 in 110 children) higher than the estimates in 2006.67 In Korea, previous studies reported that the prevalence of ASD was estimated to be 2.64% (1 in 38 children) among school-aged children, that being 7- to 12-year-olds, 18.53 cases per 100,000 persons when looking at all age groups.8910 However, studies on the age-specific prevalence of ASD are limited in Korea; in particular, no study has investigated the time trends of ASD prevalence over the last 10 years.
Therefore, the aim of this study was to establish annual birth cohorts that include all infants born from 2002 to 2012 and calculate the prevalence and premature mortality statistics of ASD according to birth year using the National Health Insurance Service database.

METHODS

Data sources

We customized and used the National Health Insurance Database to test the study hypothesis. The National Health Insurance Database is managed by the National Health Insurance Service in Korea. Since universal health coverage was implemented in 1989, all citizens residing in the Republic of Korea, except for the vulnerable class, are obligated to subscribe to the national health insurance. As of April 2020, 97.2% of all citizens residing in the Republic of Korea are subscribed to the mandatory national health insurance; the remaining people are beneficiaries of the Medical Aid program funded by the government. Healthcare services provided through Medical Aid are also reimbursed by the National Health Insurance Service. Thus, theoretically, the National Health Insurance Service has the healthcare service data of all citizens of the Republic of Korea.11 We extracted information regarding sex, age, and subscription type (health insurance/Medical Aid) from the National Health Insurance Service qualification database and information regarding ASD from the detailed healthcare service database. Access to these databases was given through the Big Data Utilization Specialist Program of the National Health Insurance Service.

Study design and population

We conducted a population-based retrospective birth cohort study. ASD was defined as the inclusion of ICD-10 codes F84.0, F84.1, F84.5, F84.8, or F84.9 as the main diagnosis or additional diagnosis in the healthcare service databank of the National Health Insurance Database.51213 To estimate the 8-year prevalence of ASD, we established birth cohorts of children born from 2002 to 2012. The total and sex-specific (male/female) numbers of ASD development every year were calculated until children became 8 years of age (e.g., children born in 2002 were followed up until 2010 and children born in 2012 until 2020, etc.).
To analyze the risk for premature mortality among children diagnosed with ASD, we established three new birth cohorts: 1) a birth cohort comprising children born between 2002 and 2012 and followed until 8 years of age (2010–2020) (e.g., children born in 2002 were followed up until 2010 and children born in 2012 until 2020, etc.), 2) a birth cohort comprising children born between 2002 and 2003 and followed until 8 years of age (2010–2011), and 3) a birth cohort comprising children born between 2011 and 2012 and followed until 8 years of age (2019–2020).
We estimated 8-year ASD prevalence and mortality, considering the average age at ASD diagnosis previously reported.14 Data on death and date of death were obtained from the mortality data in the National Health Insurance Database qualification databank.

Statistical analysis

The 8-year ASD prevalence (per 1,000 births) was calculated as the number of ASD cases detected until 8 years of age in children born each year, divided by the number of total birth in the corresponding year (e.g., the 8-year ASD prevalence in 2010 was calculated as the number of children diagnosed to ASD until 2010 among those born in 2002, divided by the number of total birth in 2002). Therefore, the 8-year ASD prevalence can be summarized as follows:
Prevalencei=NumberofASDCasesUntilYeariAmongChildrenBorninYear(i8)Numberoftotalbirthsinyear(i8)×1,000jkms-37-e1-e001.jpg
i = year of interest
The risk of premature mortality among ASD patients was estimated using the above-mentioned birth cohorts through Cox proportional hazard models adjusted for sex, household income (high, middle, and low classes based on the health insurance premium quartile), area of residence (Seoul Capital area, which includes Seoul, Incheon, and Gyeonggi Province; other metropolitan areas; and other regions [cities and provinces]), and year of birth.15 The Cox proportional hazard models can be summarized as follows:
h(t) = h0(t)exp(b1Xsex + b2Xhousehold income + b3Xarea of residence + b4Xyear of birth + b5XASD diagnosis
All statistical analyses were performed using SAS Enterprise Guide 7.1. Statistical significance was defined as a two-tailed P value < 0.05.

Ethics statement

The Institutional Review Board (IRB) of Seoul National University Hospital approved the study protocol (approval No. 20180917/07-2018-27/103) and waived the requirement for informed consent because anonymized claims data were used.

RESULTS

A total of 4,989,351 children born from 2002 to 2012 were enrolled in this study. Of these, 35,529 were diagnosed with ASD until 8 years of age. Among children born in 2002, 2,467 out of 473,494 children (5.2 per 1,000 births) were diagnosed with ASD, and 8-year ASD prevalence was 2.6 times higher among boys (1,839; 7.4 per 1,000 boy births) than among girls (628; 2.8 per 1,000 girl births). Among children born in 2012, 4,378 out of 467,360 children (9.4 per 1,000 births) were diagnosed with ASD, and 8-year ASD prevalence was 2.7 times higher among boys (3,246; 13.5 per 1,000 boy births) than among girls (1,132; 5.0 per 1,000 girl births) (Table 1).
Table 1

8-year prevalence of ASD among children born from 2002 to 2012

jkms-37-e1-i001
Year of birth No. of births No. of ASD diagnoses until 8 years of age 8-year ASD prevalence (per 1,000)
Total
2002 473,494 2,467 5.2
2003 476,016 2,462 5.2
2004 456,277 2,498 5.5
2005 418,613 2,435 5.8
2006 431,444 2,684 6.2
2007 479,462 3,459 7.2
2008 453,113 3,320 7.3
2009 428,321 3,482 8.1
2010 451,572 4,070 9.0
2011 453,679 4,274 9.4
2012 467,360 4,378 9.4
Boys
2002 247,648 1,839 7.4
2003 247,472 1,853 7.5
2004 236,866 1,881 7.9
2005 216,873 1,818 8.4
2006 223,196 1,952 8.7
2007 246,812 2,511 10.2
2008 233,498 2,405 10.3
2009 220,747 2,571 11.6
2010 233,155 3,014 12.9
2011 232,955 3,191 13.7
2012 239,980 3,246 13.5
Girls
2002 225,846 628 2.8
2003 228,544 609 2.7
2004 219,411 617 2.8
2005 201,740 617 3.1
2006 208,248 732 3.5
2007 232,650 948 4.1
2008 219,615 915 4.2
2009 207,574 911 4.4
2010 218,417 1,056 4.8
2011 220,724 1,083 4.9
2012 227,380 1,132 5.0
ASD = autism spectrum disorder.
Table 2 shows the ASD cases newly diagnosed in each birth year. For most groups of children born in each year, the number of newly diagnosed ASD cases spiked at age 3 or 4 and substantially decreased after age 8 or 9.
Table 2

Total number of ASD newly diagnosed from 2002 to 2012

jkms-37-e1-i002
Year of birth Year of ASD diagnosis
2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 Total
Total
2002 37 158 265 337 373 400 545 224 128 144 106 96 101 86 95 80 86 92 81 3,434
2003 86 196 314 442 478 347 230 190 179 130 100 76 85 105 73 95 89 73 3,288
2004 67 196 360 555 441 295 216 206 162 126 96 68 101 100 101 100 69 3,259
2005 92 260 425 454 358 286 250 186 124 104 93 86 88 129 99 64 3,098
2006 123 391 447 439 416 334 210 193 131 118 97 91 99 156 76 3,321
2007 214 551 429 639 558 365 337 209 157 126 122 97 141 110 4,055
2008 202 394 448 707 516 339 334 219 161 161 141 136 113 3,871
2009 191 401 494 699 589 362 350 227 169 138 136 105 3,861
2010 281 432 526 793 601 436 481 313 207 201 123 4,394
2011 284 367 551 799 659 545 505 332 232 175 4,449
2012 176 376 544 795 736 551 587 410 203 4,378
Boys
2002 21 90 188 271 306 298 390 176 99 104 84 70 81 73 75 74 64 70 60 2,594
2003 51 127 239 342 374 278 168 144 130 98 72 54 61 81 55 66 63 62 2,465
2004 44 120 247 431 344 230 170 167 128 103 77 49 79 77 69 80 53 2,468
2005 46 142 315 364 288 221 193 151 98 74 71 71 70 99 76 46 2,325
2006 76 216 297 348 331 269 157 153 105 93 79 75 77 123 60 2,459
2007 114 323 289 506 433 287 271 160 128 106 94 75 111 78 2,975
2008 110 224 300 556 395 268 265 165 122 132 111 102 91 2,841
2009 102 231 358 548 462 285 283 169 133 108 115 82 2,876
2010 156 255 383 626 451 344 373 252 174 162 102 3,278
2011 163 203 399 632 523 414 407 267 183 142 3,333
2012 83 196 388 618 585 431 455 325 165 3,246
Girls
2002 16 68 77 66 67 102 155 48 29 40 22 26 20 13 20 6 22 22 21 840
2003 35 69 75 100 104 69 62 46 49 32 28 22 24 24 18 29 26 11 823
2004 23 76 113 124 97 65 46 39 34 23 19 19 22 23 32 20 16 791
2005 46 118 110 90 70 65 57 35 26 30 22 15 18 30 23 18 773
2006 47 175 150 91 85 65 53 40 26 25 18 16 22 33 16 862
2007 100 228 140 133 125 78 66 49 29 20 28 22 30 32 1,080
2008 92 170 148 151 121 71 69 54 39 29 30 34 22 1,030
2009 89 170 136 151 127 77 67 58 36 30 21 23 985
2010 125 177 143 167 150 92 108 61 33 39 21 1,116
2011 121 164 152 167 136 131 98 65 49 33 1,116
2012 93 180 156 177 151 120 132 85 38 1,132
ASD = autism spectrum disorder.
Regarding the risk of all-cause mortality among children with ASD (born between 2002 and 2012), the hazard ratio (HR) of death in children diagnosed with ASD was 2.340 (95% confidence interval (CI), 2.063–2.654; P < 0.001) compared to those who were not diagnosed with ASD. In the sex-stratified analyses, the HR for death according to ASD diagnosis was 4.223 (95% CI, 3.472–5.135; P < 0.001) for girls and 1.774 (95% CI, 1.505–2.090; P < 0.001) for boys, indicating that girls are at a higher risk of death from ASD (Table 3, Fig. 1). In analyses stratified by income status, the HR was not only increased in middle (2.359; 95% CI, 1.979–2.812; P < 0.001) and lower-income class (2.089; 95% CI, 1.546–2.825; P < 0.001) but also in the high-income class (2.469; 95% CI, 1.969–3.094; P < 0.001). Regarding the area of residence, the risk of premature death was higher among those residing outside the Seoul Capital area than those residing in the Seoul Capital area. In particular, the HR of death among people with ASD who were residing in areas in the Seoul Capital area was 1.961 (95% CI, 1.614–2.383; P < 0.001), that of those residing in other metropolitan areas was 2.765 (95% CI, 2.111–3.622; P < 0.001), and that of those residing in other cities and provinces was 2.692 (95% CI, 2.185–3.318; P < 0.001) (Table 3). Meanwhile, the HRs of all-cause premature mortality were 1.982 (95% CI, 1.414–2.781; P < 0.001) among children with ASD born between 2002 and 2003, and 2.391 (95% CI, 1.497–3.819; P < 0.001) among children with ASD born between 2011 and 2012.
Table 3

Risk of all-cause mortality in children with ASD compared with children without ASD, stratified by sex, household income, and area of residence

jkms-37-e1-i003
Variables Stratum Hazard ratio 95% CI P value
Totala ASD 2.340 2.063–2.654 < 0.001
No ASD Ref. Ref.
Sex
Boys ASD 1.774 1.505–2.090 < 0.001
No ASD Ref. Ref.
Girls ASD 4.223 3.472–5.135 < 0.001
No ASD Ref. Ref.
Household income
High ASD 2.469 1.969–3.094 < 0.001
No ASD Ref. Ref.
Middle ASD 2.359 1.979–2.812 < 0.001
No ASD Ref. Ref.
Low ASD 2.089 1.546–2.825 < 0.001
No ASD Ref. Ref.
Area of residence
Seoul Capital Area ASD 1.961 1.614–2.383 < 0.001
No ASD Ref. Ref.
Metropolitan Cities ASD 2.765 2.111–3.622 < 0.001
No ASD Ref. Ref.
Others ASD 2.692 2.185–3.318 < 0.001
No ASD Ref. Ref.
ASD = autism spectrum disorder, CI = confidence interval, Ref. = reference.
aCox proportional hazard models adjusted for sex, income, area of residence, and year of birth.
Fig. 1

Risk of all-cause mortality in children with autism spectrum disorder stratified by sex.

Associations were assessed using Cox regression models adjusted for household income, area of residence, and birth year.
ASD = autism spectrum disorder.
jkms-37-e1-g001

DISCUSSION

Prior to devising policies pertaining to individuals with ASD, policymakers need to ascertain the number of people affected by the disorder and the number of people who would die due to the disorder.145 To date, corresponding information on ASD in the Republic of Korea has not been properly studied. Therefore, we followed up on all newborns and estimated the prevalence and mortality of ASD among children at 8 years of age.
In this study, we established birth cohorts of children born from 2002 to 2012 using nationwide population-based claims data in the Republic of Korea, analyzed newly diagnosed ASD cases according to birth year, and assessed the trend of diagnosis according to age for each cohort. The results showed that the number of newly diagnosed ASD cases spiked at age 3 or 4 and substantially decreased after age 8 or 9. This phenomenon was evident in both boys and girls. The present study also showed that the risk for premature death from ASD was higher among girls, the high-income class, and people residing in regions outside the Seoul capital area than among boys, the low-income class, and people residing in other regions, respectively.
Although the prevalence of ASD varies by country, it is on the rise overall.61617 An increased prevalence means that there is an increased number of newly diagnosed cases if the mortality rate is consistent. The United States established the Autism and Developmental Disabilities Monitoring Network in 2000. The network analyzes the trends of ASD prevalence among 8-year-olds every 2 years.6 According to their data, the prevalence of ASD among 8-year-olds rose from 14.5 cases per 1,000 children (1 in 69 children) in 2012 to 18.5 cases per 1,000 children (1 in 54 children) in 2016.618 According to Canada’s National Autism Surveillance System, the prevalence of ASD among children aged 8 years old in Canada was 15.9 cases per 1,000 children in 2015; 28% of the children were diagnosed with ASD at or after the age of 8.19 In Sweden, the cumulative incidence of ASD is estimated to be 12 cases per 1,000 children among children aged 8 years old.20
In contrast, there is no nationwide data on the prevalence of ASD in the Republic of Korea, and the disorder is not continuously monitored.121 The prevalence of ASD among children in the Republic of Korea has been estimated based on regional epidemiology study results, as opposed to using nationwide data. The epidemiology study calculated the prevalence of ASD among elementary school children (7–12 years) to be 2.64% using an epidemiological tool. One noteworthy factor is that two-thirds of the patients with ASD, as identified using the epidemiological tool, had not been diagnosed by a physician prior to the survey.8 Even if nationwide population-based claims data, such as those used in the present study, were used in that study, the prevalence was calculated for all patients with ASD in a particular year; thus, it was difficult to identify the number of ASD diagnoses according to age.9 Thus, the present study is significant in that it is the first study to identify the annual nationwide prevalence of ASD according to age.
In a US surveillance monitoring study, the median age at ASD diagnosis among children aged 8 years old was reported to be 4.25 years.6 Among children aged 4 years old, the median age at diagnosis was 33 months, which is similar to our findings.22 As the rate of ASD diagnosis before age 4 increased from 58% in 2014 to 71% in 2018, there has been a growing emphasis on the importance and awareness of early ASD diagnosis.2223 In a nationwide study conducted in Canada, the ASD diagnosis rate was 33% among children up to age 3 and 72% among children up to age 7, indicating a lower early diagnosis rate than the US.19
The prevalence of ASD among children aged 8 years and older, the stage at which the rate of increase in diagnosis diminishes, was 5.2–9.4 cases per 1,000 population, which is lower than that reported in foreign studies and that estimated in the Republic of Korea using an epidemiological tool.681920 Previous epidemiological studies reported that two-thirds of children diagnosed with ASD using an epidemiological tool had not been diagnosed by a physician, shedding light on the reality of under-diagnosis of ASD and the consequent lack of treatment in the Republic of Korea.821 Although a previous large-scale study reported a 4–5 times higher prevalence of ASD in males than in females, the male-to-female prevalence ratio among children aged 8 years in the present study was relatively low at 2.45–2.82.61419
Our analysis showed that the risk of mortality was substantially higher among preschool-aged children with ASD than among their counterparts without ASD. In particular, the risk of premature mortality was markedly higher among girls than among boys, a finding which aligns with the findings of previous studies.1224252627 ASD is not a direct and sole cause of death. One of the hypotheses concerning the higher mortality rate associated with ASD is related to the comorbid conditions of ASD or intentional or unintentional injury.15242728 Since we analyzed all-cause mortality in this study, additional studies that include the analysis of the major comorbidities of ASD and the cause of death are needed.
When we stratified the risk of mortality from ASD according to income level, the risk of mortality was increased not only in the middle/low-income class but also in the high-income class. Previous studies reported that the rate of early ASD diagnosis and prevalence were higher in families with higher socioeconomic status, whereas delayed diagnosis and inadequate treatment in low-income families affected prognosis.293031 Thus, further studies, especially those with information regarding the cause of death, should be conducted to analyze the association between the risk of premature mortality and family income and the reason for the gap between income levels using nationwide data.
Our analysis of the association between the risk of all-cause mortality and ASD diagnosis according to the area of the residence revealed that there are regional gaps in the risk of premature mortality from ASD. In particular, the risk of premature mortality was highest among those residing in other metropolitan cities, followed by other cities and provinces and the Seoul capital area. A previous study that analyzed the utilization of healthcare by individuals with ASD in the Republic of Korea reported that these individuals utilized 36% of the healthcare facilities in Seoul and 22% of the healthcare facilities in Gyeonggi Province as of 2017.5 Although more than half of the healthcare facilities utilized are located in the Seoul capital area, the findings of the present study indicate that the risk of premature mortality from ASD is substantially higher among people residing in regions outside the Seoul capital area. This may be attributable to differences in the supply of and access to healthcare services needed for ASD across regions or a low rate of diagnosis of ASD in regions outside the Seoul capital area. Therefore, further research is needed to estimate the prevalence of ASD according to region.
In the Republic of Korea, three types of databases, namely the disability registry, the current state of individuals with disabilities, and National Health Insurance Scheme data, are used to estimate the number of individuals with developmental disabilities, including ASD. The government relies on the disability registry database to develop policies. Thus, individuals must register their disability to reap the benefits of these policies. However, there is a risk that the number of people with ASD is underestimated in the disability registry due to issues such as stigma.1432 The National Health Insurance claims data provide information on everyone in the Republic of Korea who received care for ASD. However, it is possible that the actual social burden due to ASD may be overestimated. An analysis of the 2017 health insurance claims data showed that healthcare utilization was remarkably diminished among people in their 30s and older and was virtually absent among people in their 40s and older.15 Therefore, cohorts need to be established and analyzed by linking the disability registry data and health insurance claims data to comprehensively determine the actual epidemiological features and social burden from ASD.145
Prior to this study, there has been virtually no attempt to estimate the nationwide prevalence of ASD—the most fundamental factors that need to be considered when developing and implementing relevant national policies—in the Republic of Korea. The present study confirmed that the increase in the prevalence of ASD in the Republic of Korea levels out from age 8. The current prevalence of ASD among children aged 8 years old was about 9.4 cases per 1,000 births and that the prevalence was about 2.7 times higher in boys than in girls. In addition, the risk of premature mortality was higher among children diagnosed with ASD and among girls with ASD than among boys with ASD. The significance of this study is that it generated foundational nationwide data that can be used in ASD research, policies, and decision-making. More specific studies, including analyses of causes of death, are needed to establish detailed targets and tailored policies and plans.

ACKNOWLEDGMENTS

We especially appreciate the National Health Insurance Service in Korea for sharing the invaluable national health insurance database in a prompt manner.

Notes

Funding: This study was supported by “Smile Together Foundation,” which is a non-governmental organization to help people with developmental disorders in 2020.

Disclosure: The authors have no potential conflicts of interest to disclose.

Author Contributions:

  • Conceptualization: Kim KN, Kang SC, Kim HJ, Yun JE, Lee JY.

  • Data curation: Kim KN Kang SC.

  • Formal analysis: Kim KN, Kang SC.

  • Funding acquisition: Lee JY.

  • Investigation: Kim KN, Yoo SM, Kang SC, Kim HJ, Lee JY.

  • Methodology: Kim KN, Kang SC, Lee JY.

  • Software: Kim KN, Kang SC.

  • Supervision: Lee JY.

  • Visualization: Kim KN.

  • Writing - original draft: Yoo SM, Kim KN.

  • Writing - review & editing: Yoo SM, Kim KN, Kang SC, Kim HJ, Yun JE, Lee JY.

References

1. Lee JY, Yun J. What else is needed in the Korean government’s master plan for people with developmental disabilities? J Prev Med Public Health. 2019; 52(3):200–204. PMID: 31163956.
crossref
2. Yun J. The necessity of comprehensive service institution for people with autism: Lessons from the North Carolina TEACCH program in United States. Public Health Affairs. 2019; 3(1):147–154.
crossref
3. Yun J, Lee JY. Implications for the US Medicaid role expansion for people with autistic spectrum disorder. Glob Soc Secur Rev. 2019; 9:59–67.
4. Lee JY, Yun JE, Jang WM. Barriers to estimation of number of adults with autism spectrum disorders. J Rehab Res. 2019; 23(2):1–14.
crossref
5. Yun J, Kim HJ. Trend analysis of medical care utilization among people with autistic spectrum disorder using national health insurance data. J Digit Converg. 2018; 16(11):411–418.
6. Maenner MJ, Shaw KA, Baio J, Washington A, Patrick M, DiRienzo M, EdS1; PhD-7, et al. Prevalence of autism spectrum disorder among children aged 8 years—autism and developmental disabilities monitoring network, 11 sites, United States, 2016. MMWR Surveill Summ. 2020; 69(4):1–12.
7. Autism and Developmental Disabilities Monitoring Network Surveillance Year 2006 Principal Investigators. Centers for Disease Control and Prevention (CDC). Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006. MMWR Surveill Summ. 2009; 58(10):1–20.
8. Kim YS, Leventhal BL, Koh YJ, Fombonne E, Laska E, Lim EC, et al. Prevalence of autism spectrum disorders in a total population sample. Am J Psychiatry. 2011; 168(9):904–912. PMID: 21558103.
crossref
9. Hong M, Lee SM, Park S, Yoon SJ, Kim YE, Oh IH. Prevalence and economic burden of autism spectrum disorder in South Korea using national health insurance data from 2008 to 2015. J Autism Dev Disord. 2020; 50(1):333–339. PMID: 31630294.
crossref
10. Yoo HJ. Recent increase in autism and ADHD: true or inflated? J Korean Med Sci. 2013; 28(7):974–975. PMID: 23853476.
crossref
11. National Health Insurance. Updated 2020. Accessed April 5, 2021. https://www.nhis.or.kr/nhis/policy/wbhada01700m01.do .
12. Hwang YI, Srasuebkul P, Foley KR, Arnold S, Trollor JN. Mortality and cause of death of Australians on the autism spectrum. Autism Res. 2019; 12(5):806–815. PMID: 30802364.
crossref
13. Bachmann CJ, Gerste B, Hoffmann F. Diagnoses of autism spectrum disorders in Germany: time trends in administrative prevalence and diagnostic stability. Autism. 2018; 22(3):283–290. PMID: 29671642.
crossref
14. Developmental Disabilities Monitoring Network Surveillance Year 2010 Principal Investigators. Centers for Disease Control and Prevention (CDC). Prevalence of autism spectrum disorder among children aged 8 years - autism and developmental disabilities monitoring network, 11 sites, United States, 2010. MMWR Surveill Summ. 2014; 63(2):1–21.
15. Guan J, Li G. Injury mortality in individuals with autism. Am J Public Health. 2017; 107(5):791–793. PMID: 28323463.
crossref
16. Özerk K, Cardinal D. Prevalence of autism/ASD among preschool and school-age children in Norway. Contemp Sch Psychol. 2020; 24(4):419–428.
crossref
17. Chiarotti F, Venerosi A. Epidemiology of autism spectrum disorders: a review of worldwide prevalence estimates since 2014. Brain Sci. 2020; 10(5):274.
crossref
18. Christensen DL, Braun KV, Baio J, Bilder D, Charles J, Constantino JN, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years—autism and developmental disabilities monitoring network, 11 sites, United States, 2012. MMWR Surveill Summ. 2018; 65(13):1–23. PMID: 30439868.
19. Ofner M, Coles A, Decou ML, Do MT, Bienek A, Snider J, et al. Autism Spectrum Disorder among Children and Youth in Canada 2018. Ottawa, ON: Public Health Agency of Canada;2018.
20. Schendel DE, Overgaard M, Christensen J, Hjort L, Jørgensen M, Vestergaard M, et al. Association of psychiatric and neurologic comorbidity with mortality among persons with autism spectrum disorder in a Danish population. JAMA Pediatr. 2016; 170(3):243–250. PMID: 26752506.
crossref
21. Rah SS, Hong SB, Yoon JY. Prevalence and incidence of developmental disorders in Korea: a nationwide population-based study. J Autism Dev Disord. 2020; 50(12):4504–4511. PMID: 32347466.
crossref
22. Shaw KA, Maenner MJ, Baio J, Washington A, Christensen DL, Wiggins LD, et al. EdS1. Early identification of autism spectrum disorder among children aged 4 years—Early Autism and Developmental Disabilities Monitoring Network, six sites, United States, 2016. MMWR Surveill Summ. 2020; 69(3):1–11.
23. Zuckerman KE, Broder-Fingert S, Sheldrick RC. To reduce the average age of autism diagnosis, screen preschoolers in primary care. Autism. 2021; 25(2):593–596. PMID: 33126817.
crossref
24. Gillberg C, Billstedt E, Sundh V, Gillberg IC. Mortality in autism: a prospective longitudinal community-based study. J Autism Dev Disord. 2010; 40(3):352–357. PMID: 19838782.
crossref
25. Mouridsen SE, Brønnum-Hansen H, Rich B, Isager T. Mortality and causes of death in autism spectrum disorders: an update. Autism. 2008; 12(4):403–414. PMID: 18579647.
26. Woolfenden S, Sarkozy V, Ridley G, Coory M, Williams K. A systematic review of two outcomes in autism spectrum disorder - epilepsy and mortality. Dev Med Child Neurol. 2012; 54(4):306–312. PMID: 22348343.
crossref
27. Bilder D, Botts EL, Smith KR, Pimentel R, Farley M, Viskochil J, et al. Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study. J Autism Dev Disord. 2013; 43(5):1196–1204. PMID: 23008058.
crossref
28. Hirvikoski T, Mittendorfer-Rutz E, Boman M, Larsson H, Lichtenstein P, Bölte S. Premature mortality in autism spectrum disorder. Br J Psychiatry. 2016; 208(3):232–238. PMID: 26541693.
crossref
29. Durkin MS, Maenner MJ, Meaney FJ, Levy SE, DiGuiseppi C, Nicholas JS, et al. Socioeconomic inequality in the prevalence of autism spectrum disorder: evidence from a U.S. cross-sectional study. PLoS One. 2010; 5(7):e11551. PMID: 20634960.
crossref
30. King MD, Bearman PS. Socioeconomic status and the increased prevalence of autism in California. Am Sociol Rev. 2011; 76(2):320–346. PMID: 21547238.
crossref
31. Thomas P, Zahorodny W, Peng B, Kim S, Jani N, Halperin W, et al. The association of autism diagnosis with socioeconomic status. Autism. 2012; 16(2):201–213. PMID: 21810908.
crossref
32. Kim JW, Kim HW, Moon DS, Lim YS, McDougle CJ, Howe YJ. Comparison of services for autism spectrum disorder in Massachusetts with those in Seoul. J Korean Med Sci. 2019; 34(43):e288. PMID: 31701704.
crossref
TOOLS
Similar articles