Psychiatric and Medical Conditions in Transition-Aged Individuals With ASD
Psychiatric and Medical Conditions in Transition-Aged Individuals With ASD
BACKGROUND AND OBJECTIVES: Children with autism spectrum disorder (ASD) have a variety of abstract
medical and psychiatric conditions and an increased use of health care services. There
is limited information about the prevalence of psychiatric and medical conditions in
adolescents and young adults with ASD. Our objective was to describe the frequency of
medical and psychiatric conditions in a large population of diverse, insured transition-aged
individuals with ASD.
METHODS: Participants included Kaiser Permanente Northern California members who were
enrolled from 2013 to 2015 and who were 14 to 25 years old. Individuals with ASD
(n = 4123) were compared with peers with attention-deficit/hyperactivity disorder
(n = 20 615), diabetes mellitus (n = 2156), and typical controls with neither condition
(n = 20 615).
RESULTS: Over one-third (34%) of individuals with ASD had a co-occurring psychiatric
condition; the most commonly reported medical conditions included infections (42%),
obesity (25%), neurologic conditions (18%), allergy and/or immunologic conditions (16%),
musculoskeletal conditions (15%), and gastrointestinal (11%) conditions. After controlling
for sex, age, race, and duration of Kaiser Permanente Northern California membership,
most psychiatric conditions were significantly more common in the ASD group than in each
comparison group, and most medical conditions were significantly more common in the ASD
group than in the attention-deficit/hyperactivity disorder and typical control groups but
were similar to or significantly less common than the diabetes mellitus group.
CONCLUSIONS: Although more research is needed to identify factors contributing to this excess
burden of disease, there is a pressing need for all clinicians to approach ASD as a chronic
health condition requiring regular follow-up and routine screening and treatment of medical
and psychiatric issues.
aDepartment of Pediatrics, The Permanente Medical Group, Inc, Oakland, California; bKaiser Permanente Roseville Medical Center, Roseville, California; and cDivision of Research, Kaiser
Dr Davignon helped design the study and collaborated in drafting the initial manuscript; Dr Croen conceptualized and designed the study and collaborated in
drafting the initial manuscript; Dr Massolo collaborated in the conceptualization and design of the study and reviewed and revised the manuscript; Dr Qian
conducted the initial and subsequent analyses, collaborated in creating tables and figures, and reviewed and revised the manuscript; and all authors approved the
final manuscript as submitted.
DOI: https://doi.org/10.1542/peds.2016-4300K
Accepted for publication Sep 26, 2017
Address correspondence to Meghan N. Davignon, MD, Kaiser Roseville Medical Center, 1600 Eureka Rd, Building C, Roseville, CA 95661. E-mail: meghan.davignon@
kp.org
12% in 18–21-year-olds, 19% in dependence was significantly less in children with ASD had a relatively
22–25-year-olds) and was higher in common in the ASD group than in all lower prevalence, including sleep
females (20%) than males (11%). 3 comparison groups (Table 2). Less disorders (7%), endocrine conditions
In addition to their ASD diagnosis, common disorders associated with (3%), and metabolic (3%) disorders
41% had received a developmental high morbidity or mortality were (Table 2, Fig 1).
disorder (DD) diagnosis at some also significantly more prevalent in
Compared with the TC group,
point in the past (20.7% global individuals with ASD compared with
individuals with ASD were at
delay, 23% language disorder, 11% those in the control group, including
significantly increased risk for
learning disorder, 4% motor delay). schizophrenic disorders (ASD: 1%;
most medical conditions (Table 2,
However, during the 2-year study versus TC: 0.3%, adjusted odds ratio
Fig 1). The highest risks were seen
period, only 4.3% had 1 or more of [aOR] = 3.6, 95% confidence interval
for epilepsy (aOR = 11.9), genetic
these diagnoses documented in their (CI): 2.4–5.3; versus ADHD: 0.6%,
disorders (aOR = 7.7), dyslipidemia
medical record (Table 2). aOR = 1.9, 95% CI: 1.3–2.6; versus DM:
(aOR = 4.9), constipation (aOR = 3.5),
0.7%, aOR = 2.0, 95% CI 1.1–3.8) and
endocrine conditions (aOR = 3.2),
Psychiatric Conditions suicide and self-inflicted injury (ASD:
and sleep disorders (aOR = 3.1).
0.7%; versus TC: 0.3%, aOR = 3.6, 95%
Over one-third (34%) of individuals Antipsychotic medications, a
CI: 2.4–5.3; no significant difference
with ASD had a co-occurring known risk factor for obesity and
versus ADHD [0.9%] or DM [0.9%]).
psychiatric condition; the most dyslipidemia,10 were used by 19%
common were ADHD (15%), anxiety of individuals with ASD. However,
(14%), depression (10%), and bipolar Medical Conditions among individuals who did not
disorder (6%) (Table 2). In adjusted take antipsychotic medications,
analyses, most psychiatric conditions The most common medical obesity and dyslipidemia remained
were significantly more common conditions in transition-aged significantly more common in the
in the ASD group than in each individuals with ASD included ASD group versus the TC group
comparison group, with 2 exceptions. infections (42%), obesity (25%), (obesity: 23% vs 15%, P < .0001;
Depression was significantly more neurologic conditions (18%), allergy dyslipidemia: 2.5% vs 0.7%, P <
common in the ASD group versus and/or immunology conditions .0001). Functional GI disorders,
the TC group but significantly less (16%), musculoskeletal conditions genitourinary and renal conditions,
common in the ASD group versus the (15%), and GI conditions (11%). infectious diseases as a group,
ADHD group, and drug abuse and/or Other conditions previously reported and hereditary and degenerative
S338
Condition n (%) aOR (95% CI)a
ASD, TC, ADHD, DM, ASD Versus TC ASD Versus ADHD ASD Versus DM
n = 4123 n = 20 615 n = 20 615 n = 2156
Developmental disabilityb 177 (4.3) 23 (0.1) 228 (1.1) 22 (1.0) 42.81 3.97 (3.24–4.86)c 5.56 (3.48–8.88)c
(27.56–66.50)c
Global developmental delay 77 (1.9) 11 (0.05) 64 (0.3) 9 (0.4) 38.37 5.96 (4.25–8.36)c 7.80
(20.24–72.71)c (3.78–16.12)c
Language disorder 73 (1.8) 2 (0.01) 25 (0.1) 1 (0.05) 194.76 14.51 37.20
(47.62–796.57)c (9.15–23.02)c (5.10–271.46)c
Learning disorder 27 (0.6) 9 (0.04) 130 (0.6) 8 (0.4) 16.16 1.05 (0.69–1.60) 1.82 (0.78–4.27)
(7.45–35.03)c
Psychiatric conditions (includes ADHD)b 1419 (34.4) 1905 (9.2) 8883 (43.1) 534 (24.8) 4.97 (4.58–5.39)c 0.70 (0.65–0.75)c 1.84 (1.62–2.09)c
Psychiatric conditions (without ADHDd) 1168 (28.3) 1905 (9.2) 5424 (26.3) 503 (23.3) 3.73 (3.43–4.06)c 1.14 (1.06–1.23)c 1.62 (1.42–1.85)c
Anxiety 595 (14.4) 776 (3.8) 2352 (11.4) 204 (9.5) 4.01 (3.57–4.50)c 1.33 (1.21–1.47)c 1.91 (1.59–2.30)c
ADHDd 602 (14.6) 0 (0.0) 6443 (31.2) 77 (3.6) —d —d 3.97 (3.08–5.11)c
Bipolar disorder 264 (6.4) 133 (0.6) 963 (4.7) 61 (2.8) 9.58 (7.72–11.88)c 1.48 (1.28–1.70)c 2.80 (2.07–3.79)c
Depression 410 (9.9) 821 (4.0) 2392 (11.6) 282 (13.1) 2.51 (2.21–2.85)c 0.85 (0.76–0.95)c 0.94 (0.79–1.12)
Disruptive, impulse, and conduct disorders 143 (3.5) 60 (0.3) 560 (2.7) 23 (1.1) 11.93 1.35 (1.12–1.63)c 3.91 (2.45–6.24)c
(8.75–16.26)c
Drug abuse and/or dependence 63 (1.5) 458 (2.2) 1393 (6.8) 96 (4.4) 0.65 (0.50–0.85)c 0.22 (0.17–0.29)c 0.30 (0.21–0.43)c
OCD 94 (2.3) 41 (0.2) 204 (1.0) 13 (0.6) 10.48 2.30 (1.79–2.95)c 4.05 (2.20–7.44)c
(7.21–15.24)c
Psychoses 70 (1.7) 77 (0.4) 178 (0.9) 15 (0.7) 4.83 (3.46–6.73)c 2.01 (1.52–2.66)c 2.36 (1.31–4.26)c
Tic disorder 61 (1.48) 5 (0.02) 139 (0.7) 3 (0.1) 59.36 2.18 (1.61–2.97)c 7.08
(23.69–148.73)c (2.18–22.98)c
Medical conditionb
Allergy and/or immune 666 (16.2) 2585 (12.5) 3220 (15.6) 500 (23.2) 1.33 (1.21–1.46)c 1.02 (0.93–1.12) 0.73 (0.63–0.84)c
Allergic rhinitis 154 (3.7) 498 (2.4) 659 (3.2) 68 (3.2) 1.62 (1.35–1.96)c 1.13 (0.95–1.36) 1.24 (0.90–1.70)
Atopic dermatitis and eczema 270 (6.6) 1081 (5.2) 1189 (5.8) 157 (7.3) 1.29 (1.12–1.48)c 1.08 (0.94–1.24) 1.00 (0.80–1.26)
Autoimmune disorders 148 (3.6) 456 (2.2) 705 (3.4) 1427 (66.2) 1.57 (1.30–1.90)c 1.04 (0.87–1.25) NCe
Drug allergy 83 (2.0) 226 (1.1) 464 (2.2) 95 (4.4) 1.69 (1.30–2.18)c 0.91 (0.72–1.16) 0.61 (0.44–0.85)c
Cardiovascular 248 (6.0) 545 (2.6) 817 (4.0) 522 (24.2) 2.32 (1.98–2.71)c 1.52 (1.31–1.77)c 0.25 (0.21–0.30)c
Dyslipidemia 133 (3.2) 148 (0.7) 288 (1.4) 398 (18.5) 4.88 (3.83–6.22)c 2.24 (1.81–2.77)c 0.18 (0.15–0.23)c
Endocrine 127 (3.1) 199 (1.0) 349 (1.7) 1617 (75.0) 3.20 (2.54–4.04)c 1.87 (1.52–2.31)c NC
Any endocrine without diabetesd 104 (2.5) 199 (1.0) 248 (1.2) 203 (9.4) 2.61 (2.04–3.34)c 2.16 (1.71–2.74)c 0.38 (0.29–0.49)c
DAVIGNON et al
TABLE 2 Continued
Condition n (%) aOR (95% CI)a
ASD, TC, ADHD, DM, ASD Versus TC ASD Versus ADHD ASD Versus DM
n = 4123 n = 20 615 n = 20 615 n = 2156
Renal disorders 89 (2.2) 403 (1.9) 595 (2.9) 270 (12.5) 1.07 (0.84–1.35) 0.75 (0.59–0.94)c 0.24 (0.18–0.31)c
Hematology and/or oncology 159 (3.9) 553 (2.7) 736 (3.6) 194 (9.0) 1.41 (1.17–1.69)c 1.09 (0.91–1.30) 0.64 (0.50–0.81)c
Infectious disease 1731 (42.0) 8795 (42.7) 10 608 (51.5) 1249 (57.9) 0.92 (0.81–1.04) 0.64 (0.56–0.72)c 0.55 (0.45–0.67)c
Bacterial 209 (5.1) 1138 (5.5) 1494 (7.2) 228 (10.6) 0.89 (0.76–1.04) 0.69 (0.59–0.80)c 0.56 (0.46–0.70)c
Mycoses 215 (5.2) 1311 (6.4) 1729 (8.4) 247 (11.5) 1.12 (0.97–1.29) 0.87 (0.76–1.00) 0.60 (0.49–0.73)c
Viral 54 (3.8) 335 (4.8) 456 (6.5) 81 (10.8) 0.80 (0.68–0.92)c 0.61 (0.53–0.71)c 0.46 (0.38–0.57)
Ear infections 81 (5.8) 213 (3.0) 323 (4.6) 33 (4.4) 1.70 (1.48–1.95)c 1.26 (1.11–1.45)c 1.18 (0.94–1.49)
2018
Lower respiratory
Skin infections 403 (9.8) 1685 (8.2) 2239 (10.9) 374 (17.4) 1.14 (1.01–1.28)c 0.89 (0.80–1.00) 0.59 (0.50–0.69)
Downloaded
Upper respiratory infections 788 (19.1) 3996 (19.4) 5217 (25.3) 581 (27.0) 0.93 (0.85–1.01) 0.70 (0.64–0.76)c 0.72 (0.63–0.82)
Injury 327 (7.9) 2240 (10.9) 3288 (16.0) 324 (15.0) 0.68 (0.60–0.77)c 0.47 (0.41–0.53)c 0.50 (0.42–0.60)c
Fracture 237 (5.8) 1756 (8.5) 2500 (12.1) 260 (12.1) 0.64 (0.55–0.74)c 0.45 (0.40–0.52)c 0.47 (0.38–0.58)c
Injury of head and neck 124 (3.0) 755 (3.7) 1253 (6.1) 95 (4.4) 0.77 (0.63–0.93)c 0.49 (0.41–0.60)c 0.63 (0.47–0.85)c
Metabolic 143 (3.5) 200 (1.0) 345 (1.7) 392 (18.2) 3.71 (2.97–4.64)c 2.06 (1.68–2.52)c 0.21 (0.17–0.26)c
Lipoid metabolism 100 (2.4) 100 (0.5) 199 (1.0) 297 (13.8) 5.35 (4.02–7.13)c 2.42 (1.89–3.10)c 0.21 (0.16–0.27)c
Musculoskeletal 608 (14.8) 3726 (18.1) 4770 (23.1) 482 (22.4) 0.74 (0.67–0.81)c 0.59 (0.53–0.64)c 0.67 (0.58–0.78)c
Neurology 733 (17.8) 1886 (9.2) 2909 (14.1) 470 (21.8) 2.07 (1.88–2.27)c 1.36 (1.24–1.49)c 1.03 (0.89–1.18)
Cerebral palsy and other paralytic syndromes 93 (2.3) 60 (0.3) 104 (0.5) 14 (0.6) 7.37 (5.29–10.29)c 4.65 (3.50–6.19)c 4.94 (2.73–8.93)c
Epilepsy and recurrent seizures 352 (8.5) 160 (0.8) 364 (1.8) 64 (3.0) 11.88 5.27 (4.52–6.14)c 4.10 (3.07–5.48)c
(9.78–14.43)c
Hereditary and degenerative diseases of CNS 112 (2.7) 512 (2.5) 861 (4.2) 119 (5.5) 1.03 (0.84–1.28) 0.65 (0.54–0.80)c 0.62 (0.46–0.82)c
Migraine 106 (2.6) 599 (2.9) 950 (4.6) 133 (6.2) 0.79 (0.64–0.98)c 0.57 (0.46–0.70)c 0.58 (0.44–0.78)c
Syncope 82 (2.0) 274 (1.3) 434 (2.1) 45 (2.1) 1.43 (1.11–1.84)c 0.96 (0.75–1.22) 1.06 (0.71–1.59)
Nutrition 214 (5.2) 395 (1.9) 637 (3.1) 156 (7.24) 2.84 (2.38–3.38)c 1.70 (1.45–2.00)c 0.95 (0.75–1.20)
Nutrition metabolism and development 180 (4.4) 329 (1.6) 529 (2.6) 94 (4.4) 2.81 (2.32–3.39)c 1.71 (1.44–2.04)c 1.22 (0.92–1.61)
Overweight and obesity 1821 (44.2) 6646 (32.2) 7653 (37.1) 1211 (56.2) 1.73 (1.62–1.86)c 1.37 (1.28–1.47)c 0.78 (0.70–0.88)c
Overweight 784 (19.0) 3482 (16.9) 3751 (18.2) 535 (24.8) 1.16 (1.06–1.27)c 1.05 (0.96–1.15) 0.76 (0.66–0.87)c
Obesity 1037 (25.2) 3164 (15.4) 3902 (18.9) 676 (31.4) 1.96 (1.81–2.13)c 1.49 (1.38–1.62)c 0.94 (0.83–1.07)
Ophthalmology 164 (4.0) 642 (3.1) 672 (3.3) 170 (7.9) 1.33 (1.12–1.59)c 1.13 (0.95–1.35) 0.57 (0.44–0.72)c
Pulmonary 383 (9.3) 1578 (7.6) 2582 (12.5) 313 (14.5) 1.19 (1.06–1.34)c 0.72 (0.64–0.81) 0.66 (0.55–0.78)
Asthma 318 (7.7) 1306 (6.3) 2267 (11.0) 250 (11.6) 1.19 (1.04–1.35)c 0.68 (0.60–0.76) 0.68 (0.56–0.82)
at least 1.5% in the ASD group and statistically significant findings in comparison with at least 1 comparison group (P < .05).
c Statistically significant odds ratio.
d The TC group was selected from among those who did not have an ADHD diagnosis and did not have a diabetes diagnosis; thus, comparisons between the ASD group and the TC group are not possible for these 2 conditions.
e NC because the regression model did not converge.
f Diagnosed at any time through September 2015.
S339
FIGURE 1
Percentage of psychiatric and medical conditions in 14- to 25-year-old individuals with ASD, ADHD, DM, and TCs, from KPNC, 2014–2015. A, Allergy and/or
Immune; B, Cardiovascular; C, Ear, Nose, and Throat; D, GI; E, Infectious Disease; F, Injury; G, Musculoskeletal; H, Neurology; I, Overweight and/or Obesity;
J, Psychiatric; K, Pulmonary; L, Sleep. * denotes a statistically significant difference compared with the ASD group.
disorders of the nervous system following notable exceptions: (asthma) were all significantly
occurred at equal frequency in allergy and/or immunology less prevalent in the comparisons
the ASD and TC groups; injury, conditions, diabetes, diarrhea, between the ASD group versus the
musculoskeletal conditions, and gastroesophageal reflux, hematology ADHD group (Table 2).
migraines were significantly less and/or oncology, overweight, and By contrast, compared with the DM
common in the ASD group versus the ophthalmologic conditions did not group, individuals with ASD were at
TC group (Table 2). differ in frequency between the a similar or significantly lower risk
Comparisons between the ASD ASD group and the ADHD group. GI of most medical conditions, with the
and ADHD groups were largely disorders, genitourinary and/or renal exception of hearing impairment,
similar to those between the ASD conditions, infectious diseases as a genetic disorders, cerebral palsy,
group and the TC group, with the group, and pulmonary conditions epilepsy, and dyssomnia, all of which
or treatment with psychotropic with children and adults, it is possible There are likely many contributors
medications, which in turn may that certain medical conditions are to the elevated rates of co-occurring
increase the risk of other health underrecognized and undertreated conditions seen in individuals
problems. Thus, although transition- in this age group, contributing to with ASD. Self-recognition of
aged individuals with ASD may additional medical, behavioral, and differences from others and social
experience relative health compared mental health problems. isolation may lead to anxiety and
depression, and treatments used and GI problems. In addition, transitioning, changing routines, and
to address behavioral, psychiatric, symptoms inherent to ASD, accommodating to unfamiliar people
and neurologic conditions may including sensory sensitivities and places may make it more difficult
lead to or exacerbate other medical and difficulties describing feelings for teenagers and young adults with
conditions, such as obesity, sleep, and pain, interacting with others, ASD to access adequate medical
REFERENCES
1. American Psychiatric Association 5. Croen LA, Najjar DV, Ray GT, Lotspeich 9. Denny JC, Ritchie MD, Basford MA,
(APA). Diagnostic and Statistical L, Bernal P. A comparison of health et al. PheWAS: demonstrating the
Manual of Mental Disorders. 5th ed. care utilization and costs of children feasibility of a phenome-wide scan to
Washington, DC: American Psychiatric with and without autism spectrum discover gene-disease associations.
Association; 2013 disorders in a large group-model Bioinformatics. 2010;26(9):1205–1210
2. Christensen DL, Baio J, Van Naarden health plan. Pediatrics. 2006;118(4).
10. Nicolaidis C, Kripke CC, Raymaker
Braun K, et al; Centers for Disease Available at: www.pediatrics.org/cgi/
D. Primary care for adults on the
Control and Prevention (CDC). content/full/118/4/e1203
autism spectrum. Med Clin North Am.
Prevalence and characteristics of 6. Krieger N. Overcoming the absence 2014;98(5):1169–1191
autism spectrum disorder among of socioeconomic data in medical
children aged 8 years–autism and records: validation and application of 11. Schendel DE, Overgaard M, Christensen
developmental disabilities monitoring a census-based methodology. Am J J, et al. Association of psychiatric
network, 11 sites, United States, Public Health. 1992;82(5): and neurologic comorbidity with
2012 [published correction appears 703–710 mortality among persons with
in MMWR Morb Mortal Wkly Rep. autism spectrum disorder in a
7. Lord C, Rutter M, DiLavore PC, Risi S, Danish population. JAMA Pediatr.
2016;65(15):404]. MMWR Surveill Gotham K, Bishop, SL. ADOS-2: Autism
Summ. 2016;65(3):1–23 2016;170(3):243–250
Diagnostic Observation Schedule.
3. Bauman ML. Medical comorbidities 2nd ed. Torrance, CA: Western 12. Buck TR, Viskochil J, Farley M, et al.
in autism: challenges to diagnosis Psychological Services; 2012 Psychiatric comorbidity and
and treatment. Neurotherapeutics. medication use in adults with autism
8. Karter AJ, Ferrara A, Liu JY, Moffet
2010;7(3):320–327 spectrum disorder. J Autism Dev
HH, Ackerson LM, Selby JV. Ethnic
Disord. 2014;44(12):3063–3071
4. Croen LA, Zerbo O, Qian Y, et al. The disparities in diabetic complications
health status of adults on the autism in an insured population. JAMA. 13. Magiati I, Tay XW, Howlin P. Cognitive,
spectrum. Autism. 2015;19(7):814–823 2002;287(19):2519–2527 language, social and behavioural
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