Age at diagnosis of autism spectrum disorders: is there an association with socioeconomic status and family self-education about autism?
Authors Hrdlicka M, Vacova M, Oslejskova H, Gondžová V, Vadlejchova I, Kocourkova J, Koutek J, Dudova I
Received 26 February 2016
Accepted for publication 1 April 2016
Published 6 July 2016 Volume 2016:12 Pages 1639—1644
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Roger Pinder
Michal Hrdlicka,1 Maria Vacova,1 Hana Oslejskova,2 Veronika Gondzova,2 Iveta Vadlejchova,3 Jana Kocourkova,1 Jiri Koutek,1 Iva Dudova1
1Department of Child Psychiatry, Charles University Second Faculty of Medicine and University Hospital Motol, Prague, 2Department of Child Neurology, Masaryk University Faculty of Medicine and University Hospital, Brno, 3Child Psychiatry Clinic, Chomutov, Czech Republic
Background: The marked increase in autism spectrum disorders (ASD) prevalence has stimulated worldwide interest in exploring broader circumstances of care of autistic children, including the role of socioeconomic status (SES) and family information on autism.
Methods: Our sample comprised of 160 children who participated in a diagnostic examination focused on autism, and their parents who completed a simple descriptive questionnaire focusing on the family situation as well as family self-education about autism. The diagnosis of ASD was confirmed in 120 children (75% of the sample; 94 boys, 26 girls) with mean age 6.2±2.7 years (median 5.3, range 2.2–17.2 years). In 71 autistic patients (59.2%), a diagnosis of mental retardation was also established.
Results: The age at diagnosis of ASD correlated negatively with maternal (P=0.014) and paternal (P=0.002) ages at the time of birth of the ASD child as well as with paternal (P=0.002) and maternal (P=0.050) education. The age at diagnosis of ASD did not correlate with family SES. Mothers were significantly more active in seeking information on autism than fathers or both parents equally (80 vs 9 vs 28 cases, respectively; P<0.001). The mean number of information sources on autism was 3.5±1.8 with a range 0–9. The mean number of resources did not differ among the three SES groups (3.50 vs 3.49 vs 4.25, respectively; P=0.704). The mean number of sources did not correlate with the age at diagnosis of ASD. The most often used sources were the Internet (81.7%), followed by psychologists (48.3%), books (46.7%), and child and adolescent psychiatrists (43.3%).
Conclusion: An earlier diagnosis of ASD is associated with higher parental age at birth and higher parental education but not with family SES or number of family information sources.
Keywords: autism spectrum disorders, early diagnosis, socioeconomic status, parental education, parental information
For many decades, autism was considered to be a rare condition. However, the reported prevalence of autism spectrum disorders (ASD) has considerably increased during the past decade, with recent estimates in the range of 1%–1.5%.1,2 The marked increase in ASD prevalence has stimulated worldwide interest in exploring broader circumstances of care of autistic children. A number of studies have examined the role of socioeconomic status (SES) and family self-education about autism relative to the age of the child at the time of autism diagnosis.
Data from the US indicate that higher family SES and higher parental education levels are associated with an earlier autism diagnosis and higher autism prevalence.3–7 Parents and caregivers of ASD children with higher household incomes, as well as parents and caregivers with less education, were more likely to report greater satisfaction with the diagnostic processes used by the schools that their children attended.8 Associations were also found between higher SES and a family residing in an ASD hotspot (ie, localized geographical area associated with increased relative risk of ASD).9 In a Canadian study, household income accurately predicted intellectual disability status in 67% of autistic children. The lower the household income, the greater was the probability of meeting intellectual disability criteria.10
Similar to the US studies, higher SES was found to be a possible risk factor for autism in India,11 but not in the UK12 or in Thailand.13 Additionally, parental education was also not associated with autism risk in the UK.13 A Danish study showed no significant association between risk of autism on the one hand and SES and maternal education on the other hand (paternal education was not analyzed).14 However, markedly different results came from Sweden. Children of families with lower SES and of parents with manual labor occupations were at higher risk of ASD. No important relationships with parental education levels were observed.15
A systematic review of epidemiological surveys of ASD identified over 600 studies, including studies in local languages. The reviewed evidence did not support differences in ASD prevalence by geographic region, nor was there a strong impact of ethnic, cultural, or socioeconomic factors.16 Another comprehensive review, focusing on the age at ASD diagnosis and limited to studies published in English, identified 42 studies between 1990 and 2012. Factors associated with earlier diagnosis included higher SES, symptom severity, and greater parental concern about initial symptoms.17
Greater awareness of autism has been suggested as one of the factors influencing the increase in ASD prevalence.18 This may result in earlier and more frequent contacts between the family of a potential ASD child and health professionals. Thus, information sources on autism have increasingly become a topic of research interest in the past 2 decades. In 1999, British parents most frequently reported professionals as their source of information, although other parents and voluntary organizations were also mentioned.19 However, American parents reported 6 years later that the most frequent source of information was books (88%), followed by the Internet (86%) and other parents (72%).20 On average, parents reported getting information about ASD from nearly seven different sources (mean 6.9; range 0–15). The total number of information sources also differed relative to parental or family income, with those in lower income groups (mean 5.9) using fewer information sources than either middle (mean 7.0) or upper (mean 7.2) income groups.
The main problem with the Internet serving as an information source is the extreme range in quality and reliability. US research found that websites with a “.gov” top-level domain were significantly more likely to be of higher quality than websites with a commercial oriented top-level domain (eg, “.com” or “.org”).21 Research focused on websites of advocacy groups found that the majority (61%) of the claims about treatment safety and efficacy were unsubstantiated.22 Instead, a range of rhetorical strategies were used to imply scientific support. Many websites did not meet criteria for quality health information and failed to cite evidence supporting described interventions.23
Regarding the situation in the Czech Republic, the first systematic diagnostic programs for autism were launched in the late 1990s. Two older studies reported a mean age at diagnosis of 9.1 years in 200424 and 6.8 years in 2007.25 No specific studies on the prevalence of autism or on the socioeconomic factors associated with the age at ASD diagnosis have been conducted in the Czech Republic.
The aims of our study were to determine if family situation, including SES and access to information resources on autism, influenced the age at diagnosis of ASD in daily clinical practice in the Czech Republic.
We created a simple descriptive questionnaire focusing on two topics: 1) general family situation and 2) family self-education about autism.
In the first part, we collected family information including 1) parental ages at the time of the examination and age and at the time of birth of the ASD-affected child, 2) educational level of parents, 3) household, 4) marital status, and 5) family SES. We divided the participant families into three SES groups based on Czech State legal definitions at the time the study was initiated. These definitions provide clear upper limits for low income and clear lower limits for high income families.
Low family SES: The total family income was below 2.4 multiples of the “Living Minimum Amount”; the family gets, according to this criterion, a financial allowance from the state for each child.
Middle family SES: Family income exceeds criterion A, but is less than criterion C.
High family SES: At least one of the parents has an income of at least four multiples of the average salary in the Czech Republic (ie, 100,000 Czech crowns at minimum), or the sum of the incomes of both parents exceeds this amount.
In the second part, parents were questioned about whether they came to the examination with the expectation that their child had autism and whether they had sought information about autism prior to the examination. They were asked to identify all their information sources on autism and specify the number of sources they used in self-education. Multiple entries were allowed. They could choose from the following: 1) pediatrician; 2) child and adolescent psychiatrist; 3) physician of other specialty; 4) psychologist; 5) school nurse from a nursery school, school teacher, or special education teacher; 6) Internet; 7) books; 8) media (television, newspapers, journals); 9) people with similar problems in the family; and 10) other sources.
Finally, we asked the parents who had been more active in seeking information on autism whether or not they were satisfied with the information they had found on autism.
Responders were parents of 160 children (mean age at examination 6.5±2.9 years; 123 boys, 37 girls) who attended a diagnostic examination focused on autism. The examination took place at three facilities: the Department of Child Psychiatry, University Hospital Motol, Prague (132 cases); the Department of Child Neurology, University Hospital, Brno (19 cases); and the Child Psychiatry Clinic, Chomutov (nine cases). Families were consecutively recruited from November 2012 to January 2016. The study was approved by the Multicentre Ethics Committee of the University Hospital Motol, and the Multicentre Ethics Committee of the University Hospital Brno. Parents who agreed to participate in the study also signed informed consents.
The questionnaires were completed, in the vast majority of cases, by mothers (N=142; 88.8%). Fathers completed the questionnaires in 16 cases (10.0%), while “other” caregivers completed the questionnaires in two cases (1.2%).
The International Classification of Diseases, 10th Edition,26 was used to make a clinical diagnosis, and experienced clinicians with expertise in the autism diagnosis were involved in the study. The diagnosis was further supported using age-appropriate modules from the Autism Diagnostic Observation Schedule27 and/or the Autism Diagnostic Interview – Revised28 in the Department of Child Psychiatry, or by the Autism Diagnostic Interview – Revised alone in the Department of Child Neurology. A diagnosis of ASD was confirmed in 120 children (75% of the sample; 94 boys, 26 girls), and only this particular subgroup was used in the analysis that is presented in the “Results” section. The mean age at examination of children with a confirmed ASD diagnosis was 6.2±2.7 years (median 5.3, range 2.2–17.2 years). Diagnoses according International Classification of Diseases, 10th Edition included 88 patients with childhood autism, 24 patients with atypical autism, seven patients with Asperger syndrome, and one patient with other childhood disintegrative disorder. In 71 autistic patients (59.2%), a diagnosis of mental retardation (MR) was also established. Of these, 35.2% had mild MR, 31% moderate MR, 2.8% severe MR, and 31% unspecified MR.
The diagnosis in 40 children, where the ASD diagnosis was ruled out, included specific developmental disorders of speech and language (15 cases), hyperkinetic disorder (eleven cases), MR (eleven cases), abnormal personality development (four cases), and hyperkinetic conduct disorder (two cases). Other mixed disorders of conduct and emotions, phobic anxiety disorder of childhood, combined vocal and multiple motor tic disorder, and adjustment disorder were represented by one case of each. Several patients suffered from combined diagnoses.
Statistical analysis was performed using the Statistical Package for the Social Sciences, v22 (IBM Corporation, Armonk, NY, USA). Descriptive statistics for the sample were used. The Spearman’s correlation analysis was used to explore relationships between the age at diagnosis and parental education and family SES (ie, ordinal data). The Pearson’s correlation analysis was used to explore relationships between the age at diagnosis and parental age at the time of birth of the affected child and the mean number of information sources used for self-education about autism (ie, continuous data).The one-sample chi-square test was used to compare activities of family members in seeking information about autism. The Mann–Whitney independent samples U test was used for comparison of the number of information sources between families who suspected ASD and those who did not. The Kruskal–Wallis independent samples test was used for comparison of the number of information sources relative to the three SES groups.
Family demographic and socioeconomic status
Data on the demographic and SES of families are presented in Table 1. The age at diagnosis of ASD correlated negatively with maternal and paternal ages at the time of birth of the affected child as well as with paternal and maternal education; that is, an earlier diagnosis of ASD was associated with higher parental age at birth and higher parental education. The age at diagnosis of ASD did not correlate with family SES (Table 2).
Table 1 Family characteristics of the sample (n=120)
Table 2 Correlation between age at diagnosis of autism spectrum disorders and sociodemographic variables
Parental views and activity
The majority of families (75.8%) came to the diagnostic examination with the opinion that their child was autistic: 47 parents (39.2%) gave the answer “definitely agree” and 44 parents (36.7%) gave the answer “slightly agree”. Only 16 parents (13.3%) answered “slightly disagree” and one family (0.8%) responded “definitely disagree”. Twelve families (10.0%) reported that there was no preestablished opinion within the family.
The vast majority of families (114/120, 95%) sought information on autism prior to the diagnostic procedure. Mothers were significantly more active in seeking information on autism than fathers or both parents equally (80 vs 9 vs 28 cases, respectively; χ2=69.282, df=2, P<0.001). Three families did not respond to the question. Thirty-nine responders (32.5%) considered the information they found on autism to be sufficient; 80 responders (66.7%) reported that they found the information inadequate. In one case (0.8%), the answer was missing.
Information sources on autism
The mean number of sources on autism was 3.5±1.8 (range 0–9), and the median number of sources was 3. Taking into account only those families who expressed a defined opinion about whether their child was autistic or not (n=108), it was found that the mean number of sources was significantly higher in parents who had suspected ASD compared to those who had not (3.75 vs 2.82, respectively, U=524.0, P=0.042). The mean number of resources did not differ among the three SES groups (3.50 vs 3.49 vs 4.25, respectively; H=0.703, df=2, P=0.704). The mean number of sources did not correlate with the age at diagnosis of ASD (r=-0.145, P=0.118).
Table 3 specifies sources of information. The most often used information sources were found on the Internet (81.7%), followed by psychologists (48.3%), books (46.7%), and child and adolescent psychiatrists (43.3%). In the subgroup of physicians with other specialties, neurologists and pediatric neurologists were the most common (12/20, 60.0%).
Table 3 Sources of family information about autism
Our finding that higher education of both parents correlated with a younger age at diagnosis of ASD agrees with studies published in the US.3–7 On the other hand, our finding that family SES was not associated with an earlier diagnosis of ASD was inconsistent with several US studies3–7 and also with the results from a comprehensive review by Daniels and Mandell.17 Our results on SES are more in line with findings from certain developed European countries with general health insurance and an open health care system, eg, Denmark.14 Significant negative correlations between the age at ASD diagnosis and parental age at delivery and parental education were not surprising – older and better educated parents are obviously more experienced and able to manage health care of their children more efficiently. However, it must be noted that the correlation coefficients (range 0.180–0.286) indicated a rather small effect size for all variables that were significantly correlated with the age at diagnosis, according to the Cohen’s classification.29
Czech parents were active in seeking information about autism prior to the diagnostic examination (95% of the sample). It was of no surprise that mothers were significantly more active in seeking information than fathers; even so, our findings showed that with regard to fathers the numbers were unexpectedly very low (N=9, 7.7%). In certain ways our results correspond with a study by Johnson and Simpson,30 who found that 63.5% of mothers with autistic children reported having a spouse who had not been willing to participate in some type of research survey. According to the authors, this indifference may indicate a lack of paternal involvement not only in self-education regarding autism but also in the day-to-day care of children with ASD.
The mean number of information sources used for self-education about autism was lower in Czech families (3.5) compared to US families (6.9), which was reported in a study by Mackintosh et al.20 Unlike the Mackintosh et al study, the total number of information sources did not differ among the SES groups defined in our study. However, the passing of 11 years between publication of the Mackintosh et al study and our study probably did influence the preference of information sources. In the US study, books were the most often used resource (88%), followed closely by the Internet (86%) and then by other parents having children with ASD (72%).20 In our study, the Internet was the main source of information (81.7%), whereas books came in third place with 46.7%. Additionally, the number of sources of information coming from those with similar family problems was also very low compared to the US study (14.2% vs 72%). The difference may reflect different social and cultural traditions in both countries. Of particular interest was the low involvement of pediatricians in providing families with information on autism (21.7%), which may point to a specific gap in the Czech system of primary pediatric care.
Our data also pointed to a decrease in both the age at diagnosis and proportion of intellectual disability in ASD individuals over time, generally speaking. In two Czech studies from the 2000s, mean ages at diagnosis were 9.1 years24 and 6.8 years,25 whereas the mean age was 6.2 years in the current study. In the 1990s, approximately 75%–80% of children with autism were described as mentally retarded,31 and in a study from 2004, the number remained high, at 79.7%.24 However, a recent meta-analysis by Elsabbagh et al reported that the proportion of participants with normal IQ was in the range of 15.6%–86.7% for autistic disorder and 45%–85.3% for pervasive developmental disorders.16 Our current study found the proportion of children with normal IQ to be 40.8%, which corresponds with Elsabbagh et al meta-analysis.16
A possible limitation of our study involves the relatively few families in our study that reported being in the high SES group (3.3%), which could have led to a misrepresentation of this group. One explanation could be that the design of our study did not provide anonymous data collection; thus, some families might have not been willing to reveal their true SES. Alternatively, it is possible that families with higher incomes may prefer diagnostic examinations in private facilities, which exist outside of the general health insurance system; all three facilities that took part in this study were part of the general health insurance system. Regrettably, objective means to verify either of these speculative explanations were not available.
Earlier diagnosis of ASD was associated with higher parental age at the time of birth of the ASD-affected child and higher parental education. The age at diagnosis of ASD did not correlate with family SES. Mothers were significantly more active in seeking information on autism than fathers or both parents equally. An earlier diagnosis was not associated with the number of information sources that the family used for self-education about ASD.
This work was supported by the Project (Ministry of Health, Czech Republic) for Conceptual Development of Research Organization 00064203 (University Hospital Motol, Prague, Czech Republic), and by the Ministry of Health of the Czech Republic, grant number 16-31754A. All rights are reserved. The authors would like to thank Prof Tomas Urbanek, for statistical consultation, and Thomas Secrest, for his assistance with the English version of the manuscript.
The authors report no conflicts of interest in this work.
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