The probabilities of failing any ASQ domain and of the specific domains are shown. The longitudinal crude probabilities of failure by infertility treatment status for all children and stratified by plurality were estimated by generalized linear mixed-effects models using ASQ data from 4 to 36 months in the Upstate KIDS Study.
eTable. ASQ Responses and Screening Fails in Upstate KIDS
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Yeung EH, Sundaram R, Bell EM, et al. Examining Infertility Treatment and Early Childhood Development in the Upstate KIDS Study. JAMA Pediatr. 2016;170(3):251–258. doi:10.1001/jamapediatrics.2015.4164
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An increasing percentage of births are conceived with assisted reproductive technology (ART) and other infertility treatment. Despite findings that such treatments may be associated with diminished gestation and birth size, scarce data exist regarding infertility treatments and children’s development in the United States.
To assess the use and type of infertility treatment in relation to children’s development through age 36 months.
Design, Setting, and Participants
Prospective cohort study (conducted 2008-2014) that sampled based on infertility treatment and plurality. Included in the study were infants born between 2008 and 2010 in New York state (excluding New York City) whose parents completed developmental screening instruments through 36 months of age. A total of 4824 mothers (97% of 4989) completed 1 or more developmental screening instruments for 5841 children, including 1830 conceived with infertility treatment and 2074 twins.
Maternal self-report of any infertility treatment was further categorized into ART and ovulation induction/intrauterine insemination. Assisted reproductive technology use was previously validated by linkage with the Society for Assisted Reproductive Technology–Clinical Outcome Reporting System.
Main Outcomes and Measures
Five developmental domains (fine motor, gross motor, communication, personal-social functioning, and problem-solving ability), as measured by the parental completion of the Ages and Stages Questionnaires at 4, 8, 12, 18, 24, 30, and 36 months of age. Generalized linear mixed modeling techniques estimated adjusted odds ratios (aORs) and 95% CIs for use and type of infertility treatment in relation to failing a developmental domain. Data were stratified by plurality and weighted for the sampling scheme.
There were 1422 mothers (29.5%; mean [SD], age, 34.1 [5.2] years) who underwent infertility treatment. Infertility treatment was not associated with risk of their children failing any developmental domain (aOR, 1.33; 95% CI, 0.94-1.89). Assisted reproductive technology was associated with increased risk for failing any developmental domain but only when singletons and twins were evaluated together (aOR, 1.81; 95% CI, 1.21-2.72). Adjustment for birth weight further attenuated this estimate (aOR, 1.26; 95% CI, 0.82-1.93). After stratifying by plurality, type of treatment also was not significantly associated with failing any developmental domain for ovulation induction/intrauterine insemination (aOR, 1.00; 95% CI, 0.57-1.77 for singletons and aOR, 1.30; 95% CI, 0.76-2.21 for twins) or ART (aOR, 1.38; 95% CI, 0.78-2.43 for singletons and aOR, 1.58; 95% CI, 0.94-2.65 for twins).
Conclusions and Relevance
After considering plurality, children’s development through age 3 years was similar irrespective of infertility treatment or specific type. To our knowledge, these findings are among the first to focus on non-ART treatments in the United States.
Infertility treatment, including assisted reproductive technology (ART), has helped many people become parents.1,2 In 2011, 1.5% of US births were conceived with ART.1 Conceptions by ovulation induction were estimated to be much higher, accounting for 3% to 7% of US births.3,4
Concern about the neurodevelopment of children conceived with such modalities is longstanding, given the potential for developmental “programming” at any stage of treatment including in vitro culture5 and intracytoplasmic sperm injection (ICSI).6 Conception by fertility drugs may also be relevant owing to ovarian stimulation possibly impacting endometrium receptivity and placentation.7 Observations that children conceived by infertility treatment are born earlier and with lower birth weight add to concerns.8,9
Many studies, as reviewed elsewhere,10-12 have investigated neurodevelopmental outcomes with ART but the evidence remains equivocal and largely based on a few follow-up studies conducted outside of the United States. In Sweden, a small significant association with 18% higher risk for intellectual disabilities was found, driven by procedures with ICSI,6 whereas in Denmark, no association was observed.13 Other studies investigating cognitive or neuromotor function have largely found no difference.11 One linkage study from the United States observed an increased risk for autism associated with ART,14 which seemed largely due to socioeconomic differences in surveillance,15 and no significant associations were found in large registry studies from Scandinavia.6,13,16
Studies investigating non-ART infertility treatments and children’s development remain rare. One study found a small increased risk in any mental disorders for children conceived with ovulation induction (OI), with or without intrauterine insemination (IUI), relative to children conceived without any treatment using registry data from Denmark.13 These results contradict earlier studies from Finland,17 the United States,18 and the United Kingdom that found no differences with respect to children conceived by OI/IUI.19
In response to critical data gaps, we designed the Upstate KIDS Study to specifically assess the association between the mode of conception and children’s development through age 3 years. Because ART technique differs between the United States and abroad (eg, including the number of embryos transferred or use of assisted hatching),20 our findings are particularly important for communicating with US couples seeking infertility treatment.
The Upstate KIDS Study, which recruited mothers and their children from New York state (excluding New York City) between 2008 and 2010, was designed to assess the association between the mode of conception and children’s development through age 3 years.
Use of any infertility treatment was not associated with risk for failing any developmental domain as assessed by the Ages and Stages Questionnaire.
Specific treatment using ovulation induction with or without intrauterine insemination was not associated with failing any developmental domain.
Conception by assisted reproductive technology was associated with failing any domain, but not significantly, after accounting for plurality.
No difference in parental reports of children using developmental services or referral for Early Intervention Program evaluation was found relative to infertility treatment or the specific types.
The Upstate KIDS Study recruited infants born to women delivering in New York state (excluding New York City) between 2008 and 2010.21 All infants whose birth certificates indicated infertility treatment use comprised the exposure cohort and their parents were invited to participate. All multiples were also invited to participate. Singletons not conceived with infertility treatment were recruited at a 3:1 ratio to the exposure cohort frequency matched on the state’s perinatal region of birth. In total, 5034 mothers (27% of 18 479 approached) of 6171 children enrolled in the study, with higher response (32%) among exposed mothers.21 We have described recruitment and follow-up procedures, as well as demonstrated the validity of this sampling framework relative to birth certificate information and the absence of major differences in baseline characteristics by participation status.21 The New York State Department of Health and the University at Albany (State University of New York) institutional review boards approved the study and served as the institutional review boards designated by the National Institutes of Health under a reliance agreement. All parents provided written informed consent.
At 4 months post partum, mothers selected all medical services or medications used to become pregnant on the questionnaire. Two subcategories of exposure were defined: (1) ART use consisted of in vitro fertilization (with or without ICSI), assisted hatching, frozen embryo transfer, zygote intrafallopian transfer, gamete intrafallopian transfer, and/or donor eggs or embryos and (2) OI via oral or injectable medications with or without IUI.21 Maternal report was linked with the Society for Assisted Reproductive Technology–Clinical Outcome Reporting System (SART-CORS), a database of ART outcomes reported from member US clinics to the Centers for Disease Control and Prevention. The sensitivity and specificity of maternal report compared with SART-CORS were high (93% and 99%, respectively).22 Given the absence of a registry for verifying OI/IUI and geographic limitation of the SART linkage, we used maternal report for all infertility treatment information and relied on birth certificate data only when missing (n = 147; 3%).
The Ages and Stages Questionnaire (ASQ) is a validated developmental screening instrument recommended for early identification of developmental delays.23-25 The ASQ encourages parents to perform activities with their children to accurately respond to questions capturing 5 developmental domains (ie, fine motor, gross motor, communication, personal-social functioning, and problem-solving ability). Parents completed the ASQ at 4, 6, 8, 12, 18, 24, 30, and 36 months of age, corrected for gestational age.26,27 We implemented the ASQ–second edition27 for screening at ages 4 to 12 months and the third edition26 from ages 18 months onwards as ASQ-3 became available in 2009.
Each item was scored as recommended26,27 (“yes” = 10 points, “sometimes” = 5 points, and “not yet” = 0 points) and summed for each domain (0-60 points). Domain-specific fails were defined as scores 2 SDs below the mean for normative data.26,27 Study personnel followed up with parents when the child failed any of the 5 domains or parental concern was noted. Trained specialists implemented an age-appropriate follow-up ASQ for the domain(s) that failed or discussed concerns. We defined age at fail as the time of the initial fail. When follow-up was incomplete after an initial fail, the child remained as failing that ASQ. Screening instruments were considered valid only if completed in the specified age windows.26,27 For children who failed any ASQ domain, a referral was made to the New York State Early Intervention Program (EIP), which provides free developmental services as needed after clinical evaluation.28
We linked EIP data to assess whether the proportions of children referred for developmental evaluation differed by infertility treatment exposure. Records were matched on identifiers (ie, birth dates and names). The Early Intervention Program provided aggregate tables for proportions of Upstate KIDS children referred for evaluation stratified by plurality and infertility treatment status. Individual-level data from EIP required parental consent, which was solicited from those whose child failed a previous ASQ and were received for 478 children.
Questionnaires accompanying the ASQ at 30 and 36 months also asked mothers to report whether their children received any developmental services. The positive and negative predictive values of reported use of developmental services compared against EIP linkage were high for the 478 infants (86.2% and 95.0%, respectively).
Last, a subgroup of 314 singletons (8%) and 132 twin pairs (12%) underwent clinical diagnostic examinations at 3 to 4 years of age. For this assessment, children who failed the ASQ screening (at 30 or 36 months) and the Modified Checklist for Autism in Toddlers29 (at 18 months) were invited along with a random sample of children with no history of fails. Based on this evaluation, clinicians provided diagnostic codes for each child. Developmental disability was defined as having 1 or more of these diagnoses: autism spectrum disorder (ASD); attention-deficit/hyperactivity disorder; language, learning, and speech disorders; cognitive deficits; cerebral palsy; and/or sensory impairments.
Covariate information came from vital records (ie, maternal and paternal ages, insurance status, plurality, previous live birth, prepregnancy body mass index [BMI, calculated as weight in kilograms divided by height in meters squared], birth weight; and gestational age) or by baseline maternal report (ie, paternal BMI, marital status, race/ethnicity, education, and smoking and alcohol use during pregnancy).
Sociodemographic characteristics relative to infertility treatment were compared using χ2 and t tests. Infant characteristics are shown for all singletons and a randomly selected twin of each sibling pair. Triplets and quadruplets from 45 families were excluded owing to small numbers (n = 134 children).
We first evaluated the prospective associations between infertility treatment exposure (yes/no) and failing any ASQ domain and then by each of the 5 domains. Treatment type was further assessed separating ART and OI/IUI. Children conceived without infertility treatment were the reference group in all analyses. We used generalized linear mixed-effects models with a logit link to estimate the associations between infant treatment and failing the ASQ. These models provided adjusted odds ratios (aORs) and 95% CIs. All models included maternal-level random intercepts and nested infant-level random intercepts to account for the correlation owing to repeated measures and clustering of infants within mothers.30 In models based only on singletons or primary cohort where only 1 infant was included from each mother, an infant-level random intercept was included to account for repeated measures of infants. Sampling weights were applied to account for the study’s design of oversampling infants conceived with infertility treatment and twins.21 Weights were derived using New York state birth certificate data on infertility treatment, plurality, and region of birth for all infants born during the period of recruitment. Time was modeled assuming a nonlinear trajectory of the odds of failing. The estimation was based on weighted likelihood function, which was computed using an adaptive quadrature and the standard errors were calculated based on sandwich-type variance estimation. Our longitudinal methods accounted for children’s varying developmental stages and varying failures over the course of follow-up, allowing flexibility of children to fail at any point in time but not necessarily subsequent follow-up screenings.
A priori factors known to be associated with development (such as socioeconomic status or smoking)31,32 and associated with infertility treatment were adjusted for including maternal age, race/ethnicity, education, insurance, married/living as married, previous live birth, and smoking during pregnancy. Birth weight was included in a separate model to avoid potential overadjustment bias.33 Missing data on marital status (n = 206 infants) and prior live birth (n = 43) were completed using multiple imputations after creating 10 data sets based on a Bernoulli distribution, with probabilities dependent on their observed distributions by infertility treatment type. For variables where few (n <10) were missing (such as smoking or insurance), the missing were imputed using the most frequent response.
Because the ASQ is a screening rather than diagnostic tool, we also evaluated cross-sectional associations between infertility treatment and maternal reported use of developmental services reported at 30 and/or 36 months of age, using logistic regression and adjusting for similar covariates and weighted for the sampling framework. Analyses accounted for missing questionnaire data by inverse probability weighting.34 To construct the weights for missing data, a regression model was run to determine the probability of missing data at 30 and 36 months (yes/no) by infertility treatment exposure and plurality. Sampling weights were multiplied to missing weights to further take into account missing data. Total weights were trimmed at the 95th percentile. For twins, generalized estimating equations were used to account for the correlation between twin pairs. Last, for the children with diagnostic information at 3 to 4 years, χ2 tests of the frequencies were made with respect to developmental diagnoses among singletons (n = 314) and 1 twin of each pair (n = 132). All analyses were performed using SAS version 9.3 (SAS Institute Inc).
In total, 3402 mothers (of 4011 children) unexposed and 1422 mothers (of 1830 children) exposed to infertility treatment were included in our analysis. Six to 10 percent of children failed at least 1 of the ASQ developmental domains at each screen (eTable in the Supplement). Domain-specific fails were fewer, ranging from 2% to 5% per screen. Longitudinal follow-up decreased over time in the families. However, almost all children had at least 1 valid ASQ screen between 4 and 36 months. Mothers (n = 4824; 97% of 4989) who returned the ASQ were more frequently white (81% vs 65%) compared with mothers who never returned one (n = 165; 3%) but did not otherwise differ.
Table 1 shows the differences in characteristics by use of any infertility treatment. Differences between the specific treatment types were also observed, with older parental ages; more twin births; higher education and paternal BMI; and lower maternal prepregnancy BMI, birth weight, and gestational age in the ART group compared with the OI/IUI group.
The unadjusted longitudinal trajectories of the ASQ failures were similar, irrespective of infertility treatment among all children and after stratifying by plurality (Figure). Adjustment for covariates strengthened associations but they did not reach statistical significance (aOR, 1.33; 95% CI, 0.94-1.89; Table 2). Assisted reproductive technology was associated with an increased risk for failing any developmental domain (aOR, 1.81; 95% CI, 1.21-2.72) and, specifically, the personal-social (aOR, 2.03; 95% CI, 1.15-3.59) and problem-solving (aOR, 2.33; 95% CI, 1.15-4.74) domains. However, given the higher probability of failing the ASQ among twins and the higher proportion of twins in the ART group (34% vs 19%) than the unexposed group, results were further stratified by plurality. No statistically significant differences were observed for any of the 5 domains and even when further adjusting for birth weight among singletons or twins.
When we linked our cohort with the state’s EIP data, we observed no significant differences in the percentages of children referred for evaluation by infertility treatment status. That is, among 3904 singletons, 21.2% of children conceived with treatment and 20.7% of children not conceived with treatment were referred. Among 1084 nonrelated twins, 40.8% of children conceived with treatment and 38.6% of children not conceived with treatment were referred. In addition, no differences were found in maternal report of children’s use of developmental services (eg, aOR, 1.26; 95% CI, 0.69-2.30 for any treatment) (Table 3).
Among children who completed diagnostic evaluations at 3 to 4 years, 73 (16%) had a developmental disability that included 1 or multiple of the following: language-, learning-, or speech-related disorders (n = 49), ASD (n = 17), attention-deficit/hyperactivity disorder and its subtypes (n = 16), cognitive deficits (n = 6), cerebral palsy (n = 2), and sensory impairments (n = 2). Frequency of any disability did not differ by infertility treatment exposure; 18% of children without treatment (n = 266) and 13% of children conceived by infertility treatment (n = 180) had a diagnosis (P = .15). Similarly, further stratifying by type of treatment showed no differences: 16% among children conceived with OI/IUI (n = 89) having a diagnosis and 11% of children conceived with ART (n = 91) (P = .25).
In the first US birth cohort designed specifically to assess infertility treatment and children’s development through 3 years of age, we observed that ART was associated with increased risk for developmental delays but associations were primarily owing to the higher twinning rate associated with ART and were not statistically significant after stratifying by plurality. We also observed no difference in parental reports of children using developmental services or referral for EIP evaluation relative to infertility treatment. Moreover, the prevalence of clinically diagnosed developmental disabilities at 3 to 4 years of age was not associated with infertility treatment in a subsample of children undergoing clinical evaluations. These findings suggest that infertility treatment is not associated with developmental delays through 3 years of age, irrespective of treatment type, after accounting for plurality.
Studies on children conceived by infertility treatment in the United States remain scarce and have predominantly focused on the risk for ASD, mostly finding no association.12,15,18,35 In particular, several analyses based on linkages between the National ART Surveillance System and developmental services among Californian children (born 1997-2006) have been conducted to evaluate autism risk in relation to ART.14,15,20 Although a higher risk was found in association with ART,14 socioeconomic factors related to surveillance may largely explain this finding.15 However, further analyses by the same authors found that ICSI was associated with an increased risk for autism in the first 5 years of life (adjusted hazard ratio, approximately 1.65 among singletons and multiples) compared with in vitro fertilization.20 According to our SART-CORS linkage, more than 70% of ART children were conceived with ICSI and fewer with in vitro fertilization, prohibiting further comparisons of the techniques. Our cohort was systematically followed up through age 3 years and will continue through age 8 years, allowing for a more complete assessment of development including disabilities that may not manifest until later ages.
Our findings of the OI/IUI group suggest that these non-ART treatments are also not likely to lead to large short-term differences in a child’s development (ie, up to 3 years of age). Other studies have also found no statistically significant differences in developmental disorders,17 cognitive development,19 or autism.12,18 A registry study from Denmark suggested a small increased risk for mental disorders associated with OI/IUI.13 Specifically, risks were observed for ASD (hazard ratio, 1.20; 95% CI, 1.05-1.37) but not intellectual disabilities (1.02; 95% CI, 0.81-1.28).13 Although our study could not evaluate autism given the follow-up through 3 years, the ASQ was designed to screen for developmental delays associated with intellectual disabilities or ASD.36 However, given our relatively smaller sample size in comparison with the study from Denmark (approximately 33 000 exposed), we were unable to rule out weak associations with certainty, although some of the ASQ domains were found to have associations in the 1.20 range for OI/IUI.
Of note, the ASQ was designed as a screening not diagnostic instrument, and its concurrent validity in comparison with other clinically administered developmental assessment tools varies.23,26,27,37,38 For the Upstate KIDS Study, cutoffs at 2 SDs below the average were used to maximize specificity and minimize overreferral that might result in undue parental distress. A small Iranian study using the ASQ at 60 months similarly reported no differences in the failure of domains among 61 singleton term infants conceived by ART compared with 61 infants spontaneously conceived after adjusting for education and birth weight.39
Our findings are strengthened by the multiple methods used to evaluate childhood development (which is important given that children can develop in an uneven manner), the demonstrated validity of maternal-reported ART treatment data compared with clinical data from SART-CORS,22 and our ability to link children with the state’s EIP. Still, our study had limitations including attrition over time, particularly for the unexposed cohort and twins, and missing data stemming from ASQs being completed by parents outside of established age ranges as observed in a previous study.28 However, we accounted for missing data via generalized linear mixed-effects modeling40 and by inverse probability weighting for missing responses.34 The sample sizes of the 2 specific treatment groups, particularly among twins, were underpowered to detect small associations that could not be ruled out by our analysis. The low initial enrollment rate and its difference by exposure status (32% among exposed vs 26% among nonexposed) may limit generalizability.
We found no evidence suggesting that children’s development through age 3 years—using a standardized parental rating instrument and augmented by registry linkage for developmental services—is associated with any type of infertility treatment in comparison with children conceived without such treatments after accounting for plurality. The elevated probability of delay associated with multiple births remains a risk to be weighed given the higher twinning rate after use of ART. Continued follow-up of children conceived by infertility treatment is needed to ensure the absence of later-onset conditions.
Corresponding Author: Edwina H. Yeung, PhD, ScM, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Blvd, 7B03, Rockville, MD 20852 (firstname.lastname@example.org).
Accepted for Publication: November 5, 2015.
Published Online: January 4, 2016. doi:10.1001/jamapediatrics.2015.4164.
Author Contributions: Drs Yeung and Xie had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Bell, Kus, Buck Louis.
Acquisition, analysis, or interpretation of data: Yeung, Sundaram, Bell, Druschel, Ghassabian, Bello, Xie, Buck Louis.
Drafting of the manuscript: Yeung, Buck Louis.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Yeung, Sundaram, Bell, Xie.
Obtained funding: Druschel, Buck Louis.
Administrative, technical, or material support: Yeung, Bell, Kus, Ghassabian, Buck Louis.
Study supervision: Yeung.
Conflict of Interest Disclosures: None reported.
Funding/Support: This study was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (contracts HHSN275201200005C and HHSN267200700019C).
Role of the Funder/Sponsor: The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Contributions: We thank all of the Upstate KIDS Study participants and staff for their important contributions, as well as Donna M. Noyes, PhD, Kirsten Siegenthaler, PhD, MSPH, and Daniel Kellis from the New York State Department of Health, Bureau of Early Intervention who performed the New York State Early Intervention Program linkage and provided aggregated data frequencies. None received compensation for their contribution.
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