Abstract
Information available on the risks of neurodevelopmental disorders (NDs) associated with in utero exposure to valproate (VPA) and to other antiepileptic drugs (AEDs) is limited. A nationwide population-based cohort study was conducted based on comprehensive data of the French National Health Data System (SNDS). Liveborn infants without brain malformation, born between January 2011 and December 2014, were followed from birth up to December 2016. NDs were identified based on diagnoses of mental or behavioural disorders and utilization of speech therapy, orthoptic or psychiatric services. The risk of NDs was compared between children exposed in utero to AED monotherapy and unexposed children, using Cox proportional hazard models adjusted for maternal and neonatal characteristics. The cohort included 1,721,990 children, 8848 of whom were exposed in utero to AED monotherapy. During a mean follow-up of 3.6 years, 15,458 children had a diagnosis of mental or behavioural disorder. In utero exposure to VPA was associated with an increased risk of NDs overall (aHR: 3.7; 95% CI 2.8–4.9) and among children born to a mother without mental illness (aHR 5.1; 95% CI 3.6–7.3). A dose–response relationship was demonstrated and the risk of NDs was more particularly increased for an exposure to VPA during the second or third trimesters of pregnancy. Among the other AEDs, only pregabalin was consistently associated with an increased risk of NDs (aHR: 1.5; 95% CI 1.0–2.1). This study confirms a four to fivefold increased risk of early NDs associated with exposure to VPA during pregnancy. The risk associated with other AEDs appears much lower.
Subject terms: Epidemiology, Neurodevelopmental disorders, Adverse effects
Introduction
Epilepsy is one of the most common conditions affecting women of reproductive age1,2, and most of them need antiepileptic drugs (AED) to avoid the harmful effects of uncontrolled seizures on themselves and their offspring3. However, in utero AED exposure is associated with congenital malformations of varying degrees of severity4,5 and with neurodevelopmental disorders (NDs). In utero exposure to valproate (VPA) is associated with poorer educational attainment6–8, poorer cognitive skills (IQ9,10 and language10–13, motor13,14, attentional13,15,16, behavioural12,14,16–18 and social skills14–17) and various NDs (mental retardation18, language disorders12, motor disorders13, attention-deficit/hyperactivity disorder15 and autism spectrum disorders19). These disorders may affect 30 to 40% of exposed children16, and their frequency increases with the dose of VPA administered to the mother20,21. However, previous studies have failed to determine whether the risk differs according to the period of exposure during pregnancy. Data concerning other AEDs are heterogeneous and insufficient to allow any definitive conclusions concerning the risk of NDs18,20,21. Although a number of studies have been conducted on this topic, it is difficult to draw firm conclusions given the variety of methods and outcomes considered, related to cognitive skills (e.g. IQ or language skills), NDs (e.g. autism spectrum disorders, or attention-deficit/hyperactivity disorder) or school performance.
The aim of the present study was to assess the risk of early NDs associated with in utero exposure: (1) to VPA used in epilepsy, in particular according to dose and period of exposure during pregnancy; and (2) to other AEDs.
Methods
Data sources
This study was conducted using the French national health data system (SNDS), including health insurance claim and hospital discharge databases linked by a unique patient identifier. The system covers the entire French population and contains comprehensive data on all reimbursements for health-related expenditures22, including dispensed drugs (coded using the Anatomical Therapeutic Chemical, ATC, classification) with date of dispensing and outpatient care performed by healthcare professionals, as well as demographic data such as sex, age, area of residence, vital status, and Complementary Universal Health Insurance scheme (CMU-C, a system providing free access to healthcare for people with an annual income below 50% of the poverty threshold). Patients’ status for 100% reimbursement of care related to a severe and costly long-term disease (LTD) is recorded and coded according to the International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD-10). The hospital discharge database provides detailed information about all admissions to French public and private hospitals since 2006. Diagnoses (ICD-10 coded) and medical or surgical procedures performed during hospital stays are available. Mother–child data linkage, possible since 2011 for deliveries in a public institution and since 2012 for all deliveries, was available for 94% of all deliveries in 2014.
This study was approved by the French Data Protection Supervisory Authority (Commission Nationale de l’Informatique et des Libertés). No informed consent is required for studies based on French administrative medical databases, as these data are anonymous.
Study population and follow-up
All liveborn singleton children born between 1st January 2011 and 31st December 2014 were eligible for inclusion. The mother had to be covered by the national health insurance general scheme for salaried workers (which represents 75% of the French population) and to have had at least one health expenditure reimbursement over the 2 years preceding the onset of pregnancy. We excluded children who could not be linked to their mother’s data, those with missing data for sex, gestational age and birth weight and those with a diagnosis of brain malformation (ICD-10 codes Q00 to Q04 and Q05.0 to Q05.4) during their stay in the maternity unit. When the mother had several deliveries during the study period, only the first single liveborn child during the study period was included.
Children were followed from birth until 31/12/2016 (study end date) or until the first of the following conditions, when it occurred before the end of the study: (i) occurrence of the event of interest; (ii) child lost to follow-up, defined as a period of more than 12 months without any reimbursement; (iii) child’s death.
Exposures
Among VPA products, only those indicated for the treatment of epilepsy, i.e. those containing valproic acid and sodium valproate, were considered. The other AEDs considered were lamotrigine and carbamazepine (also indicated in bipolar disorder), clonazepam, pregabalin and gabapentin (also indicated in neuropathic pain), levetiracetam, oxcarbazepine, phenobarbital, and topiramate (also indicated in migraine). In utero exposure to each AED was defined by at least one dispensing of the drug to the mother between the beginning of the month preceding onset of pregnancy and the end of pregnancy. Children considered to be exposed to each AED were those whose mother had used this drug as monotherapy, defined by the use of a single drug indicated for epilepsy during pregnancy (children whose mother had used several AEDs during pregnancy were excluded due to the major difficulty of measuring the respective association of each drug with the risk of NDs). The period of exposure to the AED during pregnancy was categorized as follows: exposure exclusively during the 1st trimester, exposure during the 1st trimester and during the 2nd or 3rd trimester, exposure exclusively during the 2nd or 3rd trimester. The mean daily dose and the cumulative dose of each AED during pregnancy were estimated from the total quantity of drug substance dispensed and the number of days covered during pregnancy, and categorized according to the tertiles of their distributions.
Outcomes
NDs were assessed based on diagnoses (and age at first diagnosis) of mental and behavioural disorders, identified by the attribution of LTD status and/or hospital admission (ICD-10 code F70 to F98). The following diagnostic categories were distinguished: “pervasive developmental disorders” (F84, corresponding to autism spectrum disorders in ICD-11 [6A02]), “mental retardation” (F70–F79), “disorders of psychological development” (F80–F89, including language, motor, learning and autism spectrum disorders), and “behavioural and emotional disorders with onset usually occurring in childhood and adolescence” (F90–F98). Despite the imperfect match with ICD-11 categories, for convenience we collectively refer to categories F70–F98 as “neurodevelopmental disorders” in this paper. We also assessed health care utilization (and age of first utilization) in office medicine or in the outpatient department of a public hospital, identified by reimbursement of at least (i) one speech therapy session; (ii) one orthoptist consultation; (iii) one psychiatrist or child psychiatrist consultation.
Covariates
Information was available on the following characteristics known or likely to be related to both AED therapy in the mother and NDs in the offspring: mother’s age and CMU-C status at the time of delivery, mean monthly salary over the 3 months preceding maternity leave, year of the end of pregnancy, folic acid supplementation (folic acid dispensing during the month preceding pregnancy or the first trimester of pregnancy), alcohol use during the year preceding pregnancy or during pregnancy (in the mother: diagnosis of alcohol-related disease and/or dispensing of a drug indicated for the treatment of alcohol abuse; or in the neonate: diagnosis of maternal use of alcohol or foetal alcohol syndrome), tobacco use during the year preceding pregnancy or during pregnancy (in the mother: diagnosis of tobacco-related disease and/or dispensing of nicotine replacement therapy, a drug indicated for the treatment of tobacco dependence or a bronchodilator exclusively indicated in the treatment of chronic obstructive pulmonary disease; or in the neonate: diagnosis of maternal tobacco use), diagnosis of mental illness other than tobacco or alcohol use disorders, dispensing of psychotropic drugs (antidepressants, especially selective serotonin reuptake inhibitors [SSRI], antipsychotics, anxiolytics, hypnotics) during the year preceding pregnancy or during pregnancy, number of ATC classes of psychotropic drugs dispensed during the year preceding pregnancy (used as an indicator of severity of psychiatric morbidity); and child gestational age, sex, birth weight and neonatal diseases (diagnosis of cerebrovascular disease, intra-uterine hypoxia, birth asphyxia, intracranial haemorrhage).
Statistical analysis
In the main analysis, incidence rate of the various outcomes was estimated for each exposure group and the risk was compared between children exposed in utero to monotherapy with each AED considered and unexposed children. The comparison group for VPA and AEDs not indicated in bipolar disorder (clonazepam, gabapentin, levetiracetam, oxcarbazepine, phenobarbital, pregabalin and topiramate) was composed of children not exposed to any AED during pregnancy. The comparison group for lamotrigine and carbamazepine was composed of children not exposed to either AED or any drugs for bipolar disorder during pregnancy. All these comparisons were performed globally for the overall study population, and by restricting the population to children born to a mother with no known mental illness, i.e. with no history of diagnosed mental illness and no dispensing of psychotropic drugs during the year preceding pregnancy.
In complementary analyses, the risk associated with each event studied was compared between: children exposed to VPA monotherapy and children exposed to lamotrigine monotherapy (i.e. with no other associated drug indicated for the treatment of epilepsy); between children exposed to VPA monotherapy categorized according to the dose of VPA during pregnancy and unexposed children; between children exposed to VPA monotherapy categorized according to the trimester of exposure to VPA during pregnancy and unexposed children.
Cox proportional hazard regression models were used to estimate adjusted hazard ratios (aHRs) and their 95% confidence intervals (CI) comparing the risk of the events studied according to AED exposure. All models were adjusted for the mother’s sociodemographic and medical characteristics (age, CMU-C status, folic acid supplementation, alcohol use, tobacco use, history of mental illness other than tobacco or alcohol use disorders, severity of psychiatric morbidity, psychotropic drugs during the year preceding pregnancy, selective serotonin reuptake inhibitor during pregnancy) and neonatal characteristics (sex, gestational age, birth weight).
Ethics approval and consent to participate
This study was approved by the Commission Nationale de l'Informatique et des Libertés (French data protection agency) (regulatory decision DE-2011–078).
Ethical publication statement
All authors confirm that they have read the Journal’s position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.
Results
The study population was composed of 1,721,990 single liveborn children between 01/01/2011 and 31/12/2014 (Fig. 1). Among the mothers who had used an AED during pregnancy (N = 11,549), 3862 had used lamotrigine, 1491 VPA, 1,777 pregabalin, 1559 clonazepam, 1210 levetiracetam, 791 carbamazepine, 697 topiramate, 467 gabapentin, 250 oxcarbazepine, and 154 phenobarbital. AEDs were predominantly used as monotherapy during pregnancy (Supplementary Table 1).
Figure 1.
Flowchart of the study population.
The majority (60.6%) of children exposed to VPA, lamotrigine, carbamazepine, levetiracetam, oxcarbazepine and phenobarbital during pregnancy were exposed for prolonged periods, i.e. during the 1st trimester and at least the 2nd or 3rd trimester of pregnancy. In contrast, in children exposed to clonazepam, gabapentin, pregabalin and topiramate, exposure was usually limited to the 1st trimester of pregnancy (Supplementary Table 3). Children included in the cohort were followed until a mean age of 3.6 years (maximum: 5 years) (Supplementary Table 3).
A total of 15,270 children (0.9%) were identified with NDs during follow-up, mainly based on a diagnosis of the “disorders of psychological development” category (10,010 cases, 0.6%), including 4280 cases (0.3%) of “pervasive developmental disorders”; and, to a lesser degree, a diagnosis of the “behavioural and emotional disorders with onset usually occurring in childhood and adolescence” (4398 cases, 0.3%) or “mental retardation” (3398 cases, 0.2%) categories. The majority of diagnoses (62%) were derived from hospitalisation data (Supplementary Table 4). A total of 72,498 children (4.2%) utilized speech therapy services, 204,693 (11.9%) utilized orthoptic services and 22,539 (1.3%) utilized psychiatric services (Supplementary Table 5).
Exposure to VPA
Mothers of children exposed to VPA were older, more socioeconomically deprived, more often received folic acid supplementation, more often users of alcohol or tobacco, antidepressants, antipsychotics, anxiolytics and hypnotics (both before and during pregnancy) than mothers of unexposed children. Children exposed to VPA were more often born preterm, with a birth weight less than 2500 g and were small for gestational age (Table 1). These differences tended to be less pronounced or tended to disappear in children born to a mother with no known mental illness (Supplementary Table 6).
Table 1.
Maternal and neonatal characteristics by exposure group—overall study population. N (%) are shown.
| Unexposed* | Exposed to valproate | Exposed to lamotrigine | Exposed to carbamazepine | Exposed to clonazepam | Exposed to gabapentin | Exposed to levetiracetam | Exposed to oxcarbazepine | Exposed to phenobarbital | Exposed to pregabalin | Exposed to topiramate | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| (N = 1,710,441) | (N = 991) | (N = 2,813) | (N = 468) | (N = 1,246) | (N = 378) | (N = 621) | (N = 143) | (N = 84) | (N = 1,627) | (N = 477) | ||
| Maternal characteristics | ||||||||||||
| Age at the end of pregnancy (years) | Mean (standard deviation) | 29.8 (5.3) | 31.0 (5.7) | 29.9 (5.1) | 31.7 (5.6) | 32.1 (5.5) | 32.2 (5.5) | 29.3 (5.3) | 30.6 (5.7) | 31.4 (6.6) | 32.3 (5.7) | 30.5 (5.3) |
| < 25 | 276,843 (16.2) | 137 (13.8) | 424 (15.1) | 50 (10.7) | 118 (9.5) | 32 (8.5) | 119 (19.2) | 23 (16.1) | 18 (21.4) | 139 (8.5) | 66 (13.8) | |
| [25–30] | 562,803 (32.9) | 259 (26.1) | 916 (32.6) | 111 (23.7) | 302 (24.2) | 90 (23.8) | 212 (34.1) | 32 (22.4) | 15 (17.9) | 414 (25.4) | 144 (30.2) | |
| [30–35] | 547,199 (32.0) | 310 (31.3) | 942 (33.5) | 156 (33.3) | 380 (30.5) | 125 (33.1) | 181 (29.1) | 52 (36.4) | 20 (23.8) | 495 (30.4) | 153 (32.1) | |
| ≥ 35 | 323,596 (18.9) | 285 (28.8) | 531 (18.9) | 151 (32.3) | 446 (35.8) | 131 (34.7) | 109 (17.6) | 36 (25.2) | 31 (36.9) | 579 (35.6) | 114 (23.9) | |
| Complementary Universal Health Insurance scheme | 270,199 (15.8) | 311 (31.4) | 446 (15.9) | 92 (19.7) | 303 (24.3) | 82 (21.7) | 134 (21.6) | 36 (25.2) | 27 (32.1) | 404 (24.8) | 79 (16.6) | |
| Salary reconstituted from the sum of maternity leave allowances | Missing data | 660,198 (38.6) | 552 (55.7) | 1,157 (41.1) | 218 (46.6) | 577 (46.3) | 162 (42.9) | 264 (42.5) | 67 (46.9) | 50 (59.5) | 701 (43.1) | 190 (39.8) |
| < €1000 ** | 75,800 (7.2) | 58 (13.2) | 161 (9.7) | 32 (12.8) | 58 (8.7) | 17 (7.9) | 43 (12.0) | 7 (9.2) | 6 (17.6) | 117 (12.6) | 27 (9.4) | |
| €1000–1499 ** | 156,470 (14.9) | 102 (23.2) | 256 (15.5) | 43 (17.2) | 126 (18.8) | 50 (23.1) | 73 (20.4) | 18 (23.7) | 9 (26.5) | 177 (19.1) | 63 (22.0) | |
| €1500–1999 ** | 349,119 (33.2) | 144 (32.8) | 612 (37.0) | 91 (36.4) | 216 (32.3) | 81 (37.5) | 118 (33.1) | 26 (34.2) | 10 (29.4) | 366 (39.5) | 103 (35.9) | |
| €2000–2499 ** | 222,451 (21.2) | 74 (16.9) | 310 (18.7) | 53 (21.2) | 135 (20.2) | 34 (15.7) | 56 (15.7) | 17 (22.4) | 7 (20.6) | 136 (14.7) | 61 (21.3) | |
| €2500–2999 ** | 118,169 (11.3) | 38 (8.7) | 160 (9.7) | 19 (7.6) | 48 (7.2) | 19 (8.8) | 37 (10.4) | 5 (6.6) | 1 (2.9) | 74 (8.0) | 16 (5.6) | |
| ≥ €3000 ** | 128,234 (12.2) | 23 (5.2) | 157 (9.5) | 12 (4.8) | 86 (12.9) | 15 (6.9) | 30 (8.4) | 3 (3.9) | 1 (2.9) | 56 (6.0) | 17 (5.9) | |
| Year of end of pregnancy | 2011 | 321,046 (18.8) | 243 (24.5) | 490 (17.4) | 121 (25.9) | 601 (48.2) | 59 (15.6) | 90 (14.5) | 32 (22.4) | 15 (17.9) | 230 (14.1) | 93 (19.5) |
| 2012 | 488,371 (28.6) | 333 (33.6) | 778 (27.7) | 134 (28.6) | 500 (40.1) | 90 (23.8) | 147 (23.7) | 50 (35.0) | 32 (38.1) | 412 (25.3) | 118 (24.7) | |
| 2013 | 471,047 (27.5) | 233 (23.5) | 793 (28.2) | 134 (28.6) | 83 (6.7) | 116 (30.7) | 202 (32.5) | 27 (18.9) | 23 (27.4) | 465 (28.6) | 128 (26.8) | |
| 2014 | 429,977 (25.1) | 182 (18.4) | 752 (26.7) | 79 (16.9) | 62 (5.0) | 113 (29.9) | 182 (29.3) | 34 (23.8) | 14 (16.7) | 520 (32.0) | 138 (28.9) | |
| Folic acid | 482,209 (28.2) | 525 (53.0) | 1,978 (70.3) | 268 (57.3) | 360 (28.9) | 139 (36.8) | 396 (63.8) | 89 (62.2) | 32 (38.1) | 440 (27.0) | 179 (37.5) | |
| Indicator of alcohol use | 5,503 (0.3) | 22 (2.2) | 27 (1.0) | 2 (0.4) | 35 (2.8) | 6 (1.6) | 13 (2.1) | 1 (0.7) | 2 (2.4) | 21 (1.3) | 7 (1.5) | |
| Indicator of tobacco use | 137,968 (8.1) | 136 (13.7) | 283 (10.1) | 53 (11.3) | 165 (13.2) | 66 (17.5) | 69 (11.1) | 13 (9.1) | 8 (9.5) | 257 (15.8) | 43 (9.0) | |
| Diagnosis of mental illness other than tobacco and alcohol use disorders | 41,553 (2.4) | 96 (9.7) | 287 (10.2) | 74 (15.8) | 216 (17.3) | 43 (11.4) | 51 (8.2) | 36 (25.2) | 15 (17.9) | 169 (10.4) | 54 (11.3) | |
| Antidepressants before pregnancy | 105,848 (6.2) | 107 (10.8) | 399 (14.2) | 84 (17.9) | 494 (39.6) | 143 (37.8) | 68 (11.0) | 37 (25.9) | 13 (15.5) | 603 (37.1) | 185 (38.8) | |
| Antidepressants during pregnancy | 38,561 (2.3) | 58 (5.9) | 239 (8.5) | 67 (14.3) | 393 (31.5) | 100 (26.5) | 30 (4.8) | 29 (20.3) | 7 (8.3) | 422 (25.9) | 113 (23.7) | |
| SSRI during pregnancy | 27,188 (1.6) | 33 (3.3) | 168 (6.0) | 36 (7.7) | 201 (16.1) | 42 (11.1) | 23 (3.7) | 22 (15.4) | 5 (6.0) | 172 (10.6) | 55 (11.5) | |
| Antipsychotics before pregnancy | 12,497 (0.7) | 49 (4.9) | 131 (4.7) | 32 (6.8) | 123 (9.9) | 24 (6.3) | 15 (2.4) | 31 (21.7) | 6 (7.1) | 79 (4.9) | 30 (6.3) | |
| Antipsychotics during pregnancy | 11,281 (0.7) | 37 (3.7) | 77 (2.7) | 24 (5.1) | 109 (8.7) | 17 (4.5) | 8 (1.3) | 24 (16.8) | 5 (6.0) | 67 (4.1) | 27 (5.7) | |
| Anxiolytics before pregnancy | 243,326 (14.2) | 284 (28.7) | 980 (34.8) | 176 (37.6) | 522 (41.9) | 150 (39.7) | 232 (37.4) | 59 (41.3) | 28 (33.3) | 659 (40.5) | 188 (39.4) | |
| Anxiolytics during pregnancy | 106,177 (6.2) | 206 (20.8) | 675 (24.0) | 120 (25.6) | 389 (31.2) | 112 (29.6) | 173 (27.9) | 50 (35.0) | 23 (27.4) | 429 (26.4) | 103 (21.6) | |
| Hypnotics before pregnancy | 69,084 (4.0) | 93 (9.4) | 246 (8.7) | 44 (9.4) | 287 (23.0) | 72 (19.0) | 57 (9.2) | 20 (14.0) | 12 (14.3) | 315 (19.4) | 71 (14.9) | |
| Hypnotics during pregnancy | 18,314 (1.1) | 46 (4.6) | 94 (3.3) | 28 (6.0) | 157 (12.6) | 32 (8.5) | 28 (4.5) | 15 (10.5) | 4 (4.8) | 149 (9.2) | 34 (7.1) | |
| Indicator of severity of psychiatric morbidity (number of ATC classes of psychotropic drugs) | 0 | 1,406,243 (82.2) | 653 (65.9) | 1,640 (58.3) | 263 (56.2) | 492 (39.5) | 157 (41.5) | 366 (58.9) | 65 (45.5) | 53 (63.1) | 701 (43.1) | 217 (45.5) |
| 1 | 184,570 (10.8) | 180 (18.2) | 658 (23.4) | 107 (22.9) | 283 (22.7) | 91 (24.1) | 138 (22.2) | 33 (23.1) | 10 (11.9) | 355 (21.8) | 92 (19.3) | |
| 2 | 67,558 (3.9) | 67 (6.8) | 247 (8.8) | 34 (7.3) | 149 (12.0) | 49 (13.0) | 54 (8.7) | 14 (9.8) | 8 (9.5) | 227 (14.0) | 69 (14.5) | |
| 3 | 27,762 (1.6) | 28 (2.8) | 106 (3.8) | 26 (5.6) | 102 (8.2) | 40 (10.6) | 28 (4.5) | 5 (3.5) | 4 (4.8) | 133 (8.2) | 36 (7.5) | |
| 4 | 12,338 (0.7) | 17 (1.7) | 71 (2.5) | 11 (2.4) | 81 (6.5) | 14 (3.7) | 11 (1.8) | 4 (2.8) | 5 (6.0) | 83 (5.1) | 32 (6.7) | |
| ≥ 5 | 11,970 (0.7) | 46 (4.6) | 91 (3.4) | 27 (5.8) | 139 (11.2) | 27 (7.2) | 24 (3.9) | 22 (15.4) | 4 (4.8) | 128 (7.9) | 31 (6.5) | |
| Neonatal characteristics | ||||||||||||
| Gestational age at birth | Mean (standard deviation) | 39.1 (1.7) | 39.0 (1.8) | 39.0 (1.7) | 39.1 (1.8) | 38.9 (1.9) | 38.6 (2.1) | 38.9 (2.0) | 38.8 (1.9) | 38.8 (2.0) | 38.9 (1.9) | 39.0 (2.1) |
| 22–26 WA | 2041 (0.1) | 1 (0.1) | 2 (0.1) | 0 (0.0) | 1 (0.1) | 0 (0.0) | 1 (0.2) | 1 (0.7) | 0 (0.0) | 3 (0.2) | 1 (0.2) | |
| 27–31 WA | 8584 (0.5) | 6 (0.6) | 9 (0.3) | 3 (0.6) | 9 (0.7) | 2 (0.5) | 6 (1.0) | 0 (0.0) | 1 (1.2) | 9 (0.6) | 6 (1.3) | |
| 32–34 WA | 20,638 (1.2) | 19 (1.9) | 40 (1.4) | 7 (1.5) | 28 (2.2) | 23 (6.1) | 11 (1.8) | 3 (2.1) | 1 (1.2) | 37 (2.3) | 10 (2.1) | |
| 35–36 WA | 59,992 (3.5) | 45 (4.5) | 124 (4.4) | 12 (2.6) | 55 (4.4) | 21 (5.6) | 33 (5.3) | 6 (4.2) | 3 (3.6) | 61 (3.7) | 19 (4.0) | |
| ≥ 37 WA | 1,619,186 (94.7) | 920 (92.8) | 2638 (93.8) | 446 (95.3) | 1153 (92.5) | 332 (87.8) | 570 (91.8) | 133 (93.0) | 79 (94.0) | 1517 (93.2) | 441 (92.5) | |
| Sex | Male | 873,972 (51.1) | 496 (50.1) | 1471 (52.3) | 243 (51.9) | 597 (47.9) | 206 (54.5) | 292 (47.0) | 65 (45.5) | 43 (51.2) | 847 (52.1) | 254 (53.2) |
| Weight at birth | Mean (standard deviation) | 3,288 (513) | 3,209 (550) | 3,262 (515) | 3,274 (542) | 3,220 (553) | 3,190 (600) | 3,152 (540) | 3,218 (597) | 3,087 (593) | 3,263 (563) | 3,257 (579) |
| < 2500 g | 91,455 (5.3) | 88 (8.9) | 172 (6.1) | 31 (6.6) | 105 (8.4) | 47 (12.4) | 60 (9.7) | 12 (8.4) | 12 (14.3) | 118 (7.3) | 32 (6.7) | |
| 2500–2999 g | 337,541 (19.7) | 227 (22.9) | 606 (21.5) | 103 (22.0) | 278 (22.3) | 73 (19.3) | 152 (24.5) | 30 (21.0) | 20 (23.8) | 324 (19.9) | 90 (18.9) | |
| 3000–3499 g | 704,348 (41.2) | 389 (39.3) | 1,156 (41.1) | 176 (37.6) | 485 (38.9) | 140 (37.0) | 251 (40.4) | 60 (42.0) | 35 (41.7) | 630 (38.7) | 203 (42.6) | |
| ≥ 3500 g | 577,097 (33.7) | 287 (29.0) | 879 (31.2) | 158 (33.8) | 378 (30.3) | 118 (31.2) | 158 (25.4) | 41 (28.7) | 17 (20.2) | 555 (34.1) | 152 (31.9) | |
| Small for gestational age | 167,376 (9.8) | 149 (15.0) | 284 (10.1) | 48 (10.3) | 159 (12.8) | 45 (11.9) | 82 (13.2) | 14 (9.8) | 17 (20.2) | 177 (10.9) | 55 (11.5) | |
| Neonatal condition | 222,201 (13.0) | 119 (12.0) | 349 (12.4) | 59 (12.6) | 197 (15.8) | 53 (14.0) | 85 (13.7) | 17 (11.9) | 9 (10.7) | 231 (14.2) | 74 (15.5) | |
*Not exposed to any antiepileptic drug during pregnancy. ** among those for whom the information was available.
In multivariable analysis, children exposed to VPA, compared to unexposed children, were at higher risk of NDs (aHR, 3.7; 95% CI 2.8–4.9)—especially pervasive developmental disorders (aHR, 4.6; 95% CI 2.9–7.5), disorders of psychological development (aHR, 4.7; 95% CI 3.5–6.4) and mental retardation (aHR, 5.1; 95% CI 3.1–8.5)—and utilization of speech therapy (aHR, 1.7; 95% CI 1.4–2.1). These estimates were similar or higher among children born to a mother with no known mental illness (Table 2). Comparison with children exposed to lamotrigine showed three to fourfold increased risks of pervasive developmental disorders, mental retardation and disorders of psychological development with VPA (Supplementary Table 7).
Table 2.
Incidence of early neurodevelopmental disorders during follow-up according to exposure to valproate during pregnancy (compared to unexposed children) in the overall study population and among children born to a mother with no known mental illness.
| Overall population | Children born to a mother with no known mental illness | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Children exposed to valproate during pregnancy (N = 991) |
Unexposed children (N = 1,710,441) |
aHR [95%CI]* | Children exposed to valproate during pregnancy (N = 619) |
Unexposed children (N = 1,382,288) |
aHR [95%CI]* | |||||
| N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
|||
| Diagnosis | ||||||||||
| Mental and behavioural disorders (F70–F98) | 50 | 13.5 | 15,270 | 2.5 | 3.7 [2.8–4.9] | 31 | 13.4 | 11,012 | 2.2 | 5.1 [3.6–7.3] |
| Pervasive developmental disorders (F84) | 17 | 4.5 | 4,280 | 0.7 | 4.6 [2.9–7.5] | 11 | 4.7 | 3,131 | 0.6 | 6.4 [3.5–11.5] |
| Mental retardation (F70–F79) | 15 | 4.0 | 3,398 | 0.6 | 5.1 [3.1–8.5] | 8 | 3.4 | 2,544 | 0.5 | 5.5 [2.7–11.0] |
| Disorders of psychological development (F80–F89) | 41 | 11.0 | 10,010 | 1.6 | 4.7 [3.5–6.4] | 28 | 12.1 | 7,315 | 1.5 | 6.9 [4.8–10.0] |
| Behavioural and emotional disorders with onset usually occurring in childhood and adolescence (F90–F98) | 7 | 1.8 | 4,398 | 0.7 | 1.7 [0.8–3.5] | 4 | 1.7 | 2,976 | 0.6 | 2.4 [0.9–6.3] |
| Health care utilization | ||||||||||
| Speech therapy | 93 | 25.1 | 72,012 | 11.9 | 1.7 [1.4–2.1] | 62 | 27.0 | 55,532 | 11.3 | 2.1 [1.6–2.7] |
| Orthoptics | 135 | 38.4 | 203,489 | 35.6 | 1.1 [0.9–1.3] | 79 | 36.0 | 162,427 | 35.3 | 1.0 [0.8–1.3] |
| Psychiatry | 22 | 5.8 | 22,365 | 3.7 | 1.2 [0.8–1.9] | 12 | 5.1 | 16,018 | 3.3 | 1.4 [0.8–2.5] |
Bold values indicate statistically significant associations, i.e. with a p-value ≤ 0.05.
IR Incidence rate, HR Hazard ratio, 95%CI 95% confidence interval, PY person-year.
*Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, diagnosis of mental illness other than tobacco and alcohol use disorders, antipsychotic drug use during the year preceding pregnancy, indicator of severity of psychiatric morbidity, indicator of tobacco use, indicator of alcohol use, folic acid, SSRI during pregnancy, child’s sex, gestational age and birth weight.
The risk of NDs and health care utilization during follow-up among children exposed to VPA differed according to the period of in utero exposure (Table 3). Prolonged exposures during pregnancy (1st trimester and at least during the 2nd or 3rd trimester) were associated with higher risks, whereas exposure exclusively during the 1st trimester of pregnancy was not associated with an increased risk of any of the diagnostic categories or health care utilizations studied (but only a limited number of cases were observed). Highest risks were also observed with highest doses of VPA, but the risks of mental retardation and disorders of psychological development were increased even in the lower tertiles of VPA doses (Supplementary Table 8).
Table 3.
Incidence of early neurodevelopmental disorders during follow-up according to the period of exposure to VPA during pregnancy in the overall study population (compared to unexposed children).
| Unexposed children (N = 1,710,441) |
Children exposed to valproate only during the 1st trimester of pregnancy (N = 232) |
Children exposed to valproate during the 1st trimester and the 2nd or 3rd trimester of pregnancy (N = 601) |
Children exposed to valproate only during the 2nd or 3rd trimester of pregnancy (N = 158) |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| N | IR per 1,000 PY | N | IR per 1,000 PY | aHR [95%CI]* | N | IR per 1,000 PY | aHR [95%CI]* | N | IR per 1,000 PY | aHR [95%CI]* | |
| Diagnosis | |||||||||||
| Mental and behavioural disorders (F70–F98) | 15,270 | 2.5 | 4 | 4.6 | 1.0 [0.4–2.6] | 40 | 17.7 | 5.5 [4.0–7.4] | 6 | 10.1 | 3.0 [1.3–6.6] |
| Pervasive developmental disorders (F84) | 4,280 | 0.7 | 1 | 1.1 | 0.9 [0.1–6.7] | 14 | 6.1 | 7.0 [4.1–11.8] | 2 | 3.3 | 3.4 [0.8–13.4] |
| Mental retardation (F70–F79) | 3,398 | 0.6 | 2 | 2.3 | 2.5 [0.6–9.9] | 10 | 4.3 | 6.0 [3.2–11.1] | 3 | 5.0 | 6.8 [2.2–21.1] |
| Disorders of psychological development (F80–F89) | 10,010 | 1.6 | 2 | 2.3 | 0.8 [0.2–3.1] | 33 | 14.5 | 6.9 [4.9–9.7] | 6 | 10.0 | 4.4 [2.0–9.9] |
| Behavioural and emotional disorders with onset usually occurring in childhood and adolescence (F90–F98) | 4,398 | 0.7 | 2 | 2.3 | 1.5 [0.4–5.9] | 5 | 2.2 | 2.2 [0.9–5.3] | 0 | 0.0 | - |
| Health care utilization | |||||||||||
| Speech therapy | 72,012 | 11.9 | 17 | 19.9 | 1.3 [0.8–2.0] | 70 | 31.3 | 2.2 [1.8–2.8] | 6 | 9.9 | 0.7 [0.3–1.5] |
| Orthoptics | 203,489 | 35.6 | 24 | 29.3 | 0.8 [0.5–1.2] | 98 | 46.5 | 1.3 [1.0–1.5]a | 13 | 22.2 | 0.7 [0.4–1.2] |
| Psychiatry | 22,365 | 3.7 | 5 | 5.8 | 1.2 [0.5–2.8] | 14 | 6.0 | 1.3 [0.8–2.2] | 3 | 5.0 | 1.2 [0.4–3.8] |
Bold values indicate statistically significant associations, i.e. with a p-value ≤ 0.05.
IR Incidence rate, HR Hazard ratio, 95%CI 95% confidence interval.
*Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, diagnosis of mental illness other than tobacco and alcohol use disorders, antipsychotics during the year preceding pregnancy, indicator of severity of psychiatric morbidity, indicator of tobacco use, indicator of alcohol use, folic acid, SSRI during pregnancy, child’s sex, gestational age and birth weight.
ap = 0.03.
Exposure to lamotrigine and carbamazepine
As for VPA, mothers exposed to lamotrigine and especially carbamazepine were more socioeconomically deprived, more often users of alcohol or tobacco, psycholeptics and psychoanaleptics, their children more often had a lower birth weight and were more often small for gestational age (Table 1); and these differences were less pronounced (carbamazepine) or disappeared (lamotrigine) in children born to a mother with no known mental illness (Supplementary Table 6).
In multivariable analysis, children exposed to lamotrigine, compared to unexposed children, were at higher risk of NDs (aHR, 1.6; 95% CI 1.2–2.1), especially disorders of psychological development (aHR, 1.5; 95% CI 1.0–2.1) and mental retardation (aHR, 2.4; 95% CI 1.4–4.0). These estimates slightly decreased and were no longer significant among children born to a mother with no known mental illness, except for utilization of speech therapy (aHR, 1.3; 95% CI 1.0–1.6) (Table 4). Children exposed to carbamazepine, compared to unexposed children, were at higher risk of NDs (aHR, 1.9; 95% CI 1.0–3.4), especially disorders of psychological development (aHR, 2.0; 95% CI 1.0–4.1) and behavioural and emotional disorders retardation (aHR, 3.2; 95% CI 1.4–7.1) (Supplementary Table 9). There was no increased risk for any of the outcomes among children born to a mother with no known mental illness.
Table 4.
Incidence of early neurodevelopmental disorders during follow-up according to exposure to lamotrigine during pregnancy (compared to unexposed children) in the overall study population and among children born to a mother with no known mental illness.
| Overall population | Children born to a mother with no known mental illness | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Children exposed to lamotrigine during pregnancy (N = 2,813) |
Unexposed children (N = 1,707,707) |
aHR [95%CI]* | Children exposed to lamotrigine during pregnancy (N = 1,586) |
Unexposed children (N = 1,382,176) |
aHR [95%CI]** | |||||
| N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
|||
| Diagnosis | ||||||||||
| Mental and behavioural disorders (F70–F98) | 47 | 4.7 | 15,165 | 2.5 | 1.6 [1.2–2.1] | 17 | 3.0 | 11,010 | 2.2 | 1.4 [0.9–2.2] |
| Pervasive developmental disorders (F84) | 10 | 1.0 | 4,254 | 0.7 | 1.3 [0.7–2.4] | 5 | 0.9 | 3,131 | 0.6 | 1.4 [0.6–3.5] |
| Mental retardation (F70–F79) | 15 | 1.5 | 3,385 | 0.6 | 2.4 [1.4–4.0] | 4 | 0.7 | 2,544 | 0.5 | 1.4 [0.5–3.8] |
| Disorders of psychological development (F80–F89) | 27 | 2.7 | 9,949 | 1.6 | 1.5 [1.0–2.1]a | 12 | 2.1 | 7,315 | 1.5 | 1.5 [0.8–2.6] |
| Behavioural and emotional disorders with onset usually occurring in childhood and adolescence (F90–F98) | 10 | 1.0 | 4,352 | 0.7 | 1.0 [0.6–1.9] | 1 | 0.2 | 2,974 | 0.6 | 0.3 [0.0–2.1] |
| Health care utilization | ||||||||||
| Speech therapy | 149 | 14.9 | 71,832 | 11.8 | 1.2 [1.0–1.4]b | 85 | 15.1 | 55,527 | 11.3 | 1.3 [1.0–1.6]d |
| Orthoptics | 410 | 44.1 | 203,120 | 35.6 | 1.1 [1.0–1.2]c | 214 | 40.5 | 162,414 | 35.3 | 1.1 [0.9–1.2] |
| Psychiatry | 49 | 4.9 | 22,261 | 3.6 | 1.0 [0.7–1.3] | 17 | 3.0 | 16,015 | 3.3 | 0.8 [0.5–1.3] |
Bold values indicate statistically significant associations, i.e. with a p-value ≤ 0.05.
IR Incidence rate, HR Hazard ratio, 95%CI 95% confidence interval.
*Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, diagnosis of mental illness other than tobacco and alcohol use disorders, antipsychotic drug use during the year preceding pregnancy, indicator of severity of psychiatric morbidity, indicator of tobacco use, indicator of alcohol use, folic acid, SSRI during pregnancy, child’s sex, gestational age and birth weight.
**Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, indicator of tobacco use, indicator of alcohol use, folic acid, child’s sex, gestational age and birth weight.
ap = 0.05, bp = 0.07, cp = 0.02, dp = 0.03.
Exposure to other AEDs not indicated in bipolar disorder
Mothers of children exposed to other AED were generally older (except for levetiracetam), more socioeconomically deprived (particularly those using phenobarbital), and more often users of alcohol, tobacco antidepressants, antipsychotics, anxiolytics and hypnotics than mothers of unexposed children. However, no marked differences in terms of any of the child characteristics was observed between the two groups (Table 1 and Supplementary Table 6).
The risks of NDs and health care utilization during follow-up associated with these AEDs are presented in Table 5 (pregabalin) and in Supplementary Tables 10–15 (other AEDs). No consistent association was found for these AEDs, except for pregabalin, which was associated with a 1.5-fold increased risk of NDs (aHR: 1.5, 95% CI 1.0 to 2.1) with, in particular, an increased risk of mental retardation (aHR: 3.1, 95% CI 1.2 to 8.3) and utilization of orthoptic services in the absence of maternal mental illness; and phenobarbital, which was associated with a sevenfold higher risk of a diagnosis of “behavioural and emotional disorders with onset usually occurring in childhood and adolescence” among children born to a mother with no known mental illness (aHR: 7.6, 95% CI 1.1 to 53.6). However, in utero exposures to levetiracetam, oxcarbazepine or topiramate were associated with increased health care utilization (orthoptics for levetiracetam and oxcarbazepine, speech therapy for topiramate and psychiatry for levetiracetam).
Table 5.
Incidence of early neurodevelopmental disorders during follow-up according to exposure to pregabalin during pregnancy (compared to unexposed children) in the overall study population and among children born to a mother with no known mental illness.
| Overall population | Children born to a mother with no known mental illness | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Children exposed to pregabalin during pregnancy (N = 1,627) |
Unexposed children (N = 1,710,441) |
aHR [95%CI]* | Children exposed to pregabalin during pregnancy (N = 674) |
Unexposed children (N = 1,382,288) |
aHR [95%CI]** | |||||
| N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
N | IR per 1,000 PY |
|||
| Diagnosis | ||||||||||
| Mental and behavioural disorders (F70–F98) | 28 | 5.0 | 15,270 | 2.5 | 1.5 [1.0–2.1]a | 7 | 3.1 | 11,012 | 2.2 | 1.3 [0.6–2.7] |
| Pervasive developmental disorders (F84) | 7 | 1.2 | 4,280 | 0.7 | 1.4 [0.7–2.9] | 1 | 0.4 | 3,131 | 0.6 | 0.7 [0.1–4.8] |
| Mental retardation (F70–F79) | 7 | 1.2 | 3,398 | 0.6 | 1.7 [0.8–3.6] | 4 | 1.7 | 2,544 | 0.5 | 3.1 [1.2–8.3] |
| Disorders of psychological development (F80–F89) | 16 | 2.9 | 10,010 | 1.6 | 1.3 [0.8–2.2] | 4 | 1.7 | 7,315 | 1.5 | 1.1 [0.4–3.0] |
| Behavioural and emotional disorders with onset usually occurring in childhood and adolescence (F90–F98) | 9 | 1.6 | 4,398 | 0.7 | 1.4 [0.8–2.8] | 2 | 0.9 | 2,976 | 0.6 | 1.4 [0.3–5.5] |
| Health care utilization | ||||||||||
| Speech therapy | 61 | 11.0 | 72,012 | 11.9 | 0.9 [0.7–1.2] | 24 | 10.5 | 55,532 | 11.3 | 1.0 [0.7–1.5] |
| Orthoptics | 225 | 43.3 | 203,489 | 35.6 | 1.2 [1.1–1.4] | 98 | 46.0 | 162,427 | 35.3 | 1.4 [1.1–1.6] |
| Psychiatry | 23 | 4.1 | 22,365 | 3.7 | 0.9 [0.6–1.3] | 7 | 3.1 | 16,018 | 3.3 | 1.0 [0.5–2.1] |
Bold values indicate statistically significant associations, i.e. with a p-value ≤ 0.05.
IR Incidence rate, HR hazard ratio, 95% CI 95% confidence interval.
*Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, diagnosis of mental illness other than tobacco and alcohol use disorders, antipsychotics during the year preceding pregnancy, indicator of severity of psychiatric morbidity, indicator of tobacco use, indicator of alcohol use, folic acid, SSRI during pregnancy, child’s sex, gestational age and birth weight.
**Cox models adjusted for: mother’s age, Complementary Universal Health Insurance scheme, indicator of tobacco use, indicator of alcohol use, folic acid, child’s sex, gestational age and birth weight.
ap = 0.04.
Discussion
This large nationwide cohort study provides new information on the risks of early NDs associated with in utero exposure to VPA and the other main AEDs currently used. Firstly, it shows a four to fivefold higher risk of early NDs following exposure to VPA, more specifically concerning pervasive developmental disorders, mental retardation and disorders of psychological development. Exposure to VPA, which was found to have a dose–response relationship with occurrence of NDs, also had a different impact according to the period of exposure: children exposed during the second and/or third trimesters of pregnancy had a markedly increased risk of early NDs, unlike children exposed to VPA only during the first trimester. Secondly, the risk associated with other AEDs appeared to be much lower than that associated with VPA. The slight increases in the risk of several mental and behavioural disorders with lamotrigine and carbamazepine were no longer observed when the analysis was confined to children born to a mother with no known mental illness, suggesting an effect of maternal mental illness or associated characteristics rather than exposure to these drugs. The associations observed between pregabalin and phenobarbital and mental retardation, behavioural and emotional disorders and utilization of orthoptic services were based on limited or very limited sample sizes. For the other AEDs, either no increased risk was observed (clonazepam or gabapentin) or only associations with health care utilizations services (oxcarbazepine, levetiracetam, topiramate), often at the limit of significance.
The results for VPA confirm published data concerning both the level of increased risk of NDs associated with exposure during pregnancy, the nature of these disorders and the dose-dependent nature of this risk. Several studies have demonstrated a five to sevenfold increased risk of autism spectrum disorders10,16,19,23–25, a four to eightfold increased risk of special educational needs6,9, and a two to threefold increased risk of language delay11–13 related to in utero exposure to VPA. Moreover, lower IQ, attention and memory scores have been reported among 6-year-old children exposed to VPA in utero10. Prenatal exposure to VPA has also been associated with an increased risk of attention-deficit/hyperactivity disorder15 and decreased sociability and communication scores14,17 and school performances in 6-year-old children7 and adolescents8. Previous studies have reported the existence of a dose–effect relationship20,21, and one study even suggested a threshold effect, with no observed effect for doses lower than 800 mg/day9. In contrast, in our study the risks of NDs were increased even at low VPA doses. Experimental data suggest that VPA, which acts on GABA signalling, induces hippocampal and cortical dysplasia26.
This study also provides new data concerning the heterogeneous level of risk of early NDs according to the period of exposure to VPA during pregnancy. Although some studies have suggested that the increased risk of NDs is predominantly observed following exposure during the third trimester27,28, others have reported harmful effects regardless of the period of exposure during pregnancy29. Our results suggest that the exposure period associated with an increased risk of early NDs essentially corresponds to the second and/or third trimesters of pregnancy, although no definitive conclusions can be drawn due to the limited number of cases.
Our results concerning lamotrigine support published data, generally suggesting no impact of exposure to lamotrigine during pregnancy on the risks of NDs, particularly on the risk of mental retardation18,20,21. However, some studies have suggested an impact of in utero exposure to lamotrigine on the risk of impaired motor and sensory capacities30, disorders of eye-hand coordination31, or language delay or onset of autistic trait13, and experimental data are not completely reassuring32. Longer-term follow-up of our cohort may enable us to more reliably detect the potential effects of lamotrigine on these disorders.
Regarding carbamazepine, phenobarbital and topiramate, although experimental studies have not demonstrated any effects26,32, increased risks of cognitive and motor disorders have been reported in children exposed prenatally9,10,13,15,27,33–35. Our results suggest a possible increased risk of early NDs associated with exposure to carbamazepine and phenobarbital but not with topiramate. However, these results were based on limited numbers of cases among exposed children and should be interpreted with caution.
Almost no data concerning the risks of NDs associated with the other AEDs considered in our study are available in the literature. The results of the present study do not suggest an increased risk of a diagnosis of NDs associated with exposure to clonazepam, gabapentin, levetiracetam or oxcarbazepine during pregnancy. However, our finding of an increased risk of mental retardation and utilization of orthoptic services among children exposed to pregabalin constitutes a signal that needs to be further investigated.
Strengths and limitations
This study, based on the largest cohort of children exposed to AEDs in utero, constitutes a major source of information on the risk of NDs associated with prenatal exposure to these drugs. Up until now, studies on this risk have generally been limited to a small number of drugs and much smaller sample sizes. Linking the mother and child data from the national SNDS databases allowed this study to be conducted on a large unselected population, for which exposure to AEDs was measured without memory bias, in contrast with previous studies generally based on retrospective exposure data derived from registries. The data available in the SNDS also allowed the analysis of various indicators of NDs based on diagnoses or health care utilization. Finally, the available information allowed to account for differences in terms of sociodemographic characteristics, maternal health status and neonatal characteristics according to exposure to the various AEDs considered.
However, this study comprises some limitations. Firstly, as identification of NDs was based on diagnoses established during a hospitalisation or for management of a LTD, or utilization of speech therapy, orthoptic or psychiatric services, any case not associated with this type of event would not be identified. Furthermore, the limited follow-up in the study (up until a mean age of 3.6 years) probably resulted in identifying only the most severe cases, while less severe cases would need a longer follow-up to be detected. These limitations would have led to underestimate the incidence of NDs, especially those that typically manifest at later stages of development (eg, learning disorders or ADHD), and this underestimation may differ according to the exposure group, as the time to diagnosis could be shorter among children exposed in utero to VPA due to closer follow-up. Furthermore, due to the lack of specificity of the indicators of health care utilization, results based on these indicators must be interpreted cautiously.
Moreover, due to the observational nature of the data, reported differences according to AED exposure must be interpreted cautiously. Differences between children exposed to each drug versus those not exposed to any AED during pregnancy could partly reflect an effect of maternal epilepsy on the risk of NDs in the offspring. However, previous studies suggest that such an effect, if any, would be very limited9,13,31,36. In addition, the increased risk of NDs in children exposed to VPA persisted even when compared to children exposed to lamotrigine. Women with genetic epilepsy syndromes (also having genetic vulnerability to NDs) are often prescribed valproate as first line therapy; however, it is unlikely that these syndromes were common enough to explain the large (four to fivefold) increase in risk of NDs associated with VPA observed in this study.
Maternal psychiatric morbidity and comedications, which constitute major risk factors for NDs37, could also explain the observed differences between AED exposure groups. However, maternal psychiatric morbidity and comedications were accounted for in the analyses using information available in the SNDS. In addition, analyses were systematically conducted both in the overall population and in the subpopulation of children born to a mother with no known mental illness. The increased risk of NDs associated with VPA persisted or was even amplified in this restricted analysis, suggesting that the observed association cannot be explained by differences in terms of maternal psychiatric morbidity.
Information available in the SNDS on folic acid supplementation is probably subject to measurement errors since dispensing of folic acid is not always reimbursed by national health insurance. Thus, analyses may have failed to fully account for the putative protective effect10,38–41 of folic acid supplementation on the risk of NDs. Other potential confounding factors, such as characteristics of maternal epilepsy or parental IQ, could not be taken into account, as this information is not available in the SNDS.
Lastly, due to limited sample size and events in the group of women taking 200–800 mg/day of VPA, our study, which was restricted to AEDs used in monotherapy, was not powered to identify thresholds of risk within this range. Other studies would be necessary to document the safety of low doses of VPA as they may be currently used (in association with levetiracetam or lamotrigine for example) to limit the teratogenicity of VPA.
Conclusions
This study confirms a four to fivefold increased risk of early NDs (before the age of 6 years), especially pervasive developmental disorders and mental retardation, associated with exposure to VPA indicated in epilepsy during pregnancy, with a marked dose effect. It also provides new data suggesting that the exposure period associated with an increased risk of early NDs is more particularly situated during the second and/or third trimesters of pregnancy. The risk of early NDs associated with other AEDs, especially lamotrigine, appears to be much lower. However, the risk of NDs after in utero exposure to pregabalin deserves further investigations.
Supplementary information
Author contributions
J.C., R.D.S., S.M., A.W. and M.Z. planned the study. P.O.B. performed statistical analyses. J.C. drafted the manuscript. Y.M., H.P. and F.R. contributed to the analysis and reviewed the manuscript. All authors had full access to all of the study data (including statistical reports and tables) and take responsibility for the integrity of the data and the accuracy of the data analysis. J.C. and R.D.S. are the guarantors.
Data availability
Data cannot be shared publicly because access to French administrative medical databases is regulated by the French Data Protection Supervisory Authority (Commission Nationale de l'Informatique et des Libertés, CNIL). Data are available from the Commission Nationale de l'Informatique et des Libertés, CNIL (contact via https://www.cnil.fr/) for researchers who meet the criteria for access to confidential data.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
is available for this paper at 10.1038/s41598-020-74409-x.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Data cannot be shared publicly because access to French administrative medical databases is regulated by the French Data Protection Supervisory Authority (Commission Nationale de l'Informatique et des Libertés, CNIL). Data are available from the Commission Nationale de l'Informatique et des Libertés, CNIL (contact via https://www.cnil.fr/) for researchers who meet the criteria for access to confidential data.