Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

The impact of the use of antiepileptic drugs on the growth of children

BMC Pediatrics volume 13, Article number: 211 (2013) Cite this article

Abstract

Background

This study investigated whether long-term treatment with antiepileptic drugs (AEDs) had negative effects on statural growth and serum calcium levels in children with epilepsy in Taiwan.

Methods

Children with epilepsy treated with one prescription of AEDs (monotherapy) for at least 1 year were selected. The AEDs included valproic acid (VPA; Deparkin) in 27 children (11 boys and 16 girls) aged 4-18 years, oxcarbazepine (Trileptal) in 30 children (15 boys and 15 girls) aged 5-18 years, topiramate (Topamax) in 19 children (10 boys and 9 girls) aged 6-18 years, and lamotrigine (Lamicta) in eight children (5 boys and 3 girls) aged 5-13 years. Patients with a history of febrile convulsions were selected as the controls.

Results

One year of VPA treatment significantly impaired the statural growth of pediatric patients with epilepsy (p < 0.005) compared with the control group. The underlying mechanism may have been due to the direct effect of VPA on the proliferation of growth plate chondrocytes rather than alterations of serum calcium.

Conclusions

These results raise serious concerns about the growth of pediatric epilepsy patients who use AEDs, and potentially the need to closely monitor growth in children with epilepsy and adolescents under AED treatment, especially VPA.

Peer Review reports

Background

The skeletal system determines a person’s height. Although stiff and unyielding, bone is a living tissue that continuously remodels throughout life. Specialized cells are engaged in the bone remodeling and turnover processes, such as osteoblasts initiating bone formation, osteocytes monitoring bone mechanical stresses, and osteoclasts absorbing bone [1]. The growth plate is at the end of long bones, is made up of chondrocytes at different stages of differentiation, and is divided histologically into three distinct zones: resting, proliferative, and hypertrophic [2]. Longitudinal bone growth is primarily achieved through the action of chondrocytes in the proliferative and proliferative zones of the growth plate [3]. Apart from the effects of circulating systemic and local hormones, calcium and other chemicals, which are mainly provided by bone to maintain the intra-and extracellular mineral pools, can work in cohort with osteoblasts, osteocytes, and extracellular matrix proteins to mineralize osteoid [4]. Calcium is crucial for normal epiphyseal growth plate development, and changes in extracellular calcium modulate the function of chondrocytes [5]. Proliferation of epiphyseal growth plates results from a complex interplay among a net effect of hormones and growth factors, which may directly or indirectly affect the serum levels of calcium and the condition of those cells, leading to final stature.

Epilepsy is a chronic condition characterized by recurrent clinical events or epileptic seizures, which occur in the absence of a metabolic or toxic disease or fever [6]. In addition, the diagnosis of epilepsy can possibly be made after only one epileptic seizure if an “endearing predisposition of the brain to future seizures” exists. The World Health Organization (2001) estimates a prevalence of 0.8% in the general population, and the prevalence in Taiwan has been reported to be 0.28% [7]. Epilepsy often requires long-term antiepileptic drug (AED) therapy. However, prolonged AED administration is associated with a number of problems such as behavioral and psychiatric disorders, metabolic and endocrine disorders, idiosyncratic reactions, and drug interaction effects [8]. Although some studies suggest that patients with epilepsy treated with AEDs have an increased risk of fractures, low bone mineral density (BMD), and abnormalities in bone metabolism, skeletal diseases associated with long-term AED treatment are seriously unrecognized [9, 10]. In a survey of >1000 adult and pediatric neurologists designed to assess the awareness of the effects of AED therapy on bone health, only 28% of adult and 41% of pediatric neurologists reported screening their patients for bone diseases [11]. A lack of consensus between physicians concerning the impact of AED therapy on bone may put epilepsy patients at risk, especially children, with regard to bone health or developing bone diseases.

Evidence suggests that patients with epilepsy are predisposed to bone problems and fractures [12]. However, one meta-analysis concluded that the deficit in bone mineral density was too small to explain the increase in the risk of fractures in patients with epilepsy [13]. Bone abnormalities such as short stature, abnormal dentition, rickets, and osteomalacia have been reported to be linked to the use of AEDs [12, 14, 15]. The mechanisms through which AEDs cause abnormal bone metabolism and increase fractures are not fully understood. Reports have shown that hypocalcemia is an important biochemical abnormality in patients receiving cytochrome P450 enzyme-inducing AEDs, which potentially increase the catabolism of vitamin D to inactive metabolites, leading to reduction of calcium [9, 10, 16]. However, some non-enzyme-reducing AEDs have also been linked with low bone mass [10, 17, 18]. A new generation of AEDs, including oxcarbazepine (OXA), topiramate (TPM), and lamotrigine (LTG), have been approved as therapeutic options for epilepsy. However, to date, there is no consensus about the effect on bone metabolism in individuals receiving these AEDs, and no definitive guidelines for evaluation or treatment have yet been determined. Most epileptic patients are diagnosed and treated in childhood and adolescence, and this period is crucial in attaining peak bone mass. Therefore, it is worth investigating whether AEDs affect bone growth in pediatric patients with epilepsy.

The maintenance of growth and bone health is a complex process that can be influenced by the underlying diseases and nutritional status of a patient, but also by chemical factors. If AED treatment is associated with disturbance of statural growth and calcium metabolism, clinical parameters such as serum calcium levels and statural growth may reveal abnormalities after AED therapy in pediatric patients with epilepsy. The aim of this study was to evaluate the effects of AED monotherapy including VPA, OXA, TPM, and LTG on alterations in serum calcium levels and statural growth in drug-naïve, Taiwanese pediatric patients newly diagnosed with epilepsy. To gain further insight into the mechanism of action of AEDs on linear bone growth, we examined the effects of AEDs on cultured growth plate chondrocytes in vitro on cell proliferation using a tetrazolium methylthiotetrazole (MTT) assay. Our results showed that, instead of affecting serum calcium levels, VPA may interfere with the proliferation of growth plate chondrocytes in a direct manner and significantly affect the statural growth of children with epilepsy. These results raise serious concerns about the growth of pediatric epilepsy patients who use AEDs, and potentially the need to closely monitor growth in epileptic children and adolescents under AED treatment, especially VPA.

Methods

Study subjects

From February 2009 to January 2011, children with newly diagnosed seizures, which were classified according to the report of the International League Against Epilepsy (ILAE) Commission on Classification and Terminology 2005 [19], including generalized, tonic-clonic (ICD-9-CM diagnosis code 345.10), absence (ICD-9-CM diagnosis code 345.0), myoclonic (ICD-9-CM diagnosis code 345.1), clonic (ICD-9-CM diagnosis code 345.1), tonic (ICD-9-CM diagnosis code 345.1), atonic (ICD-9-CM diagnosis code 345.1), and focal (ICD-9-CM diagnosis code 345.5) seizures. The children were attending the pediatric outpatient department, emergency department, or were admitted to the pediatric ward and started on standard recommended doses of valproic acid (VPA; Deparkine solution; Sanofi Winthrop Industrie, Paris, France; starting dose 20 mg/kg/day, maintenance dose 20-40 mg/kg); OXA (Trileptal suspension form; Novartis, Rueil-Malmaison, France; starting dose 5-10 mg/kg/day, maintenance dose 20-40 mg/kg); TPM (Topamax 100 mg tablets, Janssen-Cilag, Baar, Switzerland; starting dose 0.5-1 mg/kg/day, maintenance dose 3-9 mg/kg); or LTG (Lamictal 50 mg tablets, GlaxoSmithKline, Zeist, Netherlands; starting dose 0.5 mg/kg/day, maintenance dose 5-15 mg/kg) for at least 1 year. All children were ambulatory and without any dietary restrictions. The serum levels of patients taking VPA were routinely monitored, and the levels were within the therapeutic range (50-100 μg/mL). Patients were excluded if they had: (1) a history of taking AEDs or other medications that affect bone metabolism (e.g., steroids, diuretics, vitamin D, calcium supplements, bisphosphonates, or calcitonin); (2) any endocrine or medical disorders (e.g., hypothyroidism or renal diseases); (3) a history of nutritional deficiency; (4) limitations in ambulation or daily physical activity; (5) any progressive neurological disorders other than epilepsy; and (6) clinical/biochemical evidence of rickets or growth retardation. All of the children resided in Taipei, were ambulatory, had normal age-appropriate activity, and nutritionally adequate diets. Subjects with a history of simple febrile convulsions (ICD-9-CM diagnosis code 780.31) were selected as the control group. Body height, weight, and body mass index (BMI) were recorded. All patients were followed up every 3-6 months at the pediatric outpatient department.

Estimation of serum calcium

Five-milliliter venous blood samples were collected from all patients for the measurement of serum total and ionized calcium levels. Cobas c501 (Roche Diagnostics, Mannheim, Germany) and NOVA CCX (NovaBiomedical, Waltman, MA, USA) were used for the measurement of serum total and ionized calcium levels, respectively.

Consent and ethical approval

The current study was approved by the scientific and ethics committees of Tri-Service General Hospital and National Defense Medical Centre, Taipei, Taiwan (TSGHIRB approval number 100-05-239). All parents, guardians, or legal representatives signed an informed consent form before participation in the study.

Reagents

Dulbecco’s Modified Eagle’s Medium/Nutrient Mixture F-12 HAM Medium (DMEM/F-12) were purchased from Gibco Life Technologies (Carlsbad, CA, USA). Dimethylsulfoxide (DMSO), fetal bovine serum (FBS), and MTT were purchased from Sigma (St. Louis, MO, USA). All other reagents were purchased from Sigma and were tissue culture grade. The drugs were obtained as described above. In the in vitro study, the choice of AED concentration was based on therapeutic plasma concentrations of the respective drug in the patients. The following concentrations were used: VPA, 415 μM (60 μg/mL); OXA, 30 μM (7 μg/mL); TPM, 30 μM (10 μg/mL); LTG, 20 μM (5 μg/mL) [20].

Cell isolation

Chondrocytes were isolated and cultured as described previously [21]. Male 3-week-old Sprague–Dawley rats (50-60 g each) were obtained from BioLASCO Taiwan (Taipei, Taiwan). All experiments were approved by the local institutional animal care and use committee, Tri-Service General Hospital and National Defense Medical centre, Taipei, Taiwan, ROC (IACUC-12-233). The epiphyseal growth plate of the tibia was separated by cleaning the cartilage plate of muscular tissue, periosteum, and perichondrium. The proximal epiphysis was divided by a transverse cut with a sharp scalpel, and the cartilage plate was separated distally from the calcification zone of the tibial metaphysis. Isolated growth plates were digested with 3 mg/mL collagenase type H (Sigma) for 3 h at 37°CC. After thorough washing, cells were counted using a Neubauer chamber. Cell viability, examined by trypan blue exclusion, was >95%.

Monolayer cultures

Cell monolayers were cultured in DMEM/F-12 medium supplemented with 10% FBS, 100 IU/mL penicillin (Gibco), and 100 mg/mL streptomycin (Gibco). The cells were grown in 75-cm2 plastic culture flasks (Corning, Corning, New York, NY, USA) and incubated at 37°CC until confluence. They were then washed three times with phosphate-buffered saline (PBS), harvested using trypsin-EDTA (Gibco), and subcultured at a 1:3 ratio. Chondrocytes were immunopositive for anti-S100 protein (data not shown). Growth-plate chondrocytes grown to passages 3 and 5 were then plated at 1 × 104 cells/mL into 96-well plates for the MTT assay. The medium with the AEDs was changed daily and cells were collected for assay on Day 5. All cells were maintained in an atmosphere of 5% CO2 and 95% air at 37°CC.

Evaluation of rat chondrocyte proliferation by a MTT assay

Cell viability was determined by measuring the activity of cellular dehydrogenase that could cleave MTT (3-(4,5-dimethylthiazol-2-il)-2,5-diphenyl tetrazolium bromide) (Sigma) in a colorimetric assay as described previously [22]. Activate dehydrogenase reduced MTT in viable cells to form insoluble formazan, which was then dissolved in DMSO and quantified spectrophotometrically at 540 nm. Growth-plate chondrocytes (1 × 104 cells/mL) were seeded into 96-well plates (Corning) in triplicate and kept under 5% CO2 at 37°CC. After 24 h incubation, the cell culture medium was replaced daily by one containing fresh complete medium or fresh complete medium with 0.1% DMSO as a vehicle, or fresh complete medium with an AED for 5 days. Two hundred microliters of MTT (0.5 mg/mL) was then added to each well and the mixture was left to incubate for 3 h at 37°CC. The reaction was then stopped by injecting 200 μL DMSO per well. The plates were shaken for 5 min, and then the optical density at 540 nm was determined on a microplate reader (μQuant, BIO-TEK Instruments Inc., Winooski, VT, USA) with KC Junior analysis software, version 1.5 (BIO-TEK Instruments). At least three such experiments were performed for each treatment.

Statistical analysis

All statistical analyses were performed using SPSS software, version 13.0 (Chicago, IL, USA). Age, sex, weight, BMI, AED, and levels of calcium were expressed as the mean ± standard deviation (SD). Comparisons of the data were conducted by one-way analysis of variance (ANOVA). The Student’s paired t test was used to compare serial changes in serum calcium after 1-year treatment with AEDs and the control group. Comparisons of the data from cell proliferation studies were carried out by ANOVA. A p value <0.05 was considered statistically significant; *represents p < 0.05 and **p < 0.005.

Results

Clinical characteristics

The demographic characteristics of the patients are shown in Table 1. There were no significant differences between the control and study patients in age, sex, height, weight, or BMI.

Table 1 Clinical parameters of children with epilepsy
Full size table

Changes in statural growth

A statistically significantly lower body height was found in patients treated with VPA compared with the controls (p < 0.005; Figure 1). However, there were no significant differences between the control group and patients treated with OXA, TPM, or LTG.

Figure 1
figure 1

VPA significantly affected growth of children with epilepsy. Comparison of changes in body height among the control group and children with epilepsy treated for 1 year with AEDs, including VPA, OXA, TPM, and LTG. The bars represent means, and the whiskers represent standard errors. Significant differences (**, p < 0.005) were found between the control group and the group with VPA treatment.

Full size image

Serum total and ionized calcium levels

Levels of serum total and ionized calcium did not differ significantly among the patients treated with VPA, OXA, TPM, and LTG compared with the controls (p > 0.05; Figure 2). None of the drugs affected the level of serum calcium in the epilepsy patients.

Figure 2
figure 2

AEDs did not affect the level of calcium in children with epilepsy. Comparison in the changes of serum total (A) and ionized (B) calcium concentration among the control group and children with epilepsy treated for 1 year with AED, including VPA, OXA, TPM, and LTG. The bars represent means, and the whiskers represent standard errors.

Full size image

Evaluation of growth-plate chondrocyte proliferation

The influence of the vehicle (0.1% DMSO) and AEDs, including VPA, OXA, LTG, or TPM on growth-plate chondrocyte proliferation was expressed as a percentage of cell growth in six independent experiments. In comparison with the controls, the cell proliferation rate was significantly decreased to 84.45 ± 2.3% when the cells were exposed to VPA. However, there were no significant effects on the proliferation of the chondrocytes with OXA, LTG, or TPM (Figure 3).

Figure 3
figure 3

VPA significantly reduced the proliferation of rat growth-plate chondrocytes. The influence of vehicle (0.1% DMSO) and AEDs, including VPA, OXA, LEV, LTG, and TPM on chondrocytes of rat growth-plate proliferation in MEM:HAM-F12 (1 : 1) medium with 10% FBS, expressed as cell growth percentages. The mean values are presented on top of the bars with the standard error value. (**, p < 0.005).

Full size image

Discussion

In the current study, there were significant reductions in statural growth in the epilepsy patients who were treated with VPA for 1 year compared with the control group. However, there were no significant differences in statural growth in those who were treated with OXA, LTG, or TPM. In support of our findings, Sheth et al. [23] and Kafali et al. [24] reported decreased bone mass in the lumbar spine and middle of the distal radius in children without physical handicaps who were treated with VPA for ≥6 [23] or 18 [24] months. This suggests that VPA can disturb bone growth. Childhood and adolescence are crucial periods in which to attain peak bone mass, and most patients with epilepsy are diagnosed and treated in this period, therefore, AEDs, and especially VPA, should be used with caution in pediatric patients with epilepsy.

Calcium is crucial for normal epiphyseal growth plate development. However, hypocalcemia is reported to affect 3–30% of patients with epilepsy treated with AEDs [25], and this has been postulated to explain AED-associated bone disease. Theoretically, AEDs that induce cytochrome P450 enzymes may cause reduced levels of bioavailable vitamin D, leading to decreased absorption of calcium in the gut, resulting in hypocalcemia and an increase in circulating parathyroid hormone, which then increases the mobilization of bone calcium stores and subsequent bone turnover [9, 10, 26]. In the current study, no significant changes in serum total and ionized calcium concentrations were found in the patients after 1 year treatment with VPA, OXA, LTG, or TPM. In addition, vitamin D deficiency has been reported to not affect low BMD in epilepsy patients after correcting for age and duration on AEDs [27]. These results and others [28, 29] support the notion that AEDs can cause bone loss without inducing hypocalcemia and vitamin D deficiency, suggesting that other mechanisms may be responsible.

VPA, a cytochrome P450 enzyme inhibitor, is widely used for the management of epilepsy [30]. In the current study, the statural growth of pediatric patients was significantly affected by the use of VPA compared with the control subjects, and this was not through alterations in the concentration of calcium. The reported effects of VPA on bone loss in patients with epilepsy are diverse, including accelerated or no bone loss [30–33], hyper- and hypocalcemia [33, 34], or normal serum calcium level [35, 36]. To clarify these contradictions, we examined the effects of AEDs on the proliferation of cultured growth plate chondrocytes in vitro, and showed that cell proliferation was significantly inhibited by VPA, which is similar to our clinical findings. However, also in agreement with our clinical findings, no distinct effects on the inhibition of proliferation in the growth-plate chondrocytes were seen in the patients who were treated with OXA, TPM, or LTG.

OXA, TPM, and LTG are approved for monotherapy or adjunctive therapy in patients with partial and generalized seizures. Despite being safer and having better tolerability, data regarding these new generation AEDs on bone health in children are controversial. OXA and TPM are cytochrome P450 isoenzyme inducers. Epilepsy patients treated with OXA are reported to have an increased risk of fractures [37], lower BMD [28], and decreased 25-hydroxyvitamin D3 levels [38]. TPM is associated with renal calculi, osteomalacia and/or osteoporosis [39], and mild hypocalcemia and increased bone turnover [40]. LTG does not induce or inhibit cytochrome P450 isoenzymes [41]. Children treated with LTG and/or VPA for >2 years have shorter stature, lower BMD, and reduced bone formation compared with controls [15]. However, because of combined therapy, the seizure status in those children may be more severe and their physical activity lower. A lower physical activity may cause more severe bone abnormalities than AEDs do. In fact, all available data indicate that LTG monotherapy does not alter BMD, calcium, or vitamin D levels [16, 42, 43]. Although we did not find disturbances in serum calcium and statural growth in the epilepsy patients who were treated with OXA, TPM, or LTG, our findings do not contradict previous reports. This is because OXA, TPM, and LTG may alter bone microstructure and bone turnover rate but maintain an adequate bone mass, leading to a normal statural growth rate in vivo and a normal proliferation of bone cells in vitro. Ultimately, all of these factors may have an impact on longitudinal skeletal growth and risk of fractures.

It was unclear how VPA directly interfered with the proliferation of growth-plate chondrocytes in the current study. VPA at a therapeutic dose is an effective inhibitor of histone deacetylases, producing hyperacetylation of histone tails and chromatin relaxation owing to disruption of histone–DNA and histone–histone interactions [44]. Apoptosis of chondrocytes is the main process for growth-plate remodeling, therefore, it is worth investigating whether VPA delays cell-cycle progression [45], modulates caspases and/or induces apoptosis [46], thereby causing inhibition of cell growth and proliferation, leading to short stature.

The current study had a number of limitations. First, the sample size was small and the duration of follow-up was only 1 year. It is possible that statistically significant lower statures would have been discovered after 1 year in children taking some or all of these AEDs if larger sample sizes and longer duration had been used. Second, the literature shows that enzyme-inducing AEDs increase the catabolism of vitamin D to inactive metabolites, potentially explaining why some enzyme-inducing AEDs are associated with increased risk of osteoporosis [9, 14, 15]. However, it has been reported that vitamin D deficiency may not affect BMD in epilepsy patients after correcting for age and duration on AEDs [27]. If the level of vitamin D is affected by AED, the downstream of the calcium level should be cascaded. The lack of vitamin D was a limitation of our study for a more comprehensive understanding of AED on growth. Third, rat chondrocytes in the growth plate cannot truly represent in vivo human conditions. Finally, this study was not randomized. These limitations may have led to some bias in analyzing the effects of AED on the growth of children with epilepsy.

The use of these AEDs for children and adolescents with epilepsy is growing, and the number of reported side effects of the newer AEDs is increasing. Therefore, our findings are valuable, because we performed a longitudinal study on AED monotherapy that indicated the risks of short stature in pediatric patients receiving AEDs. Early identification and proper management of AED-related growth retardation and associated bone health require greater public awareness and understanding of these adverse effects in children and adolescents.

Conclusions

AEDs are effective and necessary for children with epilepsy. However, long-term AED therapy, and especially VPA, may predispose patients to growth and bone health abnormalities. Childhood and adolescence are crucial growth periods, thus, prevention of growth retardation and adverse bone health with the use of VPA may be addressed by judicious use of AEDs coupled with improved nutrition and promotion of weight-bearing activities. Moreover, the new generation of AEDs such as OXA, LTG, and TPM may be alternative choices because of fewer adverse effects.

References

  1. Ripamonti U, Roden L: Biomimetics for the induction of bone formation. Expert Rev Med Devices. 2010, 7: 469-479. 10.1586/erd.10.17.

    Article  CAS  PubMed  Google Scholar 

  2. van der Eerden BC, Karperien M, Wit JM: Systemic and local regulation of the growth plate. Endocr Rev. 2003, 24: 782-801. 10.1210/er.2002-0033.

    Article  CAS  PubMed  Google Scholar 

  3. Rauch F: Bone growth in length and width: the Yin and Yang of bone stability. J Musculoskelet Neuronal Interact. 2005, 5: 194-201.

    CAS  PubMed  Google Scholar 

  4. Qin C, Baba O, Butler WT: Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis. Crit Rev Oral Biol Med. 2004, 15: 126-136. 10.1177/154411130401500302.

    Article  CAS  PubMed  Google Scholar 

  5. Rodriguez L, Cheng Z, Chen TH, Tu C, Chang W: Extracellular calcium and parathyroid hormone-related peptide signaling modulate the pace of growth plate chondrocyte differentiation. Endocrinology. 2005, 146: 4597-4608. 10.1210/en.2005-0437.

    Article  CAS  PubMed  Google Scholar 

  6. Fisher RS, van Emde BW, Blume W, Elger C, Genton P, Lee P, Engel J: Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). Epilepsia. 2005, 46: 470-472. 10.1111/j.0013-9580.2005.66104.x.

    Article  PubMed  Google Scholar 

  7. Chen CC, Chen TF, Hwang YC, Wen YR, Chiu YH, Wu CY, Chen RC, Chen TH, Liou HH: Population-based survey on prevalence of adult patients with epilepsy in Taiwan (Keelung community-based integrated screening no. 12). Epilepsy Res. 2006, 72: 67-74. 10.1016/j.eplepsyres.2006.07.007.

    Article  PubMed  Google Scholar 

  8. Greenwood RS: Adverse effects of antiepileptic drugs. Epilepsia. 2000, 41 (Suppl 2): S42-S52.

    Article  CAS  PubMed  Google Scholar 

  9. Pack AM, Gidal B, Vazquez B: Bone disease associated with antiepileptic drugs. Cleve Clin J Med. 2004, 71 (Suppl 2): S42-S48.

    Article  PubMed  Google Scholar 

  10. Sheth RD: Metabolic concerns associated with antiepileptic medications. Neurology. 2004, 63: S24-S29.

    Article  CAS  PubMed  Google Scholar 

  11. Valmadrid C, Voorhees C, Litt B, Schneyer CR: Practice patterns of neurologists regarding bone and mineral effects of antiepileptic drug therapy. Arch Neurol. 2001, 58: 1369-1374. 10.1001/archneur.58.9.1369.

    Article  CAS  PubMed  Google Scholar 

  12. Morijiri Y, Sato T: Factors causing rickets in institutionalised handicapped children on anticonvulsant therapy. Arch Dis Child. 1981, 56: 446-449. 10.1136/adc.56.6.446.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Vestergaard P: Epilepsy, osteoporosis and fracture risk - a meta-analysis. Acta Neurol Scand. 2005, 112: 277-286. 10.1111/j.1600-0404.2005.00474.x.

    Article  CAS  PubMed  Google Scholar 

  14. Robinson PB, Harris M, Harvey W: Abnormal skeletal and dental growth in epileptic children. Br Dent J. 1983, 154: 9-13. 10.1038/sj.bdj.4804977.

    Article  CAS  PubMed  Google Scholar 

  15. Guo CY, Ronen GM, Atkinson SA: Long-term valproate and lamotrigine treatment may be a marker for reduced growth and bone mass in children with epilepsy. Epilepsia. 2001, 42: 1141-1147.

    Article  CAS  PubMed  Google Scholar 

  16. Pack A: Bone health in people with epilepsy: is it impaired and what are the risk factors?. Seizure. 2008, 17: 181-186. 10.1016/j.seizure.2007.11.020.

    Article  PubMed  Google Scholar 

  17. Samaniego EA, Sheth RD: Bone consequences of epilepsy and antiepileptic medications. Semin Pediatr Neurol. 2007, 14: 196-200. 10.1016/j.spen.2007.08.006.

    Article  PubMed  Google Scholar 

  18. Souverein PC, Webb DJ, Weil JG, Van Staa TP, Egberts AC: Use of antiepileptic drugs and risk of fractures: case–control study among patients with epilepsy. Neurology. 2006, 66: 1318-1324. 10.1212/01.wnl.0000210503.89488.88.

    Article  CAS  PubMed  Google Scholar 

  19. Berg AT, Berkovic SF, Brodie MJ, Buchhalter J, Cross JH, van Emde BW, Engel J, French J, Glauser TA, Mathern GW, Moshe SL, Nordli D, Plouin P, Scheffer IE: Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE commission on classification and terminology, 2005–2009. Epilepsia. 2010, 51: 676-685. 10.1111/j.1528-1167.2010.02522.x.

    Article  PubMed  Google Scholar 

  20. Luna-Tortos C, Fedrowitz M, Loscher W: Evaluation of transport of common antiepileptic drugs by human multidrug resistance-associated proteins (MRP1, 2 and 5) that are overexpressed in pharmacoresistant epilepsy. Neuropharmacology. 2010, 58: 1019-1032. 10.1016/j.neuropharm.2010.01.007.

    Article  CAS  PubMed  Google Scholar 

  21. Brochhausen C, Neuland P, Kirkpatrick CJ, Nusing RM, Klaus G: Cyclooxygenases and prostaglandin E2 receptors in growth plate chondrocytes in vitro and in situ–prostaglandin E2 dependent proliferation of growth plate chondrocytes. Arthritis Res Ther. 2006, 8: R78-10.1186/ar1948.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Lee HS, Lee CH, Tsai HC, Salter DM: Inhibition of cyclooxygenase 2 expression by diallyl sulfide on joint inflammation induced by urate crystal and IL-1beta. Osteoarthritis Cartilage. 2009, 17: 91-99. 10.1016/j.joca.2008.05.010.

    Article  PubMed  Google Scholar 

  23. Sheth RD, Wesolowski CA, Jacob JC, Penney S, Hobbs GR, Riggs JE, Bodensteiner JB: Effect of carbamazepine and valproate on bone mineral density. J Pediatr. 1995, 127: 256-262. 10.1016/S0022-3476(95)70304-7.

    Article  CAS  PubMed  Google Scholar 

  24. Kafali G, Erselcan T, Tanzer F: Effect of antiepileptic drugs on bone mineral density in children between ages 6 and 12 years. Clin Pediatr (Phila). 1999, 38: 93-98. 10.1177/000992289903800205.

    Article  CAS  Google Scholar 

  25. Pack AM: The association between antiepileptic drugs and bone disease. Epilepsy Curr. 2003, 3: 91-95. 10.1046/j.1535-7597.2003.03306.x.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Ali II, Schuh L, Barkley GL, Gates JR: Antiepileptic drugs and reduced bone mineral density. Epilepsy Behav. 2004, 5: 296-300. 10.1016/j.yebeh.2004.02.005.

    Article  PubMed  Google Scholar 

  27. Andress DL, Ozuna J, Tirschwell D, Grande L, Johnson M, Jacobson AF, Spain W: Antiepileptic drug-induced bone loss in young male patients who have seizures. Arch Neurol. 2002, 59: 781-786. 10.1001/archneur.59.5.781.

    Article  PubMed  Google Scholar 

  28. Valimaki MJ, Tiihonen M, Laitinen K, Tahtela R, Karkkainen M, Lamberg-Allardt C, Makela P, Tunninen R: Bone mineral density measured by dual-energy x-ray absorptiometry and novel markers of bone formation and resorption in patients on antiepileptic drugs. J Bone Miner Res. 1994, 9: 631-637.

    Article  CAS  PubMed  Google Scholar 

  29. Weinstein RS, Bryce GF, Sappington LJ, King DW, Gallagher BB: Decreased serum ionized calcium and normal vitamin D metabolite levels with anticonvulsant drug treatment. J Clin Endocrinol Metab. 1984, 58: 1003-1009. 10.1210/jcem-58-6-1003.

    Article  CAS  PubMed  Google Scholar 

  30. Wen X, Wang JS, Kivisto KT, Neuvonen PJ, Backman JT: In vitro evaluation of valproic acid as an inhibitor of human cytochrome P450 isoforms: preferential inhibition of cytochrome P450 2C9 (CYP2C9). Br J Clin Pharmacol. 2001, 52: 547-553. 10.1046/j.0306-5251.2001.01474.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Jette N, Lix LM, Metge CJ, Prior HJ, McChesney J, Leslie WD: Association of antiepileptic drugs with nontraumatic fractures: a population-based analysis. Arch Neurol. 2011, 68: 107-112.

    Article  PubMed  Google Scholar 

  32. Verrotti A, Coppola G, Parisi P, Mohn A, Chiarelli F: Bone and calcium metabolism and antiepileptic drugs. Clin Neurol Neurosurg. 2010, 112: 1-10. 10.1016/j.clineuro.2009.10.011.

    Article  PubMed  Google Scholar 

  33. Sato Y, Kondo I, Ishida S, Motooka H, Takayama K, Tomita Y, Maeda H, Satoh K: Decreased bone mass and increased bone turnover with valproate therapy in adults with epilepsy. Neurology. 2001, 57: 445-449. 10.1212/WNL.57.3.445.

    Article  CAS  PubMed  Google Scholar 

  34. Pack AM, Morrell MJ, Marcus R, Holloway L, Flaster E, Done S, Randall A, Seale C, Shane E: Bone mass and turnover in women with epilepsy on antiepileptic drug monotherapy. Ann Neurol. 2005, 57: 252-257. 10.1002/ana.20378.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Erbayat AE, Serdaroglu A, Tumer L, Gucuyener K, Hasanoglu A: Evaluation of bone mineral metabolism in children receiving carbamazepine and valproic acid. J Pediatr Endocrinol Metab. 2000, 13: 933-939.

    Google Scholar 

  36. Gough H, Goggin T, Bissessar A, Baker M, Crowley M, Callaghan N: A comparative study of the relative influence of different anticonvulsant drugs, UV exposure and diet on vitamin D and calcium metabolism in out-patients with epilepsy. Q J Med. 1986, 59: 569-577.

    CAS  PubMed  Google Scholar 

  37. Vestergaard P, Tigaran S, Rejnmark L, Tigaran C, Dam M, Mosekilde L: Fracture risk is increased in epilepsy. Acta Neurol Scand. 1999, 99: 269-275. 10.1111/j.1600-0404.1999.tb00675.x.

    Article  CAS  PubMed  Google Scholar 

  38. Mintzer S, Boppana P, Toguri J, DeSantis A: Vitamin D levels and bone turnover in epilepsy patients taking carbamazepine or oxcarbazepine. Epilepsia. 2006, 47: 510-515. 10.1111/j.1528-1167.2006.00460.x.

    Article  CAS  PubMed  Google Scholar 

  39. Mirza N, Marson AG, Pirmohamed M: Effect of topiramate on acid–base balance: extent, mechanism and effects. Br J Clin Pharmacol. 2009, 68: 655-661. 10.1111/j.1365-2125.2009.03521.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Heo K, Rhee Y, Lee HW, Lee SA, Shin DJ, Kim WJ, Song HK, Song K, Lee BI: The effect of topiramate monotherapy on bone mineral density and markers of bone and mineral metabolism in premenopausal women with epilepsy. Epilepsia. 2011, 52: 1884-1889. 10.1111/j.1528-1167.2011.03131.x.

    Article  CAS  PubMed  Google Scholar 

  41. Khanna S, Pillai KK, Vohora D: Insights into liaison between antiepileptic drugs and bone. Drug Discov Today. 2009, 14: 428-435. 10.1016/j.drudis.2009.01.004.

    Article  CAS  PubMed  Google Scholar 

  42. Kim SH, Lee JW, Choi KG, Chung HW, Lee HW: A 6-month longitudinal study of bone mineral density with antiepileptic drug monotherapy. Epilepsy Behav. 2007, 10: 291-295. 10.1016/j.yebeh.2006.11.007.

    Article  PubMed  Google Scholar 

  43. Sheth RD, Hermann BP: Bone mineral density with lamotrigine monotherapy for epilepsy. Pediatr Neurol. 2007, 37: 250-254. 10.1016/j.pediatrneurol.2007.05.018.

    Article  PubMed  Google Scholar 

  44. Zhang CL, McKinsey TA, Olson EN: Association of class II histone deacetylases with heterochromatin protein 1: potential role for histone methylation in control of muscle differentiation. Mol Cell Biol. 2002, 22: 7302-7312. 10.1128/MCB.22.20.7302-7312.2002.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Vallo S, Xi W, Hudak L, Juengel E, Tsaur I, Wiesner C, Haferkamp A, Blaheta RA: HDAC inhibition delays cell cycle progression of human bladder cancer cells in vitro. Anticancer Drugs. 2011, 22: 1002-1009.

    CAS  PubMed  Google Scholar 

  46. Ren M, Leng Y, Jeong M, Leeds PR, Chuang DM: Valproic acid reduces brain damage induced by transient focal cerebral ischemia in rats: potential roles of histone deacetylase inhibition and heat shock protein induction. J Neurochem. 2004, 89: 1358-1367. 10.1111/j.1471-4159.2004.02406.x.

    Article  CAS  PubMed  Google Scholar 

Pre-publication history

Download references

Acknowledgments

HC Fan and HS Lee express their gratitude to the Tri-Service General Hospital and National Defense Medical Center for the grants TSGH-C100-085, TSGH-C101-028, and TSGH-C102-24.

Author information

Authors and Affiliations

  1. Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

    Herng-Sheng Lee & Shih-Yu Wang

  2. Center for Molecular Medicine, MRC IGMM, University of Edinburgh, Edinburgh, Scotland, UK

    Donald M Salter

  3. Department of Orthopaedics, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

    Chih-Chien Wang

  4. Department of Paediatrics, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

    Shyi-Jou Chen & Hueng-Chuen Fan

Authors
  1. Herng-Sheng Lee
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Shih-Yu Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Donald M Salter
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Chih-Chien Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Shyi-Jou Chen
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Hueng-Chuen Fan
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Hueng-Chuen Fan.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

HS Lee, DM Salter, and HC Fan were involved in conception and design of the study and drafting the manuscript. HS Lee and DM Salter revised the manuscript critically for important intellectual content. SY Wang, CC Wang, SJ Chen, and HC Fan made substantial contributions to acquisition, analysis, and interpretation of data. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Authors’ original file for figure 3

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Lee, HS., Wang, SY., Salter, D.M. et al. The impact of the use of antiepileptic drugs on the growth of children. BMC Pediatr 13, 211 (2013). https://doi.org/10.1186/1471-2431-13-211

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1471-2431-13-211

Keywords

BMC Pediatrics

ISSN: 1471-2431

Contact us