Evaluation of serum 25-Hydroxy vitamin D levels in children with autism Spectrum disorder

Vitamin D may play an important role in etiology of Autism Spectrum Disorders (ASDs). Vitamin D is a neuroactive steroid affecting brain development and function. It plays an essential role in myelination, which is important for connectivity in the brain. Studies have shown that decreased vitamin D levels, decreased maternal vitamin D levels during pregnancy, and decreased exposure to solar UVB might increase the risk of ASD [1].

Despite extensive studies on ASD, the etiology of this disorder is quite unknown and studies are ongoing [2, 3]. ASD has a dominant genetic origin. However, environmental and genetic factors have interaction in the incidence of this disorder [3‐5]. The results of studies have shown that in disease etiology, risk factors such as prenatal and postnatal infections [6, 7], and exposure to Valproic Acid of alcohol during pregnancy [8, 9], the age of mother [10], and abnormal nutritional and metabolic factors [3] are effective. During the recent years, the incidence of ADSs has been significantly increased. In previous studies, the incidence of this disorder was 10 in 10,000 [11], whereas the incidence of this disorder is now estimated as 90–250 in 10,000 [12‐15]. In addition, in 2010, CDC reported the incidence of autism disorder in the United States as 1 in 68 and this indicates 78% increase in the incidence level compared with 2002 [16]. However, a part of this sudden increase is probably the result of increased awareness and better reports about autism disorder as well as improved diagnostic criteria, but the exact causes for this sudden increase should be determined in future studies [17]. Increased incidence of the disease can impose a heave financial burden on the society. It is estimated that medication costs for each patient will be 40,000 to 60,000 dollar per year [16]. During the past decades, numerous studies were conducted on the role of vitamin D in neuropsychological disorders [18‐23]. The findings of these studies showed that vitamin D deficiency is one of the risk factors of evolutional neuropsychological disorders such as schizophrenia [24] and autism [19, 25‐28]. However, studies on the relationship between vitamin D and autism in different parts of the world such as Sweden [29], Egypt [20], Saudi Arabia [30], and China [31, 32] indicate lower 25 (OH) D level in patients with ASD in different ages compared with the control group. Moreover, some studies [33, 34] have shown different findings and no significant difference was observed between serum levels of vitamin D in ADS and control groups. To our knowledge few studies have been conducted in this regard in Iran and no study has been conducted in Ahvaz city, Southwestern Iran. Therefore, the present study aimed to evaluate the serum 25 - hydroxyl vitamin D level among children with ASDs in Ahvaz city, Iran.

It was a cross-sectional study which had conducted on 62 children in two groups: a case group (n = 31) consisted of ASD children who study in especial schools; and a control group (n = 31) of healthy children were selected from regular schools by using simple random sampling approach in Ahvaz city, Iran; 2016.

The two groups were matched in terms of gender, age, weight, height, head circumference, adequate breastfeeding (for at least six months), type and amount of food, socioeconomic status (the ratio of the number of family members to bedrooms was used as a measure of socioeconomic status) [35, 36], average income, family size, and exposure to smokers.

The finding has shown that 31 children with ASD and 31 healthy children with age range of 5–12 years old. No significant difference was observed between two groups in terms of age (P = 0.80). In addition, no significant difference was observed between the mean of mother’s age at the birth of the child in both groups (P = 0.28). Most of the subjects in the case and control groups were male (83.9 and 90.3%, respectively) and no significant difference was observed in both groups in terms of gender (P = 0.45). Most of children in the case group were Bakhtiari (35.5%) and in the control group were Arab (Table 1).

In both groups, the use of direct daily sun was equal (67.74%). No significant difference was observed between the groups in exposure to direct sun (min/day) (P-0.56) (Table 2).

Recently, the role of vitamin D deficiency is identified as an environmental risk factor for some of autoimmune disorders [37, 38]. A study by Patrick and colleagues showed that vitamin D ma influence some of social behaviors of children with autism. He emphasized that vitamin D is a gene activator that creates tryptophan hydroxylase enzyme. This enzyme converts tryptophan into serotonin in the brain. Therefore, a sufficient level of vitamin D to produce serotonin in the brain than functions as a neuron transmitter improves social behaviors by positive effects on behavior [39]. In a clinical trial study by Feng and colleagues on 37 children with autism, for three months, these children received 150,000 IU as intramuscular injection(monthly) and 400 IU orally (daily). These researchers reported that disease symptoms and behavioral checklist in children (3 years old and older) with autism improved [40]. In most of the studies conducted on ASDs and vitamin D, lower 25-hydroxyvitamine D level in children with autism was taken into consideration. Our findings showed low level 25-hydroxyvitamine D level in the ASD children, compared with the healthy counterparts. Testes et al. reported that the mean of serum 25-hydroxyvitamine D level in children with autism with different ethnicities was lower than the control group by 35 nmol/L [41]. Moreover, Duan et al. showed that serum 25-hydroxyvitamine D in patients with autism was significantly lower than the control group [31]. Bener et al. attributed some biological and lifestyle factors such as birth, kinship, body mass profile, and physical activity and 25-hydroxyvitamine D level with the incidence of autism. Their findings showed that serum 25-hydroxyvitamine D level in ASD children was lower than the control group with similar ethnicity, age, and gender (P = 0.004) [42]. This finding was supported by the study of Meguid et al. [20]. Saad et al. [18] reported an inverse relationship between the averaged serum 25-hydroxyvitamine D level and severity of ASD (P > 0.001), which was not evaluated in our study. In another study in Saudi Arabia on comparing serum 25-hydroxyvitamine D level and MAG among 50 children with autism (5–12 years old) and 30 healthy children, a significant negative relationship was observed between serum 25-hydroxyvitamine D level and incidence of autism (P > 0.001) [30]. Neumeyer and colleagues reported that the ration of male children with ASD with serum 25-hydroxyvitamine D level lower than 80 nmol/L was higher than healthy subjects (77% against 37% and p = 0.02). However, the results of a study by Molloy [33] and Esparham [3] in the United States showed that there is not significant relationship between serum 25-hydroxyvitamine D level in two groups of children with ASD and without ASD. Ugur and colleagues investigated vitamin D3 level of 54 children with autism and 54 healthy children between 3 and 8 years old in Turkey. They did not observe any significant difference t vitamin D3 serum level between these two groups [35]. The results of a study by Hashemzeh and colleagues in Iran showed no significant difference between vitamin D in children with autism and healthy children. Also, no significant relationship was observed between serum vitamin D level and severity of the disease symptoms [34].

There significant difference was observed between serum 25-hydroxyvitamine D levels in two groups of this study and different studies confirm that and also there was no significant difference between two groups in time of exposure to sun. Therefore it is recommended to use vitamin D supplement in children with ASDs under medical care.