Table 5 tabulates the results of the chi-square test (OR: 52.76; 95% CI: 6.58-423.01; P < 0.001). The results indicated that infantile anorexia and cognitive development had a statistically significant relationship (P < 0.05). The strength parameter of the OR relationship was 52.76. This finding showed that children with infantile anorexia were 52.76 times more likely to have cognitive development disorders than children with no eating disorders. The results of this study are in line with the results of a study conducted by Chatoor et al., indicating that children with infantile anorexia had lower cognitive values (
30).
The relationship is supported by the opinion of Rosales et al. that food is significantly related to the body, especially at the stages of physical growth, development, and intelligence of school children (
31). The number of cells in the brain decreases, and imperfections in biochemical organizations in the brain occur. This situation affects the growth and development of children. Eating disorders are focused on regulating appetite in the hypothalamus, which controls neurochemical mechanisms specifically for eating and satiety. Serotonin is considered to be involved in the pathophysiology of eating disorders, although this study is still in its developmental stage (
32). Serotonin plays a role in memory, learning process, sleep pattern, mood, and appetite. Higher serotonin levels are in accordance with the levels of anxiety and obsessive behavior (
33).
A study conducted by Kaye et al. (2009) reported that starvation could improve mood by lowering serotonin levels. However, when starvation continuously existed, the compensatory mechanism of the brain occurred through elevating the level of serotonin receptors. This soaring level of serotonin can cause extreme anxiety and emotional disturbance, difficult to recover without any sufficient support (
34).
One of the genetic factors believed to be susceptible to eating disorders is the serotonin transporter (5-HTT) gene. A study reported that the low expression of 5-HTTLPR allele polymorphism had a relationship with anorexia (
35). This has an important role in the susceptibility of subtypes or endophenotypes to eating disorders (
36).
The subsequent discussion brings up other factors affecting children’s cognitive impairment, one of which is iron in the blood. Iron is a nutrient that is important for children’s growth, mental development, and motor and cognitive function. Iron deficiency anemia is associated with poor performance in neonates, low scores in cognitive function tests in preschool children, and low school learning achievement (
37,
38).
Other effective factors in cognitive impairment among children are still closely related to the profile of hematology, one of which is the content of iodine in the blood. Iodine is a nutrient in thyroid hormone, which is responsible for regulating thyroid function, supporting healthy metabolism, and helping growth and development (
39,
40). Iodine is also important for brain development over a period affecting neurogenesis, neuron and glial cell differentiation, myelination, neuron migration, and synaptogenesis. Iodine supplementation from mothers to children requires adequate attention. The adequate consumption of iodine can avoid cognitive impairment in children (
41,
42).