The pathophysiology of febrile seizure (FS) is not fully understood, and research results have revealed a complex interaction of inflammation, genetic tendency and cytokines. Tumor necrosis factor alpha (TNF-α), interleukin 1 beta (IL-1β) and interleukin 6 (IL-6) are the main cytokines involved in the pathophysiology of FS. 1,2 MicroRNAs (miRNAs) are small non-coding RNAs, and their main target is messenger RNAs (mRNAs). More than two thousand miRNAs have been identified thus far, and more than half of these are expressed in the human brain. 3 Alteration in the expression levels of specific miRNAs has been suggested as a possible cause in the pathophysiology of different diseases, such as cancer, Parkinson disease and epilepsy. 3,4 miRNAs have emerged as potent regulators of inflammation. 4,5 For example, miRNA-146a is the first inflammation-associated miRNA.