Gastroesophageal reflux disease is one of the most public digestive diseases, and its prevalence is relatively high in Iran. Its economic burden is high, so it is estimated that Americans spend more than 10 billion dollars per year on proton pump inhibitors (PPIs) for its treatment (
15). The reduction of the quality of life and the occurrence of many problems such as absenteeism, reduction of leisure time programs, and increase of problems related to doing household chores are among the problems of patients with GERD. However, most cases of GERD (79.2%) are non-complicated (
16).
Today, there are various methods for diagnosing this disease, some of which do not have sufficient sensitivity and specificity. Therefore there is still no gold standard diagnostic test for GERD, and the diagnosis is based on a combination of PPI tests, ambulatory pH monitoring, and esophagogastroduodenoscopy (EGD). Other methods, such as barium esophagogram, high-resolution esophageal manometry, and gastric emptying studies can help rule out other diseases that may contribute to or mimic the signs of GERD (
17). Most of these diagnostic methods are expensive. Therefore, finding a solution to diagnose this cost-effective disease seems necessary. In the pathophysiology of GERD, dysfunction of various mechanisms known as the "anti-reflux barrier" occurs, one of the most obvious of which is the dysfunction of the autonomic nervous system, especially the parasympathetic nerves, so that parasympathetic activity is impaired in all patients (
6,
7). Inflammation motivates the “cholinergic anti-inflammatory pathway,” which motivates the release of Ach (
18). Ach can suppress inflammation in both CNS and peripheral tissues (
19). Acetylcholine affects macrophages through the α7 nicotinic receptor, which results in stopping the NF-κB nuclear transmission signaling pathway, which leads to a decrease in the making of pro-inflammatory cytokines. In this way, the cholinergic system with a reflex mechanism can quickly recover inflammation by getting evidence from various body parts (
11,
18).
Cholinesterase activity is reduced in various chronic and severe inflammatory diseases (
9-
13). Since cholinesterases are made in the liver, their amount decreases in liver patients and malnutrition (
19-
21). Also, cholinesterase activity in acquired immunodeficiency syndrome (AIDS) (
22), burns (
20), in patients with gingivitis and periodontitis (
23), cancer (
24), brain damage (
25), ischemic stroke (
26), anorexia nervosa (
27), Alzheimer’s disease (
28) and multiple sclerosis (MS) (
29) is reduced. Regulating the systemic level of Ach requires continuous control of the balance between the production of Ach by the vagus nerve and its hydrolysis by acetylcholinesterase and butyrylcholinesterase. Since the serum levels of cholinesterase reflect fluctuations in the body’s total capacity to hydrolyze Ach; therefore, the reduction in the serum level of cholinesterase is related to the downregulation of cholinesterase activity as a compensatory reaction of the body to increase the anti-inflammatory activity of acetylcholine (
18).
The acid and pepsin contents of the stomach can cause damage to the esophagus and mouth and then lead to an increase in inflammatory factors and the occurrence of inflammation. Since the level of cholinesterase activity decreases in inflammatory diseases, it can justify the decrease in the serum level of cholinesterase activity in patients with GERD. The results showed that the cut-off point of cholinesterase activity in serum was significant for distinguishing GERD. Therefore, assessing cholinesterase activity may be helpful in the diagnosis of GERD.