China team makes key breakthrough on deafness
Print Edition
Chinese researchers recently made a breakthrough in discovering a gene responsible for deafness, providing a target for treating hearing impairment.
The study published online earlier this month in the international journal Genetics in Medicine described the gene as ABCC1, which has variants associated with hearing loss and plays a key role in maintaining cochlear function.
The cochlea is a spiral tube shaped like a snail shell.
It is the auditory area of the inner ear and enables effective hearing.
Using gene screening, sequencing and other genetic analysis methods, researchers from Xiangya Hospital affiliated to the Central South University in Hunan Province found the variants in gene ABCC1 could work as a pump to extrude toxic substances and metabolic waste products from the inner ear.
In experiments done on mice, they found the dysfunction of these variants could lead to hearing loss.
Hearing impairment is the most common sensory deficit, with an incidence of one in 500 individuals worldwide. Aging and chronic exposure to loud noises are the main factors that contribute to hearing loss.
Early warning signs
Since the discovery of several genes responsible for deafness in the 1990s, the role of genetic factors has received increasing attention in the scientific community.
Revealing the mechanism of how these single gene variants function can help scientists provide early warning and develop a new treatment for millions of patients who lost their hearing, said lead researcher Feng Yong.
Feng has conducted deafness gene researches for more than two decades.
His team has reported pathogenic mutations of over 20 deafness genes. The discovery was inspired by one of Feng鈥檚 patients.
The research team visited the patient鈥檚 hometown, conducted family surveys and at last identified the new gene in a process which lasted for more than three years.
鈥淥ur data also has implications for future molecular and clinical diagnosis of hearing loss,鈥 Feng said.
Further research should be performed to determine the potential contribution of the gene to hearing loss, which will be beneficial for future treatment strategies, according to researchers.
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