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Scientists discover a hidden gene mutation that causes deafness—and a way to fix it

New research ties CPD gene mutations to hearing loss—and points to potential cures using arginine and even Viagra.

Date:
October 25, 2025
Source:
University of Chicago
Summary:
Scientists have identified mutations in the CPD gene as a key cause of a rare congenital hearing loss, revealing how disruptions in arginine and nitric oxide signaling damage sensory cells in the ear. Using mouse and fruit fly models, the team showed that restoring arginine levels or using sildenafil improved cell survival and hearing function.
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Genetic Breakthrough Could Help Restore Hearing
A newly identified CPD gene mutation causes congenital hearing loss by disrupting arginine metabolism and nitric oxide signaling. Promising treatments using arginine or sildenafil may one day help restore hearing in affected individuals. Credit: Shutterstock

Mutations in a gene called CPD have been found to play a key role in a rare inherited form of hearing loss, according to an international research collaboration. Scientists from the University of Chicago, the University of Miami, and several institutions in Turkiye published the discovery in theJournal of Clinical Investigation. The study reveals that the CPD gene, which is typically known for modifying proteins, also affects the inner ear. Researchers not only identified the genetic mechanism behind this effect but also found two possible treatment strategies.\

"This study is exciting because we found a new gene mutation that's linked to deafness, and more importantly we have a therapeutic target that can actually mitigate this condition," said lead author Rong Grace Zhai, PhD, Jack Miller Professor for the Study of Neurological Diseases of Neurology at UChicago. Although the study focused on individuals with a rare combination of mutations to the CPD gene, there could be broader implications if single mutations are linked to age-related hearing loss, she added.

The connection between CPD and hearing loss

Researchers began investigating CPD after identifying an unusual combination of mutations in three unrelated Turkish families affected by sensorineural hearing loss (SNHL), a congenital and hereditary condition that causes permanent deafness.

SNHL is typically diagnosed in early childhood and has long been considered irreversible. Hearing aids and cochlear implants can help improve perception of sound, but no direct medical treatment exists to repair the underlying damage.

When the scientists expanded their search through genetic databases, they discovered that individuals with other CPD mutations also showed signs of early-onset hearing loss, strengthening the link between this gene and auditory function.

How CPD protects sensory cells

To understand how CPD influences hearing, the team conducted experiments using mice. The CPD gene normally produces an enzyme responsible for generating the amino acid arginine, which then helps create nitric oxide, a key neurotransmitter involved in nerve signaling. In the inner ear, mutations in CPD disrupted this process, triggering oxidative stress and the death of delicate sensory hair cells that detect sound vibrations.

"It turns out that CPD maintains the level of arginine in the hair cells to allow a quick signaling cascade by generating nitric oxide," Zhai explained. "And that's why, although it's expressed ubiquitously in other cells throughout the nervous system, these hair cells in particular are more sensitive or vulnerable to the loss of CPD."

Fruit fly experiments reveal possible treatments

The researchers also used fruit flies as a model to explore how CPD mutations affect hearing. Flies with the defective gene exhibited behaviors consistent with inner ear dysfunction, such as impaired hearing and balance issues.

To test potential treatments, scientists tried two approaches. One was to provide arginine supplements to replace what was lost due to the gene defect. The other was to use sildenafil (Viagra), a drug known to stimulate one of the signaling pathways disrupted by reduced nitric oxide. Both treatments improved cell survival in patient-derived cells and reduced hearing-loss symptoms in the fruit flies.

"What makes this really impactful is that not only do we understand the underlying cellular and molecular mechanism for this kind of deafness, but we also found a promising therapeutic avenue for these patients. It is a good example of our efforts to repurpose FDA approved drugs for treating rare diseases," Zhai said.

The study also demonstrates the value of fruit fly models for studying neurological diseases, including age-related conditions, Zhai noted. "They give us the capability to not only understand disease pathology, but also to identify therapeutic approaches," she said.

Expanding the research to broader populations

The researchers plan to continue studying how nitric oxide signaling functions in the inner ear's sensory system. They also aim to investigate how common CPD mutations are in larger populations and whether they might contribute to other forms of hearing loss.

"How many people carry variants in this gene and is there a susceptibility to deafness or age-dependent hearing loss?" she said. "In other words, is this a risk factor for other types of sensory neuropathy?"

The study included collaborators from multiple institutions, including the University of Miami, Ege University, Ankara University, Yüzüncü Yıl University, Memorial Şişli Hospital, the University of Iowa, and the University of Northampton (UK).


Story Source:

Materials provided byUniversity of Chicago.Note: Content may be edited for style and length.


Journal Reference:

  1. Memoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, Amanda G. Lobato, Tahir Atik, Clemer Abad, Nirmal Vadgama, Duygu Duman, Nazım Bozan, Enise Avcı Durmuşalioǧlu, Sunny Greene, Shengru Guo, Suna Tokgöz-Yılmaz, Merve Koç Yekedüz, Fatma Tuba Eminoğlu, Mehmet Aydın, Serhat Seyhan, Ioannis Karakikes, Vladimir Camarena, Maria Camila Robayo, Tijana Canic, Güney Bademci, Gaofeng Wang, Amjad Farooq, Mei-ling Joiner, Katherina Walz, Daniel F. Eberl, Jamal Nasir, R. Grace Zhai, Mustafa Tekin.Carboxypeptidase D deficiency causes hearing loss amenable to treatment.Journal of Clinical Investigation, 2025; DOI:10.1172/JCI192090

Cite This Page:

University of Chicago. "Scientists discover a hidden gene mutation that causes deafness—and a way to fix it." ScienceDaily. ScienceDaily, 25 October 2025. <www.sciencedaily.com/releases/2025/10/251024041752.htm>.
University of Chicago. (2025, October 25). Scientists discover a hidden gene mutation that causes deafness—and a way to fix it.ScienceDaily. Retrieved October 26, 2025 from www.sciencedaily.com/releases/2025/10/251024041752.htm
University of Chicago. "Scientists discover a hidden gene mutation that causes deafness—and a way to fix it." ScienceDaily. www.sciencedaily.com/releases/2025/10/251024041752.htm (accessed October 26, 2025).

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