A novel anxiety-associated SNP identified in LYNX2 (LYPD1) is associated with decreased protein binding to nicotinic acetylcholine receptors
2024

New Genetic Variant Linked to Anxiety

Sample size: 624 publication 10 minutes Evidence: moderate

Author Information

Author(s): Kristin R. Anderson, Wenpeng Cao, Hui Sun Lee, Mark A. Crenshaw, Talulla B. Palumbo, Ethan Fisher-Perez, Amanda DeGraaf, Peter Rogu, Maria A. Beatty, Gabrielle M. Gracias, Avani V. Pisapati, Katie Hoffman, Krystle J. McLaughlin, Almut Hupbach, Im Wonpil, X. Frank Zhang, Julie M. Miwa

Primary Institution: Lehigh University

Hypothesis

Does the LYNX2 gene variant affect anxiety levels in humans?

Conclusion

The LYNX2 Q39H variant is associated with increased anxiety levels comparable to those seen in diagnosed anxiety disorders.

Supporting Evidence

  • A specific LYNX2 SNP is linked to a reduced binding affinity between the LYNX2 protein and nicotinic acetylcholine receptors.
  • Individuals with the Q39H mutation reported anxiety levels similar to those diagnosed with anxiety disorders.
  • The study identified a novel SNP in the LYNX2 gene that had not been previously reported.

Takeaway

Some people have a gene change that makes them feel more anxious, like when you're scared of the dark. This study found that this change can make them feel anxious even if they don't have a doctor's label for it.

Methodology

Participants completed anxiety questionnaires and DNA analysis was performed to identify SNPs in the LYNX2 gene.

Potential Biases

The study relied on self-reported anxiety measures, which can be subjective.

Limitations

The study's population was primarily young adults, which may not represent older individuals with anxiety disorders.

Participant Demographics

The cohort consisted of 624 participants, with an average age of 20.7 years, including 179 males and 416 females.

Statistical Information

P-Value

p<1.0 × 10–4

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.3389/fnbeh.2024.1347543

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