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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 1
2011 pubmed 14 citations

A novel p.S34N mutation of CAMP gene in patients with periodontal disease.

Türkoğlu. Oya O; Berdeli. Afig A; Emingil. Gülnur G; Atilla. Gül G

Key Findings

  • A novel missense mutation (p.S34N) in the CAMP gene was identified in 25 subjects.
  • The p.S34N mutation was significantly more frequent in generalized aggressive periodontitis patients than in chronic periodontitis patients or controls.
  • Individuals with generalized aggressive periodontitis were about 5.3 times more likely to carry the mutation after adjusting for age, gender, and bleeding on probing.

Practical Outcomes

  • For most biohackers, the finding isn’t directly actionable—there’s no new supplement or protocol to try. It suggests that genetic testing for this mutation might help explain severe gum disease in a few cases, but no specific LL‑37‑based interventions are supported yet.

Summary

Researchers found a new genetic change (p.S34N) in the CAMP gene that makes the immune peptide LL‑37 slightly different, and this change is much more common in people with a severe, fast‑progressing gum disease called generalized aggressive periodontitis, but not in regular chronic gum disease or healthy people.

Abstract

Recent studies have showed that genetic factors involved in the host responses might determine the severity of periodontitis. hCAP-18/LL-37 is a part of the innate immune response in the oral cavity. The aim of the present study was to investigate the mutation of CAMP gene encoding hCAP-18/LL-37 in the patients with different periodontal diseases. Seventy-eight chronic periodontitis, 72 generalized aggressive periodontitis, and 149 controls were analysed for mutation of CAMP gene using direct DNA sequencing method. Frequencies of p.S34N mutation were compared by Pearson chi-square test. Logistic regression analysis was used to analyse the association between periodontitis and p.S34N mutation adjusting for bleeding on probing, age and gender. Twenty-five subjects had a novel missense mutation of CAMP gene. Single base substitution (c.101G>A) in exon 1 led to p.S34N mutation. All amino acid substitutions were heterozygous mutation. The patients with generalized aggressive periodontitis had significantly higher p.S34N mutation prevalence compared to the others, whilst there was no significant difference in prevalence of p.S34N mutation between the patients with chronic periodontitis and the control subjects. Logistic regression analysis adjusted for BOP, age and gender revealed that the patients with generalized aggressive periodontitis were 5.32 times more likely to have p.S34N mutation compared to the controls (OR=5.32, 95% CI: 1.3-22.1). We report a novel missense mutation of CAMP gene. p.S34N mutation in CAMP gene seems to be contributing factor for generalized aggressive periodontitis, but not for chronic periodontitis.

Study Information

Provider

pubmed

Year

2011

Date

2011-01-05T00:00:00.000Z

DOI

10.1016/j.archoralbio.2010.11.016

Citations

14

References

35