Science and Research

Genetic Risk Factors for Spontaneous Pneumothorax in Birt-Hogg-Dube Syndrome

BACKGROUND: Birt-Hogg-Dube syndrome (BHDS) is a genetic tumor syndrome characterized by lung cysts, spontaneous pneumothorax, fibrofolliculomas, and renal cell cancer. Because of its rarity and clinical heterogeneity, much is still unknown regarding the course of the disease and individual risk assessment. Therefore, we studied nonenvironmental risk factors for pneumothorax in a large sample of patients with BHDS. METHODS: Clinical data were available from 197 patients with BHDS (male patients, 103; female patients, 94) belonging to 63 unrelated families. The FLCN coding region including adjacent intronic sequences was analyzed by PCR and subsequent Sanger sequencing as well as by multiplex ligation-dependent probe amplification. Statistical analyses were performed, using adequate methods to account for familial clustering. RESULTS: Patients who had only a single spontaneous pneumothorax were significantly older at the time of occurrence than those with multiple pneumothoraces (mean, 38.93 vs 29.74 years; P value, .010). The risk for three or more pneumothoraces drastically increased after the second event. Significantly increased pneumothorax risks were found for mutations c.1300G>C (59%) and c.250-2A>G (77%), compared with FLCN hotspot mutation c.1285dup (37% risk) (P value, .02). CONCLUSIONS: We observed significant differences for the spontaneous pneumothorax risk regarding both age and sex in patients with BHDS. Furthermore, two FLCN mutations were identified that are associated with significantly increased pneumothorax risk. Thus, formerly unknown individual predictors have been identified that provide improved risk stratification for patients with BHDS.

  • Sattler, E. C.
  • Syunyaeva, Z.
  • Mansmann, U.
  • Steinlein, O. K.

Keywords

  • Birt-Hogg-Dube syndrome
  • FLCN gene
  • genotype-phenotype correlation
  • pneumothorax
Publication details
DOI: 10.1016/j.chest.2019.12.019
Journal: Chest
Pages: 1199-1206 
Number: 5
Work Type: Original
Location: CPC-M
Disease Area: LC
Partner / Member: LMU
Access-Number: 31958439
See publication on PubMed

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