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TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis.

Justin M OldhamShwu-Fan MaFernando J MartinezKevin J AnstromGanesh RaghuDavid A SchwartzEleanor ValenziLeah WittCathryn LeeRekha VijYong HuangMary E StrekImre Nothnull null
Published in: American journal of respiratory and critical care medicine (2016)
NAC may be an efficacious therapy for individuals with IPF with an rs3750920 (TOLLIP) TT genotype, but it was associated with a trend toward harm in those with a CC genotype. A genotype-stratified prospective clinical trial should be conducted before any recommendation regarding the use of off-label NAC to treat IPF.
Keyphrases
  • idiopathic pulmonary fibrosis
  • clinical trial
  • transcription factor
  • interstitial lung disease
  • open label
  • randomized controlled trial
  • rheumatoid arthritis
  • systemic sclerosis
  • phase iii