Alpha-1 antitrypsin deficiency: outstanding questions and future directions.
María Torres-DuránJosé Luis Lopez-CamposMiriam BarrechegurenMarc MiravitllesBeatriz Martinez-DelgadoSilvia CastilloAmparo EscribanoAdolfo BaloiraMaría Mercedes Navarro-GarciaDaniel PellicerLucía BañulsMaría MagallónFrancisco CasasFrancisco DasíPublished in: Orphanet journal of rare diseases (2018)
2) Several clinical and etiological aspects of the disease are yet to be resolved. New strategies for early detection and biomarkers for patient outcome prediction are needed to reduce morbidity and mortality in these patients; 3) Augmentation therapy is the only specific approved therapy that has shown clinical efficacy in delaying the progression of emphysema. Regrettably, some countries reject registration and reimbursement for this treatment because of the lack of larger randomised, placebo-controlled trials. 4) Alternative strategies are currently being investigated, including the use of gene therapy or induced pluripotent stem cells, and non-augmentation strategies to prevent AAT polymerisation inside hepatocytes.
Keyphrases
- gene therapy
- placebo controlled
- induced pluripotent stem cells
- end stage renal disease
- double blind
- ejection fraction
- clinical trial
- newly diagnosed
- chronic kidney disease
- study protocol
- chronic obstructive pulmonary disease
- open label
- randomized controlled trial
- peritoneal dialysis
- squamous cell carcinoma
- stem cells
- replacement therapy
- mesenchymal stem cells
- lung function
- patient reported outcomes
- bone marrow
- atomic force microscopy
- locally advanced