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http://purl.uniprot.org/citations/37777755http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37777755http://www.w3.org/2000/01/rdf-schema#comment"

Background

Idiopathic pulmonary fibrosis (IPF) has an unknown aetiology and limited treatment options. A recent meta-analysis identified three novel causal variants in the TERT, SPDL1, and KIF15 genes. This observational study aimed to investigate whether the aforementioned variants cause clinical phenotypes in a well-characterised IPF cohort.

Methods

The study consisted of 138 patients with IPF who were diagnosed and treated at the Helsinki University Hospital and genotyped in the FinnGen FinnIPF study. Data on > 25 clinical parameters were collected by two pulmonologists who were blinded to the genetic data for patients with TERT loss of function and missense variants, SPDL1 and KIF15 missense variants, and a MUC5B variant commonly present in patients with IPF, or no variants were separately analysed.

Results

The KIF15 missense variant is associated with the early onset of the disease, leading to progression to early-age transplantation or death. In patients with the KIF15 variant, the median age at diagnosis was 54.0 years (36.5-69.5 years) compared with 72.0 years (65.8-75.3 years) in the other patients (P = 0.023). The proportion of KIF15 variant carriers was 9- or 3.6-fold higher in patients aged < 55 or 65 years, respectively. The variants for TERT and MUC5B had similar effects on the patient's clinical course, as previously described. No distinct phenotypes were observed in patients with the SPDL1 variant.

Conclusions

Our study indicated the potential of KIF15 to be used in the genetic diagnostics of IPF. Further studies are needed to elucidate the biological mechanisms of KIF15 in IPF."xsd:string
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http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Hollmen M."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Koskela J."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Kaarteenaho R."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Myllarniemi M."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Ainola M."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Sutinen E."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Laaka A."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/author"Partanen J.J."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/name"Respir Res"xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/pages"240"xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/title"KIF15 missense variant is associated with the early onset of idiopathic pulmonary fibrosis."xsd:string
http://purl.uniprot.org/citations/37777755http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/37777755http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/37777755
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