| CPC G01N 33/537 (2013.01) [C12Q 1/6883 (2013.01); G01N 33/68 (2013.01); G01N 33/6893 (2013.01); G16B 40/00 (2019.02); G16B 40/30 (2019.02); G16C 99/00 (2019.02); G16H 50/30 (2018.01); C12Q 2600/118 (2013.01); C12Q 2600/158 (2013.01); C12Q 2600/16 (2013.01); G01N 2333/54 (2013.01); G01N 2333/705 (2013.01); G01N 2333/70503 (2013.01); G01N 2333/70535 (2013.01); G01N 2333/70596 (2013.01); G01N 2333/924 (2013.01); G01N 2333/96486 (2013.01); G01N 2400/40 (2013.01); G01N 2800/122 (2013.01); G01N 2800/125 (2013.01); G01N 2800/127 (2013.01); G01N 2800/50 (2013.01)] | 5 Claims |
|
1. A method of treating a subject having cystic fibrosis and at risk for severe pulmonary exacerbation, the method comprising
a. obtaining a whole blood sample from the subject;
b. detecting the mRNA expression level of each of the following genes in a gene panel consisting of: TLR2, ADAM9, PLXND1, CD163, CD36, CD64, CSPG2, IL32, HPSE, and HCA112;
c. determining the subject's risk for severe pulmonary exacerbation by calculating a risk score of mild, moderate or severe pulmonary exacerbation based on the subject's combined mRNA expression level of the genes from step (b), wherein the subject's calculated risk score correlates to a risk score for mild, moderate or severe pulmonary exacerbation; and
d. treating the subject determined to be at risk for severe exacerbation with treatments effective for treating severe pulmonary exacerbations.
|