TY - JOUR
T1 - Use of endotypes, phenotypes, and inflammatory markers to guide treatment decisions in chronic rhinosinusitis
AU - Staudacher, Anna G.
AU - Peters, Anju T.
AU - Kato, Atsushi
AU - Stevens, Whitney W.
N1 - Funding Information:
Funding: This study was funded by grants K23AI141694, PO1AI145818, and R01AI137174 from the National Institutes of Health and the Ernest S. Bazley Foundation.
Publisher Copyright:
© 2020 American College of Allergy, Asthma & Immunology
PY - 2020/4
Y1 - 2020/4
N2 - Objective: With the advent of new treatment options for Chronic Rhinosinusitis (CRS) comes the ability for physicians to provide more individualized patient care. Physicians are now tasked with identifying who may be the best candidate for a particular therapy. In this review, existing biomarkers and potentially new methods that could guide treatment choices in CRS patients will be discussed. Data Sources: Published literature obtained through PubMed searches. Study Selection: Studies relevant to inflammatory endotypes, phenotypes, and biomarkers in CRS were included. Results: Currently, there are no clinically validated tools that determine the best therapeutic modality for CRS patients with or without nasal polyps (CRSwNP or CRSsNP). Patients with CRS can be classified into three endotypes based on the presence of type 1, type 2, or type 3 inflammation. CRS endotypes can be influenced by age and geographic location. Clinical application however may be limited since endotyping current requires basic research laboratory support. Clinical symptoms may also predict inflammatory endotypes with smell loss being indicative of type 2 inflammation. Numbers of tissue and/or peripheral eosinophils as well as levels of IgE may predict disease severity in CRSwNP but not necessarily treatment responses. Unique clinical phenotypes or biomarkers are especially lacking that predict type 1 or type 3 inflammation in CRSwNP or type 1, type 2, or type 3 inflammation in CRSsNP. Conclusion: While significant progress has been made in characterizing endotypes, phenotypes, and biomarkers in CRS, additional studies are needed to determine if and how these factors could assist physicians in providing more individualized clinical care.
AB - Objective: With the advent of new treatment options for Chronic Rhinosinusitis (CRS) comes the ability for physicians to provide more individualized patient care. Physicians are now tasked with identifying who may be the best candidate for a particular therapy. In this review, existing biomarkers and potentially new methods that could guide treatment choices in CRS patients will be discussed. Data Sources: Published literature obtained through PubMed searches. Study Selection: Studies relevant to inflammatory endotypes, phenotypes, and biomarkers in CRS were included. Results: Currently, there are no clinically validated tools that determine the best therapeutic modality for CRS patients with or without nasal polyps (CRSwNP or CRSsNP). Patients with CRS can be classified into three endotypes based on the presence of type 1, type 2, or type 3 inflammation. CRS endotypes can be influenced by age and geographic location. Clinical application however may be limited since endotyping current requires basic research laboratory support. Clinical symptoms may also predict inflammatory endotypes with smell loss being indicative of type 2 inflammation. Numbers of tissue and/or peripheral eosinophils as well as levels of IgE may predict disease severity in CRSwNP but not necessarily treatment responses. Unique clinical phenotypes or biomarkers are especially lacking that predict type 1 or type 3 inflammation in CRSwNP or type 1, type 2, or type 3 inflammation in CRSsNP. Conclusion: While significant progress has been made in characterizing endotypes, phenotypes, and biomarkers in CRS, additional studies are needed to determine if and how these factors could assist physicians in providing more individualized clinical care.
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U2 - 10.1016/j.anai.2020.01.013
DO - 10.1016/j.anai.2020.01.013
M3 - Review article
C2 - 32007571
AN - SCOPUS:85079905062
SN - 1081-1206
VL - 124
SP - 318
EP - 325
JO - Annals of Allergy, Asthma and Immunology
JF - Annals of Allergy, Asthma and Immunology
IS - 4
ER -