Evidence map›Paper›PMID 41004123›Full record

ArticleInternational forum of allergy & rhinology2026

Factor Analysis-Based Quantitative Endotyping Improves Associations With CRS Cross-Sectional and Longitudinal Outcomes.

Brooke N Gleason, Zhidi Luo, Aditi Agarwal, Siyuan Dong, Regan L Harmon, Junqin Bai, Chun-Kang Liao, Julia Huang, David B Conley, Kevin C Welch and 7 more

Abstract read
In one paragraph

Article in International forum of allergy & rhinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Brooke N GleasonDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0009-0008-5614-4990
Zhidi LuoDepartment of Psychiatry and Behavioral Science, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Aditi AgarwalDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0009-0006-8532-6094
Siyuan DongDepartment of Preventive Medicine (Biostatistics and Informatics), Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Regan L HarmonDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Junqin BaiDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-6012-2809
Chun-Kang LiaoDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Julia HuangDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
David B ConleyDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kevin C WelchDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Robert C KernDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Stephanie S SmithDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-0605-3993
Anju T PetersDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-0745-2379
Whitney S StevensDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-2608-6610
Atsushi KatoDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Lutfiyya N MuhammadDepartment of Preventive Medicine (Biostatistics and Informatics), Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Bruce K TanDepartment of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-9210-5050

Funding

Population-based CRS epidemiology: sex differences, natural history, and long-term outcomes based on clinically-defined phenotypes and biologically-based endotypes - GeisingerP01AI145818 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KATO, ATSUSHI · 2019 to 2023
$9.3M
Type-2 inflammation mediates olfactory loss in Chronic Rhinosinusitis: mechanisms and therapeutic opportunitiesR01DC016645 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TAN, BRUCE K · 2018 to 2022
$3.0M
Autoantibody mediated pathogenesis in chronic rhinosinusitis with nasal polyps: mechanisms and consequencesR01AI134952 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TAN, BRUCE K · 2018 to 2022
$2.0M
NIAID NIH HHS P01 AI145818NIAID NIH HHS R01 AI134952NIDCD NIH HHS R01 DC016645NIH HHS R01 AI134952NIH HHS R01 DC016645
6 · The paper itself

Abstract

backgroundChronic rhinosinusitis (CRS) is a heterogeneous inflammatory disease characterized by persistent sinonasal inflammation. There is increasing interest in endotype-based classification, which categorizes CRS based on underlying inflammatory pathways. We applied factor analysis to facilitate continuous endotype assignment to CRS patients and assess cross-sectional and longitudinal CRS outcomes.

methodsWe prospectively enrolled 203 patients (52 controls, 88 CRSsNP, and 63 CRSwNP) undergoing endoscopic nasal or sinus surgery (ESS). Middle meatal mucus biomarkers were analyzed pre-ESS (V0) and 6-12 months post-ESS (V1). Factor analysis was performed to identify latent factors. Factor scores were generated, and statistical analyses were conducted to assess correlations with radiographic (Lund-Mackay [LM]) and patient-reported (SNOT-22, CRS-PRO) outcomes measured at V0, V1, and V2 (1.5-5 years post-ESS).

resultsFour factors were identified: Type 1 (T1), Type 2 (T2), Type 3 (T3), and macrophage-associated (M). CRSwNP patients had higher T2 and M factor scores than CRSsNP and controls. T2, T3, and M factor scores demonstrated stronger or equivalent associations with radiographic and patient-reported outcomes compared to individual biomarkers. Following ESS, median T2 and M factor scores significantly declined, while T1 and T3 remained stable. V0 T1 and T2 were weakly associated with long-term (V2) radiographic and symptom scores. V1 factor scores were more consistently predictive of long-term (V2) outcomes, with T2, T3, and M demonstrating modest correlations with radiographic severity and CRS-PRO.

conclusionsFactor analysis identifies distinct, quantifiable patterns of inflammation in CRS, offering improved associations with cross-sectional and longitudinal outcomes compared to individual biomarkers.

Indexed as

RhinitisSinusitisAdultAgedBiomarkersChronic DiseaseCross-Sectional StudiesEndoscopyFactor Analysis, StatisticalFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective StudiesBiomarkersbiomarkerchronic rhinosinusitisdisease severityendoscopic sinus surgeryendotypepatient reported outcomes

Identifiers

PMID41004123
PMCPMC12755909

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.