Evidence map›Paper›PMID 41330703›Full record

ArticleAllergy, asthma & immunology research2025

Impact of Biologics on Nasal Symptoms in Severe Asthmatics: Findings From the PRISM Study.

Ji-Su Shim, Hyunkyoung Kim, Jae-Woo Kwon, So-Young Park, Sujeong Kim, Byung-Keun Kim, Young-Hee Nam, Min-Suk Yang, Mi-Ae Kim, Sae-Hoon Kim and 20 more

Abstract read
In one paragraph

Article in Allergy, asthma & immunology research, 2025. 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
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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

30 authors.

Ji-Su Shim *Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8846-0364
Hyunkyoung Kim *Department of Allergy and Clinical Immunology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0065-9214
Jae-Woo KwonDepartment of Allergy and Clinical Immunology, Kangwon National University School of Medicine, Chuncheon, Korea.ORCID https://orcid.org/0000-0003-1639-3606
So-Young ParkDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-5224-3077
Sujeong KimDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Korea.ORCID https://orcid.org/0000-0002-2494-9216
Byung-Keun KimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-5147-6306
Young-Hee NamDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.ORCID https://orcid.org/0000-0001-8759-2982
Min-Suk YangDepartment of Internal Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-9861-0530
Mi-Ae KimDepartment of Pulmonology, Allergy and Critical Care Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.ORCID https://orcid.org/0000-0003-1253-6075
Sae-Hoon KimDivision of Allergy and Clinical Immunology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0002-2572-5302
Byung-Jae LeeDepartment of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-6940-0836
Taehoon LeeDepartment of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.ORCID https://orcid.org/0000-0002-9224-0866
Sang-Ha KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID https://orcid.org/0000-0002-1763-5366
Young-Joo ChoDepartment of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9414-5934
Sang Min LeeDivision of Respiratory Disease and Allergy, Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Korea.ORCID https://orcid.org/0000-0002-9568-2096
Chan Sun ParkDepartment of Internal Medicine, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.ORCID https://orcid.org/0000-0003-0113-8354
Jae-Woo JungDepartment of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3411-735X
Han-Ki ParkDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Korea.ORCID https://orcid.org/0000-0002-5460-9917
Joo-Hee KimDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea.ORCID https://orcid.org/0000-0002-1572-5149
Jeong-Hee ChoiDepartment of Pulmonology and Allergy, Hallym University Dongtan Sacred Heart Hospital, Hwaseong, Korea.ORCID https://orcid.org/0000-0002-0599-875X
Ji-Yong MoonDepartment of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2459-3448
Kyoung-Hee SohnDepartment of Internal Medicine, Kyung Hee University Medical Center, Seoul, Korea.ORCID https://orcid.org/0000-0001-8407-8080
Gyu Young HurDepartment of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-5039-0199
Sang Hoon KimDepartment of Internal Medicine, Nowon Eulji Hospital, Eulji University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4105-0552
Hye-Kyung ParkDepartment of Internal Medicine, Pusan National University Hospital, Pusan National University College of Medicine, Busan, Korea.ORCID https://orcid.org/0000-0003-4065-2962
Sunyoung YoonDepartment of Allergy and Pulmonology in Internal Medicine, Chungnam National University, Chungnam National University Sejong Hospital, Sejong, Korea.ORCID https://orcid.org/0000-0002-4205-1434
Hyun Jung JinDivision of Pulmonology and Allergy, Department of Internal Medicine, Yeungnam University Medical Center, College of Medicine, Yeungnam University, Daegu, Korea.ORCID https://orcid.org/0000-0003-2888-420X
Min-Hye KimDepartment of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea. mineyang81@ewha.ac.kr.ORCID https://orcid.org/0000-0002-1775-3733
Tae-Bum KimDepartment of Allergy and Clinical Immunology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. tbkim@amc.seoul.kr.ORCID https://orcid.org/0000-0001-5663-0640
Precision Intervention in Severe Asthma (PRISM) Study Investigators

Funding

Korea Health Industry Development Institute RS-2024-00403700National Research Foundation of Korea 2019M3E5D3073365
6 · The paper itself

Abstract

purposeThe sino-nasal outcome test (SNOT-22) is a patient-reported outcome measure for chronic rhinosinusitis (CRS), assessing treatment response after 6 months of biologic uses in patients with severe CRS. We investigated score changes in each domain of SNOT-22 with biologics in patients with severe asthma.

methodsA total of 229 patients with severe asthma and nasal symptoms were enrolled from a prospective, observational, multicenter cohort study. After 6 months of treatment with biologics or conventional GINA Step 4-5 management, SNOT-22 changes were evaluated by analyzing total and rhinological, extranasal rhinological, ear/facial, psychological, and sleep domain scores.

resultsThe adjusted odds ratio (OR) of being a responder was significantly higher for dupilumab in the total (OR, 2.29; 95% confidence interval [CI], 1.08-4.87), extranasal rhinological (OR, 2.80; 95% CI, 1.20-6.56), physiologic (OR, 2.23; 95% CI, 1.03-4.83), and sleep dysfunction (OR, 2.50; 95% CI, 1.14-5.47) domain scores of SNOT-22 than those for conventional or anti- interleukin (IL)-5 antibody treatment. After adjusting for the history of CRS diagnosis, dupilumab users had higher ORs for total SNOT-22 (OR, 2.20; 95% CI, 1.02-4.77) and extranasal rhinological (OR, 2.77; 95% CI, 1.16-6.60) scores. When SNOT-22 was plotted by the type of treatment at 0, 1, and 6 months, an overall trend of decreased total/domain scores of SNOT-22 was observed in the biologic-treated group compared to the conventional group, with the most pronounced decrease in dupilumab-treated group.

conclusionsDupilumab demonstrates a significant improvement not only in total SNOT-22 scores but also in the extranasal rhinological, physiologic, and sleep dysfunction domain scores compared to conventional or anti-IL-5 treatment in patients with severe asthma and nasal symptoms.

Indexed as

Asthmamonoclonal antibodiesrhinosinusitissino-nasal outcome test-22treatment outcome

Identifiers

PMID41330703
PMCPMC12683743

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