Evidence map›Paper›PMID 42264002›Full record

ArticleAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology2026

Unique and shared patterns of chemosensory dysfunction distinguish chronic COVID-19 and aspirin-exacerbated respiratory disease.

Dante G Minichetti, Tiffany Dharia, Amelia Boyd, Alyson Brown, Alexander Perniss, Evan Lemire, Adam L Haber, Rachel E Roditi, Stella E Lee, Valentina Parma and 3 more

Abstract read
In one paragraph

Article in Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Dante G MinichettiDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Tiffany DhariaDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Amelia BoydDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Alyson BrownDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Alexander PernissDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Evan LemireDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Adam L HaberDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Rachel E RoditiDivision of Otolaryngology-Head and Neck Surgery, Brigham and Women's Hospital, Boston, Massachusetts; Department of Surgery, Harvard Medical School, Boston, Massachusetts.
Stella E LeeDivision of Otolaryngology-Head and Neck Surgery, Brigham and Women's Hospital, Boston, Massachusetts; Department of Surgery, Harvard Medical School, Boston, Massachusetts.
Valentina ParmaMonell Chemical Senses Center, Philadelphia, Pennsylvania.
Kathleen M BuchheitDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Tanya M LaidlawDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Lora G BankovaDivision of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts. Electronic address: lbankova@bwh.harvard.edu.

Funding

Therapeutic Control of Aspirin-Exacerbated Respiratory DiseaseU19AI095219 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Joshua A Boyce · 2011 to 2026
$29.1M
Immune dysregulation mechanisms of persistent post-COVID19 olfactory dysfunctionR01DC021425 · NIDCD · BRIGHAM AND WOMEN'S HOSPITAL · PI Lora Bankova · 2024 to 2026
$1.9M
The Role of IL-5 and Local Nasal Polyp Immunoglobulin Production in Aspirin-Exacerbated Respiratory DiseaseK23AI139352 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BUCHHEIT, KATHLEEN MARY · 2019 to 2023
$1.0M
Patient-Oriented Research Mentorship and Training in Upper Airway Allergic and Inflammatory DiseasesK24AI180296 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Tanya Maria Laidlaw · 2024 to 2026
$522k
Biomarkers predicting nasal polyp recurrence in aspirin-exacerbated respiratory diseaseR21AI182809 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Kathleen Mary Buchheit · 2025 to 2026
$484k
Allergen-elicited signaling cascades in olfactory microvillous tuft cellsR21AI185057 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BANKOVA, LORA · 2024 to 2025
$476k
Brush cell sensing of aeroallergen-elicited stress signals promotes epithelial cell activationR21AI154345 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BANKOVA, LORA · 2021 to 2022
$437k
NIAID NIH HHS K23 AI139352NIAID NIH HHS K24 AI180296NIAID NIH HHS R21 AI154345NIAID NIH HHS R21 AI182809NIAID NIH HHS R21 AI185057NIAID NIH HHS U19 AI095219NIDCD NIH HHS R01 DC021425
6 · The paper itself

Abstract

backgroundPersistent chemosensory dysfunction (CSD) occurs in both COVID‑19 and aspirin-exacerbated respiratory disease (AERD). The similarities and differences in the chemosensory experiences of these 2 conditions remain undefined and poorly understood.

objectiveTo compare qualitative and quantitative chemosensory alterations and quality-of-life impact in individuals with COVID-19-associated vs AERD-associated CSD.

methodsParticipants from the Brigham and Women's Hospital COVID-19 CSD registry (n = 406) and the Brigham and Women's Hospital AERD registry (n = 389) completed online questionnaires assessing CSD characteristics and sinonasal disease-related quality of life.

resultsCOVID‑19 CSD showed a distinct qualitative phenotype. Overall, 60% of COVID‑19 participants reported that odors smelled different from how they recalled them, vs 19% with AERD (P < .001). Unpleasant odor perception was experienced by more than 20% of COVID‑19 participants, but by less than 5% of AERD participants. COVID‑19 CSD involved selective impairment and unpleasant distortion of sour, bitter, and umami tastes, whereas AERD exhibited a uniform quantitative reduction across taste modalities. Flavor distortions, particularly for foods with bitter or fatty components (eg, coffee, chocolate, and nut butter) and chemesthetic flavors (eg, spicy, mint, alcohol, garlic, and ginger), were significantly more common in COVID‑19 CSD (average: 25%) than in AERD (average: 0%). Both conditions were associated with impaired quality of life, including odor and food safety-related concerns.

conclusionBoth COVID‑19 CSD and AERD cause profound chemosensory disruption. However, COVID‑19 CSD is distinguished by marked qualitative distortions in smell, taste, flavor, and chemesthesis. In contrast, AERD CSD reflects a more generalized sensory reduction. Incorporating these characteristic sensory profiles into routine evaluations may improve diagnostic accuracy and guide patient counseling for ongoing chemosensory care.

Indexed as

Asthma, Aspirin-InducedCOVID-19Olfaction DisordersAdultAgedChronic DiseaseFemaleHumansMaleMiddle AgedQuality of LifeSARS-CoV-2SmellSurveys and QuestionnairesTasteTaste Disorders

Identifiers

PMID42264002
PMCPMC13453728

What Socratic holds

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Registered trials

None linked

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 Socratic graph.