Evidence map›Paper›PMID 42704614›Full record

ArticleIrish journal of medical science2026

Clinical and hematological parameters associated with omalizumab response in chronic spontaneous urticaria.

Hacer Vural Karatoprak, Serpil Sener, Dursun Turkmen, Mehmet Enes Güner, Nihal Altunisik, Zekiye Kanat, Tuba Vural

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Article in Irish journal of medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hacer Vural KaratoprakFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye.
Serpil SenerFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye.
Dursun TurkmenFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye. dursun.turkmen@inonu.edu.tr.ORCID http://orcid.org/0000-0001-9076-4669
Mehmet Enes GünerFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye.
Nihal AltunisikFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye.
Zekiye KanatFaculty of Medicine, Department of Dermatology, Inonu University, Malatya, Türkiye.
Tuba VuralIsparta City Hospital, Immunology and Allergy Diseases Clinic, Isparta, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the clinical efficacy of omalizumab treatment and its effects on hematological, inflammatory, and coagulation parameters, as well as the relationship between these parameters and treatment response, in patients with chronic spontaneous urticaria (CSU) resistant to antihistamines.

methodsThe study included 30 adult CSU patients unresponsive to four-fold dose antihistamine treatment. Patients received 300 mg of subcutaneous omalizumab every 28 days. Clinical response was assessed using the 7-day Urticaria Activity Score (UAS7). Hematological (leukocyte, neutrophil, lymphocyte counts, NLR), inflammatory (CRP, ESR), and coagulation (D-dimer, aPTT, PT, fibrinogen) parameters, as well as total IgE levels, were measured before treatment and at 3 months.

resultsA statistically significant decrease in UAS7 scores was observed after omalizumab treatment (p = 0.001). Treatment resulted in a significant decrease in leukocyte and neutrophil counts, NLR, CRP, ESR, and D-dimer levels, while a slight prolongation of aPTT was observed (p < 0.05). Total IgE, PT, fibrinogen, lymphocyte, monocyte, eosinophil, and basophil counts showed no significant changes. No significant correlation was found between baseline laboratory parameters and clinical response.

conclusionOmalizumab provides clinical improvement in CSU, as well as improvement in parameters reflecting systemic inflammation and coagulation activation. However, our study showed that baseline laboratory values were insufficient to predict treatment response. These findings suggest that the effects of omalizumab are not limited to symptom control but may have more systemic immunomodulatory effects.

Indexed as

Hematological parametersOmalizumabUAS7Urticaria

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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.