ALL Metrics
-
Views
-
Downloads
Get PDF
Get XML
Cite
Export
Track
Review

Advances in Understanding and Managing Chronic Urticaria

[version 1; peer review: 2 approved]
PUBLISHED 16 Feb 2016
Author details Author details
OPEN PEER REVIEW
REVIEWER STATUS

Abstract

There have been recent advances in the classification and management of chronic urticaria. The new term chronic spontaneous urticaria (CSU) has replaced chronic idiopathic urticaria and chronic autoimmune urticaria. In addition, chronic inducible urticaria (CINDU) has replaced physical urticaria and includes other forms of inducible urticaria, such as cholinergic and aquagenic urticaria. Furthermore, novel research has resulted in a new understanding with guidelines being revised in the past year by both the American Academy of Allergy, Asthma, and Immunology (AAAAI) and the European Academy of Allergy and Clinical Immunology (EAACI)/Global Allergy and Asthma European Network (GA2LEN)/European Dermatology Forum (EDF)/World Allergy Organization (WAO). There are some differences in the recommendations, which will be discussed, but the core updates are common to both groups. The basic treatment for chronic urticaria involves second-generation non-sedating non-impairing H1 antihistamines as first-line treatment. This is followed by up to a 4-fold increase in the licensed dose of these H1 antihistamines. The major therapeutic advance in recent years has been in third-line treatment with omalizumab, a humanized monoclonal anti-immunoglobulin E (anti-IgE) antibody that prevents binding of IgE to the high-affinity IgE receptor. Several multicenter randomized controlled trials have shown safety and efficacy of omalizumab for CSU. There are also some small studies showing efficacy of omalizumab in CINDU. While there were previously many treatment options which were lacking in strong evidence, we are moving into an era where the treatment algorithm for chronic urticaria is simplified and contains more evidence-based, effective, and less toxic treatment options.

Keywords

Chronic Urticaria, Classification, Management, Antihistamines, Up-dosing, Omalizumab

Introduction

Urticaria (hives) is a relatively common condition, with a point prevalence of about 0.5–1%1. The peak incidence is in the range of 20–40 years. Urticaria is the general term for a cutaneous response characterized by wheals and swellings. A deeper localized swelling often associated with urticaria is called angioedema. Urticaria is mediated by mast cell degranulation. Mast cells can be activated by immunologic and non-immunologic mechanisms, which lead to degranulation of inflammatory mediators including histamine, leukotrienes, and prostaglandins. Release of these mediators causes the characteristic pruritus, vascular permeability, and edema.

Classification

Acute urticaria is defined as hives that last less than 6 weeks, while chronic urticaria refers to urticaria that occurs intermittently for at least 6 weeks, typically on most days of the week. Acute urticaria can occur spontaneously or in response to a trigger. Triggers of acute urticaria are typically acute viral infections or allergic reactions to foods, medications, latex, or insects. Chronic urticaria can also be spontaneous or inducible, though the triggers of inducible urticaria are different compared to those of acute urticaria. Inducible urticaria involves hiving responses resulting from physical stimuli including scratch (dermographism) and cold contact urticaria. Additional triggers of chronic urticaria include pressure, temperature change, sun exposure, water exposure, and exercise (Figure 1, Table 1)25.

e42d1361-53a0-4d13-8a53-059dee31a545_figure1.gif

Figure 1. Classification of Urticaria.

The revised classification of urticaria divides chronic urticaria into chronic spontaneous urticaria (CSU), with no external trigger, and chronic inducible urticaria (CINDU), with an identifiable trigger. Acute urticaria remains as that which lasts less than 6 weeks.

Table 1. Triggers of Acute Urticaria and Chronic Inducible Urticaria.

The triggers of acute and chronic urticaria are different and are outlined in this table.

ClassificationAcute Urticaria
(<6 weeks)
Chronic Inducible Urticaria
(>6 weeks)
TriggersInfectionDermographism
FoodCholinergic
MedicationCold-induced
VenomSolar
LatexAquagenic
ContactVibration
IdiopathicDelayed-pressure

New terminology

While the pathogenesis of urticaria remains incompletely understood, our knowledge of the etiology of chronic urticaria has increased. We are able to differentiate the older terminology of chronic autoimmune urticaria or chronic idiopathic urticaria from physically induced urticaria6. However, now physical urticaria has been revised to chronic inducible urticaria (CINDU) to reflect the external trigger and inducible nature. The term CINDU also includes cholinergic, aquagenic, and contact urticaria. The remaining forms of urticaria, which occur without an external trigger and instead via an endogenous mechanism, are classified as chronic spontaneous urticaria (CSU). This is simplified and more specific than the term chronic idiopathic urticaria, which is now falling out of use2 (Figure 1).

Assessing disease severity and impact on quality of life

The primary symptom of urticaria is pruritus. Urticaria generally causes significant disability adversely affecting an individual’s life. New tools have been developed to quantify the effect of urticaria on quality of life. One such tool is the Urticaria Activity Score (UAS7), which is a validated score recommended by urticaria guidelines7. In the UAS7, the patient records the severity of itching and the number of wheals daily for 7 days. A score of <7 in 1 week indicates control of disease, whereas a score of >28 per week indicates severe disease. This tool allows for efficient clinical practice, maximizing the information gathered during patient visits while minimizing the use of resources and time. While the UAS7 is a prospective tool, a retrospective tool was also developed, the Urticaria Control Test (UCT)8. Additional questionnaires have been developed and are recommended for use to assess the impact of urticaria on quality of life. The recently developed tools include the Chronic Urticaria Quality of Life Questionnaire (CU-Q2oL)9 and the Urticaria Severity Score10. These tools were designed specifically for urticaria since other more generic questionnaires do not capture the nuances of the impact of urticaria on one’s quality of life (Table 2).

Table 2. Tools to assess the impact of chronic urticaria on quality of life.

There are a number of recently developed tools specifically for urticaria to assess severity and impact on quality of life.

ToolDescription
Urticaria Activity Score (UAS7)Prospective tool, patients record severity of itch and
number of wheals daily, must be recorded by patient
for 7 consecutive days, assesses disease activity7
Urticaria Control Test (UCT)Retrospective tool, four-item questionnaire to
determine control of disease8
Chronic Urticaria Quality of Life
Questionnaire (CU-Q2oL)
Retrospective tool, 23-item questionnaire, assesses
quality of life9
Urticaria Severity Score (USS)Instrument for monitoring severity, 12 questions10

Advances in management

Recently, new guidelines have been published by the American Academy of Allergy, Asthma, and Immunology (AAAAI) and the European Academy of Allergy and Clinical Immunology (EAACI)/Global Allergy and Asthma European Network (GA2LEN)/European Dermatology Forum (EDF)/World Allergy Organization (WAO) that update what is currently understood about urticaria35. There are several other published regional guidelines with similar recommendations, including Canadian11. With the exception of the American guidelines, the other organizations put forth a similar algorithm. That is, the following stepwise approach: first-line treatment includes second-generation H1 antihistamines, second-line therapy involves up-dosing the second-generation H1 antihistamine, and third-line treatment includes a new medication, omalizumab, which we recommend to be used before a more toxic medication, cyclosporine A.

One of the notable differences in the guidelines put forth by the American versus European/World guidelines is the role for first-generation H1 antihistamines. The AAAAI keeps first-generation H1 antihistamines in the treatment algorithm. The EAACI/GA2LEN/EDF/WAO guidelines specifically recommend avoiding first-generation H1 antihistamines based on the benefit-to-risk ratio of these agents. The known risks are cited as well as the high underestimated risk potential when these agents are taken in the evening, such as changes in REM sleep patterns and impairment of cognitive functions12. For similar reasons, the EAACI/GA2LEN/EDF/WAO guidelines do not address a role for hydroxyzine or doxepin, whereas the AAAAI guidelines include these medications as options if up-dosing of non-sedating, non-impairing H1 antihistamines is not successful at complete control of symptoms.

The EAACI/GA2LEN/EDF/WAO guidelines do not include H2 antihistamines in their algorithm due to a recent Cochrane review that shows lack of evidence of efficacy of these medications13. Thus, H2 antihistamines are advised only on an individual case basis but not as first-, second- or third-line treatment. The AAAAI guidelines, however, consider the options of up-dosing second-generation H1 antihistamines, adding other second-generation H1 antihistamines, and adding H2 antagonists, leukotriene receptor antagonists or first-generation H1 antihistamines at bedtime to all be equally weighted second-line options3. In doing this, however, the adverse reaction profile would increase.

Both guidelines recommend that corticosteroids should be considered only for the short-term intervention and avoided as long-term treatments due to the significant number of side effects and alternative options for treatment. Both guidelines also acknowledge a role for cyclosporine A as an add-on treatment for patients who have refractory chronic urticaria that is not responsive to the above mentioned treatments3,5.

Both guidelines have also incorporated a new third-line treatment option, omalizumab, a subcutaneously injected, biologic medication3,5. There is a large body of new data showing efficacy of omalizumab in various subtypes of chronic urticaria with a relatively low level of adverse effects1824. Omalizumab is a recombinant humanized immunioglobulin G1 (IgG1) monoclonal antibody that binds to IgE. In binding IgE, omalizumab inhibits binding of IgE to the high-affinity IgE receptor (FcεRI) found on the surface of mast cells and basophils. By inhibiting binding of IgE to the receptor, the release of inflammatory mediators such as histamine, leukotrienes, and prostaglandins is limited, thus blunting the inflammatory response14. By inhibiting IgE from binding the FcεRI receptor, omalizumab also has the effect of down-regulating the FcεRI receptor on the surface of mast cells and basophils. This monoclonal antibody has also been shown to decrease the release of circulating interleukin-6 and tumor necrosis factor α and to decrease the recruitment of T cells, eosinophils, and macrophages in the inflammatory response15. The overall effect of omalizumab is to prevent urticaria and angioedema14.

Omalizumab was approved in Europe and North America in 2014 for the treatment of CSU in adults and adolescents 12 years of age and older who do not respond to H1 antihistamines16,17. This approval was based on three phase III randomized clinical trials evaluating over 1000 patients’ treatment response with inadequately controlled CSU1820. There have also been several published real life trials demonstrating efficacy and safety2123. Additionally, there are smaller case studies assessing the efficacy of omalizumab in various subtypes of CINDU, and while the number of overall cases is low, all have shown notable improvement in urticaria symptoms24. Future research is, therefore, required to evaluate the role of omalizumab in the various subtypes of chronic urticaria as well as to establish standardized protocols for dosing and monitoring adverse effects of long-term therapy.

Conclusion

A number of notable changes have occurred recently in the guidelines for managing chronic urticaria. Overall, the classification and management have become more simplified. There are new tools to track and monitor the quality of life of patients with this challenging disease. Furthermore, the recent addition of omalizumab to the treatment algorithm for CSU has offered a more effective and less toxic treatment option to those suffering with refractory disease to older treatment strategies. With the many trials currently underway for CINDU, the outlook is optimistic.

Comments on this article Comments (0)

Version 1
VERSION 1 PUBLISHED 16 Feb 2016
Comment
Author details Author details
Competing interests
Grant information
Copyright
Download
 
Export To
metrics
Views Downloads
F1000Research - -
PubMed Central
Data from PMC are received and updated monthly.
- -
Citations
CITE
how to cite this article
Moolani Y, Lynde C and Sussman G. Advances in Understanding and Managing Chronic Urticaria [version 1; peer review: 2 approved]. F1000Research 2016, 5(F1000 Faculty Rev):177 (https://doi.org/10.12688/f1000research.7246.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
track
receive updates on this article
Track an article to receive email alerts on any updates to this article.

Open Peer Review

Current Reviewer Status: ?
Key to Reviewer Statuses VIEW
ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions
Version 1
VERSION 1
PUBLISHED 16 Feb 2016
Views
5
Cite
Reviewer Report 16 Feb 2016
Riccardo Asero, Ambulatorio di Allergologia, Clinica San Carlo, Milan, Italy 
Approved
VIEWS 5
I confirm that I have read this submission and believe that I have an ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Asero R. Reviewer Report For: Advances in Understanding and Managing Chronic Urticaria [version 1; peer review: 2 approved]. F1000Research 2016, 5(F1000 Faculty Rev):177 (https://doi.org/10.5256/f1000research.7807.r12468)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
Views
12
Cite
Reviewer Report 16 Feb 2016
Richard Warrington, Department of Medicine & Immunology, University of Manitoba, Winnipeg, MB, Canada 
Approved
VIEWS 12
I confirm that I have read this submission and believe that I have an ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Warrington R. Reviewer Report For: Advances in Understanding and Managing Chronic Urticaria [version 1; peer review: 2 approved]. F1000Research 2016, 5(F1000 Faculty Rev):177 (https://doi.org/10.5256/f1000research.7807.r12467)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.

Comments on this article Comments (0)

Version 1
VERSION 1 PUBLISHED 16 Feb 2016
Comment
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
Sign In
If you've forgotten your password, please enter your email address below and we'll send you instructions on how to reset your password.

The email address should be the one you originally registered with F1000.

Email address not valid, please try again

You registered with F1000 via Google, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Google account password, please click here.

You registered with F1000 via Facebook, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Facebook account password, please click here.

Code not correct, please try again
Email us for further assistance.
Server error, please try again.