Cholinergic urticaria explained
Cholinergic urticaria |
Symptoms: | Tiny "itchy" wheals and small papular bumps on a reddish background.[1] |
Causes: | Unclear (triggered by heat) |
Treatment: | Medications, sweat therapy |
Cholinergic urticaria or also known as (CholU) and CU, is a rare form of hives (urticaria) that is triggered by an elevation in body temperature, breaking a sweat, or exposure to heat. It is also sometimes called exercise-induced urticaria or heat hives. The condition is considered to be one of the many rarest forms of allergies known to medical science.[2]
Symptoms
Cholinergic urticaria typically presents with a number of small papular hives all over the body, that involve cutaneous inflammation (wheals) and severe nerve pain, which usually develops in response to exercise, bathing, staying in a heated environment, spicy foods, or emotional stress.[3] [4] The symptoms subside and manifest rapidly on and off throughout the day with no notice. Cholinergic urticaria may significantly impair quality of life, especially in relation to normal day to day activities. It is caused by an overreaction of the immune system to the release of histamine, mast cells, and other chemicals in response to the small nerve fibers throughout the body due to the increase in body temperature being allergic to sweat.[5]
Causes
Subtypes
Sweat hypersensitivity
This subtype of CU refers to those who are hypersensitive to their own sweat.
Diagnosis
Diagnosis is made by injecting autologous (the person's own) sweat into the skin.[6]
Features
The hives are observed to coincide with perspiration points of sweating.[7]
Pathophysiology
Tanaka et al. found that the sweat hyper-sensitivities of CU and atopic dermatitis seem to be virtually the same, and therefore, the sweat-induced histamine release from basophils may also be mediated by a specific IgE for sweat in atopic dermatitis as well as CU.[7]
Treatment
- Sweat Therapy: Forced perspiration by excessive body warming (sauna, hot bath, or exercise) used daily may reduce the symptoms through exhaustion of inflammatory mediators.[8]
- Antihistamines: are a commonly prescribed first-line treatment for conventional urticaria, but its effectiveness in the treatment of CU is rather limited in most cases.[9]
- Treatment(s) with mixed success: omalizumab (anti-IgE therapy),[10] [11] danazol (synthetic androgen),[12] propranolol (beta blocker),[13] [14] zileuton (antileukotriene).
- (Other) Proposed first-line treatment: Rapid desensitization protocol using autologous sweat.
Acquired anhidrosis and/or hypohidrosis
This subtype of CU refers to those who have abnormally reduced sweating. Forced perspiration by excessive body warming (hot bath or exercise) used daily may reduce the symptoms through exhaustion of inflammatory mediators.
Diagnosis
Sweat is readily visualized by a topical indicator such as iodinated starch or sodium alizarin sulphonate. Both undergo a dramatic colour change when moistened by sweat. A thermoregulatory sweat test evaluates the body's response to a thermal stimulus by inducing sweating through the use of a hot box ⁄ room, thermal blanket or exercise. Failure of the topical indicator to undergo a colour change during thermoregulatory sweat testing can indicate anhidrosis and/or hypohidrosis (see Minor test).[15]
A skin biopsy may reveal cellular infiltrates in sweat glands or ducts.[7]
Features
Severe heat intolerance (e.g., nausea, dizziness, and headache), and tingling, pricking, pinchy or burning pain over the entire body on exposure to hot environments or prolonged exercise which improve after cooling the body. Occurs in the absence of any causative skin, metabolic, or neurological disorders.[16]
Pathophysiology
[17] The wheals, hypohidrosis, and pain seems to result from the low expression levels of acetylcholinesterase (AchE) and cholinergic receptor, muscarinic 3 (CHRM3) in the eccrine gland epithelial cells.
Elevated expression levels of CCL2/MCP-1, CCL5/RANTES and CCL17/TARC which result in chemoattracted CD4+ and CD8+ T cell populations to the surrounding area may be responsible for exerting a downmodulatory effect on the AchE and CHRM3 expressions.
Corticosteroid inhibits the expressions of CCL2/MCP-1, CCL5/RANTES and CCL17/TARC. This further support the notion that CCL2/MCP-1, CCL5/RANTES and CCL17/TARC play a crucial role.
Treatment
- First-line treatment: H1RAs are first-line therapy for patients with CholU, but many patients show only a mild to moderate response to standard H1RA doses. The addition of an H2RA was reported to be effective in patients with refractory CholU that was unresponsive to up-dosing of an H1RA. Other studies have demonstrated the efficacy of scopolamine butylbromide (an anticholinergic agent); combinations of propranolol (a b2-adrenergic blocker), antihistamines, and montelukast; and treatment and injection with botulinum toxin. [18]
- Non-pharmacological treatment: In the absence of sweat, cold-water sprays and wet towels can be used to increase the evaporative loss of heat from the skin. Shifting to a cooler or air-conditioned environments when necessary can also reduce discomfort. In the event of severe hyperthermia (body temperature >106 °F/41 °C), drastic measures such as immersion in ice-cold water are necessary to prevent irreversible brain damage.[19]
Idiopathic
Unknown or unclassified at this time. This represents those who do not fall under any of the above categories.
Prevalence
Though overall research is limited, various studies indicate that CU is relatively common across populations with prevalence rates reportedly ranging from 5% to 20% (depending on locale, race, and age).[20] [21] [22] The condition is more common in young adults, and prevalence appears to peak in adults aged 26–28 (up to 20%).[20] The vast majority of cases are reported to be mild, and proportionally few individuals seek medical attention regarding the condition.
History
Cholinergic urticaria was first described by Duke[23] in 1924 as "urticaria calorica". The term cholinergic is derived from the finding that hives similar to those of CU can be evoked using cholinergic agonists (e.g. methacholine).
See also
Notes and References
- Book: James . William D. . Elston . Dirk . Treat . James R. . Rosenbach . Misha A. . Neuhaus . Isaac . Andrews' Diseases of the Skin: Clinical Dermatology . 2020 . Elsevier . 978-0-323-54753-6 . 151–152 . 13th . https://books.google.com/books?id=UEaEDwAAQBAJ&dq=Cholinergic+urticaria&pg=PA151 . en . 7. Erythema and urticaria.
- Web site: Do You Know These 8 Rare Allergies? . 2024-06-05 . Health . en.
- 10.1111/j.1365-2133.1968.tb11948.x . Moore-Robinson . M. . Warin . R. P. . Some clinical aspects of cholinergic urticaria . The British Journal of Dermatology . 80 . 12 . 794–799 . 1968 . 5706797. 58415911 .
- Hirschmann . J. V. . Lawlor . F. . English . J. S. . Louback . J. B. . Winkelmann . R. K. . Greaves . M. W. . Cholinergic urticaria. A clinical and histologic study . Archives of Dermatology . 123 . 4 . 462–467 . 1987 . 3827277 . 10.1001/archderm.1987.01660280064024.
- Poon . E. . Seed . P. T. . Greaves . M. W. . Kobza-Black . A. . 1999 . The extent and nature of disability in different urticarial conditions . The British Journal of Dermatology . 140 . 4 . 667–671 . 10.1046/j.1365-2133.1999.02767.x . 10233318 . 731524.
- Kozaru . T. . Fukunaga . A. . Taguchi . K. . Ogura . K. . Nagano . T. . Oka . M. . Horikawa . T. . Nishigori . C. . 10.2332/allergolint.10-OA-0269 . Rapid Desensitization with Autologous Sweat in Cholinergic Urticaria . Allergology International . 60 . 3 . 277–281 . 2011 . 21364312 . free .
- Bito . T. . Sawada . Y. . Tokura . Y. . Pathogenesis of cholinergic urticaria in relation to sweating . Allergology International . 61 . 4 . 539–544 . 2012 . 10.2332/allergolint.12-RAI-0485 . 23093795 . free .
- Kobayashi . H. . Aiba . S. . Yamagishi . T. . Tanita . M. . Hara . M. . Saito . H. . Tagami . H. . 2002 . Cholinergic urticaria, a new pathogenic concept: Hypohidrosis due to interference with the delivery of sweat to the skin surface . Dermatology . 204 . 3 . 173–178 . 10.1159/000057877 . 12037443 . 43259005.
- Nakamizo . S. . Egawa . G. . Miyachi . Y. . Kabashima . K. . 2012 . Cholinergic urticaria: Pathogenesis-based categorization and its treatment options . Journal of the European Academy of Dermatology and Venereology . 26 . 1 . 114–116 . 10.1111/j.1468-3083.2011.04017.x . 21371134 . 35802279. free .
- Metz . M. . Bergmann . P. . Zuberbier . T. . Maurer . M. . Successful treatment of cholinergic urticaria with anti-immunoglobulin E therapy . 10.1111/j.1398-9995.2007.01591.x . Allergy . 63 . 2 . 247–249 . 2008 . 18186820 . 8657377 .
- Sabroe . R. A. . Failure of omalizumab in cholinergic urticaria . 10.1111/j.1365-2230.2009.03748.x . Clinical and Experimental Dermatology . 35 . 4 . e127–e129 . 2010 . 19925484 . 37421783 .
- La Shell . M. S. . England . R. W. . Severe refractory cholinergic urticaria treated with danazol . Journal of Drugs in Dermatology . 5 . 7 . 664–667 . 2006 . 16865874.
- Pachor . M. L. . Lunardi . C. . Nicolis . F. . Cortina . P. . Accordini . C. . Marchi . G. . Corrocher . R. . De Sandre . G. . Usefulness of propranolol in the treatment of cholinergic urticaria . La Clinica Terapeutica . 120 . 3 . 205–210 . 1987 . 2973859.
- Ammann . P. . Surber . E. . Bertel . O. . Beta blocker therapy in cholinergic urticaria . The American Journal of Medicine . 107 . 2 . 191 . 1999 . 10460061 . 10.1016/S0002-9343(99)00038-8.
- Chia . K. Y. . Tey . H. L. . 10.1111/jdv.12014 . Approach to hypohidrosis . Journal of the European Academy of Dermatology and Venereology . 799–804. 2012 . 23094789 . 27 . 7 . 206038609 .
- Nakazato . Y. . Tamura . N. . Ohkuma . A. . Yoshimaru . K. . Shimazu . K. . Idiopathic pure sudomotor failure: Anhidrosis due to deficits in cholinergic transmission . Neurology . 63 . 8 . 1476–1480 . 2004 . 15505168 . 10.1212/01.wnl.0000142036.54112.57. 25029977 .
- Sawada . Y. . Nakamura . M. . Bito . T. . Sakabe . J. I. . Kabashima-Kubo . R. . Hino . R. . Kobayashi . M. . Tokura . Y. . Decreased Expression of Acetylcholine Esterase in Cholinergic Urticaria with Hypohidrosis or Anhidrosis . 10.1038/jid.2013.244 . Journal of Investigative Dermatology . 2013 . 23748235 . 134 . 1 . 276–9. free .
- doi=10.1007/s10286-017-0418-6
- Thami . G. P. . Kaur . S. . Kanwar . A. J. . Acquired idiopathic generalized anhidrosis: A rare cause of heat intolerance . Clinical and Experimental Dermatology . 28 . 3 . 262–264 . 2003 . 12780708 . 10.1046/j.1365-2230.2003.01208.x. 1547067 .
- 10.1016/S0190-9622(94)70267-5 . Zuberbier . T. . Althaus . C. . Chantraine-Hess . S. . Czarnetzki . B. M. . Prevalence of cholinergic urticaria in young adults . Journal of the American Academy of Dermatology . 31 . 6 . 978–981 . 1994 . 7962780.
- Silpa-Archa . N. . Kulthanan . K. . Pinkaew . S. . 10.1111/j.1468-3083.2010.03951.x . Physical urticaria: Prevalence, type and natural course in a tropical country . Journal of the European Academy of Dermatology and Venereology . 25 . 10 . 1194–1199 . 2011 . 21175877 . 23090828 .
- Godse . K. . Farooqui . S. . Nadkarni . N. . Patil . S. . Prevalence of cholinergic urticaria in Indian adults . 10.4103/2229-5178.105493 . Indian Dermatology Online Journal . 4 . 1 . 62–63 . 2013 . 23437429 . 3573461 . free .
- DDuke . W. W. . Urticaria Caused Specifically by the Action of Physical Agents . 10.1001/jama.1924.02660010007002 . JAMA: The Journal of the American Medical Association . 83 . 3–9 . 1924 .