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Epidemiology of Vasomotor Rhinitis
World Allergy Organization Journal volume 2, pages115–118(2009)
Vasomotor rhinitis is the most common form of nonallergic rhinitis, comprising approximately 71% of all nonallergic rhinitis conditions. Although the epidemiology of this subtype of nonallergic rhinitis has not been definitively studied, it is estimated that 14 million Americans suffer from vasomotor rhinitis, with a worldwide prevalence approaching 320 million.
vasomotor rhinitis (VMR) is a subtype of nonallergic rhinitis (NAR) that is unrelated to allergy, infection, structural lesions, systemic disease, or drug abuse. Because it is, by definition, an idiopathic form of rhinitis, a diagnosis can be made only when all other forms of rhinitis have been excluded. Determination of the epidemiology of VMR is confounded by numerous challenges as shown in Table 1. The first challenge in determining the epidemiology of VMR is gaining agreement on the definition of this form of rhinopathy. As with other forms of NAR, VMR is characterized by periodic or perennial symptoms of rhinitis that are not due to IgE-dependent events. A number of consensus statements have put forth definitions of VMR, the most recent being the report of the 2008 AAAAI Joint Task Force on Practice Parameters, The diagnosis and management of rhinitis: an updated practice parameter, which defines VMR (idiopathic rhinitis) as a "heterogeneous group of patients with chronic nasal symptoms that are not immunologic or infectious in origin and are usually not associated with nasal eosinophilia." The clinical characteristics of VMR are further elaborated in the article by Bernstein in this issue.
Because VMR is a diagnosis that essentially requires the exclusion of all other forms of rhinitis, an appropriately performed epidemiological study would require protocol incorporating a multitude of standardized tests to rule out all other forms of rhinitis. Appropriate testing might include those tests listed in Table 2. The article by Benniger et al, which will appear in the next issue of this journal, describes the proposed inclusion and exclusion criteria for research studies in nonallergic rhinopathy, including VMR, as agreed upon by the participants of this roundtable meeting (see "Consensus Review and Definition of Non-allergic Rhinitis With a Focus on Vasomotor Rhinitis, Proposed To Be Known Henceforth as Nonallergic Rhinopathy: Part 1. Introduction" in this Review Series issue for the listing of participants). To date, no prospective epidemiologic studies have applied such a protocol to evaluate a large population of rhinitis patients. Consequently, current estimates regarding the prevalence of VMR are fairly crude.
A literature search was performed using the following terms: vasomotor rhinitis, nonallergic rhinitis, idiopathic rhinitis, nonallergic noninfectious rhinitis, prevalence, and epidemiology. On the basis of this search and pertinent review articles, the reported prevalence rates of NAR and subtypes were compiled and the prevalence of VMR was extrapolated.
Relative prevalence rates of allergic rhinitis versus nonallergic rhinitis
Although no studies specifically designed to examine the epidemiology of NAR or VMR have been reported, 9 epidemiologic studies report data regarding the relative prevalence of NAR in comparison to that of AR (Table 3)[6–15]. Seven of the 9 studies employed skin testing with variable techniques (prick, intradermal, both, or undefined) to distinguish nonallergic rhinitis from allergic rhinitis. Studies that did not discount positive skin tests unsupported by history (all except Mullarkey et al) or that employed intradermal (or undefined) skin testing[6–9] are likely to have overestimated the prevalence of allergic rhinitis and underdiagnosed VMR. Two of the studies used either history alone or ICD9 (International Classification of Diseases, Ninth Revision) data to diagnose VMR, both of which are not well-established for diagnostic purposes[12, 14]. Because none of the studies assessed for the presence of local (nasal) IgE production, known as entopy, VMR may have been overdiagnosed in some cases.
Despite the fact that some of these studies were performed in allergy outpatient settings, which would be anticipated to skew the reported prevalence rates toward the diagnosis of AR, the findings are fairly consistent and independent of the setting performed. These 9 studies, when added in total, are heavily influenced by the enormity of the data from Schatz et al, but when analyzed independently of the Schatz data, they reveal a relative prevalence rate of 76% allergic and 24% nonallergic--closely approximating a 3:1 ratio.
Three studies were identified that attempted to systematically subtype NAR by performing testing that included, at a minimum, nasal examination, skin testing for sensitivity to specific aeroallergens, total IgE, nasal cytology, and sinus x-rays (Table 4)[6, 7, 16]. Each of these 3 studies has significant limitations. Symptoms were poorly characterized, irritant triggers were not captured, skin test techniques were variably defined, sinus imaging was limited to sinus x-rays (known to have limited value), and nasal examination data were not presented. However, each of these studies did include examination of nasal cytology (albeit with variable methodologies) in an attempt to screen out NARES or eosinophilic rhinosinustits.
The data from these 3 studies, when combined, total 200 NAR subjects. VMR was identified as the most common subtype, making up 71% of NAR diagnoses, with nonallergic rhinitis with eosinophilia syndrome (NARES) making up the majority of the remaining diagnoses (Table 5). The definitions of the NAR subtypes, VMR and NARES, used in each of the 3 studies differed slightly. Sex and age demographic data suggest a 2:1 female-to-male ratio and a higher mean age (40 years old) for VMR subjects as compared with that of allergic rhinitis subjects.
Estimated prevalence of nonallergic rhinitis in the United States and worldwide
The data from rhinitis epidemiology studies suggest that the ratio of AR prevalence (pure and mixed combined) to that of pure NAR is 3:1. This ratio can be extrapolated to determine a conservative estimate of the prevalence of NAR in the United States based on established prevalence rates of AR. If the assumption is made that 20% of the population suffers from AR, then on the basis of current population estimates for the United States of just more than 300 million, the US prevalence of AR is 60 million people. Applying the 3:1 (AR/NAR) ratio, approximately 20 million Americans would be expected to suffer from NAR (or approximately 7% of the total population). Given a current world population of 6.75 billion, similar extrapolation suggests that approximately 450 million people suffer from NAR worldwide. It is not known whether VMR is equally prevalent throughout the world and whether local weather (humidity), climate, air pollution, or genetic factors affect VMR prevalence.
Estimated prevalence of VMR in the United States and worldwide
The studies by Mullarkey, Enberg, and Settipane unanimously support VMR as the most common NAR subtype, making up approximately 71% of NAR diagnoses, with NARES making up the majority of the remaining NAR conditions. Applying the 71% frequency of VMR occurrence to the 20 million Americans who suffer from NAR, it would be estimated that VMR affects 14 million people in the United States. Applying the same frequency to the 450 million worldwide population suffering from NAR yields an estimate of a worldwide prevalence of VMR of 320 million.
Further characterization of VMR
VMR is often described as being characterized by nonallergic symptom triggers, including weather (changes in temperature or relative humidity), alcohol, tobacco smoke, dusts, automotive emission fumes, nonspecific irritant stimuli such as chlorine, and odors such as bleach, perfume, or solvents. Unfortunately, no epidemiologic data exist to further categorize VMR based on trigger type. Sex and age demographic data specific to VMR is limited, but can be extrapolated from NAR data, suggesting a female predominance and an older population for NAR than for AR[4–6, 8, 14]. However, the trend toward female predominance remains unproven; it is possible that a study selection bias may have resulted if, as suspected, more females than males entered studies because of an increased likelihood to seek rhinitis care.
Data regarding the prevalence of rhinitis, regardless of the type, are difficult to interpret. Contributing to this challenge is the observation that most population surveys have flawed designs. Because skin testing or determination of serum-specific IgE is infrequently assessed in large epidemiologic studies, allergic causation is often not accurately differentiated from nonallergic causation. However, on the basis of the data that has been reported, it is clear that VMR is, by far, the most common subtype of NAR with a significant burden of illness in the United States and worldwide.
Received grant/research support from GlaxoSmithKline (GSK), Sanofi-Aventis Pharmaceuticals, Meda Pharmaceuticals, and Alcon Laboratories. He is a consultant, or on an advisory board or the speakers bureau, for GlaxoSmithKline (GSK), Sanofi-Aventis Pharmaceuticals, and Alcon Laboratories.
Presented at a roundtable conference held in December 2008 in Washington, DC. The meeting was sponsored by the TREAT Foundation (Washington, DC) and supported through an unrestricted educational grant from Meda Pharmaceuticals. The funding company did not have any input into the development of the meeting or the series, and the company was not represented at the roundtable meeting.
Wallace DV, Dykewicz MS, Bernstein DI, Blessing-Moore J, Cox L, et al: Joint Task Force on Practice; American Academy of Allergy, Asthma & Immunology; American College of Allergy, Asthma and Immunology; Joint Council of Allergy, Asthma and Immunology. The diagnosis and management of rhinitis: an updated practice parameter. J Allergy Clin Immunol. 2008, 122 (2 Suppl): S1-S84.
Rondón C, Romero JJ, López S, Antúnez C, Martín-Casañez E, et al: Local IgE production and positive nasal provocation test in patients with persistent nonallergic rhinitis. J Allergy Clin Immunol. 2007, 119: 899-905. 10.1016/j.jaci.2007.01.006.
Bernstein J: Characteristics of nonallergic vasomotor rhinitis. World Allergy Org J. 2009, 2: 102-105. 10.1097/WOX.0b013e3181a8e389. [serial online]
Bernstein IL, Li JT, Bernstein DI, Hamilton R, Spector SL, et al: American Academy of Allergy, Asthma and Immunology; American College of Allergy, Asthma and Immunology. Allergy diagnostic testing: an updated practice parameter. Ann Allergy Asthma Immunol. 2008, 100 (3 Suppl 3): S1-148.
Benninger M, Kaliner M, Farrar J: Proposed inclusion/exclusion criteria for nonallergic rhinopathy. World Allergy Org J. 2009, 2 [serial online],
Mullarkey MF, Hill JS, Webb DR: Allergic and nonallergic rhinitis: their characterization with attention to the meaning of nasal eosinophilia. J Allergy Clin Immunol. 1980, 65: 122-126. 10.1016/0091-6749(80)90196-7.
Enberg RN: Perennial nonallergic rhinitis: a retrospective review. Ann Allergy. 1989, 63: 513-516.
Togias A: Age relationships and clinical features of nonallergic rhinitis. J Allergy Clin Immunol. 1990, 85: 182-
Settipane RA, Lieberman P: Update on non-allergic Rhinitis. Ann Allergy Asthma Immunol. 2001, 86: 494-507. 10.1016/S1081-1206(10)62896-7.
Leynaert B, Bousquet J, Neukirch C, Liard R, Neukirch F: Perennial rhinitis: an independent risk factor for asthma in nonatopic subjects. Results from the European Community Respiratory Health Survey. J Allergy Clin Immunol. 1999, 104: 301-304. 10.1016/S0091-6749(99)70370-2.
Settipane RA: Rhinitis: a dose of epidemiological reality. Allergy Asthma Proc. 2003, 24: 147-154.
Mercer MJ, van der Linde GP, Joubert G: Rhinitis (allergic and nonallergic) in an atopic pediatric referral population in the grass-lands of inland South Africa. Ann Allergy Asthma Immunol. 2002, 89: 503-512. 10.1016/S1081-1206(10)62089-3.
Bachert C, van Cauwenberge P, Olbrecht J, van Schoor J: Prevalence, classification and perception of allergic and nonallergic rhinitis in Belgium. Allergy. 2006, 61: 693-698. 10.1111/j.1398-9995.2006.01054.x.
Mølgaard E, Thomsen SF, Lund T, Pedersen L, Nolte H, Backer V: Differences between allergic and nonallergic rhinitis in a large sample of adolescents and adults. Allergy. 2007, 62: 1033-1037. 10.1111/j.1398-9995.2007.01355.x.
Schatz M, Zeiger RS, Chen W, Yang SJ, Corrao MA, Quinn VP: The burden of rhinitis in a managed care organization. Ann Allergy Asthma Immunol. 2008, 101: 240-247. 10.1016/S1081-1206(10)60488-7.
Settipane GA, Klein DE: Non allergic rhinitis: demography of eosinophils in nasal smear, blood total eosinophil counts and IgE levels. N Engl Reg Allergy Proc. 1985, 6: 363-366. 10.2500/108854185779109124.
Settipane RA, Charnock DR: Epidemiology of rhinitis: allergic and nonallergic. Clin Allergy Immunol. 2007, 19: 23-34.
U.S. and World Population Clocks - POPClocks [database online]. 2006, Washington, DC: Census Bureau, Population Division, Updated November 22, 2006. Available at: http://www.census.gov/main/www/popclock.html. Accessed January 03, 2009
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Settipane, R.A. Epidemiology of Vasomotor Rhinitis. World Allergy Organ J 2, 115–118 (2009). https://doi.org/10.1097/WOX.0b013e3181ac91ae
- vasomotor rhinitis
- nonallergic rhinopathy
- nonallergic rhinitis