Skip to main content
AAN.com
Articles
April 21, 2008

Prevalence and characteristics of allodynia in headache sufferers
A population study

April 22, 2008 issue
70 (17) 1525-1533

Abstract

Objective: The authors estimated the prevalence and severity of cutaneous allodynia (CA) in individuals with primary headaches from the general population.
Methods: We mailed questionnaires to a random sample of 24,000 headache sufferers previously identified from the population. The questionnaire included the validated Allodynia Symptom Checklist (ASC) as well as measures of headache features, disability, and comorbidities. We modeled allodynia as an outcome using headache diagnosis, frequency and severity of headaches, and disability as predictor variables in logistic regression. Covariates included demographic variables, comorbidities, use of preventive medication, and use of opioids.
Results: Complete surveys were returned by 16,573 individuals. The prevalence of CA of any severity (ASC score ≥3) varied with headache type. Prevalence was significantly higher in transformed migraine (TM, 68.3%) than in episodic migraine (63.2%, p < 0.01) and significantly elevated in both of these groups compared with probable migraine (42.6%), other chronic daily headaches (36.8%), and severe episodic tension-type headache (36.7%). The prevalence of severe CA (ASC score ≥9) was also highest in TM (28.5%) followed by migraine (20.4%), probable migraine (12.3%), other chronic daily headaches (6.2%), and severe episodic tension-type headache (5.1%). In the migraine and TM groups, prevalence of CA was higher in women and increased with disability score. Among migraineurs, CA increased with headache frequency and body mass index. In all groups, ASC scores were higher in individuals with major depression.
Conclusions: Cutaneous allodynia (CA) is more common and more severe in transformed migraine and migraine than in other primary headaches. Among migraineurs, CA is associated with female sex, headache frequency, increased body mass index, disability, and depression.

Get full access to this article

View all available purchase options and get full access to this article.

REFERENCES

1.
Woolf CJ, Wall PD. Relative effectiveness of C primary afferent fibers of different origins in evoking a prolonged facilitation of the flexor reflex in the rat. J Neurosci 1986;6:1433–1442.
2.
Sivilotti L, Woolf CJ. The contribution of GABAA and glycine receptors to central sensitization: disinhibition and touch-evoked allodynia in the spinal cord. J Neurophysiol 1994;72:169–179.
3.
Burstein R, Cutrer MF, Yarnitsky D. The development of cutaneous allodynia during a migraine attack clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine. Brain 2000;123:1703–1709.
4.
Sessle BJ, Hu JW, Amano N, Zhong G. Convergence of cutaneous, tooth pulp, visceral, neck and muscle afferents onto nociceptive and non-nociceptive neurones in trigeminal subnucleus caudalis (medullary dorsal horn) and its implications for referred pain. Pain 1986;27:219–235.
5.
Wolff HG, Tunis MM, Goodell H. Studies on migraine. Arch Intern Med 1953;92:478–484.
6.
Selby G, Lance JW. Observations on 500 cases of migraine and allied vascular headache. J Neurol Neurosurg Psychiatry 1960;23:23–32.
7.
Burstein R, Yarnitsky D, Goor-Aryeh I, et al. An association between migraine and cutaneous allodynia. Ann Neurol 2000;47:614–624.
8.
Burstein R, Collins B, Jakubowski M. Defeating migraine pain with triptans: a race against the development of cutaneous allodynia. Ann Neurol 2004;55:19–26.
9.
Bigal ME, Lipton RB. Modifiable risk factors for migraine progression. Headache 2006;46:1334–1343.
10.
Jakubowski M, Silberstein S, Ashkenazi A, Burstein R. Can allodynic migraine patients be identified interictally using a questionnaire? Neurology 2005;65:1419–1422.
11.
Lipton RB, Bigal ME, Burstein R, et al. Cutaneous allodynia in the migraine population. Ann Neurol Epub 2007 Dec 4.
12.
Lipton RB, Bigal ME, Diamond M, Freitag F, Reed ML, Stewart WF, AMPP Advisory Group. Migraine prevalence, disease burden, and the need for preventive therapy. Neurology 2007;68:343–349.
13.
Diamond S, Bigal ME, Silberstein S, Loder E, Reed M, Lipton RB. Patterns of diagnosis and acute and preventive treatment for migraine in the United States: results from the American Migraine Prevalence and Prevention Study. Headache 2007;47:355–363.
14.
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders, ed 2. Cephalgia 2004;24 (suppl 1):1–15.
15.
Silberstein SD, Lipton RB, Sliwinski M. Classification of daily and near-daily headaches: field trial of revised IHS criteria. Neurology 1996;47:871–875.
16.
Lipton RB, Diamond S, Reed M, Diamond ML, Stewart WF. Migraine diagnosis and treatment: results from the American Migraine Study II. Headache 2001;41:638–645.
17.
Liebestein M, Bigal ME, Sheftell FD, et al. Validation of the chronic daily headache questionnaire. Neurology 2007;68 (suppl 1):369.
18.
Stewart WF, Lipton RB, et al. Validity of the Migraine Disability Assessment (MIDAS) score in comparison to a diary-based measure in a population sample of migraine sufferers. Pain 2000;88:41–52.
19.
Spitzer RL, Williams JB, Kroenke K, et al. Utility of a new procedure for diagnosing mental disorders in primary care: the PRIME-MD 1000 study. JAMA 1994;272:1749–1756.
20.
Lipton RB, Stewart WF, Diamond S, et al. Prevalence and burden of migraine in the United States: data from the American Migraine Study II. Headache 2001;41:646–657.
21.
Lipton RB, Stewart WF, Simon D. Medical consultation for migraine: results from the American Migraine Study. Headache 1998;38:87–96.
22.
Bigal ME, Sheftell FD, Rapoport AM, et al. Chronic migraine is the early stage of transformed migraine in adults. Neurology 2005;65:1556–1561.
23.
Samejima F. Estimating latent ability using a pattern of graded scores. Psychometrika Monograph Supplement, No. 17. Richmond, VA: The William Byrd Press, 1969:14.
24.
Lipton RB, Pan J. Is migraine a progressive brain disease? JAMA 2004;291:493–494.
25.
Bigal ME, Lipton RB. When migraine progresses: transformed or chronic migraine. Expert Rev Neurother 2006;6:297–306.
26.
Scher AI, Stewart WF, Ricci JA, Lipton RB. Factors associated with the onset and remission of chronic daily headache in a population-based study. Pain 2003;106:81–89.
27.
Bigal ME, Lipton RB. Modifiable risk factors for migraine progression. Headache 2006;46:1334–1343.
28.
Poceta JS, Dalessio DJ. Identification and treatment of sleep apnea in patients with chronic headache. Headache 1995;35:586–589.
29.
Bigal ME, Lieberman JN, Lipton RB. Obesity and migraine. A population study. Neurology 2006;66:545–550.
30.
Bahra A, Matharu MS, Buchel C, Frackowiak RS, Goadsby PJ. Brainstem activation specific to migraine headache. Lancet 2001;357:1016–1017.
31.
Moskowitz MA, Macfarlane R. Neurovascular and molecular mechanisms in migraine headaches. Cerebrovasc Brain Metab Rev 1993;5:159–177.
32.
Hoheisel U, Mense S. Long-term changes in discharge behavior of cat dorsal horn neurones following noxious stimulation of deep tissues. Pain 1989:36:239–247.
33.
Burstein R, Yamamura H, Malick A, Strassman AM. Chemical stimulation of the intracranial dura induces enhanced responses to facial stimulation in brain stem trigeminal neurons. J Neurophysiol 1998;79:964–982.
34.
Welch KMA, Nagesh V, Aurora SK, Gelman N. Periaqueductal gray matter dysfunction in migraine: cause or the burden of illness? Headache 2001;41:629–637.
35.
Gazerani P, Andersen OK, Arendt-Nielsen L. A human experimental capsaicin model for trigeminal sensitization: gender-specific differences. Pain 2005;118:155–163.
36.
Sekine Y, Suzuki K, Ramachandran PV, Blackburn TP, Ashby Jr CR. Acute and repeated administration of fluoxetine, citalopram, and paroxetine significantly alters the activity of midbrain dopamine neurons in rats: an in vivo electrophysiological study. Synapse 2007;61:72–77.
37.
Matharu MS, Goadsby PJ. Functional brain imaging in hemicrania continua: implications for nosology and pathophysiology. Curr Pain Headache Rep 2005;9:281–288.
38.
Herishanu Y, Rogowski O, Polliack A, Marilus R. Leukocytosis in obese individuals: possible link in patients with unexplained persistent neutrophilia. Eur J Haematol 2006;76:516–520.
39.
Zelissen PM, Koppeschaar HP, Lips CJ, Hackeng WH. Calcitonin gene-related peptide in human obesity. Peptides 1991;12:861–863.
40.
Bigal ME, Liberman JN, Lipton RB. Age-dependent prevalence and clinical features of migraine. Neurology 2006;67:246–251.
41.
Hasselbalch SG, Madsen K, Svarer C, et al. Reduced 5-HT(2A) receptor binding in patients with mild cognitive impairment. Neurobiol Aging Epub 2007 Jun 1.
42.
Togsverd M, Werge TM, Tanko LB, et al. Association of a dopamine beta-hydroxylase gene variant with depression in elderly women possibly reflecting noradrenergic dysfunction. J Affect Disord Epub 2007 Aug 13.
43.
Gesztelyi G, Bereczki D. Disability is the major determinant of the severity of depressive symptoms in primary headaches but not in low back pain. Cephalalgia 2005;25:598–604.
44.
Dando WE, Branch MA, Maye JP. Headache disability in orofacial pain patients. Headache 2006;46:322–326.
45.
Bigal ME, Rapoport AM, Lipton RB, Tepper SJ, Sheftell FD. Assessment of migraine disability using the migraine disability assessment (MIDAS) questionnaire: a comparison of chronic migraine with episodic migraine. Headache 2003;43:336–342.

Information & Authors

Information

Published In

Neurology®
Volume 70Number 17April 22, 2008
Pages: 1525-1533
PubMed: 18427069

Publication History

Published online: April 21, 2008
Published in print: April 22, 2008

Permissions

Request permissions for this article.

Authors

Affiliations & Disclosures

M. E. Bigal, MD, PhD
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
S. Ashina, MD
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
R. Burstein
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
M. L. Reed, PhD
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
D. Buse, PhD
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
D. Serrano, MA
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
R. B. Lipton, MD
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.
On behalf of the AMPP Group
From the Departments of Neurology (M.E.B., S.A., D.B., R.B.L.) and Epidemiology and Population Health (R.B.L.), Albert Einstein College of Medicine, Bronx; The Montefiore Headache Center (M.E.B., R.B.L.), Bronx, NY; The New England Center for Headache (M.E.B.), Stamford, CT; Harvard Medical School (R.B.), Cambridge, MA; Vedanta Research (M.L.R., D.S.), Chapel Hill, NC; and Merck Research Laboratories (M.E.B.), Whitehouse Station, NJ.

Notes

Address correspondence and reprint requests to Dr. Marcelo E. Bigal, Global Director, Scientific Affairs, Neuroscience, One Merck Drive, P.O. Box 100, Whitehouse Station, NJ 08889-0100 [email protected]

Metrics & Citations

Metrics

Citation information is sourced from Crossref Cited-by service.

Citations

Download Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Select your manager software from the list below and click Download.

Cited By
  1. Neuroanatomy and neurophysiology of migraine, Migraine Pain Management, (21-33), (2025).https://doi.org/10.1016/B978-0-443-24705-7.00002-8
    Crossref
  2. Effectiveness of a Complementary Telehealth Education Program as a Preventive Treatment for Chronic Migraine: A Randomized Pilot Study, Journal of Clinical Medicine, 13, 22, (6825), (2024).https://doi.org/10.3390/jcm13226825
    Crossref
  3. SIRT1-regulated ROS generation activates NMDAR2B phosphorylation to promote central sensitization and allodynia in a male chronic migraine rat model, Frontiers in Molecular Neuroscience, 17, (2024).https://doi.org/10.3389/fnmol.2024.1387481
    Crossref
  4. The effectiveness and predictors influencing the outcome of onabotulinumtoxinA treatment in chronic migraine: understanding from diverse patient profiles in a single session, Frontiers in Neurology, 15, (2024).https://doi.org/10.3389/fneur.2024.1417303
    Crossref
  5. Diversity, Equity, and Inclusion in Headache Care and Research, CONTINUUM: Lifelong Learning in Neurology, 30, 2, (498-511), (2024).https://doi.org/10.1212/CON.0000000000001416
    Crossref
  6. Flexible modeling of headache frequency fluctuations in migraine with hidden Markov models, Headache: The Journal of Head and Face Pain, 65, 1, (132-142), (2024).https://doi.org/10.1111/head.14782
    Crossref
  7. Machine learning identifies factors most associated with seeking medical care for migraine: Results of the OVERCOME ( US ) study , Headache: The Journal of Head and Face Pain, 64, 8, (1027-1039), (2024).https://doi.org/10.1111/head.14729
    Crossref
  8. Novel insight into atogepant mechanisms of action in migraine prevention, Brain, 147, 8, (2884-2896), (2024).https://doi.org/10.1093/brain/awae062
    Crossref
  9. Meningeal brain borders and migraine headache genesis, Trends in Neurosciences, 47, 11, (918-932), (2024).https://doi.org/10.1016/j.tins.2024.08.012
    Crossref
  10. Healthcare disparities encountered by patients with headache disorders and potential mitigation strategies, Migraine Management, (569-582), (2024).https://doi.org/10.1016/B978-0-12-823357-3.00016-1
    Crossref
  11. See more
Loading...

View Options

Login options

Check if you have access through your login credentials or your institution to get full access on this article.

Personal login Institutional Login
Purchase Options

The neurology.org payment platform is currently offline. Our technical team is working as quickly as possible to restore service.

If you need immediate support or to place an order, please call or email customer service:

  • 1-800-638-3030 for U.S. customers - 8:30 - 7 pm ET (M-F)
  • 1-301-223-2300 for customers outside the U.S. - 8:30 - 7 pm ET (M-F)
  • [email protected]

We appreciate your patience during this time and apologize for any inconvenience.

View options

PDF and All Supplements

Download PDF and Supplementary Material

Full Text

View Full Text

Full Text HTML

View Full Text HTML

Figures

Tables

Media

Share

Share

Share article link

Share