Horton’s headaches, also known as trigeminal autonomic cephalgias (TACs), are classified as one of the most uncommon primary headaches, affecting a mere 0.1% of the population. The rarity of these headaches poses a challenge in comprehending the intricacies of their underlying mechanisms, making the study of this condition notably intricate. Despite their infrequency, Horton’s headaches are acknowledged as one of the most severe types of headaches, emphasizing the critical importance of their accurate identification and effective management.

Also referred to as Cluster headache AVF, Horton’s headaches manifest as unilateral headaches with a relatively short duration, ranging from 15 minutes to 3 hours. What sets them apart is their association with at least one autonomic symptom occurring on the same side as the headache. These autonomic symptoms include watery eyes, nasal congestion, conjunctival injection, or a sensation of auditory fullness. The interplay of these symptoms contributes to the distinct clinical profile of Horton’s headaches.

Nasal congestion is a notable feature of Horton’s headaches, and it can lead to misdiagnosis, often being confused with a “sinus headache.” Unfortunately, such misdiagnoses may result in ineffective treatments, as decongestants commonly prescribed for sinus headaches prove futile in alleviating the intensity of Horton’s headaches. A characteristic pattern emerges as these headaches occur either every other day or up to eight times a day. Additionally, they exhibit a specific temporal pattern, predominantly presenting during the night. The regularity of these headaches becomes evident, often at the same time each day.

An intriguing aspect of Horton’s headaches is their episodic nature. Most individuals experience daily episodes that persist for weeks or even months, creating a considerable impact on their daily lives. However, these intense phases are interspersed with prolonged periods of remission, providing some respite from the debilitating symptoms.

Given the severity and unique characteristics of Horton’s headaches, accurate diagnosis and appropriate management become paramount. The distinction between these headaches and other types, such as sinus headaches, is crucial to ensure effective therapeutic interventions. Healthcare professionals must be attentive to the specific autonomic symptoms accompanying these headaches, steering clear of potential misdiagnoses that could lead to ineffective treatments. As research endeavors continue to unravel the complexities of Horton’s headaches, enhancing our understanding of their mechanisms, the emphasis on timely and accurate identification remains fundamental for optimizing patient outcomes.

  1. Hypothalamic dysfunction: Horton’s headaches are thought to be associated with dysfunction of the suprachiasmatic nucleus of the hypothalamus, which is involved in the regulation of circadian rhythms.
  2. Vascular problems: Some researchers believe that Horton’s headaches may be linked to vascular problems, including the sudden dilation of blood vessels in the head.
  3. Release of chemicals: It is suggested that chemicals, such as serotonin, may be involved in triggering Horton’s headaches. Abnormal levels of these substances could cause blood vessels to constrict and cause severe pain.
  4. Genetic Factors: There is a familial tendency in some cases of Horton’s headache, suggesting a genetic component.
  5. Trigeminal Hypersensitivity: The trigeminal nerve, which is responsible for facial sensation, may be hypersensitive in people with Horton’s headaches.
Tension Headache Pattern: Characterized by a band-like pressure or tension around the forehead and temples, often described as a dull and persistent pain.
Migraine Pattern: Identified by intense, throbbing pain usually on one side of the head, accompanied by nausea, and sensitivity to light (photophobia) and sound (phonophobia).
Cluster Headache Pattern: Known for severe, burning or piercing pain around one eye, often associated with redness, tearing, and nasal congestion on the same side
  1. Sudden, intense pain: The main characteristic of Horton’s headaches is extremely intense, sudden pain, often described as a burning, stinging, or stabbing sensation. The pain is usually localized on one side of the head, around the eye, temple or forehead.
  2. Short duration of attacks: Horton’s headache attacks tend to be very short but very painful. Each episode can last from 15 minutes to three hours, although some individuals may experience several attacks in a day.
  3. Frequency of Attacks: Horton’s headaches can occur very regularly during a specific period of time, called the “cluster period.” During this time, people may have several seizures per day, often at specific times.
  4. Sensitivity to light and sound: During an attack, people with Horton’s headaches may be sensitive to light (photophobia) and sound (phonophobia).
  5. Restlessness or restlessness during attacks: Some people may feel restless or restless during a Horton’s headache attack, moving around frequently or actively expressing their pain.
  6. Symptoms associated with the affected side: The pain is usually localized to one side of the head, and symptoms such as redness or watering of the eye, runny nose, or nasal congestion on the affected side may also occur.

It is important to note that Horton’s headaches are a serious medical condition and require medical evaluation and management. If you suspect that you or someone you know is suffering from Horton’s headaches, consult a healthcare professional to get an accurate diagnosis and discuss treatment options.

The pathophysiology of Horton’s headache is not completely understood, but some hypotheses have been put forward to explain the mechanisms underlying this painful condition. Here are some aspects of the pathophysiology of Horton’s headaches:

  1. Hypothalamus: It is suggested that the suprachiasmatic nucleus of the hypothalamus, which is involved in the regulation of circadian rhythms, may play a central role in Horton’s headaches. Dysfunctions in the hypothalamus could contribute to the onset of seizures.
  2. Vascular dysregulation: Changes in blood circulation and vasomotor function have been observed during Horton’s headache attacks. Some researchers believe that abrupt changes in the caliber of blood vessels, particularly those located around the periorbital region, could contribute to the severe pain.
  3. Activation of the trigeminal nerve: The trigeminal nerve, which is responsible for facial sensation, may be involved in Horton’s headaches. Abnormal activation of this nerve could contribute to pain and associated symptoms, such as nasal congestion and watery eyes.
  4. Release of chemicals: Certain neurotransmitters and chemicals, such as serotonin, have been implicated in Horton’s headaches. Abnormal release of these substances could play a role in vasodilation and pain.
  5. Role of the immune system: There are indications that the immune system may be involved in Horton’s headaches. Inflammatory markers may be present, and some patients have shown a positive response to certain immunosuppressive medications.
  6. Genetic Factors: There is a familial trend in some cases of Horton’s headache, suggesting a possible genetic component in the predisposition to this condition.

The complexity of the pathophysiology of Horton’s headache requires continued research to better understand the underlying mechanisms. Advances in this area could lead to more targeted and effective treatments to relieve symptoms of this debilitating condition. It is important to note that the pathophysiology may vary between individuals, and the precise understanding of this condition may evolve over time as more research is conducted.

Here are some potential triggers:

  1. Alcohol: Consumption of alcohol, particularly beer, red wine or hard liquor, has been linked to triggering seizures in some people.
  2. Smoking: Smoking, especially regular smoking, is a potential risk factor.
  3. Heat: Some patients report that heat can trigger or worsen seizures.
  4. Physical activity: Intense physical exercise can trigger seizures in some people.
  5. Circadian rhythms: Horton’s headaches may be associated with disruptions in the circadian rhythm, and some people may be more likely to experience attacks at specific times of the day.
  6. Certain foods: Certain foods, such as foods high in histamine (aged cheeses, certain seafood, etc.), have been suggested as potential triggers.
  7. Stress: Although the link between stress and Horton’s headaches is unclear, stress can make symptoms worse in some people.

It is important to note that these triggers do not necessarily trigger attacks in all people with Horton’s headaches, and some individuals may not have obvious triggers. Everyone reacts differently, and it can be helpful to keep a seizure diary to identify individual triggers.

  1. Alcohol: Consumption of alcohol, particularly beer, red wine or hard liquor, has been linked to triggering seizures in some people.
  2. Smoking: Smoking, especially regular smoking, is a potential risk factor.
  3. Heat: Some patients report that heat can trigger or worsen seizures.
  4. Physical activity: Intense physical exercise can trigger seizures in some people.
  5. Circadian rhythms: Horton’s headaches may be associated with disruptions in the circadian rhythm, and some people may be more likely to experience attacks at specific times of the day.
  6. Certain foods: Certain foods, such as foods high in histamine (aged cheeses, certain seafood, etc.), have been suggested as potential triggers.
  7. Stress: Although the link between stress and Horton’s headaches is unclear, stress can make symptoms worse in some people.

The diagnostic criteria for cluster headache according to the International Classification of Headache Disorders, 3rd edition (ICHD-3) are as follows.

Diagnostic criteria:

  1. At least five painful attacks: The attacks must meet criteria B to D.
  2. Severe, one-sided headache attacks: Attacks usually occur around the eye or temple.
  3. Characteristics of pain: Pain has at least two of the following characteristics:
    • Reaches maximum intensity in just a few minutes.
    • The pain is throbbing or throbbing.
    • The pain is severe or unbearable in intensity.
  4. Frequency of attacks: The frequency of attacks is at least one every two days to eight per day.

Associated characteristics that may be present:

  • Conjunctival injection or tear: Possible presence on affected side.
  • Nasal congestion or runny nose: The nostril on the affected side may be congested or runny.
  • Eyelid Edema: The eyelid on the affected side may be edematous.
  • Forehead and facial sweat: The forehead and face on the affected side may be sweaty.
  • Restlessness or need to move: Often seen during seizures.

Note: Cluster headaches can be classified into two subtypes:

  • Episodic: Attacks occur in series (clusters) followed by periods of complete remission.
  • Chronic: Attacks occur without a complete remission period or with very short remission periods (less than 3 months).

These diagnostic criteria are intended to be evaluated by qualified healthcare professionals to confirm the diagnosis of cluster headaches. If you or someone you know is experiencing similar symptoms, it is recommended that you consult a healthcare professional for a proper evaluation.

Horton’s headaches, also known as cluster headaches, are among the most excruciating types of pain a person can experience. This neurological condition is characterized by severe, debilitating pain typically around one eye, with episodes lasting from minutes to hours. Here’s a glimpse into a typical day in the life of someone suffering from Horton’s headache.

Morning: A Brutal Awakening

The day often starts abruptly for those with Horton’s headaches. These headaches frequently occur during sleep, causing a sudden and painful awakening. The pain is described as a burning or piercing sensation, usually concentrated around one eye, accompanied by symptoms like redness, tearing, and nasal congestion on the same side.

After taking an abortive treatment, such as a triptan medication or inhaling pure oxygen, the person tries to fall back asleep. However, the fear of another attack can make sleep difficult to regain. For those who wake up without pain, the morning is marked by heightened alertness and mental preparation for the possibility of an attack.

Mid-Morning: Avoiding Triggers

The mid-morning period is critical for avoiding potential triggers. Horton’s headaches can be triggered by factors such as alcohol, certain foods (like chocolate or aged cheeses), strong odors, and even temperature changes. Morning routines are carefully designed to minimize exposure to these triggers.

In addition to preventive measures, people with Horton’s headaches often have to juggle work or family obligations. Concentrating on work can be a constant challenge, especially with the looming threat of an attack. Informed colleagues and family members can offer crucial support, but maintaining normal productivity remains difficult.

Afternoon: Managing the Attacks

Attacks can occur at any time of the day. When an attack strikes, the pain is so intense that the person is often incapacitated. These episodes typically last between 15 minutes and 3 hours, but the pain can be so unbearable that immediate intervention with specific treatments, such as high-flow oxygen or injectable medications, is necessary.

During an attack, the environment must be as quiet and dark as possible. The person may need to retreat to an isolated room to manage the pain. Relaxation techniques, such as deep breathing and meditation, can help, although their effectiveness varies from person to person.

Evening: Anticipating the Night

Evenings are a time for preparing for the night ahead. Horton’s headaches often follow regular cycles, making attacks somewhat predictable. The person may avoid known evening triggers, such as alcohol, and ensure that emergency treatments are readily accessible.

Sleep is crucial, but the fear of nighttime attacks can make falling asleep difficult. Some people find it helpful to sleep in a semi-upright position to reduce the frequency of attacks. Others adopt soothing rituals, such as reading or listening to soft music, to facilitate a more peaceful transition to sleep.

Conclusion: A Daily Struggle

Living with Horton’s headaches is a daily struggle marked by intense pain and constant adaptation. Every aspect of the day, from diet to sleep routines, is influenced by the need to avoid triggers and manage attacks. Despite these challenges, those with this condition develop incredible resilience and coping strategies to navigate their daily lives.

For those unfamiliar with this condition, understanding the challenges faced by people with Horton’s headaches can foster empathy and support. Recognizing the invisible pain and the strength required to manage it can help create a more compassionate and supportive environment for everyone.

Here are some aspects of osteopathy that could be considered in the context of Horton’s headache:

  1. Muscle release: The osteopath may use muscle release techniques to reduce tension in the muscles of the neck, shoulders and skull, which can contribute to intensified pain during a Horton’s headache attack.
  2. Improved blood circulation: Osteopathy techniques aimed at improving blood circulation can be used to promote vascular regulation in the skull region.
  3. Stress management: Certain osteopathic techniques can help reduce stress and general tension in the body, which can potentially have a positive impact on the frequency and severity of Horton’s headache attacks.

However, it is crucial to emphasize that osteopathy is not a cure for Horton’s headache. This condition requires thorough medical evaluation and management by healthcare professionals, often with specific medications to relieve pain and regulate episodes.

If you suffer from Horton’s headache, it is essential to consult a neurologist or qualified healthcare professional to obtain an accurate diagnosis and discuss appropriate treatment options.

Several studies have explored the effectiveness of osteopathic treatments for various types of headaches, including migraines and tension-type headaches. Although specific research on osteopathy for cluster headaches is limited, the results of related studies are promising:

Studies on migraines:

  • A 2011 study published in “The Journal of Headache and Pain” found that osteopathic manipulative treatment (OMT) significantly reduced the frequency and intensity of migraine attacks. The study, titled “Efficacy of osteopathic manipulative treatment of female patients with migraine: results of a randomized controlled trial,” was published in the Journal of Alternative and Complementary Medicine . It involved 42 participants, with 21 in the intervention group receiving OMT and 21 in the control group receiving no additional treatment beyond their usual medication. Results showed significant improvements in the intervention group in several domains of health-related quality of life, a reduction in pain intensity, and a decrease in the number of days affected by migraines. The control group did not show such significant improvements, supporting the potential benefits of OMT in managing migraines. ( Journal of Alternative and Complementary Medicine )
  • Another study from the same year, titled “Migraine without aura and osteopathic medicine, a non-pharmacological approach to pain and quality of life: open pilot study,” published in The Journal of Headache and Pain , also suggested that osteopathic manipulative treatment (OMT) has positive effects on reducing pain and improving quality of life for patients with migraine. This study involved patients with migraine without aura and evaluated the impact of OMT on pain and quality of life. The results showed a significant reduction in the intensity and frequency of migraine attacks in participants receiving OMT. Additionally, these patients reported an improvement in their overall quality of life, including aspects such as emotional and physical well-being. The researchers observed that OMT may help modulate the autonomic nervous system, improve blood flow, and correct musculoskeletal misalignments, which may contribute to the reduction of migraines. However, the study authors stressed the need for further research with larger samples and more robust methodologies to confirm these promising results and better understand the mechanisms of action of OMT in the treatment of migraines​ ( The Journal of Headache and Pain )

Tension-type headaches:

  • A study published in the European Journal of Pain in 2014 explored the effectiveness of osteopathic manipulative treatment (OMT) for tension-type headaches. This research found that OMT can relieve these headaches through muscle relaxation and improved blood flow. The study involved patients with chronic tension-type headaches (CTTH). Participants were divided into two groups: one group receiving OMT sessions and a control group treated with amitriptyline, a medication commonly used for chronic pain. The results showed that patients in the OMT group experienced significant reductions in pain intensity, headache frequency, and headache duration, compared to the control group. Specifically, pain intensity in the OMT group decreased from 4.9 to 3.1 on a 10-point scale, headache frequency decreased from 19.8 to 8.3 days per month, and headache duration was reduced from 10 to 6 hours. These improvements were statistically significant and suggest that OMT may be an effective treatment for tension-type headaches by improving head posture and reducing muscle tension. However, the study also highlighted the need for further research with larger sample sizes to confirm these findings and better understand the mechanisms underlying OMT’s effectiveness for this type of headache.​ ( Journal of Osteopathic Medicine )

In conclusion, osteopathy presents itself as a promising and holistic approach in the management of Horton’s headaches, also known as “cluster migraines”. By focusing on the structural and functional balance of the body, osteopaths aim to relieve pain, reduce the frequency of attacks and restore the overall well-being of patients.

Osteopathy is distinguished by its consideration of the patient’s posture, mobility and blood circulation to identify physical imbalances. The gentle manual techniques used in osteopathy aim to release muscle tension and joint restrictions, thereby helping to reduce pressure on nerves and blood vessels.

This approach not only treats local symptoms, but also focuses on identifying underlying factors such as stress and other lifestyle elements that could be contributing to headaches. By taking a holistic perspective, osteopathy offers a complementary alternative for those seeking non-invasive solutions in the management of these debilitating headaches.

Thus, osteopathy represents a promising avenue for providing relief to those suffering from Horton’s headaches, highlighting the importance of treating both symptoms and underlying causes for a comprehensive approach to neurovascular health.

  1. Drummond PD. Mechanisms of autonomic disturbance in the face during and between attacks of  cluster  headache . Cephalalgia. 2006 Jun;26(6):633-41. [ PubMed ]2.
  2. Hoffmann J, May A. Diagnosis, pathophysiology, and management of  cluster  headache . Lancet Neurol. 2018 Jan;17(1):75-83. [ PubMed ]3.
  3. Weaver-Agostoni J.  Cluster  headache . Am Fam Physician. 2013 Jul 15;88(2):122-8. [ PubMed ]4.
  4. Láinez MJ, Guillamón E.  Cluster  headache  and other TACs: Pathophysiology and neurostimulation options. Headache . 2017 Feb;57(2):327-335. [ PubMed ]5.
  5. Harder AVE, Winsvold BS, Noordam R, Vijfhuizen LS, Børte S, Kogelman LJA, de Boer I, Tronvik E, Rosendaal FR, Willems van Dijk K, O’Connor E, Fourier C, Thomas LF, Kristoffersen ES,  Cluster  Headache  Genetics Working Group. Fronczek R, Pozo-Rosich P, Jensen RH, Ferrari MD, Hansen TF, Zwart JA, Terwindt GM, van den Maagdenberg AMJM. Genetic Susceptibility Loci in Genomewide Association Study of  Cluster  Headache . Ann Neurol. 2021 Aug;90(2):203-216. [ PMC free article ] [ PubMed ]6.
  6. O’Connor E, Fourier C, Ran C, Sivakumar P, Liesecke F, Southgate L, Harder AVE, Vijfhuizen LS, Yip J, Giffin N, Silver N, Ahmed F, Hostettler IC, Davies B, Cader MZ, Simpson BS, Sullivan R, Efthymiou S, Adebimpe J, Quinn O, Campbell C, Cavalleri GL, Vikelis M, Kelderman T, Paemeleire K, Kilbride E, Grangeon L, Lagrata S, Danno D, Trembath R, Wood NW, Kockum I, Winsvold BS , Steinberg A, Sjöstrand C, Waldenlind E, Vandrovcova J, Houlden H, Matharu M, Belin AC. Genome-Wide Association Study Identifies Risk Loci for  Cluster  Headache . Ann Neurol. 2021 Aug;90(2):193-202. [ PubMed ]7.
  7. Shin YW, Park HJ, Shim JY, Oh MJ, Kim M. Seasonal Variation, Cranial Autonomic Symptoms, and Functional Disability in Migraine: A Questionnaire-Based Study in Tertiary Care. Headache . 2015 Sep;55(8):1112-23. [ PubMed ]8.
  8. Waldenlind E, Gustafsson SA, Ekbom K, Wetterberg L. Circadian secretion of cortisol and melatonin in  cluster  headache  during active  cluster  periods and remission. J Neurol Neurosurg Psychiatry. 1987 Feb;50(2):207-13. [ PMC free article ] [ PubMed ]9.
  9. Akerman S, Holland PR, Summ O, Lasalandra MP, Goadsby PJ. A translational in vivo model of trigeminal autonomic cephalalgias: therapeutic characterization. Brain. 2012 Dec;135(Pt 12):3664-75. [ PubMed ]10.
  10. Waung MW, Taylor A, Qualmann KJ, Burish MJ. Family History of  Cluster  Headache : A Systematic Review. JAMA Neurol. 2020 Jul 01;77(7):887-896. [ PMC free article ] [ PubMed ]11.
  11. Fischera M, Marziniak M, Gralow I, Evers S. The incidence and prevalence of  cluster  headache : a meta-analysis of population-based studies. Cephalalgia. 2008 Jun;28(6):614-8. [ PubMed ]12.
  12. Rozen TD. Cluster  Headache  Clinical Phenotypes: Tobacco Nonexposed (Never Smoker and No Parental Secondary Smoke Exposure as a Child) versus Tobacco-Exposed: Results from the United States  Cluster  Headache  Survey. Headache . 2018 May;58(5):688-699. [ PubMed ]13.
  13. Leone M, Russell MB, Rigamonti A, Attanasio A, Grazzi L, D’Amico D, Usai S, Bussone G. Increased familial risk of  cluster  headache . Neurology. 2001 May 08;56(9):1233-6. [ PubMed ]14.
  14. Barloese MCJ, Beske RP, Petersen AS, Haddock B, Lund N, Jensen RH. Episodic and Chronic  Cluster  Headache : Differences in Family History, Traumatic Head Injury, and Chronorisk. Headache . 2020 Mar;60(3):515-525. [ PubMed ]15.
  15. Drummond PD. Dysfunction of the sympathetic nervous system in  cluster  headache . Cephalalgia. 1988 Sep;8(3):181-6. [ PubMed ]16.
  16. Wilbrink LA, Louter MA, Teernstra OPM, van Zwet EW, Huygen FJPM, Haan J, Ferrari MD, Terwindt GM. Allodynia in  cluster  headache . Bread. 2017 Jun;158(6):1113-1117. [ PubMed ]17.
  17. Headache  Classification Committee of the International  Headache  Society (IHS) The International Classification of  Headache  Disorders, 3rd edition. Cephalalgia. 2018 Jan;38(1):1-211. [ PubMed ]18.
  18. Long RJ, Zhu YS, Wang AP. Cluster  headache  due to structural lesions: A systematic review of published cases. World J Clin Cases. 2021 May 16;9(14):3294-3307. [ PMC free article ] [ PubMed ]19.
  19. Grangeon L, O’Connor E, Danno D, Ngoc TMP, Cheema S, Tronvik E, Davagnanam I, Matharu M. Is pituitary MRI screening necessary in  cluster  headache ? Cephalalgia. 2021 Jun;41(7):779-788. [ PMC free article ] [ PubMed ]