Article Text


Platelet–leukocyte interaction and platelet activation in migraine: a link to ischemic stroke?
  1. J A Zeller,
  2. K Frahm,
  3. R Baron,
  4. R Stingele,
  5. G Deuschl
  1. Department of Neurology, Christian Albrechts University Kiel, Kiel, Germany
  1. Correspondence to:
 Dr J A Zeller
 Klinikum der Christian Albrechts Universität, Klinik für Neurologie, Niemannsweg 147, D-24105 Kiel, Germany;


Objectives: Migraine has been identified as an independent risk factor for ischemic stroke. Both neurogenic inflammation and platelet activation have been linked to the pathophysiology of migraine. Increased platelet activation results in up-regulation of specific binding to leukocytes which promotes pro-inflammatory leukocyte secretion and their tethering to endothelium, a mechanism that has been demonstrated in stroke and which could provide a link to migraine. We aimed to determine whether platelet–leukocyte aggregation is increased in migraine patients outside an acute attack.

Methods: Seventy two patients with migraine according to IHS criteria were compared to a control group (n = 72). Whole blood flow cytometry was used to quantify the activation dependent P selectin on the platelet, and to assess the fraction of platelets bound to the different leukocyte subsets.

Results: Migraine patients showed significantly more platelet–leukocyte aggregates compared to the control subjects (p = 0.003). This effect was driven by an increased polymorphonuclear cell–platelet aggregation (p = 0.003) whereas platelet aggregation with monocytes and lymphocytes was not. Platelet activation was also increased (p = 0.001).

Conclusions: In migraine pro-inflammatory platelet adhesion to leukocytes occurs during the headache free interval similar to that seen in acute coronary and cerebrovascular syndromes. This may suggest a link between migraine and stroke on a cellular level.

  • cell adhesion
  • ischemic stroke
  • migraine
  • platelet activation

Statistics from

In numerous epidemiological studies, migraine has been identified as an independent risk factor for cerebral ischaemia, particularly in young females (see Crassard1 for a review). A mechanism connecting the two disease entities has not yet been identified. For many years platelet dysfunction has been linked to the pathophysiology of migraine. Several investigators found indirect evidence for increased platelet activation during migraine attacks and the headache free period (see Kitano2 for reference). In addition, aggregometric studies suggested decreased platelet responsiveness after ex vivo stimulation,3,4 which has been attributed to an “exhaustion” of platelets following in vivo stimulation.

Platelet activation not only propagates mutual and endothelial adhesion and aggregation but also plays an important role in up-regulating inflammatory processes by interacting with leukocytes, especially monocytes and neutrophils.5–7 The intercellular binding is mediated mainly between the platelets’ activation dependent P selectin epitope and the P selectin glycoprotein ligand 1 (PSGL-1) on the leukocyte.8 This results in increased leukocyte superoxide anion and tumour necrosis factor production, enhanced endothelial adhesion and transendothelial migration, but also increased platelet mediated aggregation and thromboxane release.9 The important role of increased platelet activation and platelet–leukocyte interaction in the development of atherothrombotic disease has been reported in thrombocythemic patients,10 in the pathophysiology of ischemic stroke,11,12 and in symptomatic coronary disease.13–16

We hypothesised that if increased platelet activation and platelet–leukocyte interaction can also be measured in migraine patients during the headache free interval, this parallel with stroke patients would highlight a possible common pathophysiological pathway in both diseases, which may contribute to the epidemiological coincidence. Although the pathophysiology of migraine is known to include neurogenic inflammation with significant intercellular signalling, the cellular interaction between leukocytes and platelets in migraine has not been investigated.

To test our hypothesis we used flow cytometry to directly test on a cellular level whether migraine patients show up-regulated platelet leukocyte interaction in addition to increased baseline platelet activation.



The study group consisted of 72 patients who sequentially attended the Kiel headache outpatient clinic with confirmed diagnosis of migraine according to IHS criteria17 and were willing to give written informed consent. The study was approved by the university’s ethics committee. Forty eight patients suffered from migraine without aura and 24 from migraine with aura; none of the patients had a history of myocardial infarction or stroke. The mean age of migraine patients was 45.6 years (standard deviation (SD) 12.4). Fifty nine patients (82%) were female, and of these 36 (61%) were premenopausal. The mean age in the control group was 43.9 years (SD 18.3) and 56% were female. In the patient group nobody reported a history of cerebral ischaemia, and one patient had one episode of suspected angina without cardiac findings in the subsequent diagnostic investigation. Three patients mentioned intermittent cardiac arrhythmia which needed no specific treatment. Two patients were diabetic without insulin treatment. Seven of the patients were smoking regularly as opposed to six members of the control group. At the time of blood sampling, 29 patients (40.3%) were taking β blockers as a single prophylactic agent, 13 (18%) were on β blockers and amitriptyline, three on a combination of β blocker and cyclandelat, and two on cyclandelat only. Twenty four patients (33.3%) were taking no medication at all. One case remained unclear with regard to drug prophylaxis. The control group consisted of volunteers from medical staff and patients who were all free from migraine or other forms of chronic or remitting headache, history of cardiac or cerebrovascular disease, diabetes, and acute infection. Both patients and controls had been free from acetylsalicylic acid or other non steroidal antiflammatory drugs for at least 2 weeks, and nobody in the control group was taking tricyclic antidepressants.


Venous blood was drawn from an antecubital vein between 10 a.m. and 1 p.m., anticoagulated with 3.8% sodium citrate and processed after 10 min of resting time without further manipulation. Blood samples were kept at body temperature at all times. For the flow cytometric assays, we used direct fluorescent markers (all commercially available; Coulter Immunotech, Krefeld, Germany). Whole blood was diluted 1:10 with warmed HEPES buffer and two aliquots of 50 μl were incubated with CD 61-PE (an activation independent subunit of the GP IIb/IIIa complex) to immunologically identify all platelets. Simultaneously, in a one step procedure, the sample for measuring platelet activation was stained with anti CD 62-P. The other sample was double stained with the panleukocytic marker CD 45 to identify leukocytes. After incubation for 5 min, the process was stopped using cold buffer, immediately followed by flow cytometry.

Platelets were identified by their size and granulation properties using forward/sideward scatter and staining with the panthrombocytic marker CD 61-PE. By double gating of CD 45 positivity, forward and sideward scatter properties we discriminated between leukocyte subsets. Then the double fluorescent particles positive for both the leukocytic CD 45 and platelet CD 61 epitope were counted as platelet–leukocyte aggregates and platelet–leukocyte subset aggregates, respectively. Since red cells are not specifically stained and unspecific fluorescence is far below detection threshold, it is not necessary in this assay to perform red cell lysis, thus avoiding further artefacts. Measurements were performed with an Epics XL cytometer (Coulter Immunotech, Krefeld, Germany). This assay is an established procedure in various academic institutions in our country and has been in routine use in our laboratory for the 3 years prior to this investigation.

Statistical analysis

All values are expressed as means (SD). The Mann–Whitney U test was used to compare groups, and p<0.05 was considered significant in two tailed tests.


A total of 72 migraine patients (59 women and 13 men) were included in this study. Two thirds of the patients suffered from migraine without aura and one third from migraine with aura, a ratio commonly seen in the distribution of migraine subtypes in specialised clinics. Within the patient group there were no significant differences regarding age or sex distribution. Since we deliberately examined migraine patients outside an acute attack, none of the subjects had experienced headaches in the 24 h prior to blood sampling. Nineteen of the 72 patients (26%) reported a migraine attack 1–3 days prior to the investigation, and 17 had used an oral or subcutaneous triptane. Recent migraine attack and triptane intake did not differ statistically between both migraine groups. In the control group (as in control groups in previous studies), there was no gender difference regarding platelet–leukocyte adhesion or platelet activation. Thus we regarded the gender mismatch between controls and migraine patients as insignificant.

Platelet–leukocyte aggregation

Migraine patients showed a significantly increased number of platelet–leukocyte aggregates (5.70% v 3.89% in controls, p = 0.003). This was due to the increased proportion of platelets aggregating with polymorphonuclear cells (7.26% v 4.98%, p = 0.002; table 1). Aggregation of platelets with monocytes and lymphocytes was, although raised, not significantly increased in this sample size. Analysis of age dependency (two groups above and below the 50th percentile) and of the influence of prophylactic medication (47 with, 24 without) revealed no statistical difference.

Table 1

 Platelet–leukocyte aggregates (percent of platelet population (SD)) and platelet activation (mean fluorescence in arbitrary units(SD))

Platelet activation

During the headache free interval investigated here, migraine patients expressed more of the activation dependent platelet epitope P selectin compared to the control subjects (1.41 (0.22) arbitrary units, p = 0.001; table 1). This was mainly influenced by the highly significant (1.42 (0.21), p<0.001) difference in patients suffering from migraine without aura; in those affected by migraine with aura the difference failed to reach significance in our sample (1.39 (0.23), p = 0.082). As seen with aggregation, values were not age or drug dependent.


This study represents the first investigation of intercellular communication between platelets and leukocytes in migraine patients. The hypothesised significant increase in intercellular platelet–leukocyte interaction does exist in migraine patients similar to that seen in many patients with acute or early post-acute cerebral ischaemia. In addition, those without aura have a higher baseline of platelet activation compared to controls.

Platelet activation has been investigated before by measuring plasma levels of the platelet secretion products or urinary platelet metabolites.2,18–20 Using a photometric technique, whole blood flow cytometry, the externalisation of activation dependent platelet epitopes can be quantified on a cell to cell level in an automated procedure. In this way, dilution effects in the whole body plasma compartment and possible artefacts by metabolic processes can be avoided. We use P selectin antibodies which quantify the surface expression of the CD 62P epitope (P selectin) on the platelet. This alpha granule protein is externalised on to the platelet surface during platelet activation. The epitope has been shown to be a reliable activation marker in cardiac and neurovascular patients.11,16,21 Also, direct detection of both leukocyte and platelet specific cell properties allows immediate ex vivo identification of aggregates without further artefact prone immunostaining and microscopy.

Cytometric measurement of activation dependent platelet epitopes aims directly at the platelets’ cellular surface with very little ex vivo manipulation, and is less prone to artefacts. The observation of augmented platelet activation in migraine patients confirms previous reports that used indirect methods. We suggest that enhanced platelet activation in migraine patients is a marker of the inflammatory process in the trigeminovascular system and cellular interaction rather than a precipitating factor in migraine pathogenesis.

As regards isolated lymphocyte properties, altered white cell function in migraine has been reported: both a significant rise in CD3+ (T lymphocyte) CD16+56+ (natural killer lymphocytes) classified lymphocytes in migraine without aura patients outside an attack were seen22 as well as raised B lymphocyte counts and decreased CD8 (T suppresser) positive lymphocytes in migraine patients when compared to controls.23 Empl et al24 described an increased CD4 (T helper) count in patients with migraine with or without aura compared to controls. In addition they found significantly higher proportions of integrin high expressing T helper cells in subjects with migraine without aura compared to migraine with aura.

Using this method, our results do not support lymphocytic reaction with memory cells, which represents a longer standing process of inflammation indicative of immunological activation in migraine patients, but acute phase leukocyte subsets (as seen by the increased neutrophil fraction attached to platelets). This suggests that even during the quiescent phase increased inflammatory signalling occurs. This may involve kinins like interferons and tumour necrosis factor and soluble adhesion molecules25 which lead in a partly self-propagating process to direct intercellular interaction among different subsets of leukocytes and between leukocytes and platelets.

Increased platelet–leukocyte adhesion has also been described in patients at risk of reocclusion after coronary stenting13 and in patients with unstable angina14; this could be reduced by blockage of the activation dependent platelet GP IIb/IIIa receptor.15

This observation of increased intercellular communication in both cardiovascular disease and migraine may provide a direct link to ischemic stroke for which migraine has been proven to be an independent risk factor, particularly in premenopausal women.26–32 In a recent review of migraine, haemostasis, and ischemic stroke in young women,1 the authors found it impossible to conclude from previous trials how migraine and cerebral ischaemia are connected because of contradicting results and conflicting techniques. Likewise, studies on the incidence of antiphospholipid antibodies or prothrombotic genetic risk factors (mainly factor V Leiden and prothrombin mutation) in migraine patients were not promising, particularly since the latter are known to mainly affect venous system thrombosis, hence not a platelet initiated mechanism. However, it seems reasonable to study risk factors for increased platelet aggregability in the light of previous reports of patients with essential thrombocythaemia and migraine whose symptoms were reduced by antiplatelet therapy.33 Additional data suggest a preventive effect of aspirin alone or in combination with dipyridamole on migraine recurrence.35–37

We strongly support this approach: patients with acute ischemic stroke of large vessel but not of cardiac origin show increased platelet activation11 and, particularly following infections, increased leukocyte–platelet aggregates.12 The role of this intercellular communication is still subject to research: possible explanations include a causative model where infection via platelet and leukocyte activation triggers thrombus formation as well as post-thrombotic processes where platelet stimulated leukocyte activation adds to excitotoxic substance release. Increased platelet activation in essential thrombocythaemia leading to stroke has also been reported.38 These coincidences of altered platelet function in migraine patients, as reported here, and those suffering from stroke, myocardial infarction, and thrombocythaemia are promising links that should be further pursued. Although primary platelet dysfunction as an initiator for migraine is unlikely, the increased activation and leukocyte, namely neutrophil, aggregation constitute a prothrombotic risk that eventually may lead to ischemic stroke. It must also be considered that inflammation and infection itself have been proven to be independent risk factors of ischemic stroke.39–41

In migraine pro-inflammatory platelet adhesion to leukocytes occurs during the headache free interval similar to that seen in acute coronary and cerebrovascular syndromes. This may suggest a link between migraine and stroke on a cellular level. Studies with correlation of this haemostasiological parameter to other indicators of altered coagulation biochemistry in migraine patients and comparisons between migraine patients with and without stroke, and subgroup analysis of data from stroke prevention trials on the efficacy of antiplatelet therapy in migraine patients will aid the understanding of underlying mechanisms and the deduction of possible prophylactic concepts.


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  • Competing interests: none declared

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