Abstract
Objective: The aim of this scoping review was to identify if the phase of the menstrual cycle was considered in observational studies comparing pressure pain sensitivity between women with migraine or tension-type headache (TTH) and headache-free women. Methods: A systematic electronic literature search in PubMed, Medline, Web of Science, Scopus, and CINAHL databases was conducted. Observational studies including one or more groups with TTH and/or migraine comparing pressure pain thresholds (PPTs) were included. The methodological quality (risk of bias) was assessed with the Newcastle-Ottawa Scale. Authors, objectives, inclusion/exclusion criteria, size sample, female sample, tool to assess PPTs, mean age, and the use of any medication were extracted and analyzed independently by two authors. Results: From a total of 1404 and 1832 identified articles for TTH and migraine, 30 and 18 studies satisfied the criteria and were included. Nineteen (63.4%) studies assessing TTH patients and eleven (61.1%) assessing migraine patients showed a high risk of bias. The most common flaws were attributed to improper selection of control and control over other additional factors. Based on the systematic review, just one study including TTH and one including migraine patients considered the menstrual cycle. Conclusion: The results of this scoping review identified that the phase of the menstrual cycle has been rarely considered in studies investigating sensitivity to pressure pain in primary headaches, such as TTH or migraine, although there is evidence showing the relevance of the phase of the menstrual cycle in pain perception.
1. Introduction
Headache is a condition ranked among the top ten causes of disability-adjusted-life-years (DALYs) [1]. Migraine and tension-type headache are probably the most prevalent primary headaches. Tension-type headache (TTH) is the second most prevalent disorder worldwide [2]. Similarly, migraine has been ranked the third-highest cause of disability worldwide in both genders under the age of 50 years [3]. Both headaches feature the presence of pressure pain hyperalgesia [4,5]. This assumption is based on the results from several studies investigating sensitivity to pressure pain in both TTH [5,6,7,8,9,10,11] and migraine [12,13,14,15]. Additionally, migraine is also characterized by an increased sensitivity to visual or auditory stimulus during but also outside of the headache attack [4,16].
It is suggested that the menstrual cycle influences pain sensitivity [17]. During the luteal phase, the estrogen levels decrease and the levels of progesterone increase. In the luteal phase, pain thresholds are higher than in the follicular phase and during the menstruation [18]. In addition, pain inhibition is also higher during the ovulatory phase as compared to the menstrual and luteal phases [19]. Higher concentrations of progesterone decrease sensory neurotransmission since GABAergic tone is higher during the luteal phase and declines prior to the menstrual bleeding [20,21]. The role of the GABAergic system involves reducing the neuronal excitability of the nervous system [20,21]. Therefore, since the menstrual cycle affects pain sensitivity, studies investigating pressure hyperalgesia in primary headaches, such as migraine and TTH, should consider this “status”. For instance, studies comparing pain sensitivity between women with TTH or migraine and headache-free women should assess all participating women in the same phase of the cycle (e.g., menstruation-bleeding, luteal phase, ovulation, or follicular phase) to decrease the influence of the menstrual cycle on pain sensitivity between the comparisons. This is highly relevant since both TTH and migraine are more prevalent in women and gender differences are commonly seen [22,23].
No review has previously investigated if studies investigating pressure pain sensitivity in women with migraine or TTH have systematically considered the menstrual cycle. Therefore, the objective of this scoping review was to identify if the phase of the menstrual cycle was considered in observational studies comparing pressure pain sensitivity between women with migraine or TTH and headache-free women.
2. Materials and Methods
This scoping review was conducted following The Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews (PRISMA-ScR) [24]. It was prospectively registered on the Open Science Framework Registry with the identifier DOI 10.17605/OSF.IO/SAFPQ and the link https://osf.io/r4uak (accessed on 18 December 2020).
2.1. Identify the Research Question
The main research question of the current scoping review was: Is the menstrual cycle taken into consideration in observational studies comparing pressure pain hyper-sensitivity between women with TTH or migraine and headache-free women?
With the aim of providing the most updated data, we considered any phase of the menstrual cycle (e.g., menstruation-bleeding, luteal phase, ovulation, or follicular phase) in women with regular or irregular cycles, in premenopausal women, and those with hormonal use.
2.2. Identify Relevant Studies
A systematic literature search was conducted with no data limitation to 31 December 2020 in the following electronic databases: PubMed, Medline, Web of Science, Scopus, and CINAHL. The database literature search was conducted by two different researchers (FCM, DPRdS). In case of disagreement, a third researcher (FAS) participated in the decision. The search strategy for TTH is shown in Table 1 and for migraine in Table 2.
Table 1.
Search Strategy for Tension-Type Headache Studies.
Table 2.
Search Strategy for Migraine Studies.
2.3. Study Selection
This review used the PCC mnemonic (population, concept, and context) to define the inclusion criteria [25].
Population: Adult women (aged >18 years) diagnosed with TTH or migraine according to any edition of International Headache Society (IHS) criteria [26,27,28,29].
Concept: Comparison of pressure pain thresholds (PPT) between women with TTH or migraine and headache-free women.
Context: Observational studies including one or more groups with primary headache, such as TTH and/or migraine. Systematic reviews, narrative reviews, and meta-analyses or clinical trials were excluded.
Articles identified from the different databases were independently reviewed by two authors (FCM, DPRdS) with the assistance of the StArt program (copyright_version) designed by Federal University of Sao Carlos (Brazil). Authors were required to achieve a consensus on the included trials. In the case of discrepancy between the reviewers, a third author (CFdlP) decided the final inclusion or exclusion of the study.
2.4. Inclusion Criteria
- (1)
- A group of women (age >18 years) diagnosed with TTH or migraine according to the IHS criteria. Studies including both women and men were also included but the main analysis, obviously, considered just the female group.
- (2)
- A control group of healthy women without history of headache.
- (3)
- Full text report published in Spanish or English as a journal article.
- (4)
- Pressure pain sensitivity evaluated with PPTs assessed with a pressure algometer or dynamometer as the primary outcome.
2.5. Exclusion Criteria
- (1)
- Studies assessing pain sensitivity with manual palpation or with other outcomes rather than an algometer (e.g., Von-Frey monofilament).
- (2)
- Experimental-induced pain models (healthy subjects receiving a hypertonic saline injection or similar) of TTH or migraine.
- (3)
- In those studies, evaluating different quantitative sensory tests, such as thermal or electrical pain thresholds, only PPTs measured with an algometer or dynamometer were included.
2.6. Data Charting Process
Data extraction was conducted using the Mendeley Desktop program. A data chart-ing form was developed for this scoping review to identify the variables that correspond with the research question. Data were extracted independently by two authors (FCM, DPRdS) using a data charting form, including title, authors, objectives, inclusion and exclusion criteria, size sample, size female sample, recruitment process, tool to assess PPT, average age of sample, and the use of any medication. Two researchers (FCM, DPRdS) completed the chart data and had to achieve a consensus on every item. In case of disagreement, a third researcher (FAS) participated in the decision to reach a resolution.
2.7. Methodological Quality
We used the Newcastle-Ottawa Scale, a star rating system, for evaluating the quality and the risk of bias of observational studies included in the review. The Newcastle-Ottawa Scale for case control studies consists of three items: selection (with 4 sections), comparability (1 section), and exposure (3 sections). Every section is formed by 2, 3, or 4 options and some of them are awarded a star if that criterion is clearly satisfied. The maximum score is nine stars. A score ≥7 stars means a study with low risk of bias [30].
3. Results
3.1. Study Selection
The initial search for TTH revealed a total of 1404 identified articles. After removing duplicates (n = 634), 770 were initially screened. A total of 611 studies were excluded after reading the title and another 116 after reading the abstract since they were not directly related to pressure pain sensitivity in TTH. After reading the full-text of the remaining 43 studies, the last 13 were excluded because: results were not provided by TTH or migraine [31,32,33,34], text did not provide the required data [35], they were experimental-induced pain models [36,37,38], it was written in Korean [39], results were not separated by gender [40,41,42], or PPT was not assessed with an algometer or dynamometer [43]. Finally, 30 studies satisfied all inclusion criteria and were included in the review of TTH (Figure 1) [6,7,8,9,10,11,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67].
Figure 1.
TTH process. PRISMA Extension for Scoping Reviews (PRISMA-ScR) flow diagram.
The initial search for migraine revealed a total of 1832 identified articles. After removing duplicates (n = 1003), 829 were initially screened. A total of 666 studies were excluded after reading the title and another 136 after reading the abstract since they were not directly related to pressure pain sensitivity in migraine. After reading full-text of the remaining 27 studies, another nine were excluded because: results were not divided into TTH or migraine [31,32,34], text did not include the required data [68], it was an experimental-induced pain model [36], results were not separated by gender [69,70], PPT was not assessed with algometer or dynamometer [43], or due to the absence of IHS criteria [71]. Finally, 18 studies satisfied all inclusion criteria and were included in the review of migraine (Figure 2) [7,12,13,14,15,52,55,60,63,66,72,73,74,75,76,77,78,79].
Figure 2.
Migraine process. PRISMA Extension for Scoping Reviews (PRISMA-ScR) flow diagram.
3.2. Study Characteristics
Table 3 summarizes the characteristics of the studies investigating pressure pain sensitivity in women with TTH. The total sample of patients with TTH included in the studies was 1525 (986 women, 64.6%). A large number of women (≥50% of the sample) participated in the majority of the studies (n = 27, 93.34%) [6,8,9,10,11,23,44,45,46,47,48,50,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66], except for just three where more males than females participated [48,51,67]. Six articles only recruited women [8,9,10,11,44,61]. The mean age of the sample was 38.8 years (SD 9.15, range from 18 to 76 years). Most of the selected studies used a pressure algometer, except for two studies using a dynamometer [9,62]. A headache diary [80] was used in fourteen articles to confirm the diagnosis of TTH or collect the clinical features of headache [10,11,15,44,45,47,48,49,50,51,53,54,64,65].
Table 3.
Characteristics of studies including women with tension-type headache (TTH).
Patients with TTH were recruited from specific headache centres [64], random sampling from the general population [55,66], Danish Civil Registration [67], university centres or student population [9,44,45,46], advertisements in local media or newspapers [6,10,45,47,58,63], regular hospitals [9,11,48,49,50,51,56], outpatient clinics [52,53,54,57,59,65], tertiary care hospital [8], and university centres of ageing [63].
In nineteen (63.34%) studies, patients were asked for avoiding taking medication such analgesics or muscle relaxants 24–48 h before examination [7,9,10,11,44,45,46,47,48,49,50,51,52,53,58,59,60,61,63,64]. The remaining eleven (36.7%) did not take into account medication during the assessment procedure [6,8,54,55,56,57,62,63,65,66,67].
Table 4 summarizes the characteristics of the studies investigating pressure pain sensitivity in women with migraine. The total sample was 1000 patients with migraine (771 women, 77.1%). More women participated in the majority of these studies, except for one of them in which the same number of females and males participated [75]. Five articles only recruited women with migraine [12,13,14,15,73].
Table 4.
Characteristics of studies including women with migraine.
The average age of the sample with migraine was 39.7 with an SD of 8.77 years. Most of the selected studies used the pressure algometer, except for some of them reporting the use of dynamometer [14,73]. A diagnostic headache diary over two or four weeks [80] was not used in any study of migraine.
The recruitment process of the patients with migraine was done from tertiary hospitals [14,15,72], outpatient clinics [52,73], hospitals [75,77], pain clinics [79], advertisements at universities or local newspapers [63,74,78,79], university centres of ageing [63], random sample population [55,66], and social media such as Facebook [78,79].
Several studies excluded patients who had taken medication, such as analgesics or muscle relaxants, 24–48 h before examination [7,12,13,14,15,52,60,72,73,74,75,77,78,79], except for four in which this consideration was not taken into account [55,63,66,76]. Garrigós-Pedrón et al. [77] permitted the use of abortive pharmacological treatment during the assessment.
3.3. Methodological Quality
Table 5 shows the Newcastle-Ottawa Scale on each TTH study included in the review. A total of 19 (63.4%) studies showed a high risk of bias and the remaining 11 (36.7%) had aa low risk of bias according to the Newcastle-Ottawa Scale. The most common flaws were a failure to observe proper selection of controls and to control for other additional factors (Figure 3).
Table 5.
Risk of bias (the Newcastle-Ottawa Scale) of the included tension-type headache (TTH) studies.
Figure 3.
Percentage of assigned stars in tension-type headache (TTH) studies.
Table 6 shows the Newcastle-Ottawa Scale on each migraine study included in the review. A total of 11 (61.1%) studies showed a high risk of bias and the remaining seven (38.9%) had a low risk of bias according to the Newcastle-Ottawa Scale. The most common flaw was a failure to properly select controls (Figure 4).
Table 6.
Risk of bias (the Newcastle-Ottawa Scale) of the included studies in including women with migraine.
Figure 4.
Percentage of assigned stars in migraine studies.
3.4. Consideration of Menstrual Cycle
The days since the last menstruation were just recorded in one of the thirty studies (3.3%) investigating pressure pain sensitivity in TTH [47]. No other data of menstrual information were recorded in any other study. Importantly, the lack of consideration of the menstrual cycle was not considered as a limitation in any of the articles. Engstrom et al. collected the days since last menstruation in both women with and without TTH [47]. Twenty TTH patients (11 females) and 29 controls (15 females), comparable for age and sex, were included in this study. In the control group, the average number days since menstrual cycle was 16.7 (SD 9.2) days, whereas in the TTH group it was 11.3 (6.4) days. Menstrual data were not compared or associated with any other feature. Nothing else related with menstrual cycle was reported [47].
Similarly, the number of days since last menstruation were only recorded in one study including women with migraine, interestingly conducted by the same group [74]. In this case, two studies recognized that not recording the menstrual aspect was considered as a limitation [77,78]. In addition, Garridos-Pedrón et al. also considered as a limitation not reporting oral contraceptive use of the female participants [77]. Engstrom et al. [74] collected data about the number of days since last menstruation in controls (mean: 18.9 days, SD: 8.6 days), interictal migraine (mean: 14.2, SD: 7.6 days), preictal migraine (mean: 15.0, SD: 13.9 days), and postictal migraine (mean: 13.8, SD: 10.1 days) moments. Again, this menstrual data were not compared or associated with anything and no further data related with menstrual cycle were provided.
Interestingly, Strupf et al. included four patients (20% of their total sample size) with menstrual migraine [79], whereas Sales Pinto et al. included women with menstrual migraine associated with another primary headache [13]. Neither study considered the moment of the menstrual cycle in their assessments.
4. Discussion
4.1. Findings
This scoping review aimed to identify if the phase (menstruation-bleeding, luteal phase, ovulation, or follicular phase) of the menstrual cycle was considered as a cofounder factor in studies investigating pressure pain sensitivity between patients with TTH or migraine and healthy controls. The results of this review identified that the phase of the menstrual cycle has not been consistently considered in studies published to date investigating sensitivity to pressure pain in primary headaches, such as TTH or migraine, although evidence supports a potential relevance of the menstrual cycle in pain perception [17,18,81]. Only one study including individuals with TTH [47] and one including migraine patients [74] considered it relevant to include data about the last day since menstruation (but without specifying more data about this). However, these data were not compared or associated with anything else in these studies.
Similarly, an interesting finding was that just two studies including women with migraine considered the lack of menstrual information as a limitation [77,78]. Considering that more women are included in studies investigating primary headache, menstruation could be an important factor influencing pain sensitivity. We do not currently know if differences between women with migraine or TTH and headache-free women are due to “pain status” or influenced by a “menstrual status”. For instance, if headache patients are assessed in a follicular phase or other of the menstrual cycle, whereas control women are assessed during menstruation, ovulation, or a different phase of the menstrual cycle, between-group differences observed in PPTs can be related to the headache status (headache or control) but also to the menstrual cycle. In fact, this would be highly important in studies investigating pain sensitivity in women with chronic migraine, since menstrual-cycle disorders and dysmenorrhea are more prevalent in this population [82]. Future studies comparing women with migraine or TTH (no menstrual migraine) and healthy women should consider this and evaluate all participants, either patients or controls, in the same phase of the menstrual cycle and if differences between patients and controls are different depending on the phase of the menstrual cycle. This could be highly relevant since the menstrual cycle exhibits cyclic variations with an increased pain sensitivity during menstruation, suggesting that females could have lower PPTs during luteal and ovulation phases due to low levels of progesterone [81].
In fact, it has been already considered that females and males could have comparable detection thresholds for cold pain and ischemic pain while PPTs could be lower in females than males [83]. Similarly, Teepker et al. found that conditioned pain modulation inhibition neither differed between women with migraine and healthy women nor varied over the menstrual cycle [84].
4.2. Strengths and Limitations
The result from this scoping review should be extrapolated according to its strengths and limitations. The first strength was the use of different databases to avoid limiting the search and to include all articles fulfilling eligibility criteria. The second strength was the inclusion of studies without a limit date of publication. Third, we systematically evaluated all studies for determining the risk of bias and the inclusion of phase of menstrual cycle as a factor for being considered in PPT assessments. Among the limitations, although we included a total of 30 studies with TTH and 18 with migraine, almost 60% of the studies exhibited high risk of bias. Secondly, most studies were cross-sectional and no longitudinal studies investigating the time course of PPT have been conducted. Finally, the sample size of some of the studies was small, although this limitation does not restrict the extrapolation of our results in relation to the consideration of the phase of the menstrual cycle. In fact, the lack of information in relation to the investigated topic permits to determine different research lines for future studies.
4.3. Reliability and Validity of Pressure Pain Thresholds
Pressure pain threshold (PPT) is a static measure of pain reflecting the basal state of pain perception in relation to the pressure experienced a patient [85]. In fact, PPT is one of the quantitative sensory tests most commonly used for characterization of TTH [5] and migraine [4]. Nevertheless, its reliability and validity are controversial. Several studies reported good to excellent intra- and inter-rater reliability (intraclass correlation coefficient (ICC) > 0.70) when PPT are assessed on healthy subjects [86] or in individuals with different pain conditions [87,88]. Most studies calculate PPT as the mean of three consecutive trials assessed on the same point. However, evidence suggests that scores obtained at the first assessment are usually significantly higher than the two succeeding ones [89]. If this difference reaches 50kPa, it is recommended to conduct a fourth measurement and discard the highest value, although this is a recommendation not justified by evidence. More recent studies suggest that two measurements reduces the measurement error and presents excellent reliability (ICC ranging from 0.80 to 0.97) [90,91]. Most studies included in this scoping review conducted three measurements and calculated the means, but they did not calculate their internal reliability of PPT assessments. Therefore, results should be considered with caution. It would be recommended that futures studies comparing pressure sensitivity between women with headache and headache-free women calculate their own reliability data.
Another important topic is to determine if differences between headache patients and controls are clinically relevant and should be considered real. This is a topic of current debate since minimal detectable change (MDC) for PPT depends on the area of assessment and the population. For instance, Mailloux et al. 2021 [91] reported that the MDC for PPT ranged from 28.71 to 50.56 kPa in healthy subjects in the lumbar spine and the upper extremity. Walton et al. 2011 [87] found an MDC of 42.7 kPa for the cervical spine and of 86.3kPa for the tibialis anterior in asymptomatic subjects. In headache patients, Romero-Morales et al. [59] determined that a difference of 16.18kPa in the temporalis muscle and of 78.94kPa within the upper trapezius could be considered as real difference between people with TTH and headache-free subjects. Therefore, the comparison of pressure pain hyperalgesia between women with TTH or migraine against headache-free women should be accounted for according to these considerations.
This discussion increases in relevance when, in addition, considering the phase of the menstrual cycle, since some between-group variations could be related to the fact that two participating women are in a different phase of the cycle. Nevertheless, as will be discussed in the next section, studies determining the time course of pressure pain sensitivity throughout the different phases of the menstrual cycle are clearly needed. According to available data on MDC, the variations observed in PPTs between the different phases of the menstrual cycle should range between 50kPa and 100kPa depending on the area of assessment for determining real differences in sensitivity to pressure pain during the different phases of the menstrual cycle.
4.4. Future Research Directions
This review highlights the lack of information regarding consideration of the phase of the menstrual cycle in studies comparing pressure pain sensitivity between women with primary headaches, such as TTH or migraine, and healthy women and opens several questions for future research. First, further studies are needed to systematically determine if pain sensitivity is different throughout the different phases, e.g., menstruation-bleeding, luteal phase, ovulation, or follicular phase, of the menstrual cycle in both healthy women and women with headaches. In such a scenario, proper determination of the phase of the menstrual cycle when women are assessed will be highly important. For instance, determining the phase of the cycle by monitoring follicular development with ultrasound and measurement of estrogen/progestin blood measurements would be of high importance. With that information, future studies assessing pain sensitivity in women with migraine or TTH should evaluate all participants in the same phase of the menstrual cycle for avoiding an effect of this cofounder factor.
Similarly, medication intake of analgesics or muscle relaxants modifies pain perception as assessed with PPTs. In fact, a high proportion of studies included in this scoping review excluded patients who had taken analgesics or muscle relaxants 24–48 h before examination. However, regular consumption was not regularly controlled in most studies. This cofounder factor should be also considered in future studies. In such a scenario, another aspect to consider would be the use of hormonal contraception. Although the use of oral contraceptives is associated with an increased migraine intensity (at least at the end of menstruation), no effects on detection and pain thresholds has been observed in a small sample of migraineurs [81]. We believe that the differences in pain sensitivity in this group of women using any type of contraception may require separate studies.
Similarly, another subgroup of women to be considered is those with menstrual migraine. A review of studies applying neurophysiological procedures to test pain-related changes during the menstrual cycle in women with menstrual migraine found a fluctuation of the central modulation of pain across the menstrual phases, with a prevalence of excitatory versus inhibitory control in the premenstrual period [17]. Therefore, we do not know if the effect of menstrual cycle would be similar in this group of patients.
5. Conclusions
This scoping review found that observational studies examining sensitivity to pressure pain in women with TTH or migraine did not consistently consider the phase of the menstrual cycle, suggesting that the influence of menstrual cycle phase in observational studies on headache may likely be underestimated. Consequently, ignoring the effects of this cofounder factor may result in differences in PPTs between these primary headaches and healthy controls that could be related to the phase of the menstrual cycle and not just to the patient condition. Future studies investigating pressure pain sensitivity in TTH or migraine should consider the phase of the menstrual cycle in their evaluations.
Author Contributions
Conceptualization, F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; methodology, F.C.-M., F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; software, all authors; validation, all authors.; formal analysis, F.C.-M., F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; investigation, F.C.-M., F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; resources, F.C.-M., F.A.-S., and D.P.R.-d.-S.; data curation, all authors.; writing—original draft preparation, F.C.-M. and D.P.R.-d.-S.; writing—review and editing, F.C.-M., F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; visualization, F.C.-M., F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; supervision, F.A.-S., D.P.R.-d.-S., and C.F.-d.-l.-P.; project administration, C.F.-d.-l.-P. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Data Availability Statement
The data presented in this study are available on request from the corresponding author.
Conflicts of Interest
The authors declare no conflict of interest.
References
- GBD 2019 Diseases and Injuries Collaborators. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet 2020, 396, 1204–1222. [Google Scholar] [CrossRef]
- Global Burden of Disease Study 2013 Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: A systematic analysis for the Global Burden of Disease Study 2013. Lancet 2013, 386, 743–800. [Google Scholar] [CrossRef] [Green Version]
- Steiner, T.J.; Stovner, L.J.; Vos, T. GBD 2015: Migraine is the third cause of disability in under 50s. J. Headache Pain 2016, 17, 104. [Google Scholar] [CrossRef] [Green Version]
- Nahman-Averbuch, H.; Shefi, T.; Schneider, V.J.; Li, D.; Ding, L.; King, C.D.; Coghill, R.C. Quantitative sensory testing in patients with migraine: A systemic review and meta-analysis. Pain 2018, 159, 1202–1223. [Google Scholar] [CrossRef]
- Fernández-de-las-Peñas, C.; Plaza-Manzano, G.; Navarro-Santana, M.J.; Olesen, J.; Jensen, R.H.; Bendtsen, L. Evidence of localized and widespread pressure pain hypersensitivity in patients with tension-type headache: A systematic review and meta-analysis. Cephalalgia 2020, 41, 256–273. [Google Scholar] [CrossRef]
- Malo-Urriés, M.; Estébanez-de-Miguel, E.; Bueno-Gracia, E.; Tricás-Moreno, J.M.; Santos-Lasaosa, S.; Hidalgo-García, C. Sensory function in headache: A comparative study among patients with cluster headache, migraine, tension-type headache, and asymptomatic subjects. Neurol. Sci. 2020, 41, 2801–2810. [Google Scholar] [CrossRef] [PubMed]
- Bovim, G. Cervicogenic headache, migraine, and tension-type headache. Pressure-pain threshold measurements. Pain 1992, 51, 169–173. [Google Scholar] [CrossRef]
- Palacios Ceña, M.; Castaldo, M.; Kelun, W.; Torelli, P.; Pillastrini, P.; Fernández-de-las-Peñas, C.; Arendt-Nielsen, L. Widespread pressure pain hypersensitivity is similar in women with frequent episodic and chronic tension-type headache: A blinded case–control study. Headache 2016, 57, 217–225. [Google Scholar] [CrossRef]
- De Cássia Correia Kälberer Pires, R.; Salles da Rocha, N.; Esteves, J.E.; Rodrigues, M.E. Use of pressure dynamometer in the assessment of the pressure pain threshold in trigger points in the craniocervical muscles in women with unilateral migraine and tension-type headache: An observational study. Int. J. Osteopath. Med. 2017, 26, 28–35. [Google Scholar] [CrossRef]
- Fernández-De-Las-Peñas, C.; Ge, H.Y.; Cuadrado, M.L.; Madeleine, P.; Pareja, J.A.; Arendt-Nielsen, L. Bilateral pressure pain sensitivity mapping of the temporalis muscle in chronic tension-type headache. Headache 2008, 48, 1067–1075. [Google Scholar] [CrossRef]
- Fernández-De-Las-Peñas, C.; Madeleine, P.; Caminero, A.B.; Cuadrado, M.L.; Arendt-Nielsen, L.; Pareja, J.A. Generalized neck-shoulder hyperalgesia in chronic tension-type headache and unilateral migraine assessed by pressure pain sensitivity topographical maps of the trapezius muscle. Cephalalgia 2010, 30, 77–86. [Google Scholar] [CrossRef] [PubMed]
- Fernández-De-Las-Peñas, C.; Madeleine, P.; Cuadrado, M.L.; Ge, H.Y.; Arendt-Nielsen, L.; Pareja, J.A. Pressure pain sensitivity mapping of the temporalis muscle revealed bilateral pressure hyperalgesia in patients with strictly unilateral migraine. Cephalalgia 2009, 29, 670–676. [Google Scholar] [CrossRef] [PubMed]
- Sales Pinto, L.M.; Freitas de Carvalho, J.J.; Cunha, C.; dos Santos Silva, R.; Fiamengui-Filho, J.F.; Rodrigues Conti, P.C. Influence of myofascial pain on the pressure pain threshold of masticatory muscles in women with migraine. Clin. J. Pain 2013, 29, 362–365. [Google Scholar] [CrossRef]
- Florencio, L.L.; Giantomassi, M.C.M.; Carvalho, G.F.; Gonçalves, M.C.; Dach, F.; Fernández-de-las-Peñas, C.; Bevilaqua-Grossi, D. Generalized pressure pain hypersensitivity in the cervical muscles in women with migraine. Pain Med. 2015, 16, 1629–1634. [Google Scholar] [CrossRef] [Green Version]
- Palacios-Ceña, M.; Florencio, L.L.; Ferracini, G.N.; Barón, J.; Guerrero, Á.L.; Ordás-Bandera, C.; Arendt-Nielsen, L.; Fernández-de-las-Peñas, C. Women with chronic and episodic migraine exhibit similar widespread pressure pain sensitivity. Pain Med. 2016, 17, 2127–2133. [Google Scholar] [CrossRef] [Green Version]
- Coppola, G.; Di Lorenzo, C.; Schoenen, J.; Pierelli, F. Habituation and sensitization in primary headaches. J. Headache Pain 2013, 14, 65. [Google Scholar] [CrossRef]
- De Tommaso, M. Pain perception during menstrual cycle. Curr. Pain Headache Rep. 2011, 15, 400–406. [Google Scholar] [CrossRef]
- Alves, B.; Ibuki, F.; Gonçalves, A.S.; Teixeira, M.J.; Siqueira, S.R.D.T. Influence of sexual hormones on neural orofacial perception. Pain Med. 2017, 18, 1549–1556. [Google Scholar] [CrossRef] [PubMed]
- Tousignant-Laflamme, Y.; Marchand, S. Excitatory and inhibitory pain mechanisms during the menstrual cycle in healthy women. Pain 2009, 146, 47–55. [Google Scholar] [CrossRef]
- Martin, V.T. Ovarian hormones and pain response: A review of clinical and basic science studies. Gend. Med. 2009, 6, 168–192. [Google Scholar] [CrossRef] [PubMed]
- Limmroth, V.; Lee, W.S.; Moskowitz, M.A. GABAA-receptor-mediated effects of progesterone, its ring-A-reduced metabolites and synthetic neuroactive steroids on neurogenic oedema in the rat meninges. Br. J. Pharmacol. 1996, 117, 99–104. [Google Scholar] [CrossRef] [Green Version]
- Palacios-Ceña, D.; Albaladejo-Vicente, R.; Hernández-Barrera, V.; Lima-Florencio, L.; Fernández-de-Las-Peñas, C.; Jimenez-Garcia, R.; López-de-Andrés, A.; de Miguel-Diez, J.; Perez-Farinos, N. Female gender is associated with a higher prevalence of chronic neck pain, chronic low back pain, and migraine: Results of the Spanish National Health Survey, 2017. Pain Med. 2021, 22, 382–395. [Google Scholar] [CrossRef]
- Fuensalida-Novo, S.; Jiménez-Antona, C.; Benito-González, E.; Cigarán-Méndez, M.; Parás-Bravo, P.; Fernández-De-Las-Peñas, C. Current perspectives on sex differences in tension-type headache. Expert Rev. Neurother. 2020, 20, 659–666. [Google Scholar] [CrossRef] [PubMed]
- Tricco, A.C.; Lillie, E.; Zarin, W.; O’Brien, K.K.; Colquhoun, H.; Levac, D.; Moher, D.; Peters, M.D.J.; Horsley, T.; Weeks, L.; et al. PRISMA extension for scoping reviews (PRISMA-ScR): Checklist and explanation. Ann. Intern. Med. 2018, 169, 467–473. [Google Scholar] [CrossRef] [Green Version]
- Peters, M.D.J. In no uncertain terms: The importance of a defined objective in scoping reviews. JBI Database Syst. Rev. Implement. Reports 2016, 14, 1–4. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders: 2nd edition. Cephalalgia 2004, 24, 9–160.
- Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition. Cephalalgia 2018, 38, 1–211. [CrossRef] [PubMed]
- Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache Classification Committee of the International Headache Society. Cephalalgia 1988, 1–96.
- The International Classification of Headache Disorders, 3rd edition (beta version). Cephalalgia 2013, 33, 629–808. [CrossRef] [PubMed] [Green Version]
- Wells, G.; Shea, B.; O’Connell, D.; Peterson, J.; Welch, V.; Losos, M.; Tugwell, P. The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomized Studies in Meta-Analyses. Available online: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed on 11 November 2020).
- Ashina, S.; Bendtsen, L.; Buse, D.C.; Lyngberg, A.C.; Lipton, R.B.; Jensen, R. Neuroticism, depression and pain perception in migraine and tension-type headache. Acta Neurol. Scand. 2017, 136, 470–476. [Google Scholar] [CrossRef]
- Ashina, S.; Lipton, R.B.; Bendtsen, L.; Hajiyeva, N.; Buse, D.C.; Lyngberg, A.C.; Jensen, R. Increased pain sensitivity in migraine and tension-type headache coexistent with low back pain: A cross-sectional population study. Eur. J. Pain 2018, 22, 904–914. [Google Scholar] [CrossRef]
- Hylleraas, S.; Male Davidsen, E.; Saltyte Benth, J.; Gulbrandsen, P.; Dietrichs, E. The usefulness of testing head and neck muscle tenderness and neck mobility in acute headache patients. Funct. Neurol. 2010, 25, 27–31. [Google Scholar] [PubMed]
- Sand, T.; Zwart, J.A.; Heide, G.; Bovim, G. The reproducibility of cephalic pain pressure thresholds in control subjects and headache patients. Cephalalgia 1997, 17, 748–755. [Google Scholar] [CrossRef] [PubMed]
- Göbel, H.; Weigle, L.; Christiani, K. Headache characteristics in patients with tension-type headache in relationship to pericranial muscle pain sensitivity. Cephalalgia 1991, 11, 79–80. [Google Scholar] [CrossRef]
- Göbel, H.; Weigle, L.; Kropp, P.; Soyka, D. Pain sensitivity and pain reactivity of pericranial muscles in migraine and tension-type headache. Cephalalgia 1992, 12, 142–151. [Google Scholar] [CrossRef] [PubMed]
- Lipchik, G.; Holroyd, K.; O’Donnell, F.; Cordingley, G.; Waller, S.; Labus, J.; Davis, M.; French, D. Exteroceptive suppression periods and pericranial muscle tenderness in chronic tension-type headache: Effects of psychopathology, chronicity and disability. Cephalalgia 2000, 20, 638–646. [Google Scholar] [CrossRef]
- Neufeld, J.D.; Holroyd, K.A.; Lipchik, G.L. Dynamic assessment of abnormalities in central pain transmission and modulation in tension-type headache sufferers. Headache 2000, 40, 142–151. [Google Scholar] [CrossRef]
- Kim, M.-J.; Kang, W.-C.; Hong, K.-E. Analysis of the change of the pressure pain threshold in chronic tension-type headache and control. J. Korean Inst. Herb. Acupunct. 2009, 12, 41–50. [Google Scholar] [CrossRef]
- Kim, H.S.; Chung, S.C.; Kim, Y.K.; Lee, S.W. Pain-pressure threshold in the head and neck region of episodic tension-type headache patients. J. Orofac. Pain 1995, 9, 357–364. [Google Scholar]
- Drummond, P.D. Scalp tenderness and sensitivity to pain in migraine and tension headache. Headache J. Head Face Pain 1987, 27, 45–50. [Google Scholar] [CrossRef]
- Jensen, R.; Rasmussen, B.K. Muscular disorders in tension-type headache. Cephalalgia 1996, 16, 97–103. [Google Scholar] [CrossRef]
- Sandrini, G.; Proietti Cecchini, A.; Milanov, I.; Tassorelli, C.; Buzzi, M.G.; Nappi, G. Electrophysiological evidence for trigeminal neuron sensitization in patients with migraine. Neurosci. Lett. 2002, 317, 135–138. [Google Scholar] [CrossRef]
- Caamaño-Barrios, L.H.; Galan-Del-Rıo, F.; Fernandez-De-las-Peñas, C.; Plaza-Manzano, G.; Arendt-Nielsen, L.; Ortega-Santiago, R. Widespread pressure pain sensitivity over nerve trunk areas in women with frequent episodic tension-type headache as a sign of central sensitization. Pain Med. 2019, 21, 1408–1414. [Google Scholar] [CrossRef]
- Cathcart, S.; Pritchard, D. Daily stress and pain sensitivity in chronic tension-type headache sufferers. Stress Health 2008, 24, 123–127. [Google Scholar] [CrossRef]
- Drummond, P.D.; Knudsen, L. Central pain modulation and scalp tenderness in frequent episodic tension-type headache. Headache 2011, 51, 375–383. [Google Scholar] [CrossRef] [PubMed]
- Engstrøm, M.; Hagen, K.; Bjørk, M.; Stovner, L.J.; Stjern, M.; Sand, T. Sleep quality, arousal and pain thresholds in tension-type headache: A blinded controlled polysomnographic study. Cephalalgia 2014, 34, 455–463. [Google Scholar] [CrossRef] [Green Version]
- Fernández-de-las-Peñas, C.; Coppieters, M.W.; Cuadrado, M.L.; Pareja, J.A. Patients with chronic tension-type headache demonstrate increased mechano-sensitivity of the supra-orbital nerve. Headache 2008, 48, 570–577. [Google Scholar] [CrossRef]
- Fernández-de-las-Peñas, C.; Cuadrado, M.L.; Arendt-Nielsen, L.; Ge, H.Y.; Pareja, J.A. Increased pericranial tenderness, decreased pressure pain threshold, and headache clinical parameters in chronic tension-type headache patients. Clin. J. Pain 2007, 23, 346–352. [Google Scholar] [CrossRef]
- Fernández-de-las-Peñas, C.; Ge, H.Y.; Arendt-Nielsen, L.; Cuadrado, M.L.; Pareja, J.A. The local and referred pain from myofascial trigger points in the temporalis muscle contributes to pain profile in chronic tension-type headache. Clin. J. Pain 2007, 23, 786–792. [Google Scholar] [CrossRef] [PubMed]
- Fernández-de-las-Peñas, C.; Ge, H.Y.; Arendt-Nielsen, L.; Cuadrado, M.L.; Pareja, J.A. Referred pain from trapezius muscle trigger points shares similar characteristics with chronic tension type headache. Eur. J. Pain 2007, 11, 475–482. [Google Scholar] [CrossRef]
- Filatova, E.; Latysheva, N.; Kurenkov, A. Evidence of persistent central sensitization in chronic headaches: A multi-method study. J. Headache Pain 2008, 9, 295–300. [Google Scholar] [CrossRef] [Green Version]
- Jensen, R. Mechanisms of spontaneous tension-type headaches: An analysis of tenderness, pain thresholds and EMG. Pain 1995, 64, 251–256. [Google Scholar] [CrossRef]
- Jensen, R.; Bendtsen, L.; Olesen, J. Muscular factors are of importance in tension-type headache. Headache 1998, 38, 10–17. [Google Scholar] [CrossRef] [PubMed]
- Jensen, R.; Rasmussen, B.K.; Pedersen, B.; Olesen, J. Muscle tenderness and pressure pain thresholds in headache. A population study. Pain 1993, 52, 193–199. [Google Scholar] [CrossRef]
- Langemark, M.; Jensen, K.; Jensen, T.S.; Olesen, J. Pressure pain thresholds and thermal nociceptive thresholds in chronic tension-type headache. Pain 1989, 38, 203–210. [Google Scholar] [CrossRef]
- Mazzotta, G.; Sarchielli, P.; Gaggioli, A.; Gallai, V. Study of pressure pain and cellular concentration of neurotransmitters related to nociception in episodic tension-type headache patients. Headache 1997, 37, 565–571. [Google Scholar] [CrossRef]
- Peddireddy, A.; Wang, K.; Svensson, P.; Arendt-Nielsen, L. Stretch reflex and pressure pain thresholds in chronic tension-type headache patients and healthy controls. Cephalalgia 2009, 29, 556–565. [Google Scholar] [CrossRef] [PubMed]
- Romero-Morales, C.; Jaén-Crespo, G.; Rodríguez-Sanz, D.; Sanz-Corbalán, I.; López-López, D.; Calvo-Lobo, C. Comparison of pressure pain thresholds in upper trapezius and temporalis muscles trigger points between tension type headache and healthy participants: A case–control study. J. Manipulative Physiol. Ther. 2017, 40, 609–614. [Google Scholar] [CrossRef]
- Sandrini, G.; Antonaci, F.; Pucci, E.; Bono, G.; Nappi, G. Comparative study with EMG, pressure algometry and manual palpation in tension-type headache and migraine. Cephalalgia 1994, 14, 451–457. [Google Scholar] [CrossRef]
- Schoenen, J.; Bottin, D.; Hardy, F.; Gerard, P. Cephalic and extracephalic pressure pain thresholds in chronic tension-type headache. Pain 1991, 47, 145–149. [Google Scholar] [CrossRef]
- Stroppa-Marques, A.E.Z.; De Melo-Neto, J.S.; Do Valle, S.P.; Pedroni, C.R. Muscular pressure pain threshold and influence of craniocervical posture in individuals with episodic tension-type headache. Coluna Columna 2017, 16, 137–140. [Google Scholar] [CrossRef]
- Uthaikhup, S.; Sterling, M.; Jull, G. Widespread sensory hypersensitivity is not a feature of chronic headache in elders. Headache 2009, 50, 677–678. [Google Scholar] [CrossRef] [PubMed]
- Ashina, S.; Babenko, L.; Jensen, R.; Ashina, M.; Magerl, W.; Bendtsen, L. Increased muscular and cutaneous pain sensitivity in cephalic region in patients with chronic tension-type headache. Eur. J. Neurol. 2005, 12, 543–549. [Google Scholar] [CrossRef] [PubMed]
- Bendtsen, L.; Jensen, R.; Olesen, J. Decreased pain detection and tolerance thresholds in chronic tension-type headache. Arch. Neurol. 1996, 53, 373–376. [Google Scholar] [CrossRef]
- Buchgreitz, L.; Lyngberg, A.C.; Bendtsen, L.; Jensen, R. Frequency of headache is related to sensitization: A population study. Pain 2006, 123, 19–27. [Google Scholar] [CrossRef]
- Buchgreitz, L.; Lyngberg, A.C.; Bendtsen, L.; Jensen, R. Increased pain sensitivity is not a risk factor but a consequence of frequent headache: A population-based follow-up study. Pain 2008, 137, 623–630. [Google Scholar] [CrossRef]
- Güven, H.; Çilliler, A.E.; Çomoǧlu, S.S. Cutaneous allodynia in patients with episodic migraine. Neurol. Sci. 2013, 34, 1397–1402. [Google Scholar] [CrossRef]
- Gonçalves, M.C.; Chaves, T.C.; Florencio, L.L.; Carvalho, G.F.; Dach, F.; Fernández-De-Las-Peñas, C.; Bevilaqua-Grossi, D. Is pressure pain sensitivity over the cervical musculature associated with neck disability in individuals with migraine? J. Bodyw. Mov. Ther. 2015, 19, 67–71. [Google Scholar] [CrossRef]
- Burstein, R.; Yarnitsky, D.; Goor-Aryeh, I.; Ransil, B.; Bajwa, Z. An association between migraine and cutaneous allodynia. Ann. Neurol. 2000, 47, 614–624. [Google Scholar] [CrossRef]
- Wolff, H.G.; Tunis, M.M.; Goodell, H. Studies on headache: Evidence of tissue damage and changes in pain sensitivity in subjects with vascular headaches of the migraine type. AMA Arch. Intern. Med. 1953, 92, 478–484. [Google Scholar] [CrossRef] [PubMed]
- Barón, J.; Ruiz, M.; Palacios-Ceña, M.; Madeleine, P.; Guerrero, Á.L.; Arendt-Nielsen, L.; Fernández-de-las-Peñas, C. Differences in topographical pressure pain sensitivity maps of the scalp between patients with migraine and healthy controls. Headache 2016, 57, 226–235. [Google Scholar] [CrossRef]
- Bevilaqua Gossi, D.; Chaves, T.C.; Gonçalves, M.C.; Moreira, V.C.; Canonica, A.C.; Florencio, L.L.; Bordini, C.A.; Speciali, J.G.; Bigal, M.E. Pressure pain threshold in the craniocervical muscles of women with episodic and chronic migraine: A controlled study. Arq. Neuropsiquiatr. 2011, 69, 607–612. [Google Scholar] [CrossRef]
- Engstrøm, M.; Hagen, K.; Bjørk, M.H.; Stovner, L.J.; Gravdahl, G.B.; Stjern, M.; Sand, T. Sleep quality, arousal and pain thresholds in migraineurs: A blinded controlled polysomnographic study. J. Headache Pain 2013, 14, 50. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Fernández-De-Las-Peńas, C.; Arendt-Nielsen, L.; Cuadrado, M.L.; Pareja, J.A. Generalized mechanical pain sensitivity over nerve tissues in patients with strictly unilateral migraine. Clin. J. Pain 2009, 25, 401–406. [Google Scholar] [CrossRef] [PubMed]
- Fernández-De-Las-Peñas, C.; Cuadrado, M.L.; Arendt-Nielsen, L.; Pareja, J.A. Side-to-side differences in pressure pain thresholds and pericranial muscle tenderness in strictly unilateral migraine. Eur. J. Neurol. 2008, 15, 162–168. [Google Scholar] [CrossRef]
- Garrigós-Pedrón, M.; La Touche, R.; Navarro- Desentre, P.; Gracia-Naya, M.; Segura-Ortí, E. Widespread mechanical pain hypersensitivity in patients with chronic migraine and temporomandibular disorders: Relationship and correlation between psychological and sensorimotor variables. Acta Odontol. Scand. 2019, 77, 224–231. [Google Scholar] [CrossRef] [PubMed]
- Scholten-Peeters, G.G.M.; Coppieters, M.W.; Durge, T.S.C.; Castien, R.F. Fluctuations in local and widespread mechanical sensitivity throughout the migraine cycle: A prospective longitudinal study. J. Headache Pain 2020, 21, 16. [Google Scholar] [CrossRef] [Green Version]
- Strupf, M.; Fraunberger, B.; Messlinger, K.; Namer, B. Cyclic changes in sensations to painful stimuli in migraine patients. Cephalalgia 2018, 39, 585–596. [Google Scholar] [CrossRef]
- Phillip, D.; Lyngberg, A.C.; Jensen, R. Assessment of headache diagnosis. A comparative population study of a clinical interview with a diagnostic headache diary. Cephalalgia 2007, 27, 1–8. [Google Scholar] [CrossRef]
- Teepker, M.; Peters, M.; Kundermann, B.; Vedder, H.; Schepelmann, K.; Lautenbacher, S. The effects of oral contraceptives on detection and pain thresholds as well as headache intensity during menstrual cycle in migraine. Headache 2011, 51, 92–104. [Google Scholar] [CrossRef]
- Spierings, E.L.H.; Padamsee, A. Menstrual-cycle and menstruation disorders in episodic vs chronic migraine: An exploratory study. Pain Med. 2015, 16, 1426–1432. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Racine, M.; Tousignant-Laflamme, Y.; Kloda, L.A.; Dion, D.; Dupuis, G.; Choinire, M. A systematic literature review of 10 years of research on sex/gender and experimental pain perception—Part 1: Are there really differences between women and men? Pain 2012, 153, 602–618. [Google Scholar] [CrossRef] [PubMed]
- Teepker, M.; Kunz, M.; Peters, M.; Kundermann, B.; Schepelmann, K.; Lautenbacher, S. Endogenous pain inhibition during menstrual cycle in migraine. Eur. J. Pain 2014, 18, 989–998. [Google Scholar] [CrossRef]
- Arendt-Nielsen, L.; Yarnitsky, D. Experimental and clinical applications of quantitative sensory testing applied to skin, muscles and viscera. J. Pain 2009, 10, 556–572. [Google Scholar] [CrossRef] [PubMed]
- Waller, R.; Straker, L.; O’Sullivan, P.; Sterling, M.; Smith, A. Reliability of pressure pain threshold testing in healthy pain free young adults. Scand. J. Pain 2015, 9, 38–41. [Google Scholar] [CrossRef]
- Walton, D.; Macdermid, J.; Nielson, W.; Teasell, R.; Chiasson, M.; Brown, L. Reliability, standard error, and minimum detectable change of clinical pressure pain threshold testing in people with and without acute neck pain. J. Orthop. Sports Phys. Ther. 2011, 41, 644–650. [Google Scholar] [CrossRef] [Green Version]
- Van Wilgen, P.; Van der Noord, R.; Zwerver, J. Feasibility and reliability of pain pressure threshold measurements in patellar tendinopathy. J. Sci. Med. Sport 2011, 14, 477–481. [Google Scholar] [CrossRef]
- Lacourt, T.E.; Houtveen, J.H.; van Doornen, L.J.P. Experimental pressure-pain assessments: Test-retest reliability, convergence and dimensionality. Scand. J. Pain 2012, 3, 31–37. [Google Scholar] [CrossRef] [PubMed]
- Balaguier, R.; Madeleine, P.; Vuillerme, N. Intra-session absolute and relative reliability of pressure pain thresholds in the low back region of vine-workers: Effect of the number of trials. BMC Musculoskelet. Disord. 2016, 17, 350. [Google Scholar] [CrossRef] [Green Version]
- Mailloux, C.; Beaulieu, L.D.; Wideman, T.H.; Massé-Alarie, H. Within-session test-retest reliability of pressure pain threshold and mechanical temporal summation in healthy subjects. PLoS ONE 2021, 16, 1–17. [Google Scholar] [CrossRef]
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