Skip to main content

Translation, cross-cultural adaptation and measurement proprieties of the German version of the Allodynia Symptom Checklist (ASC-12)

Abstract

Background

Cutaneous allodynia is highly prevalent among migraineurs and is associated with a poor prognosis. The Allodynia Symptom Checklist (ASC-12) is a comprehensive questionnaire to identify the presence and severity of allodynia. Our aim was to translate and adapt the ASC-12 to German and evaluate its measurement properties.

Methods

Following the COSMIN guidelines, 80 migraine patients were enrolled in the study to evaluate the stages of translation (n=30) and measurement propriety assessment (n=50), respectively. After reaching a final version, the German ASC-12 was assessed for structural validity, internal consistency, test-retest reliability, construct validity and absolute agreement, using mechanical and thermal pain thresholds as reference method.

Results

The German version of the ASC-12 presented an adequate structural validity compatible with the original version of the questionnaire. Its internal consistency ranged from 0.70 to 0.80 considering the total score and the thermic, static and dynamic mechanic subdomains. The total score presented excellent reliability (ICC: 0.85) with a standard error of measurement of 1.15 points and smallest detectable change of 3.40 points. ASC-12 total scores were correlated with headache intensity (r=0.38, p=0.004), headache disability (r=0.37, p=0.004) and cold pain thresholds (r=0.28, p=0.025). The thermic allodynia ASC-12 scores were correlated with cold (r=0.36, p=0.005) and heat (r=-0.30, p=0.010) pain thresholds, while the static mechanical allodynia ASC-12 scores correlated with mechanical pain threshold (r=0.29, p=0.019) and with mechanical pain sensitivity (r=0.24 to 0.28, p< 0.045). Despite no significant bias between methods, quantitative sensory testing (QST) results and ASC-12 scores tend to disagree.

Conclusion

The German version of the ASC-12 is available for research and clinical settings and presented adequate measurement proprieties, as the original version. Despite the correlation between the ASC-12 and QST, one method cannot be replaced by the other.

Peer Review reports

Key findings

  • The German version of the ASC-12 exhibit semantic and idiomatic equivalence to the original English version.

  • The German ASC-12 presented adequate internal consistency, structural validity and reliability.

  • Total ASC-12 scores correlate with headache intensity, disability and cold pain thresholds

  • The QST evaluation cannot be replaced by the ASC-12 in the evaluation of cutaneous allodynia.

Introduction

Prolonged and/or repeated noxious stimuli can sensitize the nociception pathways and lead to cutaneous allodynia, defined as the perception of pain provoked by an innocuous thermic and/or mechanic stimulus applied over the skin [1, 2]. Up to 63% of patients with migraine present cutaneous allodynia during the attacks [3], but it can also occur interictally [4, 5].

The presence of cutaneous allodynia increases the risk of migraine chronification [1, 6], as it is considered a central sensitization marker [2]. Despite increased prevalence of central sensitization in patients with chronic migraine, it is also often observed among individuals with episodic migraine [1]. Cutaneous allodynia is related to poorer clinical outcomes such as increased depression and anxiety levels, higher migraine disability, lower quality of life, sleep disorders, medication overuse, and greater pain intensity [7,8,9]. It can predict refractory pharmacological treatment response since triptans are more likely to be effective if their intake precedes the onset of cutaneous allodynia [10,11,12]. Furthermore, cutaneous allodynia is considered a critical factor for suicidality, along with the presence of osmophobia [13].

The identification of cutaneous allodynia in clinical practice is crucial due to its relevance to the migraine prognosis, development of comorbidities and response to treatment. However, quantitative sensory testing (QST) – considered the gold standard to evaluate cutaneous allodynia [14] – has limited feasibility in the clinical setting due to high costs for equipment, requirement of specialized training and the time needed for testing [15]. The Allodynia 12-item questionnaire (Allodynia Symptom Checklist-12, ASC-12) was developed by Lipton and colleagues to assess the presence and severity of cutaneous allodynia [3]. It is a quick and valid tool that considers thermic, mechanical static and mechanical dynamic dimensions of pain perception [1, 3]. Despite being widely used for both research and clinical settings worldwide, it is not yet translated or adapted to German. Therefore, the aim of this study was to translate and culturally adapt the ASC-12 to German. We further aimed to assess its measurement proprieties, including structural validity, reliability, internal consistency, construct validity and agreement with the QST assessment protocol.

Materials and methods

Study design and sample

This study was performed at the University of Luebeck in Germany and approved by the local Ethics Committee (process number: 21-506). The procedure was carried out in two parts with two different samples of patients with migraine. First, the translation and cross-cultural adaptation of the ASC-12 to German was accomplished and tested in 30 patients, according to the Guidelines for the process of cross-cultural adaptation of self-reported measures [16]. Afterwards, the measurement proprieties assessment of the German version of the ASC-12 was performed in 50 patients, according to the COSMIN guidelines [17].

All participants were screened for migraine according to the ID migraine questionnaire [18] and had their diagnosis performed by a neurologist in accordance with ICHD-III criteria [19]. They were enrolled in the study if they were between 18 to 65 years old and had at least one migraine attack within the last month. Patients with concomitant pain syndromes within the last 3 months, concomitant headache diagnosis and/or neurological, cognitive or psychiatric disorders, and headache during the assessment were excluded. Demographic information, medication intake, headache characteristics and headache impact (HIT-6™ GlaxoSmithKline) [20] were informed by all participants.

Translation and cross-cultural adaptation

The ASC-12 includes 12 questions that encompass everyday activities such as combing the hair, shaving the face, wearing glasses, taking a shower, among others. The patients indicate the frequency of pain or unpleasantness during a migraine attack by rating the options: does not apply to me, never, rarely, less than half the time, and half the time or more. The response less than half of the time is scored as 1 point, and half the time or more as 2 points, while the other options do not receive any score. The sum of points equal or greater than 3 indicates the presence of cutaneous allodynia. Scores between 3 and 5 indicate mild, from 6 to 8 moderate, and 9 or greater severe cutaneous allodynia [3].

The translation process and cross-cultural adaptation of the ASC-12 to German was conducted following six stages [16]:

  1. 1.

    English to German translation, performed by two native German speakers fluent in English, who independently translated the checklist into German.

  2. 2.

    Synthesis of the translation to conceive one agreed version of the questionnaire.

  3. 3.

    Back translation, performed by two German translators, whose native language is English.

  4. 4.

    Expert committee review of the translations and consent on a pre-final version of the questionnaire. Eight members composed the expert committee, which consisted of post-graduation students, clinicians, professors in the field, and the translators involved in the previous stages.

  5. 5.

    Application of the pre-final version to 30 patients with migraine to evaluate comprehension difficulties of the questions.

  6. 6.

    Submission of the documents to the expert committee once the final version of the questionnaire was reached.

The last stage of the translation and cross-cultural adaptation was carried out between May and June of 2022 among 30 patients with migraine through the platform limesurvey.org (Table 1). The online survey was disseminated through simple random sampling in the migraine league organization. It included the pre-final version of the ASC-12 questionnaire conceived in stage 4, along with clinical and demographic questions. In addition, participants were asked if they had doubts regarding the meaning of words and understanding of the ASC-12 after its completion. In case of doubts from more than 10% of patients on the same question, a revision and rephrasing of the item(s) is required, with subsequent testing among 30 new patients with migraine [16]. At the beginning of the survey, each participant received an individual identification number through a link to “limesurvey.org” to prevent unauthorized access and multiple participation.

Table 1 Sample demographics (mean, SD and percentages) for each study stage

Measurement proprieties evaluation

Consecutive patients with migraine were recruited for an in-person appointment at the University of Luebeck, Germany. This sample was used to evaluate the questionnaire’s internal consistency, test-retest reliability, absolute agreement, structural and construct validity. Further than the collection of the self-reported outcomes previously described, patients underwent a standardized QST protocol established by the German Neuropathic Pain Research Network [21], to determine construct validity and absolute agreement. In order to match the dimensions of the ASC-12, the QST protocol consisted of evaluation of cold and heat pain thresholds, mechanical pain thresholds and mechanical pain sensitivity. To also determine reliability, the participants received one week later [22, 23] a limesurvey link via email to fill out again the final version of the German ASC-12.

Thermal pain thresholds were assessed with a thermal contact stimulator (TCS, QST.Lab, (TCS; André Dufour, University of Strasbourg). The area of stimulation of the TCS (T11) has a surface of 9cm2. The thermode was used to determine individual heat and cold thresholds starting with an initial temperature of 32°C with increments/decrements of 1°C/second, with a maximal range from 0°C to 60°C. Patients were instructed to press a stop button once the temperature change first elicited pain. The average of three repetitions for each modality was used for data analysis.

Mechanic pain threshold was determined using a set of weighted pinprick stimulators (8, 16, 32, 64, 128, 256 and 512mN, MRC Systems GmbH, Heidelberg, Germany). Five series of ascending and descending stimuli were performed and patients reported the stimulator that elicited a sharp sensation for each of the series. The geometric mean was used for analysis.

Mechanical pain sensitivity was tested using the same set of pinprick stimulators, a soft brush (BR), a cotton wisp (CW), and a Q‐tip (QT) over the skin. The CR, CW and QT were applied with a single stroke at a velocity of 2 to 3 cm/s over approximately 2cm in length of the skin. Each stimulus was applied over the skin in a randomized order and this time subjects were instructed to rate their pain intensity ranging from 0 to 100 using a numeric pain scale (NRS). The degree of pain intensity was defined using the geometric mean of the 5 trials for each type of stimulus.

All measurements were done at the distribution of V1 on the dominant headache side. If there was no dominant headache side reported, the evaluation site was chosen by simple randomization.

Statistical analysis

After the translation and cross-cultural adaptation phase, a confirmatory factor analysis [24] was used to assess the structural validity and to verify if the questionnaire exhibited the same three factors (thermic, static mechanical and dynamic mechanical allodynia) as the original ASC-12 version. The factor loading of each question with standardized values above 0.3 represents a relevant contribution to a dimension. The goodness-of-fit of the model was confirmed according to the following parameters: Tucker-Lewis-Index (TLI) and comparative fit index (CFI) above 0.9, mean square error root of approximation (RMSEA) and standardized root mean square residual (SRMR) below 0.08 [25]. A path diagram was used to present the standardized coefficients of each question and each dimension.

The test-retest ASC-12 reliability was assessed using two-way random-effects, absolute agreement Intraclass Correlation Coefficient (ICC), based on total scores and scores of each of the subscales in the first and second application of the German version of the ASC-12. ICCs with values below 0.45 indicated poor reliability, between 0.50 and 0.75 satisfactory, and greater than 0.75 excellent reliability [22]. Based on the reliability results, the standard error of measurement (SEM, SEM = SD × √1−ICC) and smallest detectable change on an individual level (SDC, SDCind = SEM × 1.96 × √2) [25] were calculated. The German version of the ASC-12 was assessed for internal consistency using Cronbach’s alpha coefficient for each dimension and for the total score. Values between 0.70 and 0.95 were considered adequate, as lower values indicate a lack of correlation between the items and high values indicate item redundancy [25].

The construct validity of the ASC-12 was analyzed using a two-tailed Pearson’s correlation test between the ASC-12 and clinical outcomes. The correlation of total scores was evaluated using the HIT-6 questionnaire scores, headache intensity, frequency and onset, mechanical pain sensitivity, mechanical, cold and heat pain thresholds. Correlations between the thermal allodynia scores with cold and heat were also evaluated. Furthermore, correlations between static and dynamic mechanical allodynia scores were performed by testing mechanical pain thresholds and mechanical pain sensitivity. Correlation values below 0.30 were considered weak, between 0.31 and 0.70 moderate, above 0.71 strong correlations [24].

We further tested the absolute agreement between ASC-12 scores with mechanical, cold and heat pain thresholds through Bland-Altman analysis. The mean difference of methods (bias) in relation to the maximum agreement based on normalized scores of outcomes was estimated. Limits of agreements (LoA) were calculated considering the mean difference of both methods ± 1.96 SD [26]. The presence of zero within the 95%CI bias indicates no systematic bias [23]. In addition, the hypothesis test of agreement proposed by Shieh was tested, and the conclusion of method agreement was reached by rejecting the null hypothesis [25].

The confirmatory factor analysis and absolute agreement analysis were performed using the software JAMOVI (version 2.3.21, The Jamovi Project, Sydney, Australia). The SPSS software (version 26.0, IBM, New York, USA) was used to perform the remaining analyses. An alpha level at 5% was considered and there were no missing data.

Results

Translation and cross-cultural adaptation

During the cross-cultural adaptation of the ASC-12, some English words and expressions were adapted to improve clarity. The expression “Pulling your hair back (e.g., ponytail) was adapted to “Zurückhalten der Haare (z. B. Pferdeschwanz)”. The expression “Resting your face or head on a pillow” was adapted to “beim Ablegen des Gesichts oder Kopfes auf einem Kissen”. “Exposure to heat” and “Exposure to cold” were translated to “bei Hitze” and “bei Kälte”. The classification of allodynia was adapted as follows: “None” as “keine”, “Mild” as “leichte”, “Moderate” as “moderate” and “Severe” as “schwere”. After the translation process, a consensus regarding the pre-final version of the questionnaire was reached by the expert committee and translators (Supplemental material).

Two participants (7%) reported not understanding the difference between “does not apply to me”/“betrifft mich nicht” and “never”/“Niemals”. Since there were no further comprehension doubts in same item by more than 10% (3 participants), the pre-final version was considered the German ASC-12 final version (Supplemental material). Demographic and headache characteristics of the 30 patients included in the translation and cross-cultural adaptation stage of the study can be found in Table 1.

Other comments from participants (10%) included the report of allodynia in other situations such as wearing a face mask, helmets, headphones or earplugs. Participants (13%) also reported that while having a headache they entirely avoided some activities (i.e., as wearing glasses, tight clothes, ponytail or shaving the face), since they anticipated discomfort. In this case, they considered the “does not apply to me”/“betrifft mich nicht” as the appropriate answer, since they never experienced discomfort by performing the described activity.

Measurement Proprieties

The assessment of the ASC-12 measurement proprieties took place between August and December 2022. From 51 recruited patients with migraine, one was excluded due to the concomitant diagnosis of tension-type headache. The demographic and clinical characteristics of the sample recruited in this stage of the study are shown in Table 1.

Structural validity

A confirmatory factor analysis was used to perform the structural validity assessment of the German ASC-12 according to the three pre-defined dimensions of the questionnaire: thermic allodynia, static and dynamic mechanical allodynia. The model-fit was considered adequate as all values of CFI and TLI were very close to the pre-defined thresholds. Furthermore, RMSA and SRMR were equal or below 0.08 (model 1, Table 2). Figure 1 shows the path diagram with the factor loadings of each dimension item. The standardized coefficients ranged between 0.17 and 0.68. The questionnaire items “shaving your face” and “wearing contact lenses” did not contribute significantly to the goodness-of-fit, since they presented factor loadings below 0.30. A second model without these two items was estimated (model 2, Table 2), but no improvement of the model-fit was observed.

Table 2 Model-fit of the German version of the Allodynia Symptom Checklist (ASC-12)
Fig. 1
figure 1

Structure of the German version of the ASC-12 analyzed by the confirmatory factor analysis. The standardized coefficients represent the individual contribution of each question to the model

Reliability

The mean ASC-12 score measured during the first round was 5.40 (SD: 3.20) points and 4.20 (SD: 3.40) in the second round. In the first round, 76% of the participants were classified as having allodynia, while it was 64% in the second round. The reliability of the total ASC-12 score was considered excellent with an ICC of 0.85 (95%CI: 0.64 to 0.93, p< 0.0001). The observed ICC for the thermic allodynia dimension of the questionnaire was 0.77 (95%CI: 0.52 to 0.88, p< 0.0001), 0.86 (95%CI: 0.75 to 0.92, p< 0.0001) for static mechanical allodynia dimension and 0.84 (95%CI: 0.68 to 0.91, p< 0.0001) for dynamic mechanical allodynia. The German version of the ASC-12 presented a SEM of 1.15 points and a SDC of 3.40 points.

The internal consistency measured by Cronbach’s alpha was considered adequate since 0.70 was observed for the total score, 0.70 for the thermic allodynia dimension, 0.70 for static mechanical allodynia dimension and 0.80 for dynamic mechanical allodynia dimension.

Construct validity

Weak to moderate positive correlations were found between the total scores of the ASC-12 and headache intensity (r= 0.38, p= .004), headache disability (r= 0.37, p= 0.004) and cold pain thresholds (r= 0.28, p= 0.025). The thermic allodynia dimension of the ASC-12 was moderately correlated with headache disability (r= 0.36, p= 0.005) and with both cold (r= 0.36, p= 0.005) and heat pain (r= -0.30, p= 0.010) thresholds. The static mechanical allodynia scores of the ASC-12 presented weak and positive correlations with mechanical pain threshold (r= 0.29, p= 0.019) and with mechanical pain sensitivity for all pin-prick stimulators (r values between 0.24 and 0.28, p< 0.045). Dynamic mechanical allodynia scores of the ASC-12 were positively correlated with headache intensity (r= 0.37, p= 0.004) and headache disability (r= 0.29, p= 0.023). These results are shown in Table 3.

Table 3 Correlations between clinical and QST outcomes with the German version of the Allodynia Symptom Checklist (ASC-12) total scores and respective dimensions

Agreement analysis

The LoA between the ASC-12 and mechanical pain thresholds normalized scores (A, Fig. 2) ranged from -2.8 (90%CI: -3.2 to -2.3) to 2.8 (90%CI: 2.3 to 3.2) with a non-significant bias of 0.03 (95%CI: -0.4 to 0.4). The 90%CI of the agreement hypothesis test was between -3.2 to 3.2, p> 0.05. The LoA between the ASC-12 and cold pain thresholds normalized scores (B, Fig. 2) ranged from -2.4 (90%CI: -2.8 to -2.0) to 2.4 (90%CI: 2.0 to 2.8) with a non-significant bias of 0.02 (95%CI: -0.3 bis 0.3). The 90%CI of the agreement hypothesis test was between -2.7 to 2.7, p> 0.05. The LoA between the ASC-12 and heat pain thresholds normalized scores (C, Fig. 2) ranged from -3.0 (90%CI: -3.5 to -2.5) to 3.1 (90%CI: 2.6 to 3.6) with a non-significant bias of 0.02 (95%CI: -0.4 bis 0.4). The 90%CI of the agreement hypothesis test was between -3.5 to 3.5, p> 0.05. Although almost all individuals were within the 95% limits of agreement range of the Bland-Altman plots for all three analysis and no systematic bias was observed, the agreement hypothesis test was rejected, indicating overall disagreement between ASC-12 and mechanical, cold and heat pain thresholds.

Fig. 2
figure 2

Bland-Altman plots exhibiting the agreement between the Z-scores of the ASC-12 and mechanical pain thresholds (A), cold pain thresholds (B) and heat pain thresholds (C)

Discussion

In this study, we successfully translated and adapted the English version of the ASC-12 to German, considering semantic and idiomatic equivalence to the original version. In addition, the German version of the ASC-12 demonstrated adequate measurement proprieties, despite the lack of agreement with thermal and mechanic thresholds.

For the cross-cultural comparison between different languages, the translation process has to be rigorous to ensure the equivalence of versions, and has to include assessments of the translation quality by an expert committee [27]. To this date, the ASC-12 was available only in English [3], Portuguese [28] and Turkish [29]. The German and the Portuguese versions of the ASC-12 were developed based on the same translation and cross-cultural guideline described by Beaton et al [16]. Nonetheless, a standardized process does not ensure equivalent measurement proprieties to the original version. For this reason, the assessment of validity and reliability of the adapted version are still required [30].

The structural validity analysis of the German ASC-12 confirmed the same original three questionnaire domains [3], as also observed in the Turkish version [29]. The items “combing your hair” and “pulling your hair back” demonstrated the highest contribution to the model fit, similar to Lipton et al [3]. On the other hand, and similar to the Turkish version [29], the items “wearing contact lenses” and “shaving your face” did not contribute significantly to the questionnaire, probably due to the low number of responses in the sample. Ashkenazi et al. also suggested that the item “shaving your face” does not add value in the identification of patients with allodynia [31]. This can be attributed to the higher prevalence of migraine among women, similar to the non-frequent use of contact lenses, especially during a migraine attack. Interestingly, the avoidance behavior towards some items of the ASC-12 during the migraine attack was confirmed by some patients during the translation and cross-cultural process of the questionnaire. This can lead to a reduction in the detection of allodynia, since patients reported not having experienced the activity and rated “does not apply to me”, despite anticipated discomfort and hence avoidance of the activity during a migraine attack.

Similar to the Turkish [29] and Portuguese [28] versions of the ASC-12, an adequate internal consistency and reliability was observed in the German version. Furthermore, the prevalence of allodynia verified in the sample is in line with previous reports [1, 3, 28, 29]. For the first time, measurement error variables of the questionnaire were calculated, which can inform about the absence of real changes over time and absence of differences between individuals [25]. The current results indicate that differences of scores lower than 1.15 points should be interpreted as an error, as well as score changes lower than 3.4 points. These results are relevant for all researchers and clinicians that may use the ASC-12, since it is crucial for an adequate interpretation of questionnaire scores. Future studies should also consider performing responsiveness analysis in order to determine minimal important change values of the ASC-12, which would indicate presence or absence of clinically relevant changes of ASC-12 scores in both future clinical trials as well as in clinical practice.

Further than adapting the ASC-12 to German, this is the first study that performed the construct validity and absolute agreement analysis in relation to the gold standard of measurement, the QST [14]. A previous study evaluated the presence of allodynia in migraineurs using the ASC-12 and a thermal stimulator, measuring heat and cold detection thresholds before and after onabotulinumtoxinA injection [32]. The authors reported improvement of ASC-12 scores after the treatment but no changes in thermal thresholds, further than no correlation between the questionnaire and the QST examination [32].

Indeed, the ASC-12 seems to be very accurate to identify patients with allodynia in contrast to the QST protocol, since - despite the questionnaire recall bias - it refers to symptoms occurring during a migraine attack [31]. Meanwhile, the QST protocol is usually performed during the interictal phase of migraine [33]. Although migraineurs often report several interictal symptoms [34], the level of hypersensitivity more likely returns to baseline in episodic patients during the headache-free period [35, 36]. In our measurement properties sample, 42% of the patients reported having a migraine attack in the previous or following 48hs of the examination. Among other factors, this may have contributed to the significant correlations between the thermal and mechanical domains of the ASC-12 with the thermal and mechanical pain thresholds, confirming the construct validity of the questionnaire. However, the absolute agreement analysis indicated that despite the absence of a significant bias, the QST and ASC-12 measures tended to disagree. It suggests that the QST cannot be replaced by the ASC-12 evaluation in research and clinical practice. Future studies may demonstrate agreement and greater correlation values by considering the same migraine phase for both assessments, i.e. performing the QST protocol during the headache phase and/or including a bigger sample of chronic migraine patients.

Further than the associations between thermic and mechanical aspects of the ASC-12 and QST, these current data showed correlations between the total scores of the ASC-12 with headache intensity, disability levels and cold pain thresholds. The association between greater migraine severity and allodynia was already demonstrated in previous reports [1, 3, 7, 29, 37]. Han et al [37] demonstrated in a populational study that the presence of allodynia was associated with higher headache frequency, headache intensity, presence of anxiety and depression. These current findings also agree with the study of Seo & Park, which showed among other factors, higher disability and headache intensity levels in migraineurs with allodynia and sensory hypersensitivity [7]. Burstein et al. reported greater changes on cold – but not heat – pain thresholds one hour after the onset of a migraine attack [38]. This suggests that cold threshold is the first modality to demonstrate abnormalities and identify allodynia in patients with migraine.

The advances in the understanding and evaluation of allodynia in patients with migraine can open perspectives and impact positively on new strategies of treatment. Recent literature links allodynia to dysfunctional analgesic mechanisms and abnormal representation of pain perception [39], which are associated with migraine chronification [40, 41] and observed more prominent during migraine attacks [42]. Interestingly, the presence of interictal allodynia can identify with 85% of accuracy non-responders of CGRP monoclonal antibodies [43]. The skin hypersensitivity can be explained by a hypofunction of the descending pain inhibitory system, which modulates the nociceptive transmission, or by a facilitation of the ascending pain system [44]. Neuroimaging studies suggest that patients with allodynia identified using the ASC-12 questionnaire demonstrate greater activation of the middle frontal gyrus, somatosensory and anterior cingulate cortex [39], along with abnormal sensorimotor connectivity [45, 46]. Despite the advances in the understanding of the hypersensitivity in migraineurs, they do not yet provide a clue to the prevention and treatment of allodynia and its influence on the course and burden of the disease. Further investigation of this phenomenon and its pathophysiology can open possibilities to address allodynia within the treatment plan, with the aim to reduce the likelihood of progression to chronic migraine in this group of patients. Since the ASC-12 can be a valuable tool not just for clinical but also neuroimaging and basic research, it is important to understand its measurement proprieties, its limitations and move towards an improvement of the tool, especially in regard to agreement with the gold standard.

It is important to highlight some limitations of the present study. The study sample was composed mainly by female patients with episodic migraine, which were assessed in a headache-free period. The predominance of females could have influenced the low contribution of the item “shaving your face” to the identification of allodynia by the questionnaire. The assessment of patients in the headache-free period and low proportion of chronic migraine patients in the sample are likely to limit the interpretation of the correlation and agreement analysis. Despite these limitations, the German version of the ASC-12 questionnaire presented similar measurement proprieties to the original in English, Portuguese and English versions, being available for both research and clinical settings in German-speaking countries.

Conclusions

The German version of the ASC-12 provides a valid and reliable tool for evaluating the presence and severity of cutaneous allodynia among German speaking patients with migraine. Despite the correlation between the ASC-12 questionnaire and the QST evaluation, one method cannot be replaced by the other in the evaluation of cutaneous allodynia.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ASC-12:

Allodynia Symptom Checklist

BR:

Brush

CFI:

Comparative fit index

CW:

Cotton Wisp

HIT-6:

Headache Impact Test Questionnaire

ICC:

Intraclass Correlation Coefficient

LOA:

Limits of agreements

RMSEA:

Mean Square Error Root of Approximation

NRS:

Numeric Pain Scale

QT:

Q‐tip

QST:

Quantitative Sensory Testing

SDC:

Smallest Detectable Change

SEM:

Standard Error of Measurement

SRMR:

Standardized Root Mean Square Residual

TCS:

Thermal Contact Stimulator

TLI:

Tucker-Lewis-Index

References

  1. Bigal ME, Ashina S, Burstein R, Reed ML, Buse D, Serrano D, Lipton RB, Group A (2008) Prevalence and characteristics of allodynia in headache sufferers: a population study. Neurology 70(17):1525–1533. https://doi.org/10.1212/01.wnl.0000310645.31020.b1

    Article  CAS  PubMed  Google Scholar 

  2. Tietjen GE, Brandes JL, Peterlin BL, Eloff A, Dafer RM, Stein MR, Drexler E, Martin VT, Hutchinson S, Aurora SK, Recober A, Herial NA, Utley C, White L, Khuder SA (2009) Allodynia in migraine: association with comorbid pain conditions. Headache 49(9):1333–1344. https://doi.org/10.1111/j.1526-4610.2009.01521.x

    Article  PubMed  Google Scholar 

  3. Lipton RB, Bigal ME, Ashina S, Burstein R, Silberstein S, Reed ML, Serrano D, Stewart WF, Advisory American Migraine Prevalence Prevention, G, (2008) Cutaneous allodynia in the migraine population. Ann Neurol 63(2):148–158. https://doi.org/10.1002/ana.21211

    Article  PubMed  PubMed Central  Google Scholar 

  4. Lovati C, D’Amico D, Bertora P (2009) Allodynia in migraine: frequent random association or unavoidable consequence? Expert Rev Neurother 9(3):395–408. https://doi.org/10.1586/14737175.9.3.395

    Article  PubMed  Google Scholar 

  5. Schwedt TJ, Krauss MJ, Frey K, Gereau RWt, (2011) Episodic and chronic migraineurs are hypersensitive to thermal stimuli between migraine attacks. Cephalalgia 31(1):6–12. https://doi.org/10.1177/0333102410365108

    Article  PubMed  Google Scholar 

  6. Kalita J, Yadav RK, Misra UK (2009) A comparison of migraine patients with and without allodynic symptoms. Clin J Pain 25(8):696–698. https://doi.org/10.1097/AJP.0b013e3181b12dd3

    Article  PubMed  Google Scholar 

  7. Seo JG, Park SP (2019) Clinical significance of sensory hypersensitivities in migraine patients: does allodynia have a priority on it? Neurol Sci 40(2):393–398. https://doi.org/10.1007/s10072-018-3661-2

    Article  PubMed  Google Scholar 

  8. Mendonca MD, Caetano A, Viana-Baptista M, Group CHS (2016) Association of depressive symptoms with allodynia in patients with migraine: A cross-sectional study. Cephalalgia 36(11):1077–1081. https://doi.org/10.1177/0333102415620285

    Article  Google Scholar 

  9. Dodick DW, Reed ML, Fanning KM, Munjal S, Alam A, Buse DC, Schwedt TJ, Lipton RB (2019) Predictors of allodynia in persons with migraine: Results from the Migraine in America Symptoms and Treatment (MAST) study. Cephalalgia 39(7):873–882. https://doi.org/10.1177/0333102418825346

    Article  PubMed  Google Scholar 

  10. Burstein R, Collins B, Jakubowski M (2004) Defeating migraine pain with triptans: a race against the development of cutaneous allodynia. Ann Neurol 55(1):19–26. https://doi.org/10.1002/ana.10786

    Article  CAS  PubMed  Google Scholar 

  11. Lipton RB, Munjal S, Buse DC, Bennett A, Fanning KM, Burstein R, Reed ML (2017) Allodynia Is Associated With Initial and Sustained Response to Acute Migraine Treatment: Results from the American Migraine Prevalence and Prevention Study. Headache 57(7):1026–1040. https://doi.org/10.1111/head.13115

    Article  PubMed  Google Scholar 

  12. Young WB, Ivan Lopez J, Rothrock JF, Orejudos A, Manack Adams A, Lipton RB, Blumenfeld AM (2019) Effects of onabotulinumtoxinA treatment in patients with and without allodynia: results of the COMPEL study. J Headache Pain 20(1):10. https://doi.org/10.1186/s10194-018-0952-1

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Park SP, Seo JG, Lee WK (2015) Osmophobia and allodynia are critical factors for suicidality in patients with migraine. J Headache Pain 16:529. https://doi.org/10.1186/s10194-015-0529-1

    Article  PubMed  Google Scholar 

  14. Keizer D, Fael D, Wierda JM, van Wijhe M (2008) Quantitative sensory testing with Von Frey monofilaments in patients with allodynia: what are we quantifying? Clin J Pain 24(5):463–466. https://doi.org/10.1097/AJP.0b013e3181673b80

    Article  PubMed  Google Scholar 

  15. Zhu GC, Böttger K, Slater H, Cook C, Farrell SF, Hailey L, Tampin B, Schmid AB (2019) Concurrent validity of a low-cost and time-efficient clinical sensory test battery to evaluate somatosensory dysfunction. Eur J Pain 23(10):1826–1838. https://doi.org/10.1002/ejp.1456

    Article  PubMed  PubMed Central  Google Scholar 

  16. Beaton DE, Bombardier C, Guillemin F, Ferraz MB (2000) Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976) 25(24):3186–3191. https://doi.org/10.1097/00007632-200012150-00014

    Article  CAS  PubMed  Google Scholar 

  17. Mokkink LB, Prinsen CA, Patrick DL, Alonso J, Bouter LM, de Vet HC, Terwee CB (2019) COSMIN Study Design checklist for Patient-reported outcome measurement instruments. Available from: https://www.cosmin.nl/wp-content/uploads/COSMIN-study-designing-checklist_final.pdf#. Accessed 16 Nov 2021

  18. Thiele A, Strauß S, Angermaier A, Kronenbuerger M, Fleischmann R (2020) Translation and validation of an extended German version of ID Migraine™ as a migraine screening tool. Cephalalgia Reports 3:2515816320962773. https://doi.org/10.1177/2515816320962773

    Article  Google Scholar 

  19. Headache Classification Committee of the International Headache Society (IHS) (2018) The International Classification of Headache Disorders, 3rd edition. Cephalalgia 38(1):1–211. https://doi.org/10.1177/0333102417738202

  20. Martin M, Blaisdell B, Kwong JW, Bjorner JB (2004) The Short-Form Headache Impact Test (HIT-6) was psychometrically equivalent in nine languages. J Clin Epidemiol 57(12):1271–1278. https://doi.org/10.1016/j.jclinepi.2004.05.004

    Article  PubMed  Google Scholar 

  21. Rolke R, Baron R, Maier C, Tolle TR, Treede DR, Beyer A, Binder A, Birbaumer N, Birklein F, Botefur IC, Braune S, Flor H, Huge V, Klug R, Landwehrmeyer GB, Magerl W, Maihofner C, Rolko C, Schaub C, Scherens A, Sprenger T, Valet M, Wasserka B (2006) Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): standardized protocol and reference values. Pain 123(3):231–243. https://doi.org/10.1016/j.pain.2006.01.041

    Article  CAS  PubMed  Google Scholar 

  22. Mokkink LB, de Vet HCW, Prinsen CAC, Patrick DL, Alonso J, Bouter LM, Terwee CB (2018) COSMIN Risk of Bias checklist for systematic reviews of Patient-Reported Outcome Measures. Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation 27(5):1171–1179. https://doi.org/10.1007/s11136-017-1765-4

    Article  CAS  PubMed  Google Scholar 

  23. Gagnier JJ, Lai J, Mokkink LB, Terwee CB (2021) COSMIN reporting guideline for studies on measurement properties of patient-reported outcome measures. Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation 30(8):2197–2218. https://doi.org/10.1007/s11136-021-02822-4

    Article  PubMed  Google Scholar 

  24. Sani F, Todman J (2006) Experimental design and statistics for psychology: a first course. Blackwell Publishing, Oxford

    Book  Google Scholar 

  25. Terwee CB, Bot SD, de Boer MR, van der Windt DA, Knol DL, Dekker J, Bouter LM, de Vet HC (2007) Quality criteria were proposed for measurement properties of health status questionnaires. J Clin Epidemiol 60(1):34–42. https://doi.org/10.1016/j.jclinepi.2006.03.012

    Article  PubMed  Google Scholar 

  26. Bland JM, Altman DG (1986) Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1(8476):307–310

    Article  CAS  PubMed  Google Scholar 

  27. Peters M, Passchier J (2006) Translating Instruments for Cross-Cultural Studies in Headache Research. Headache 46(1):82–91. https://doi.org/10.1111/j.1526-4610.2006.00298.x

    Article  PubMed  Google Scholar 

  28. Florencio LL, Chaves TC, Branisso LB, Goncalves MC, Dach F, Speciali JG, Bigal ME, Bevilaqua-Grossi D (2012) 12 item allodynia symptom checklist/Brasil: cross-cultural adaptation, internal consistency and reproducibility. Arq Neuropsiquiatr 70(11):852–856

    Article  PubMed  Google Scholar 

  29. Yalin OO, Uluduz D, Sungur MA, Sart H, Ozge A (2017) Identification of Allodynic Migraine Patients with the Turkish Version of the Allodynia Symptom Checklist: Reliability and Consistency Study. Noro Psikiyatr Ars 54(3):260–266. https://doi.org/10.5152/npa.2016.15953

    Article  PubMed  Google Scholar 

  30. Ware JE Jr., Gandek B (1998) Methods for testing data quality, scaling assumptions, and reliability: the IQOLA Project approach. International Quality of Life Assessment. J Clin Epidemiol 51(11):945–952. https://doi.org/10.1016/s0895-4356(98)00085-7

    Article  PubMed  Google Scholar 

  31. Ashkenazi A, Silberstein S, Jakubowski M, Burstein R (2007) Improved identification of allodynic migraine patients using a questionnaire. Cephalalgia 27(4):325–329. https://doi.org/10.1111/j.1468-2982.2007.01291.x

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Ozarslan M, Matur Z, Tuzun E, Oge AE (2022) Cutaneous allodynia and thermal thresholds in chronic migraine: The effect of onabotulinumtoxinA. Clinical Neurology and Neurosurgery 220:107357. https://doi.org/10.1016/j.clineuro.2022.107357

    Article  PubMed  Google Scholar 

  33. Nahman-Averbuch H, Shefi T, Schneider VJ 2nd, Li D, Ding L, King CD, Coghill RC (2018) Quantitative sensory testing in patients with migraine: a systematic review and meta-analysis. Pain 159(7):1202–1223. https://doi.org/10.1097/j.pain.0000000000001231

    Article  PubMed  Google Scholar 

  34. Vincent M, Viktrup L, Nicholson RA, Ossipov MH, Vargas BB (2022) The not so hidden impact of interictal burden in migraine: A narrative review. Front Neurol 3;13:1032103. https://doi.org/10.3389/fneur.2022.1032103

  35. Peng KP, May A (2018) Quantitative sensory testing in migraine patients must be phase-specific. Pain 159(11):2414–2416. https://doi.org/10.1097/j.pain.0000000000001353

    Article  PubMed  Google Scholar 

  36. Peng KP, May A (2019) Migraine understood as a sensory threshold disease. Pain 160(7):1494–1501. https://doi.org/10.1097/j.pain.0000000000001531

    Article  PubMed  Google Scholar 

  37. Han SM, Kim KM, Cho SJ, Yang KI, Kim D, Yun CH, Chu MK (2021) Prevalence and characteristics of cutaneous allodynia in probable migraine. Sci Rep 11(1):2467. https://doi.org/10.1038/s41598-021-82080-z

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Burstein R, Cutrer MF, Yarnitsky D (2000) The development of cutaneous allodynia during a migraine attack clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine. Brain 123(Pt 8):1703–1709. https://doi.org/10.1093/brain/123.8.1703

    Article  PubMed  Google Scholar 

  39. Russo A, Esposito F, Conte F, Fratello M, Caiazzo G, Marcuccio L, Giordano A, Tedeschi G, Tessitore A (2017) Functional interictal changes of pain processing in migraine with ictal cutaneous allodynia. Cephalalgia 37(4):305–314. https://doi.org/10.1177/0333102416644969

    Article  PubMed  Google Scholar 

  40. Louter MA, Bosker JE, van Oosterhout WP, van Zwet EW, Zitman FG, Ferrari MD, Terwindt GM (2013) Cutaneous allodynia as a predictor of migraine chronification. Brain 136(Pt 11):3489–3496. https://doi.org/10.1093/brain/awt251

    Article  PubMed  Google Scholar 

  41. Mathew PG, Cutrer FM, Garza I (2016) A touchy subject: an assessment of cutaneous allodynia in a chronic migraine population. Journal of pain research 9:101–104. https://doi.org/10.2147/JPR.S103238

    Article  PubMed  PubMed Central  Google Scholar 

  42. Schwedt TJ, Larson-Prior L, Coalson RS, Nolan T, Mar S, Ances BM, Benzinger T, Schlaggar BL (2014) Allodynia and descending pain modulation in migraine: a resting state functional connectivity analysis. Pain medicine 15(1):154–165. https://doi.org/10.1111/pme.12267

    Article  PubMed  Google Scholar 

  43. Ashina S, Melo-Carrillo A, Szabo E, Borsook D, Burstein R (2023) Pre-treatment non-ictal cephalic allodynia identifies responders to prophylactic treatment of chronic and episodic migraine patients with galcanezumab: A prospective quantitative sensory testing study (NCT04271202). Cephalalgia 43(3):3331024221147881. https://doi.org/10.1177/03331024221147881

    Article  PubMed  Google Scholar 

  44. Moulton EA, Burstein R, Tully S, Hargreaves R, Becerra L, Borsook D (2008) Interictal dysfunction of a brainstem descending modulatory center in migraine patients. PLoS One 3(11):e3799. https://doi.org/10.1371/journal.pone.0003799

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Hsiao FJ, Wang SJ, Lin YY, Fuh JL, Ko YC, Wang PN, Chen WT (2018) Somatosensory gating is altered and associated with migraine chronification: A magnetoencephalographic study. Cephalalgia 38(4):744–753. https://doi.org/10.1177/0333102417712718

    Article  PubMed  Google Scholar 

  46. Zhang J, Su J, Wang M, Zhao Y, Zhang QT, Yao Q, Lu H, Zhang H, Li GF, Wu YL, Liu YS, Liu FD, Zhuang MT, Shi YH, Hou TY, Zhao R, Qiao Y, Li J, Liu JR, Du X (2017) The sensorimotor network dysfunction in migraineurs without aura: a resting-state fMRI study. J Neurol 264(4):654–663. https://doi.org/10.1007/s00415-017-8404-4

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Open Access funding enabled and organized by Projekt DEAL. This research was funded the Medicine Research Committee of the University of Lübeck (H03-2022, FuL-Mittel 2022/2023).

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization: GFC, TMS, KL. Formal analysis: GFC; TMS. Methodology: GFC; TMS; TM; AS. Supervision: GFC, KL. Writing: original draft: TM. Writing: review & editing: GFC; TM; AS; TMS; KL.

Corresponding author

Correspondence to Kerstin Luedtke.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the University of Luebeck Ethics Committee (process number: 21-506).

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Marusich, T., Szikszay, T.M., Sennholz, A. et al. Translation, cross-cultural adaptation and measurement proprieties of the German version of the Allodynia Symptom Checklist (ASC-12). J Headache Pain 24, 160 (2023). https://doi.org/10.1186/s10194-023-01697-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s10194-023-01697-9

Keywords