| Literature DB >> 32327984 |
Antonello Viceconti1, Eleonora Maria Camerone1, Deborah Luzzi1, Debora Pentassuglia1, Matteo Pardini2,3, Diego Ristori1, Giacomo Rossettini1, Alberto Gallace4,5, Matthew R Longo6, Marco Testa1.
Abstract
Background: Pain and body perception are essentially two subjective mutually influencing experiences. However, in the field of musculoskeletal disorders and rheumatic diseases we lack of a comprehensive knowledge about the relationship between body perception dysfunctions and pain or disability. We systematically mapped the literature published about the topics of: (a) somatoperception; (b) body ownership; and (c) perception of space, analysing the relationship with pain and disability. The results were organized around the two main topics of the assessment and treatment of perceptual dysfunctions.Entities:
Keywords: body ownership; body perception; body representation; chronic pain; musculoskeletal disorders; rheumatic diseases; scoping review; somatoperception
Year: 2020 PMID: 32327984 PMCID: PMC7161420 DOI: 10.3389/fnhum.2020.00083
Source DB: PubMed Journal: Front Hum Neurosci ISSN: 1662-5161 Impact factor: 3.169
Figure 1Summary of the adopted guidance framework for scoping reviews.
Terminological definitions.
| “ | Tactile stimuli detection, precision of touch (e.g., two-point discrimination threshold), repositioning accuracy (e.g., joint position sense). | ||
| “ | Perception of body parts' size and location, the skin localization of tactile stimuli, tactile object recognition, spatial localisation of touch. | ||
| With this “umbrella term” it can be grouped a variety of functional and neural configurations about different body characteristics (e.g., sensorial, perceptual or cognitive). In this sense, the conceptual term “ | |||
| “ | Body structural description, general semantic knowledge, formation of attitudes and emotion toward the body. |
Adapted and modified from Longo et al. (.
Figure 2PRISMA flow diagram detailing the selection of sources of evidence.
Eligibility criteria for inclusion and exclusion studies.
Or full text not in English language but with the abstract in English language.
With a particular focus on studies reporting methodologies or test/measures feasible to translate in clinical practice.
The correspondent paper were searched where available; included only if the abstract was available and if was described with a rigorous methodology and with clearly reported results on the base of the construct analyzed.
Included only if it was described with a rigorous methodology, with clearly reported results on the base of the construct analyzed.
Included studies and reference lists of secondary studied were manually scanned in order to find additional sources.
Excluded from the analysis but reported in order to provide a general overview of the amount of international literature published.
Reference list of records of interest for the topic were be manually scanned.
Included in qualitative analysis only if containing additional information to an earlier or ongoing trial study report, or information about a study or experiment not reported elsewhere.
Synopsis of included assessment studies.
| Wand et al. ( | Case-control Study | CLBP patients ( | 11-NRS (0–10), RMDQ (0–24), Localization task for tactile and painful stimuli (n° of mislocalizations). | 67% of subjects with CLBP reported at least 1 mislocalization with respect to 25% of controls ( |
| Adamczyk et al. ( | Two-Case Report Study | CLBP ( | 11-NRS (0–10), ODI (0–100%), 2-PET (mm) for subject A and B; PTP test (mm) for subject A; qualitative version of the PTP test for subject B. | Patient A) overestimated the painful site compared to all non-painful locations 2-PET; range: 45–206%, and also at PTP test: 24–84%. |
| Adamczyk et al. ( | Preliminary Validation Study | CLBP patients ( | 11-NRS (0–10), ODI (0–100%), Two-Point Estimation (TPE) Task (manual and verbal version). | CLBP patients underestimated the caliper distance by 56.2% (manual version) and 45.9% (verbal version), irrespective of the examiner and location. |
| Wand et al. ( | Case-control Study | CLBP patients ( | 11-NRS (0–10), SF-36: item 3—physical function (10–30), Letter recognition error rate (n°). | Letter error rate were significantly larger in CLBP group of about 10% ( |
| Moseley ( | Exploratory case-control study | CLBP patients ( | 101-VAS (0–100 mm), Clinical interview and Body Image Drawing of the trunk. | Five out of the six patients reported difficulties in delineating the full extent of their trunk: they all verbatim refer that they “can't find it.” Two subjects reported that “It feels as though it has shrunk.” No patients drew all vertebrae and missing vertebrae coincided with the level of the lost trunk delineation and of the usual pain. There was a tendency of vertebrae displacement from the midline in body drawings. |
| Lauche et al. ( | a) Qualitative study embedded in a RCT (Lauche et al., | CNP patients ( | Themes and sub-themes emerged from interviews in which patients were asked to talk about their body image drawings, Visual interpretation of the Body Image Drawing for neck and shoulders (modified version of that described by Moseley, | Interviews: patients refer changes in body perception of the neck as a feeling of swollen or distorted in proportion. These overestimations persist even when patients were aware of their actual appearance. Body Image Drawing: at the baseline, the drawn body showed noticeable discrepancies respect to a “normal” body (missing lines and augmented dimension of shoulders and neck) in 4 out 6 subjects more symmetric and complete. |
| Mibu et al. ( | Case-control study | CNP patients ( | 101-VAS (0–100 mm), Visual interpretation of the Body Image Drawing for neck and shoulders (modified version of that described by Moseley, | Body image is significantly ( |
| Nishigami et al. ( | Case-control study | CLBP patients ( | 101-VAS (0–100 mm), RMDQ (0–24), Body Image Drawing of the trunk as described by Moseley ( | 42.8% of subjects with CLBP had a normal perceive image of the lower back, 28.5% had an expanded image, and 28.5% had a shrunken image. |
| Moreira et al. ( | Exploratory case-control Study | CNP patients ( | 11-VAS (0–10 mm), Modified version of the Body Image Drawing of the trunk as described by Moseley ( | Qualitative analysis of the body image drawing: In both groups, two subjects were not able to draw one side of the neck: comparing the drawings it seems that patients delineate neck and shoulders outline less symmetric and uniform than controls, and necks appear shorter. Moreover, two participants drew neck and shoulders more enlarged than they really were, and these perceptions coincided with pain location. Participants that not draw part of the neck, or drawing a clearly distorted neck tend to report pain of higher level and/or duration. |
| Valenzuela-Moguillansky ( | Qualitative Study | FM patients ( | Themes and sub-themes. | Interviewees refer modifications in different aspects of body perception: body size, weight, localization and ownership. They talk about enlarged, thicker and heavy body parts. They also refer that near space is perceived as smaller, as if it was shrinking while their body become larger. At the peak of the pain stage some patients described the perception that the painful body parts did not belong to them (loss of the sense of body ownership), expressing the paradoxical experience of being in extreme pain while not feeling it. Moreover, they refer the inability to localize their painful body parts and pain. |
| Wand et al. ( | Psychometric Validation Study | CLBP patients ( | 101-VAS (0–100 mm), RMDQ (0–24), FreBAQ (0–36). | Fifty of 51 (98%) CLBP patients endorsed some level of distortion in self-perception, with only one subject recording zero for all items. |
| Wand et al. ( | Cross-sectional Study | CLBP patients ( | 11-NRS (0–10), RMDQ (0–24), FreBAQ (0–36). | FreBAQ mean total score in CLBP patients was 9.8 (SD = 6.6); median score = 9.0 (IQR = 4.0–14.0) and it was correlated with disability (0.319; |
| Beales et al. ( | Case-control questionnaire based study | Post-Partum LPP patients ( | Short-form MGPQ (0–45), ODI (0–100%), FreKAQ (0–36) | FreBAQ median difference: |
| Wand et al. ( | Exploratory cross-sectional questionnaire based study | Pregnancy-related LPP patients ( | 11-NRS (0–10), PGQ (0–100), FreBAQ (0–36). | FreBAQ median difference between pain and pain-free groups: 2.5; (‡); |
| Nishigami et al. ( | Psychometric Validation Study | CLBP patients ( | 101-VAS (0–100 mm), RMDQ (0–24), FreBAQ (0–36). | FreBAQ mean total score in CLBP patients was 11.7 (6.4), and it was significantly correlated with pain in motion ( |
| Janssens et al. ( | Psychometric Validation Study | CLBP patients ( | 11-NRS (0–10), ODI (0–100%), FreBAQ (0–36). | FreBAQ mean total score in CLBP group ( |
| Ehrenbrusthoff et al. ( | Psychometric Validation Study | CLBP patients ( | Short Form BPI: Pain Severity (0–10), Pain Interference (0–7), RMDQ (0–24), FreBAQ (0–36). | Global FreBAQ mean total score was significantly different in CLBP group ( |
| Nishigami et al. ( | Psychometric Validation Study | Knee OA patients ( | 101-VAS (0–100 mm), OKSQ (0–48), FreKAQ (0–36) | FreKAQ mean total score was significantly higher in knee patients vs. healthy controls: 12.4 (7.6) vs. 3.4 (4.4); ( |
| Magni et al. ( | Case-Control Study | Hand OA Patients ( | 11-NRS (0–10), DASH (0–100), NLSQ (5–30). | The hand OA group reported neglect-like symptoms (median score: 5.5; IQR: 3) significantly |
| Hirakawa et al. ( | Longitudinal Study | Total Knee Arthroplasty for Knee OA patients ( | 101-VAS (0–100 mm), NLSQ (0–500): Motor Neglect (MN) and Cognitive Neglect (CN) sub-scales. | The percentage of patients with a total NLSQ ≥100 was 36% (MN, 40%; CN, 18%) at 3 w and 19% (MN, 19%; CN, 5%) at 6 w. The MN subscale of NLS was associated with Pain at 3 w (β = 0.50; |
| Gilpin et al. ( | Case-control Study | Hand OA patients ( | Visual size estimation task (% of the real hand size). | Hand size estimations were significantly smaller for the OA group: −8.01 (3.07 to 12.94); t(22) = 2.39, |
| Martínez et al. ( | Case-control Study | FM patients ( | 11-VAS (0–100 mm), Short-form BPI (0–20), FIQ (0–100), 5-point Likert Scale measuring proprioceptive drift (0.35), ownership (0–35) and agency (0–30). | FM patients were more prone to experiment the misperceptions produced by the RHIP. They scored significantly ( |
| Treleaven and Takasaki ( | Case-control Study | CNP patients ( | 11-NRS (0–10), NDI (0–100%), Short Form DHI (0–13), SVV: Computerized Rod And Frame (CRAF) test as described by Takasaki et al. ( | CNP group had significantly larger variability of SVV errors vs. the other two groups: 1) VE = 0.5 (0.23 to 0.77) vs. healthy controls ( |
| Docherty et al. ( | Case-control Study | CNP patients ( | 11-NRS (0–10), NDI (0–50), SVV and SVH: Computerized Rod And Frame (CRAF) test (°). | In absence of surrounding frame, significant difference were found in mean errors |
| (Grod and Diakow, | Cohort study | Acute or recurrent NP patients ( | Computerized Rod And Frame (CRAF) test as used by Docherty et al. ( | Statistically significant differences in SVV and SVO were found between symptomatic and asymptomatic subjects (F = 13.37, p = |
ACR, American College of Rheumatology; CLBP, Chronic Low Back Pain; LPP, Lumbo-Pelvic Pain; FM, Fibromyalgia; OA, Osteoarthritis; NP, Neck Pain; CNP, Chronic Neck Pain; VAS, Visual Analog Scale; NRS, Numeric Rating Scale; Chronic Pain Grade, CPG; BPI, Brief Pain Inventory; MGPQ, McGill Pain Questionnaire; ODI, Oswestry Disability Index; RMDQ, Roland Morris Disability Questionnaire; DASH, NDI, Neck Disability Index; DHI, Dizziness Handicap Inventory; BPQ, Body Perception Questionnaire; Disabilities of the Arm, Shoulder and Hand Questionnaire; PGQ, Pelvic Girdle Questionnaire; TSK, Tampa Scale of Kinesiophobia; PCS, Pain Catastrophizing Scale; FPQ, Fear of Pain Questionnaire; HADS, Hospital Anxiety and Depression Scale; BDI, Beck Depression Inventory; DASS, Depression Anxiety Stress Scale; STAI, State-Trait Anxiety Inventory; FIQ, Fibromyalgia Impact Questionnaire; SIQ, Symptoms Impact Questionnaire; OKSQ, Oxford Knee Score Questionnaire; MAIA, The Multidimensional Assessment of Interceptive Awareness; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders IV; PU, Pain Unpleasantness; PI, Pain Intensity; PeT, Perception Threshold; PT, Pain Threshold; PTo, Pain Tolerance; FreKAQ, Fremantle Knee Awareness Questionnaire; NLSQ, Neglect-like symptoms questionnaire, TPT, Tactile Perception Threshold; 2PDT, 2-Point Discrimination Threshold; PTP, Poin-to-Poin Test; 2-PET, two Point Estimation Test; ROM, Range Of Motion; JPS, Joint Position Sense; TEMPA, Test d'Evaluation de la performance des Membres Supérieurs des Personnes Agées; BMI, Body Mass Index; RHIP, Rubber Hand Illusion Paradigm; SVV, Subjective Visual Vertical; SVH, Subjective Visual Horizontal; AE, Absolute Error; VE, Variable Error; AE, Absolute Error; VE, Variable Error; AE, Absolute Error; VE, Variable Error; DE, Direction of Error; RMSE, Root Mean Square Error; MDC, Minimal Detectable Change; ICC, Interclass Correlation Coefficients; MD, Mean Difference; NR, not reported; NA, Not Applicable; SD, Standard Deviation; IQR, Interquartile Range; SEM, Standard Error of Measurement; CI95%, Confidence Interval; +, p-value not reported; ‡, 95% CI not reported; SD, statistical difference; y, year/s; m, month/s; h, hour/s, min., minute; s, second/s, ms, millisecond. .
Synopsis of included intervention studies.
| Wand et al. ( | Randomized COT | CLBP patients ( | 1) Patients were assigned to: | a) Pain was significantly lower in both groups at the end of treatment, regardless of treatment order ( |
| Louw et al. ( | Case-series | CLBP patients ( | It was administered a perceptual localization task of 5 min. in a single session. | a) Pain was lower after treatment (11-NRS: – |
| Barker et al. ( | Single-blinded, RCNIT | CLBP patients ( | It was tested the non-inferiority of the FairMed (device for sensory discrimination training), administered for 30 min (twice a day, for 3 weeks), respect to the TENS (same dosage). | a) Both groups improved in pain scores: 0–11 VAS = −0.8 (−1.5 to −0.1) for EG; – |
| Wand et al. ( | Three single-case study | CLBP patients ( | It was tested a mixed treatment program composed by education and graded perceptual retraining program (localization and graphaestesia training) combined with graded motor retraining (minimum 10 w of home exercises). | Both Pain and Disability improves with clinical and statistical significance: 11-NRS = – |
| (Ryan et al., | Mixed-methods pilot RCT | CLBP patients ( | Patients were assigned to: | Tactile acuity training was not superior to sham therapy. Both groups improved pain and disability post-treatment but only values for CG were statistically significant (101-VAS: – |
| Morone et al. ( | Single-blinded, RCT | CLBP patients ( | Patients were assigned to: | Both groups treated with SuPeR and with Back School obtain an overall improvement both for Pain and Disability at T1 and T3: 11-VAS = – |
| Paolucci et al. ( | Single-blinded, RCT | CLBP patients ( | Patients were assigned to: | The SuPereR treatment reduce pain more than the CG performing the Back School program, but the difference was not statistically significant: MGPQ = 44 ± 24% for EG† and 39 ± 15% for CG†; |
| Vetrano et al. ( | Single-blind, RCT | CLBP patients ( | Patients were assigned to: | Both groups improved pain and disability scores at T1 and T3 respect to the baseline: 11-VAS: −2* (‡) at T1, – |
| Lauche et al. ( | Qualitative study embedded in a RCT (Lauche et al., | CNP patients ( | Patients were interviewed before and 3 d after a single traditional cupping treatment (for half of the patients); the other half of patients were in waiting list. | Interviews: subjects in EG refer a reduction in neck size (smaller) as a relief from pain.Body Image Drawing: Body image appears to be changed in EG after treatment (smaller dimension of body parts, and lines more symmetric and complete). Even the CG subjects improve in drawings their own's body, but they were no more complete, nor matched a “normal” silhouette. |
| Preston and Newport ( | Exploratory experimental study | Hand OA patients ( | Patients were administered the MIRAGE system: visuo-tactile illusion involving manipulations (stretching or shrinking) of patient's hand (affected and unaffected) while experimenter gently pulling or pushing on part of the hand. | 85% of patients reported reduction in pain for at least one of the experimental conditions (stretching and shrinking), but only manipulating visual appearance of the affected hand. |
| Diers et al. ( | Experimental study | Bilateral TP patients ( | Patients were administered: | There was no significant influence on Electric and Pressure PU ( |
| Stanton et al. ( | Pilot-experimental study | Knee OA patients ( | Patients were administered the MIRAGE system as described in Preston and Newport ( | VT illusion decreased pain by an average of 7.8 points (2.0 to 13.5), corresponding to a 25% reduction in pain both in CO (t1, 11 =2.96, |
| Nishigami et al. ( | Pilot-experimental study | CLBP patients ( | Patients were administered the MIRAGE system as described in Preston and Newport ( | Visual illusion of a strong back vs. normal condition reduce pain and fear only in subject having distorted explicit perceptual representation of his back (FreBAQ: 29/36): 101-NRS for pain = – |
ACR, American College of Rheumatology; CLBP, Chronic Low Back Pain; LBP, Low Back Pain; TP, Thoracic Pain; CNP, Chronic Neck Pain; OA, Osteoarthritis; MPQ, VAS, Visual Analog Scale; 11-NRS, 11-point Numeric Rating Scale; MGPQ, McGill Pain Questionnaire; ODI, Oswestry Disability Index; RMDQ, Roland Morris Disability Questionnaire; TSK, Tampa Scale of Kinesiophobia; RCT, randomized controlled trial; SuPeR, Surface for Perceptive Rehabilitation; TENS, Transcutaneous Electrical Nerve Stimulation; NSAIDs, Nonsteroidal Anti-Inflammatory Drug; TrP, Trigger Point; PU, Pain Unpleasantness; PI, Pain Intensity; PeT, Perception Threshold; PT, Pain Threshold; PTo, Pain Tolerance; RCT, Randomized Controlled Trial; COT, Cross-Over Trial; RCNIT, Randomized Controlled Non-Inferiority Trial; N.R., not reported; SD, Standard Deviation; MD, Mean Difference; CI95%, Confidence Interval; .
Figure 3Summary of the distribution of included studies for clinical conditions examined.
Figure 4Summary of the distribution of domain investigated for study typology.
Figure 5Summary of the distribution of evaluation studies for research design adopted.
Figure 6Summary of the distribution of intervention studies for research design adopted.
Figure 7Summary of the evaluation for clinical relevance of included assessment studies.
Figure 8Summary of the evaluation for clinical relevance of included treatment studies.