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Dive into the research topics where Mayienne Bakkers is active.

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Featured researches published by Mayienne Bakkers.


Journal of The Peripheral Nervous System | 2010

Intraepidermal nerve fiber density at the distal leg: a worldwide normative reference study

Giuseppe Lauria; Mayienne Bakkers; Christoph Schmitz; Raffaella Lombardi; Paola Penza; Grazia Devigili; A. Gordon Smith; Sung Tsieh Hsieh; Svein Ivar Mellgren; Thirugnanam Umapathi; Dan Ziegler; Catharina G. Faber; Ingemar S. J. Merkies

The diagnostic reliability of skin biopsy in small fiber neuropathy depends on the availability of normative reference values. We performed a multicenter study to assess the normative values of intraepidermal nerve fiber (IENF) density at distal leg stratified by age deciles. Eight skin biopsy laboratories from Europe, USA, and Asia submitted eligible data. Inclusion criteria of raw data were healthy subjects 18 years or older; known age and gender; 3‐mm skin biopsy performed 10‐cm above the lateral malleolus; bright‐field immunohistochemistry protocol, and quantification of linear IENF density in three 50‐µm sections according to published guidelines. Data on height and weight were recorded, and body mass index (BMI) was calculated in subjects with both available data. Normative IENF density reference values were calculated through quantile regression analysis; influence of height, weight, or BMI was determined by regression analyses. IENF densities from 550 participants (285 women, 265 men) were pooled. We found a significant age‐dependent decrease of IENF density in both genders (women p < 0.001; men p = 0.002). Height, weight, or BMI did not influence the calculated 5th percentile IENF normative densities in both genders. Our study provides IENF density normative reference values at the distal leg to be used in clinical practice.


Annals of Oncology | 2013

The chemotherapy-induced peripheral neuropathy outcome measures standardization study: from consensus to the first validity and reliability findings

Guido Cavaletti; David R. Cornblath; Ingemar S. J. Merkies; T. J. Postma; Emanuela Rossi; Barbara Frigeni; Paola Alberti; Jordi Bruna; Roser Velasco; Andreas A. Argyriou; H. P. Kalofonos; Dimitri Psimaras; Damien Ricard; Andrea Pace; Edvina Galiè; Chiara Briani; C. Dalla Torre; Catharina G. Faber; R. Lalisang; W. Boogerd; Dieta Brandsma; Susanne Koeppen; J. Hense; Dawn J. Storey; S. Kerrigan; Angelo Schenone; Sabrina Fabbri; Maria Grazia Valsecchi; A. Mazzeo; A. Toscano

BACKGROUND Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating and dose-limiting complication of cancer treatment. Thus far, the impact of CIPN has not been studied in a systematic clinimetric manner. The objective of the study was to select outcome measures for CIPN evaluation and to establish their validity and reproducibility in a cross-sectional multicenter study. PATIENTS AND METHODS After literature review and a consensus meeting among experts, face/content validity were obtained for the following selected scales: the National Cancer Institute-Common Toxicity Criteria (NCI-CTC), the Total Neuropathy Score clinical version (TNSc), the modified Inflammatory Neuropathy Cause and Treatment (INCAT) group sensory sumscore (mISS), the European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30, and CIPN20 quality-of-life measures. A total of 281 patients with stable CIPN were examined. Validity (correlation) and reliability studies were carried out. RESULTS Good inter-/intra-observer scores were obtained for the TNSc, mISS, and NCI-CTC sensory/motor subscales. Test-retest values were also good for the EORTC QLQ-C30 and CIPN20. Acceptable validity scores were obtained through the correlation among the measures. CONCLUSION Good validity and reliability scores were demonstrated for the set of selected impairment and quality-of-life outcome measures in CIPN. Future studies are planned to investigate the responsiveness aspects of these measures.BACKGROUND Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating and dose-limiting complication of cancer treatment. Thus far, the impact of CIPN has not been studied in a systematic clinimetric manner. The objective of the study was to select outcome measures for CIPN evaluation and to establish their validity and reproducibility in a cross-sectional multicenter study. PATIENTS AND METHODS After literature review and a consensus meeting among experts, face/content validity were obtained for the following selected scales: the National Cancer Institute-Common Toxicity Criteria (NCI-CTC), the Total Neuropathy Score clinical version (TNSc), the modified Inflammatory Neuropathy Cause and Treatment (INCAT) group sensory sumscore (mISS), the European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30, and CIPN20 quality-of-life measures. A total of 281 patients with stable CIPN were examined. Validity (correlation) and reliability studies were carried out. RESULTS Good inter-/intra-observer scores were obtained for the TNSc, mISS, and NCI-CTC sensory/motor subscales. Test-retest values were also good for the EORTC QLQ-C30 and CIPN20. Acceptable validity scores were obtained through the correlation among the measures. CONCLUSION Good validity and reliability scores were demonstrated for the set of selected impairment and quality-of-life outcome measures in CIPN. Future studies are planned to investigate the responsiveness aspects of these measures.


Neurology | 2009

Intraepidermal nerve fiber density and its application in sarcoidosis

Mayienne Bakkers; I. S. J. Merkies; Giuseppe Lauria; Grazia Devigili; Paola Penza; Raffaella Lombardi; Mieke C. E. Hermans; S. I. van Nes; M. De Baets; Catharina G. Faber

Background: Intraepidermal nerve fiber density (IENFD) is considered a good diagnostic tool for small fiber neuropathy (SFN). Objectives: To assess stratified normative values for IENFD and determine the reliability and validity of IENFD in sarcoidosis. Methods: IENFD was assessed in 188 healthy volunteers and 72 patients with sarcoidosis (n = 58 with SFN symptoms, n = 14 without SFN symptoms). Healthy controls were stratified (for age and sex), resulting in 6 age groups (20–29, 30–39, … up to ≥70 years) containing at least 15 men and 15 women. A skin biopsy was taken in each participant 10 cm above the lateral malleolus and analyzed in accordance with the international guidelines using bright-field microscopy. Interobserver/intraobserver reliability of IENFD was examined. In the patients, a symptoms inventory questionnaire (SIQ; assessing SFN symptoms) and the Vickrey Peripheral Neuropathy Quality-of-Life Instrument-97 (PNQoL-97) were assessed to examine the discriminative ability of normative IENFD values. Results: There was a significant age-dependent decrease of IENFD values in healthy controls, with lower densities in men compared with women. Good interobserver/intraobserver reliability scores were obtained (κ values ≥0.90). A total of 21 patients with sarcoidosis had a reduced IENFD score (<5th percentile; 19 [32.8%] in patients with SFN symptoms, 2 [14.3%] in patients without SFN symptoms). The validity of the normative IENFD values was demonstrated by distinguishing between the SIQ scores and various PNQoL-97 values for the different patient groups. Conclusion: This study provides clinically applicable distal intraepidermal nerve fiber density normative values, showing age- and sex-related differences.


Molecular Genetics and Metabolism | 2012

Small fiber neuropathy in Fabry disease

Marieke Biegstraaten; Carla E. M. Hollak; Mayienne Bakkers; Catharina G. Faber; Johannes M. F. G. Aerts; Ivo N. van Schaik

Previous studies have explicitly shown that small nerve fibers are affected in Fabry disease which is assumed to cause the severe neuropathic pain that patients may have from childhood on. Neuropathic pain and small fiber neuropathy characteristics have therefore been considered as appropriate study endpoints in studies on the efficacy of enzyme replacement therapy. However, the relationship between small fiber neuropathy characteristics and pain, as well as the course of small fiber neuropathy in Fabry disease is still uncertain. In this article a comprehensive overview of the existing literature on small nerve fiber function and structure and the relationship with pain, age and disease severity is presented supplemented with data from the Dutch Fabry cohort, with the aim to identify consensus as well as controversies and to propose a hypothesis on the evolution of neuropathy in Fabry disease.


Neurology | 2013

Incidence and prevalence of small-fiber neuropathy: A survey in the Netherlands

Martine J.H. Peters; Mayienne Bakkers; Ingemar S. J. Merkies; Janneke G. J. Hoeijmakers; Elisabeth P.M. van Raak; Catharina G. Faber

adults is a risk factor for DLB and not for Alzheimer disease. It is striking that these symptoms were not mentioned in the article by Boot et al. since our results need confirmation. Regardless, we think that the greater likelihood of having a history of depression or anxiety in patients with diagnosis of DLB would support our findings because the diagnosis of ADHD is often confused or overlaps with depression and anxiety. Comorbidity between these entities and the possibility of bias is well known. In this study, the possibility of such bias is heightened because the data for depression or anxiety were generated solely from medical history and ADHD is usually underreported.


Journal of The Peripheral Nervous System | 2013

Temperature threshold testing: a systematic review

Mayienne Bakkers; Catharina G. Faber; Martine J. H. Peters; Jos P. H. Reulen; Hessel Franssen; Tanya Z. Fischer; Ingemar S. J. Merkies

The diagnosis of small fiber neuropathy (SFN) has been recently defined as typical symptoms due to small nerve fiber dysfunction accompanied by reduced intra‐epidermal nerve fiber density (IENFD) or abnormal temperature threshold testing (TTT). Guidelines have been published for the assessment of IENFD. However, international guidelines for TTT are lacking. This paper presents a systematic literature review on reported TTT methods and provides recommendations for its future use in studies evaluating patients. A total of 164 papers fulfilled pre‐defined requirements and were selected for review. Over 15 types of instruments are currently being used with a variety of methodological approaches for location, stimulus application, and sensation qualities examined. Consensus is needed to standardize the use of TTT as a diagnostic and follow‐up tool in patients.


Journal of The Peripheral Nervous System | 2015

Improving assessment in small fiber neuropathy

Brigitte A. Brouwer; Mayienne Bakkers; Janneke G. J. Hoeijmakers; Catharina G. Faber; Ingemar S. J. Merkies

Interval measures at the impairment level addressing symptoms and at the activity/participation level addressing daily and social restrictions have not been developed for small fiber neuropathy (SFN). We developed an SFN‐specific Rasch‐built overall disability scale (SFN‐RODS©), an activity/participation scale at the interval level. A preliminary SFN‐RODS containing 146 activity/participation items was assessed twice (reliability studies) in 238 patients with SFN. The ordinal‐based 13‐item SFN‐symptoms inventory questionnaire (SFN‐SIQ©) and pain‐visual‐analogue‐scale were also assessed (validity studies). The pre‐SFN‐RODS and SFN‐SIQ data were subjected to the Rasch analyses. The pre‐SFN‐RODS did not meet Rasch model expectations. Based on requirements, such as misfit statistics, differential item functioning, and local dependency, items were systematically removed and model fit improved. Finally, a 32‐item SFN‐RODS© scale was constructed that fulfilled all Rasch requirements, demonstrating acceptable reliability and validity scores. The 13‐item SFN‐SIQ© was successfully transformed to an interval Rasch‐built measure fulfilling models requirements. In conclusion, the 32‐item SFN‐RODS© is a disease‐specific interval measure suitable for detecting activity limitations and participation restrictions in patients with SFN. The 13‐item SFN‐SIQ© was transformed through Rasch to an interval measure. The use of these scales is recommended in future clinical interventional trials involving patients with SFN.


Muscle & Nerve | 2015

Optimizing temperature threshold testing in small-fiber neuropathy.

Mayienne Bakkers; Catharina G. Faber; Jos P. H. Reulen; Janneke G. J. Hoeijmakers; Els K. Vanhoutte; Ingemar S. J. Merkies

Introduction: We examined optimization of a temperature threshold testing (TTT) protocol for patients with suspected small‐fiber neuropathy (SFN) to lessen the burden for both patients and technicians, without sacrificing accuracy. Methods: Data from 81 patients with SFN (skin biopsy and TTT abnormal) and 81 without SFN (skin biopsy and TTT normal) were used. Warm, cold, and heat pain sensation thresholds were determined bilaterally on the thenar eminence and foot dorsum by methods of limits and levels. Diagnostic accuracy was determined for various sensory modality combinations through comparative corresponding area under the receiver‐operator characteristic curves. Results: Assessment of warm and cold thresholds in all extremities by the method of levels showed the best discriminatory ability (area under the curve 0.95, sensitivity 84.2%, specificity 93.8%). Conclusions: These assessments are suggested for TTT examination in possible SFN patients. By applying this combination, the time needed for TTT can be reduced, maintaining diagnostic accuracy. Muscle Nerve 51: 870–876, 2015


European Journal of Cancer | 2013

Rasch-built Overall Disability Scale for patients with chemotherapy-induced peripheral neuropathy (CIPN-R-ODS)

D. Binda; Els K. Vanhoutte; Guido Cavaletti; David R. Cornblath; Tjeerd J. Postma; Barbara Frigeni; Paola Alberti; Jordi Bruna; Roser Velasco; Andreas A. Argyriou; H. P. Kalofonos; Dimitri Psimaras; Damien Ricard; Andrea Pace; Edvina Galiè; Chiara Briani; C. Dalla Torre; R. Lalisang; Willem Boogerd; Dieta Brandsma; Susanne Koeppen; J. Hense; Dawn J. Storey; Simon Kerrigan; Angelo Schenone; Sabrina Fabbri; Emanuela Rossi; Maria Grazia Valsecchi; Catharina G. Faber; Ingemar S. J. Merkies


Journal of The Peripheral Nervous System | 2015

Grip strength comparison in immune-mediated neuropathies: Vigorimeter vs. Jamar

Thomas H P Draak; Mariëlle H. J. Pruppers; Sonja I. Van Nes; Els K. Vanhoutte; Mayienne Bakkers; Kenneth C. Gorson; W. Ludo van der Pol; Richard A. Lewis; Nicolette C. Notermans; Eduardo Nobile-Orazio; Jean Marc Léger; Peter Van den Bergh; Giuseppe Lauria; Vera Bril; Hans D. Katzberg; Michael P. Lunn; Jean Pouget; Anneke J. van der Kooi; Leonard H. van den Berg; Pieter A. van Doorn; David R. Cornblath; Angelika F. Hahn; Catharina G. Faber; Ingemar S. J. Merkies

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Giuseppe Lauria

Carlo Besta Neurological Institute

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Dieta Brandsma

Netherlands Cancer Institute

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R. Lalisang

Maastricht University Medical Centre

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