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Dive into the research topics where Pascale De Becker is active.

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Featured researches published by Pascale De Becker.


The American Journal of Medicine | 2000

A 37 kDa 2-5A binding protein as a potential biochemical marker for chronic fatigue syndrome.

Kenny De Meirleir; Catherine Bisbal; Isabelle Campine; Pascale De Becker; Tamim Salehzada; Edith Demettre; Bernard Lebleu

PURPOSE Recent studies have revealed abnormalities in the ribonuclease L pathway in peripheral blood mononuclear cells of patients with the chronic fatigue syndrome. We conducted a blinded study to detect possible differences in the distribution of 2-5A binding proteins in the cells of patients with chronic fatigue syndrome and controls. PATIENTS AND METHODS We studied 57 patients with chronic fatigue syndrome and 53 control subjects (28 healthy subjects and 25 patients with depression or fibromyalgia). A radioactive probe was used to label 2-5A binding proteins in unfractionated peripheral blood mononuclear cell extracts and to compare their distribution in the three groups. RESULTS A 37 kDa 2-5A binding polypeptide was found in 50 (88%) of the 57 patients with chronic fatigue syndrome compared with 15 (28%) of the 53 controls (P < 0.01). When present, the amount of 37 kDa protein was very low in the control groups. When expressed as the ratio of the 37 kDa protein to the 80 kDa protein, 41 (72%) of the 57 patients with chronic fatigue syndrome had a ratio > 0.05, compared with 3 (11%) of the 28 healthy subjects and none of the patients with fibromyalgia or depression. CONCLUSION The presence of a 37 kDa 2-5A binding protein in extracts of peripheral blood mononuclear cells may distinguish patients with chronic fatigue syndrome from healthy subjects and those suffering from other diseases.


The American Journal of Medicine | 1998

Autonomic testing in patients with chronic fatigue syndrome

Pascale De Becker; Paul Dendale; Kenny De Meirleir; Isabelle Campine; Krista Vandenborne; Yves Hagers

The purpose of this study was to determine whether chronic fatigue syndrome (CFS) patients show autonomic dysfunction at the cardiac level and if so, to discover whether these abnormalities explain the fatiguability and/or other symptoms in CFS. The study population consisted of 21 CFS patients (Centers for Disease Control and Prevention [CDC] criteria, 1988) and 13 age- and sex-matched healthy controls. The autonomic testing consisted of: (1) postural challenge: registration of heart rate and blood pressure (BP) and heart rate variability in supine and in upright position (tilted to 70 degrees); (2) Valsalva maneuver; (3) handgrip test; (4) cold pressor test; and (5) heart rate response to deep breathing. Statistical analysis was performed using the Mann Whitney rank sum test; results of the test were considered significant at the 0.05 level. After tilting heart rate was significantly higher in CFS patients compared with healthy controls (mean CFS = 88.9 beats/min vs control = 77.9 beats/min; P <0.01). Low frequency power after tilting was significantly higher in CFS patients compared with controls (mean CFS = 0.603 vs control = 0.428; P = 0.02). There was a trend toward an increased heart rate during the cold pressor test. Other parameters did not differ between the CFS and control populations. The observed changes point toward a sympathetic overactivity in CFS patients when they are exposed to stress. Parasympathetic abnormalities could not be observed. Therefore, our findings provide no real explanation for the fatigue and intolerance to physical exertion in these patients.


Clinical Rehabilitation | 2008

Can exercise limits prevent post-exertional malaise in chronic fatigue syndrome? An uncontrolled clinical trial

Jo Nijs; Freya Almond; Pascale De Becker; Steven Truijen; Lorna Paul

Objective: It was hypothesized that the use of exercise limits prevents symptom increases and worsening of their health status following a walking exercise in people with chronic fatigue syndrome. Design: An uncontrolled clinical trial (semi-experimental design). Setting: Outpatient clinic of a university department. Subjects: Twenty-four patients with chronic fatigue syndrome. Interventions: Subjects undertook a walking test with the two concurrent exercise limits. Each subject walked at an intensity where the maximum heart rate was determined by heart rate corresponding to the respiratory exchange ratio = 1.0 derived from a previous submaximal exercise test and for a duration calculated from how long each patient felt they were able to walk. Main outcome measures: The Short Form 36 Health Survey or SF-36, the Chronic Fatigue Syndrome Symptom List, and the Chronic Fatigue Syndrome — Activities and Participation Questionnaire were filled in prior to, immediately after and 24 hours after exercise. Results: The fatigue increase observed immediately post-exercise (P= 0.006) returned to pre-exercise levels 24 hours post-exercise. The increase in pain observed immediately post-exercise was retained at 24 hours post-exercise (P=0.03). Fourteen of the 24 subjects experienced a clinically meaningful change in bodily pain (change of SF-36 bodily pain score ≥10); 6 indicated that the exercise bout had slightly worsened their health status, and 2 had a clinically meaningful decrease in vitality (change of SF-36 vitality score ≥20). There was no change in activity limitations/participation restrictions. Conclusion: It was shown that the use of exercise limits (limiting both the intensity and duration of exercise) prevents important health status changes following a walking exercise in people with chronic fatigue syndrome, but was unable to prevent short-term symptom increases.


JAMA Internal Medicine | 2000

Exercise Capacity in Chronic Fatigue Syndrome

Pascale De Becker; J. Roeykens; Masha Reynders; Neil R. McGregor; Kenny De Meirleir


Journal of Interferon and Cytokine Research | 1997

Biochemical Evidence for a Novel Low Molecular Weight 2-5A-Dependent RNase L in Chronic Fatigue Syndrome

Robert J. Suhadolnik; Daniel L. Peterson; Karen O'Brien; Paul R. Cheney; Charles Vincent Herst; Nancy L. Reichenbach; Ning Kon; Susan E. Horvath; Kathryn T. Iacono; Martin E. Adelson; Kenny De Meirleir; Pascale De Becker; Ramamurthy Charubala; Wolfgang Pfleiderer


Fems Immunology and Medical Microbiology | 2002

High prevalence of Mycoplasma infections among European chronic fatigue syndrome patients. Examination of four Mycoplasma species in blood of chronic fatigue syndrome patients

Jo Nijs; Garth L. Nicolson; Pascale De Becker; Danny Coomans; Kenny De Meirleir


Journal of Chronic Fatigue Syndrome | 2002

Activity Limitations and Participation Restrictions in Patients with Chronic Fatigue Syndrom—Construction of a Disease Specific Questionnaire

Jo Nijs; Peter Vaes; Elke Van Hoof; Pascale De Becker; Neil R. McGregor; Kenny De Meirleir


Journal of Interferon and Cytokine Research | 2002

Structural and Functional Features of the 37-kDa 2-5A-Dependent RNase L in Chronic Fatigue Syndrome

Susan E. Shetzline; Camille Martinand-Mari; Nancy L. Reichenbach; Zivjena Buletic; Bernard Lebleu; Wolfgang Pfleiderer; Ramamurthy Charubala; Kenny De Meirleir; Pascale De Becker; Daniel L. Peterson; Charles Vincent Herst; Patrick Englebienne; Robert J. Suhadolnik


Chest | 2003

Associations Between Bronchial Hyperresponsiveness and Immune Cell Parameters in Patients With Chronic Fatigue Syndrome

Jo Nijs; Pascale De Becker; Kenny De Meirleir; Christian Demanet; Walter Vincken; Daniel Schuermans; Neil R. McGregor


Journal of Chronic Fatigue Syndrome | 2003

Monitoring a Hypothetical Channelopathy in Chronic Fatigue Syndrome: Preliminary Observations

Jo Nijs; Christian Demanet; Neil R. McGregor; Pascale De Becker; Michel Verhas; Patrick Englebienne; Kenny De Meirleir

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Kenny De Meirleir

Vrije Universiteit Brussel

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Jo Nijs

Vrije Universiteit Brussel

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Patrick Englebienne

Université libre de Bruxelles

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Christian Demanet

Vrije Universiteit Brussel

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Elke Van Hoof

Vrije Universiteit Brussel

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Isabelle Campine

Vrije Universiteit Brussel

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