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Dive into the research topics where B.S. van der Meij is active.

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Featured researches published by B.S. van der Meij.


European Journal of Clinical Nutrition | 2012

Oral nutritional supplements containing n-3 polyunsaturated fatty acids affect quality of life and functional status in lung cancer patients during multimodality treatment: an RCT

B.S. van der Meij; J.A.E. Langius; Marieke D. Spreeuwenberg; S.M. Slootmaker; Marinus A. Paul; Egbert F. Smit; P.A.M. van Leeuwen

Background/Objectives:Our objective was to investigate effects of an oral nutritional supplement containing n-3 polyunsaturated fatty acids (FAs) on quality of life, performance status, handgrip strength and physical activity in patients with non-small cell lung cancer (NSCLC) undergoing multimodality treatment.Subjects/Methods:In a double-blind experiment, 40 patients with stage III NSCLC were randomised to receive 2 cans/day of a protein- and energy-dense oral nutritional supplement containing n-3 polyunsaturated FAs (2.02 g eicosapentaenoic acid+0.92 g docosahexaenoic acid/day) or an isocaloric control supplement, during multimodality treatment. Quality of life, Karnofsky Performance Status, handgrip strength and physical activity (by wearing an accelerometer) were assessed. Effects of intervention were analysed by generalised estimating equations. P-values <0.05 were regarded as statistically significant.Results:The intervention group reported significantly higher on the quality of life parameters, physical and cognitive function (B=11.6 and B=20.7, P<0.01), global health status (B=12.2, P=0.04) and social function (B=22.1, P=0.04) than the control group after 5 weeks. The intervention group showed a higher Karnofsky Performance Status (B=5.3, P=0.04) than the control group after 3 weeks. Handgrip strength did not significantly differ between groups over time. The intervention group tended to have a higher physical activity than the control group after 3 and 5 weeks (B=6.6, P=0.04 and B=2.5, P=0.05).Conclusion:n-3 Polyunsaturated FAs may beneficially affect quality of life, performance status and physical activity in patients with NSCLC undergoing multimodality treatment.


Bone Marrow Transplantation | 2013

Nutritional support in patients with GVHD of the digestive tract: state of the art

B.S. van der Meij; P. de Graaf; N. Wierdsma; J.A.E. Langius; J. Janssen; P.A.M. van Leeuwen; O.J. Visser

An important complication of allo-SCT is GVHD, which commonly affects the skin, liver and digestive tract. Clinical symptoms of GVHD of the digestive tract (GVHD-DT) include excessive diarrhoea, abdominal pain and cramps, nausea and vomiting, gastrointestinal bleeding, dysphagia, and weight loss. Treatment is complicated and regarding nutritional support, only a few guidelines are available. Our aim was to critically appraise the literature on nutritional assessment, nutritional status and nutritional support for patients with GVHD-DT. Evidence shows that GVHD-DT is often associated with malnutrition, protein losing enteropathy, magnesium derangements, and deficiencies of zinc, vitamin B12 and vitamin D. Limited evidence exists on derangements of magnesium, resting energy expenditure, bone mineral density and pancreatic function, and some beneficial effects of n-3 polyunsaturated fatty acids and pancreatic enzyme replacement therapy. Expert opinions recommend adequate amounts of energy, at least 1.5 g protein/kg body weight, supplied by total parenteral nutrition in cases of severe diarrhoea. When diarrhoea is <500 mL a day, a stepwise oral upgrade diet can be followed. No studies exist on probiotics, prebiotics, dietary fibre and immunonutrition in GVHD-DT patients. Future research should focus on absorption capacity, vitamin and mineral status, and nutritional support strategies.


OA Epidemiology | 2013

The effects of supplementation of n-3 polyunsaturated fatty acids on clinical outcome parameters in patients with cancer: a systematic review

B.S. van der Meij; Jd Bauer; Ea Isenring; T Brown; Wl Davidson; Mae van Bokhorst; Jae Langius; Pam van Leeuwen

Introduction Existing guidelines on nutrition support in patients with cancer cachexia state limited evidence for the beneficial effects of n-3 polyunsaturated fatty acids (PUFAs) on clinical outcome. In order to report on the latest evidence for n-3 PUFAs in cancer cachexia, we conducted a systematic literature review of randomized controlled trials (RCTs), comparing the effects on clinical outcome parameters of oral or enteral supplementation of n-3 PUFAs in cancer patients receiving chemotherapy, radiotherapy, surgery or palliative care. Materials and methods In PubMed, EMBASE and the Cochrane Library, search terms on cancer, n-3 PUFAs and clinical outcome parameters (nutritional status, morbidity, mortality and quality of life) were entered on 1 April 2013, using limits for adults, humans and English language. The quality and evidence of the retrieved publications were appraised by an expert team of Australian and Dutch dieticians and nutritionists, using the ADA grading system. Fifteen RCTs were retrieved. Results Nine RCTs were of positive quality, five of neutral quality and one of negative quality and were performed in patients with various types of cancer. Fair evidence shows that supplementation of n-3 PUFAs appears to be safe and may improve the quality of life and physical activity in patients with cancer. However, supplementation of n-3 PUFAs does not improve energy or protein intake, appetite or survival and does not reduce postoperative complications. The evidence for the effect on body weight, fatfree mass and performance status remains inconclusive. Conclusion Supplementation of n-3 PUFAs may have some positive effects in patients with cancer. Introduction Cancer cachexia, a complex metabolic syndrome associated with underlying illness, characterized by an increased inflammatory status and loss of muscle mass with or without loss of fat mass, is highly prevalent among patients with cancer1–7. This syndrome is a result of complex alterations in carbohydrate, lipid and protein metabolism8,9, caused by inflammatory mediators such as cytokines and tumour-derived catabolic drivers10. Proteolysis-inducing factor (PIF) is produced by the tumour and induces protein catabolism11. As a result of the acute-phase response, the liver shows an increased protein turnover for the production of inflammatory mediators, using muscle mass to release amino acids9,10. Changes in lipid metabolism in cancer include a reduction of lipogenesis, with unchanged whole-body lipolysis and mobilization of fatty acids from fat tissue. Alterations in glucose metabolism are reflected by glucose intolerance and insulin resistance8,9,11. Thus far, conventional nutritional support has been limited in its ability to stabilize body weight and maintain fat-free mass in patients with cachexia. Pharmaceutical interventions sometimes improved appetite, body weight and quality of life, but weight gain mostly consisted of fat mass12–15. n-3 Polyunsaturated fatty acids (PUFAs), especially eicosapentaenoic acid (EPA), seem to be promising agents to treat cancer cachexia. A dose of around 2 g of EPA per day (alone or combined with docosahexaenoic acid, DHA) appears to decrease the production of proinflammatory cytokines16,17 and PIF and is associated with stabilization of body weight and probably fat-free mass13,18. This has been shown in animal studies and in nonrandomized human trials in pancreatic cancer patients19,20. However, randomized controlled trials (RCTs) show contradictory results21–26. This may be due to issues related to study limitations, such as the disease severity, confounding factors and nonadherence with n-3 PUFA supplements. Also, study designs and outcome parameters differ in terms of supplementation dosage, * Corresponding author Email: [email protected] 1 Department of Nutrition and Dietetics, Internal Medicine, VU University Medical Center Amsterdam, the Netherlands 2 Centre for Dietetics Research, School of Human Movement Studies, University of Queensland, Brisbane, Australia 3 Department of Nutrition and Dietetics, Royal Brisbane & Women’s Hospital, Brisbane, Australia 4 Department of Nutrition and Dietetic Services, Princess Alexandra Hospital, Brisbane, Australia 5 Department of Surgery, VU University Medical Center Amsterdam, the Netherlands


Bone Marrow Transplantation | 2017

If the gut works, use it! But does the gut work in gastrointestinal GvHD?

B.S. van der Meij; N J Wierdsma; J. Janssen; Nicolaas E. P. Deutz; O J Visser


Clinical Nutrition Supplements | 2012

PP048-SUN IMPAIRED APPETITE AND DIETARY INTAKE IN COMMUNITY-DWELLING OLDER ADULTS

B.S. van der Meij; Hanneke A.H. Wijnhoven; Jung Sun Lee; Denise K. Houston; Trisha F. Hue; T. B. Harris; S. B. Kritchevsky; A.B. Newman; Marjolein Visser


Nederlands tijdschrift voor voeding en diëtetiek | 2013

Drinkvoeding verrijkt met n-3 vetzuren beinvloedt de kwaliteit van leven en functionele status bij patienten met longkanker tijdens chemoradiotherapie: een RCT

B.S. van der Meij; J.A.E. Langius; Marieke D. Spreeuwenberg; S.M. Slootmaker; Marinus A. Paul; Egbert F. Smit; P.A.M. van Leeuwen


Clinical Nutrition Supplements | 2012

PP124-SUN PERFORMANCE STATUS, NUTRITIONAL PARAMETERS AND ATTITUDES TOWARDS PHYSICAL EXERCISE TRAINING IN LUNG CANCER PATIENTS AT THE START OF CHEMOTHERAPY

B.S. van der Meij; G. Unver; M.A. Chung; K.M. Lankhorst; G. Houwaard; L. Stanic-Jovic; J.A.E. Langius


Clinical Nutrition Supplements | 2011

PP053-SUN THE PREVALENCE AND PROGNOSTIC VALUE OF PRE-CACHEXIA AND CACHEXIA AT DIAGNOSIS OF STAGE III NSCLC

B.S. van der Meij; C.P. Schoonbeek; J.A.E. Langius; Egbert F. Smit; Maurizio Muscaritoli; P.A.M. van Leeuwen


Clinical Nutrition Supplements | 2009

P183 HOW LONG SHOULD INDIRECT CALORIMETRY MEASUREMENT TAKE: A COMPARISON BETWEEN VMAX AND DELTATRAC

G.H. Hofsteenge; H.M. Kruizenga; B.S. van der Meij; Peter J.M. Weijs


Clinical Nutrition Supplements | 2009

P110 PLASMA AND WHITE BLOOD CELL INCORPORATION OF N-3 FATTY ACIDS AFTER LIPID INFUSION IN GRAFT-VERSUS-HOST DISEASE: A DOSE RESPONSE STUDY

B.S. van der Meij; O.J. Visser; J.A.E. Langius; M. Hacquebard; Y.A. Carpentier; P.C. Huijgens; P.A.M. van Leeuwen

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J.A.E. Langius

VU University Medical Center

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Egbert F. Smit

Netherlands Cancer Institute

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O.J. Visser

VU University Amsterdam

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N. Wierdsma

VU University Amsterdam

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H.M. Kruizenga

VU University Medical Center

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J. Janssen

VU University Amsterdam

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Marinus A. Paul

VU University Medical Center

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Peter J.M. Weijs

VU University Medical Center

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