Henk J. Veeze

ORCID: 0000-0003-0250-9380
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About
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Research Areas
  • Diabetes Management and Research
  • Diabetes and associated disorders
  • Cystic Fibrosis Research Advances
  • Pancreatic function and diabetes
  • Neonatal Respiratory Health Research
  • Tracheal and airway disorders
  • Diabetes Treatment and Management
  • Ion Transport and Channel Regulation
  • Diabetes Management and Education
  • Chronic Disease Management Strategies
  • Mobile Health and mHealth Applications
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Health Systems, Economic Evaluations, Quality of Life
  • Respiratory viral infections research
  • Clinical Nutrition and Gastroenterology
  • Pneumonia and Respiratory Infections
  • Immunodeficiency and Autoimmune Disorders
  • Ion channel regulation and function
  • Advanced Glycation End Products research
  • Diet, Metabolism, and Disease
  • Congenital Ear and Nasal Anomalies
  • Asthma and respiratory diseases
  • Obesity, Physical Activity, Diet
  • Infant Nutrition and Health
  • Magnesium in Health and Disease

IJsselland Ziekenhuis
2003-2010

Boston Children's Hospital
1995-2003

Pediatrics and Genetics
2001

Erasmus University Rotterdam
1990-2000

Erasmus MC - Sophia Children’s Hospital
1990-1998

The 65-kD isoform of glutamic acid decarboxylase (GAD65) is a major autoantigen in type 1 diabetes. We hypothesized that alum-formulated GAD65 (GAD-alum) can preserve beta-cell function patients with recent-onset diabetes.We studied 334 patients, 10 to 20 years age, diabetes, fasting C-peptide levels more than 0.3 ng per milliliter (0.1 nmol liter), and detectable serum autoantibodies. Within 3 months after diagnosis, were randomly assigned receive one three study treatments: four doses...

10.1056/nejmoa1107096 article EN New England Journal of Medicine 2012-02-01

Improving glycaemic control in people with Type 1 diabetes is known to reduce complications. Our aim was compare among using data gathered regional or national registries.Data were obtained for children and/or adults from the following countries (or regions): Western Australia, Austria, Denmark, England, Champagne-Ardenne (France), Germany, Epirus, Thessaly and Thessaloniki (Greece), Galway (Ireland), several Italian regions, Latvia, Rotterdam (The Netherlands), Otago (New Zealand), Norway,...

10.1111/dme.12676 article EN Diabetic Medicine 2014-12-15

Objective: The international SWEET registry (NCT04427189) was initiated in 2008 to improve outcomes pediatric diabetes. A 10-year follow-up allowed studying time trends of key quality indicators 22 centers from Europe, Australia, Canada, and India youth with type 1 diabetes (T1D). Methods: Aggregated data per person T1D <25 years age were compared between 2008-2010 2016-2018. Hierarchic linear logistic regression models applied. Models adjusted for gender, age-, duration groups. Results:...

10.1089/dia.2020.0618 article EN cc-by-nc Diabetes Technology & Therapeutics 2021-02-10

Cystic fibrosis is the most common lethal autosomal recessive disorder among whites. Among Dutch patients with cystic fibrosis, ΔF508 mutation and A455E second of transmembrane conductance regulator gene on chromosome 7. associated preserved pancreatic function residual secretion chloride across membranes. We investigated whether it also less severe pulmonary disease in fibrosis.

10.1056/nejm199507133330204 article EN New England Journal of Medicine 1995-07-13

To investigate the impact of chloride (Cl–) permeability, mediated by residual activity cystic fibrosis transmembrane conductance regulator (CFTR) or other Cl– channels, on manifestations (CF), we determined transport properties respiratory and intestinal tracts in ΔF508 homozygous twins siblings. In majority patients, cAMP and/or Ca2+-regulated was detected airways intestine. Our finding cAMP-mediated suggests that, vivo, at least some CFTR can reach plasma membrane affect permeability....

10.1172/jci12108 article EN Journal of Clinical Investigation 2001-12-01

Previous Ussing chamber measurements of secretagogue-provoked changes in short circuit current rectal suction biopsies cystic fibrosis (CF) patients showed that a minority chloride secretion response to cholinergic agonists is reduced but not completely absent. To assess possible relationship between this phenomenon and both the genotype phenotype, we performed experiments on 51 CF patients. The mutation was identified 89 out 102 alleles. No apparent found 30 (group I). Low residual 11 II),...

10.1172/jci116993 article EN Journal of Clinical Investigation 1994-02-01

To update and extend a previous cross-sectional international comparison of glycaemic control in people with type 1 diabetes.Data were obtained for 520,392 children adults diabetes from 17 population five clinic-based data sources countries or regions between 2016 2020. Median HbA1c (IQR) proportions individuals < 58 mmol/mol (<7.5%), 58-74 (7.5-8.9%) ≥75 (≥9.0%) compared populations aged <15, 15-24 ≥25 years. Logistic regression was used to estimate the odds ratio (OR) (<7.5%) relative ≥58...

10.1111/dme.14766 article EN Diabetic Medicine 2021-12-10

Cystic fibrosis (CF), the most common severe autosomal recessive trait among Caucasians, is caused by molecular lesions in cystic transmembrane conductance regulator gene (CFTR). The course of multi-organ disease CF highly variable, suggesting influence environmental factors and/or modulating genes other than CFTR on phenotype. To evaluate cause variability, European Twin and Sibling Study collected data two clinical parameters sensitive for prognosis CF, ie weight predicted height (wfh)%...

10.1375/136905200320565256 article EN Twin Research 2000-12-01

To analyse blood glucose control according to continuous monitoring use in data from the CareLink database, and identify factors associated with continuation of sensor during sensor-augmented pump therapy.The analysis used 10 501 people Type 1 2 diabetes mellitus, whom 7916 (61.7%) had sensors for ≥ 15 days any 6-month period over a 2-year observation period. Data were analysed extent ( < 25%, 25-49%, 50-74% 75% time). Time discontinuation was also new users sensors.Compared patients lowest...

10.1111/dme.12825 article EN cc-by-nc-nd Diabetic Medicine 2015-06-04

Background Frequent use of modern diabetes technologies increases the chance for optimal type 1 (T1D) control. Limited reimbursement influences access patients with T1D to these modalities and could worsen their prognosis. We aimed describe situation insulins, glucometers, insulin pumps (CSII) continuous glucose monitoring (CGM) children in European countries participating SWEET Project compare data from EU our previous study 2009. Methods The was conducted between March 2017 August 2017....

10.1111/pedi.12833 article EN Pediatric Diabetes 2019-02-18
Felix Reschke Stefanie Lanzinger Vivien Herczeg Priya Prahalad Riccardo Schiaffini and 90 more Dick Mul Helen Clapin Bedowra Zabeen Julie Pélicand Moshe Phillip Catarina Limbert Thomas Danne G. Todd Alonso Erinn T. Rhodes Elizabeth A. Davis Henk J. Veeze David M. Maahs Roque Cardona‐Hernandez Zdenĕk Šumnı́k Sarah Corathers Nataša Bratina Thomas Danne Evelien Gevers Zineb Imane Barbara Piccini Gun Forsander Danièle Pacaud Claudio Maffeis Fiona Campbell Riccardo Bonfanti Luisa De Sanctis Ruth Krone Péter Tóth‐Heyn Michael Witsch Ilknur Arsanoglu Craig Jefferies Alanna Landry Jacques Beltrand Shazhan Amed Birgit Rami‐Merhar Pascal Barat Agnieszka Szypowska Bedowra Zabeen Kristina Casteels Radka Savova Valentino Cherubini Martin de Bock Sladjana Todorovic Catarina Limbert Hossein Moravej Marija Pozgaj Sepac Artur Mazur Andriani Gerasimidou-Vazeou Violeta Iotova Stephen O’Riordan Agata Chobot Antje Herbst Ursula Ngwu Declan Cody Niels H. Birkebæk Ragnar Hanås Damla Gökşen Archana Sarda Jarosz Chobot Alice Mirante Erick Richmond Padilla Kyriaki Tsiroukidou Banshi Saboo Christina Kanaka‐Gantenbein Riccardo Schiaffini Deborah Foskett Sujata Jali Rasa Verkauskienė Cíntia Castro-Correia Pravesh Kumar Guness Julie Pélicand Andrew Cotterill Meena Kumari Mohan Anita Špehar Uroić Peter Goss Jannet Svensson G. D. Ramchandani R. Coutant Lucía Mantilla Alexandra Sima Jae Hyun Kim Assimina Galli‐Τsinopoulou Rogério T. Ribeiro Clodagh O’Gorman Helse Fonna Heiko Bratke Safinaz El Habashy Rutul Gokalani Mauro Scharf Pinto Vipul Chavda

OBJECTIVE To analyze whether the coronavirus disease 2019 (COVID-19) pandemic increased number of cases or impacted seasonality new-onset type 1 diabetes (T1D) in large pediatric centers globally. RESEARCH DESIGN AND METHODS We analyzed data on 17,280 T1D diagnosed during 2018–2021 from 92 worldwide participating SWEET registry using hierarchic linear regression models. RESULTS The average per center adjusted for total patients treated at year and stratified by age-groups 11.2 (95% CI...

10.2337/dc22-0278 article EN Diabetes Care 2022-09-27

Abstract Background Innovations in diabetes technology have consistently improved outcomes of persons with type1 (PWDs). However, the volumes data that these technologies yield require different workflows to alleviate healthcare professionals’ (HCPs) workload and prevent losing relevant between visits for interpretation treatment adaptations. CloudCare is a population health management tool continuously oversees from groups individual PWDs, based on remote monitoring, screening triaging...

10.1186/s12902-025-01905-4 article EN cc-by BMC Endocrine Disorders 2025-03-31

Background Seasonality at the clinical onset of type 1 diabetes (T1D) has been suggested by different studies, however, results are conflicting. This study aimed to evaluate presence seasonality T1D based on SWEET database comprising data from 32 countries. Methods The cohort included 23 603 patients (52% males) recorded in international multicenter (48 centers), with ≤20 years, year between 1980 and 2015, gender, month birth T1D-diagnosis documented. Data were stratified according four age...

10.1111/pedi.12433 article EN Pediatric Diabetes 2016-10-01

Introduction Cardiovascular disease (CVD) is the leading cause of mortality in individuals with type 1 diabetes mellitus (T1DM). risk management therefore essential T1DM. This study describes performance lipid and blood pressure T1DM using three guidelines. Research design methods Individuals ≥18 years T1DM, treated insulin for ≥1 year, visiting Diabeter or University Medical Center Groningen between January 1, 2018 December 31, 2018, were included. Lipid examined Dutch, American Diabetes...

10.1136/bmjdrc-2022-002765 article EN cc-by-nc BMJ Open Diabetes Research & Care 2022-07-01

Purpose The ‘Biomarkers of heterogeneity in type 1 diabetes’ study cohort was set up to identify genetic, physiological and psychosocial factors explaining the observed disease progression development complications people with long-standing diabetes (T1D). Participants Data samples were collected two subsets. A prospective 611 participants aged ≥16 years ≥5 T1D duration from four Dutch Diabetes clinics between 2016 2021 (median age 32 years; median 12 59% female; mean glycated haemoglobin...

10.1136/bmjopen-2023-082453 article EN cc-by-nc BMJ Open 2024-06-01

'SWEET' is an acronym standing for 'Better control in pediatric and adolescent diabeteS: Working to crEate CEnTers of Reference (CORs)' based on a partnership established national European diabetes organizations such as International Diabetes Federation, Federation Nurses Diabetes, Primary Care Europe (PCDE, www.sweet-project.eu). A three-level classification centers has been put forward. In addition local care, SWEET collaborating their way being COR have defined. Peer-audited CORs with...

10.1111/j.1399-5448.2012.00914.x article EN Pediatric Diabetes 2012-08-29

<h3>Background:</h3> Knowledge of how <i>CFTR</i> mutations other than F508del translate into the basic defect in cystic fibrosis (CF) is scarce due to low incidence homozygous index cases. <h3>Methods:</h3> 17 individuals who are for deletions, missense, stop or splice site gene were investigated clinical symptoms CF and assessed CFTR function by sweat test, nasal potential difference intestinal current measurement. <h3>Results:</h3> activity gland, upper airways distal intestine was normal...

10.1136/jmg.2007.053561 article EN Journal of Medical Genetics 2007-10-26
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