Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where S.M.A.J. Tielemans is active.

Publication


Featured researches published by S.M.A.J. Tielemans.


Journal of Human Hypertension | 2013

Intake of total protein, plant protein and animal protein in relation to blood pressure: a meta-analysis of observational and intervention studies

S.M.A.J. Tielemans; W. Altorf-van der Kuil; Mariëlle F. Engberink; Elizabeth J. Brink; M. A. van Baak; Stephan J. L. Bakker; Johanna M. Geleijnse

There is growing evidence from epidemiological studies that dietary protein may beneficially influence blood pressure (BP), but findings are inconclusive. We performed a meta-analysis of 29 observational studies and randomized controlled trials (RCTs) of dietary protein and types of protein in relation to BP or incident hypertension, published until January 2012. The analysis included eight cross-sectional studies (n=48 985), four prospective studies (n=11 761) and 17 RCTs (n=1449). A modest inverse association between total protein intake and BP (−0.20 mm Hg systolic (95% CI: −0.39, −0.01) per 25 g (∼1 s.d.)) was found in cross-sectional studies, but not in prospective studies (relative risk of 0.99 (95% CI: 0.96, 1.02)). For RCTs that used carbohydrate as a control treatment, the pooled BP effect was −2.11 mm Hg systolic (95% CI: −2.86, −1.37) for a weighed mean contrast in protein intake of 41 g per day. A non-significant inverse association of −0.52 mm Hg systolic (95% CI: −1.10, +0.05) per 11 g (∼1 s.d.) was found for plant protein in cross-sectional studies, whereas animal protein was not associated with BP. In prospective studies and RCTs, however, the associations of plant protein and animal protein with BP were broadly similar. These findings suggest that increasing the intake of protein at the expense of carbohydrates may have a beneficial effect on BP. The BP effect of specific types of protein remains to be established.


Nutrition Metabolism and Cardiovascular Diseases | 2014

Associations of plant and animal protein intake with 5-year changes in blood pressure: The Zutphen Elderly Study

S.M.A.J. Tielemans; Daan Kromhout; W. Altorf-van der Kuil; Johanna M. Geleijnse

BACKGROUND AND AIM The aim of the present study was to investigate the association of plant and animal protein intake with 5-year changes in blood pressure (BP) level. METHODS AND RESULTS Analyses were based on 702 observations of 272 men participating in the Zutphen Elderly Study. Men did not use antihypertensive medication and were initially free of cardiovascular disease, diabetes mellitus and cancer. Physical and dietary examinations were performed in 1985, 1990, 1995, and 2000. Diet was assessed using the cross-check dietary history method. Men were categorised into tertiles according to their plant and animal protein intake. BP was measured twice at each examination. The associations of plant and animal protein intake with 5-year changes in BP level were investigated by a random intercept model with first-order autoregressive (AR [1]) serial correlation and a nugget effect. Adjustments were made for age, examination year, BMI, socioeconomic status, smoking, physical activity, prescribed diet, alcohol consumption and intake of energy and nutrients. In 1985, men were 70.1 ± 4.6 years old and had a mean BP of 147/84 mmHg. Mean protein intake was 15 en%, of which one-third consisted of plant protein. The higher-intake tertiles of plant protein intake were associated with a mean 5-year change of -2.9 mmHg (95% CI: -5.6, -0.2) systolic and -1.7 mmHg (95% CI: -3.2, -0.2) diastolic, compared with the lowest-intake tertile. No associations were observed for animal protein intake. CONCLUSION Intake of plant protein, but not animal protein, was inversely associated with 5-year changes in BP level in elderly men.


American Journal of Cardiology | 2013

Joint Associations of Alcohol Consumption and Physical Activity With All-Cause and Cardiovascular Mortality

Sabita S. Soedamah-Muthu; Melissa De Neve; Nicola Shelton; S.M.A.J. Tielemans; Emmanuel Stamatakis

Individual associations of alcohol consumption and physical activity with cardiovascular disease are relatively established, but the joint associations are not clear. Therefore, the aim of this study was to examine prospectively the joint associations between alcohol consumption and physical activity with cardiovascular mortality (CVM) and all-cause mortality. Four population-based studies in the United Kingdom were included, the 1997 and 1998 Health Surveys for England and the 1998 and 2003 Scottish Health Surveys. In men and women, respectively, low physical activity was defined as 0.1 to 5 and 0.1 to 4 MET-hours/week and high physical activity as ≥5 and ≥4 MET-hours/week. Moderate or moderately high alcohol intake was defined as >0 to 35 and >0 to 21 units/week and high levels of alcohol intake as >35 and >21 units/week. In total, there were 17,410 adults without prevalent cardiovascular diseases and complete data on alcohol and physical activity (43% men, median age 55 years). During a median follow-up period of 9.7 years, 2,204 adults (12.7%) died, 638 (3.7%) with CVM. Cox proportional-hazards models were adjusted for potential confounders such as marital status, social class, education, ethnicity, and longstanding illness. In the joint associations analysis, low activity combined with high levels of alcohol (CVM: hazard ratio [HR] 1.95, 95% confidence interval [CI] 1.28 to 2.96, p = 0.002; all-cause mortality: HR 1.64, 95% CI 1.32 to 2.03, p <0.001) and low activity combined with no alcohol (CVM: HR 1.93, 95% CI 1.35 to 2.76, p <0.001; all-cause mortality: HR 1.50, 95% CI 1.24 to 1.81, p <0.001) were linked to the highest risk, compared with moderate drinking and higher levels of physical activity. Within each given alcohol group, low activity was linked to increased CVM risk (e.g., HR 1.48, 95% CI 1.08 to 2.03, p = 0.014, for the moderate drinking group), but in the presence of high physical activity, high alcohol intake was not linked to increased CVM risk (HR 1.32, 95% CI 0.52 to 3.34, p = 0.555). In conclusion, high levels of drinking and low physical activity appear to increase the risk for cardiovascular and all-cause mortality, although these data suggest that physical activity levels are more important.


PLOS ONE | 2015

Essential Amino Acids in the Gluten-Free Diet and Serum in Relation to Depression in Patients with Celiac Disease

Nathalie J. M. van Hees; Erik J. Giltay; S.M.A.J. Tielemans; Johanna M. Geleijnse; Thomas Puvill; Nadine Janssen; Willem Van der Does

Introduction Celiac disease (CD) is associated with an increased risk of major depressive disorder, possibly due to deficiencies in micronutrients in the gluten-free diet. We aimed to investigate whether essential amino acids (i.e., the precursors of serotonin, dopamine and other neurotransmitters) are depleted in the diet and serum of CD patients with major depressive disorder. Methods In a cross-sectional study we assessed dietary intake of amino acids and serum levels of amino acids, in 77 CD patients on a gluten-free diet and in 33 healthy controls. Major depressive disorder was assessed with structured interviews (using the Mini International Neuropsychiatric Interview Plus). Dietary intake was assessed using a 203-item food frequency questionnaire. Results Participants had a mean age of 55 years and 74% were women. The intake of vegetable protein was significantly lower in CD patients than in healthy controls (mean difference of 7.8 g/d; 95% CI: 4.7–10.8), as were serum concentrations of tyrosine, phenylalanine and tryptophan (all p < 0.005). However, within the CD patient group, the presence of major depressive disorder (n = 42) was not associated with intake or serum levels of essential amino acids. Conclusions Patients with CD on a long-term gluten-free diet, with good adherence, consume significantly less vegetable protein than controls, and their serum levels of several essential amino acids were also lower. Despite its potential adverse effect, intake and serum levels of essential amino acids were not related to major depression.


Journal of Human Hypertension | 2017

Blood pressure trajectories in relation to cardiovascular mortality: The Rancho Bernardo Study

S.M.A.J. Tielemans; Johanna M. Geleijnse; G.A. Laughlin; H.C. Boshuizen; E. Barrett-Connor; Daan Kromhout

The added value of blood pressure (BP) trajectories for predicting cardiovascular disease (CVD) is currently unknown. We investigated the association of systolic BP (SBP) trajectories with CVD and all-cause mortality and compared these associations with those of average SBP, taking antihypertensive medication into account. Data from 762 participants of the Rancho Bernardo Study were used. SBP from five examinations (maximum) from 1984 to 2002 was used; mortality data were obtained from 2002 to 2013. SBP trajectories were derived using group-based trajectory modelling. Cox proportional hazards analysis was used to investigate associations of trajectories and average SBP with CVD and all-cause mortality, adjusted for age, sex, cholesterol, smoking, diabetes and antihypertensive medication. Mean baseline age was 65.7 years, and 67% were women. Four trajectories were identified, in which mean SBP increased by 5–12 mm Hg during 10 years. The highest trajectories were associated with two to three times greater CVD mortality and 1.5 times greater all-cause mortality risk, compared with the lowest trajectory. Each 20 mmHg increment in average SBP was associated with 1.4 times greater CVD mortality risk and 1.2 times all-cause mortality risk. Associations were not modified by antihypertensive medication (P-interaction>0.10). SBP trajectories were not superior to average SBP in predicting CVD and all-cause mortality. In the general middle-aged and older population of the Rancho Bernardo study, SBP trajectories provided no added value to average SBP in predicting CVD and all-cause mortality. Long-term average SBP levels and trajectories were significant predictors of CVD and all-cause mortality, irrespective of prescribed antihypertensive medication (which in the 1980s–1990s mainly were diuretics and β-blockers).


Journal of Hypertension | 2013

Twenty-four hour urinary urea excretion and 9-year risk of hypertension: the PREVEND study

S.M.A.J. Tielemans; Johanna M. Geleijnse; M. A. van Baak; Mariëlle F. Engberink; Elizabeth J. Brink; P. E. De Jong; Ron T. Gansevoort; Stephan J. L. Bakker

Objectives: It is not yet clear whether dietary protein could help maintaining a healthy blood pressure (BP). We investigated the association between total protein intake, estimated from 24-h urinary urea excretion, and incident hypertension in Dutch men and women. Methods: We analyzed data of 3997 men and women (aged 28–75 years) who participated in the Prevention of Renal and Vascular Endstage Disease (PREVEND) study, a prospective cohort study. Urea excretion was assessed in two consecutive 24-h urine collections at baseline and approximately 4 years later, from which total protein intake was estimated using the Maroni method. Participants were followed for 9 years for hypertension incidence, defined as BP at least 140/90 mmHg or initiation of antihypertensive medication. Hazard ratios (HR) were obtained in sex-specific quintiles of protein intake using time-dependent Cox regression, adjusted for age, sex, BMI, smoking, alcohol use, and 24-h urinary excretions of sodium and potassium. Results: Baseline BP was on average 119/70 mmHg and 976 participants developed hypertension during follow-up. Mean protein intake (in g/kg ideal body weight) was 1.18 ± 0.26 for men and 1.12 ± 0.25 for women. Estimated protein intake was nonlinearly inversely associated with incident hypertension in the fully adjusted model, with nonsignificant HR of 0.77, 0.75, 0.82, and 0.83 in consecutive quintiles compared with the lowest quintile (P-trend: 0.52). Conclusion: Protein intake, as assessed by urinary urea excretion, was not significantly associated with 9-year hypertension incidence in Dutch men and women.


European Journal of Epidemiology | 2015

Ten-year blood pressure trajectories, cardiovascular mortality and life years lost in two extinction cohorts

S.M.A.J. Tielemans; Johanna M. Geleijnse; Alessandro Menotti; Hendriek C. Boshuizen; Sabita S. Soedamah-Muthu; David R. Jacobs; Henry Blackburn; Daan Kromhout

Healthy Living: The European Congress of Epidemiology, 2015 Esther Bols • Luc Smits • Matty Weijenberg Springer Science+Business Media Dordrecht 2015


Diabetologia | 2013

Association of physical activity with all-cause mortality and incident and prevalent cardiovascular disease among patients with type 1 diabetes: the EURODIAB Prospective Complications Study

S.M.A.J. Tielemans; Sabita S. Soedamah-Muthu; M. De Neve; Monika Toeller; Nishi Chaturvedi; J. H. Fuller; Emmanuel Stamatakis


Journal of Human Hypertension | 2017

Blood pressure trajectories in relation to cardiovascular mortality

S.M.A.J. Tielemans; Johanna M. Geleijnse; G.A. Laughlin; H.C. Boshuizen; E. Barrett-Connor; Daan Kromhout


Proceedings of the Nutrition Society | 2015

Pulse pressure trajectories in relation to cardiovascular mortality and dietary protein intake: the Zutphen Study

E. Mertens; S.M.A.J. Tielemans; Sabita S. Soedamah-Muthu; Johanna M. Geleijnse

Collaboration


Dive into the S.M.A.J. Tielemans's collaboration.

Top Co-Authors

Avatar

Johanna M. Geleijnse

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar

Daan Kromhout

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar

Sabita S. Soedamah-Muthu

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar

Mariëlle F. Engberink

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar

Stephan J. L. Bakker

University Medical Center Groningen

View shared research outputs
Top Co-Authors

Avatar

Wieke Altorf-van der Kuil

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Hendriek C. Boshuizen

Wageningen University and Research Centre

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge