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  1. AU="Binnenmars, S H"
  2. AU="Promjampa, Wachinee"
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  1. Article ; Online: Use of maximal dosage renin-angiotensin-aldosterone system inhibitors in a real life population of complicated type 2 diabetes - contraindications and opportunities.

    Gant, C M / Oosterwijk, M M / Binnenmars, S H / Navis, G J / Haverkate, H / Bakker, S J L / Laverman, G D

    BMC nephrology

    2023  Volume 24, Issue 1, Page(s) 240

    Abstract: Objective: Pharmacological inhibition of the renin-angiotensin-aldosterone-system (RAASi) is the cornerstone of hypertension treatment, renoprotection and secondary prevention of cardiovascular disease in patients with type 2 diabetes. Although there is ...

    Abstract Objective: Pharmacological inhibition of the renin-angiotensin-aldosterone-system (RAASi) is the cornerstone of hypertension treatment, renoprotection and secondary prevention of cardiovascular disease in patients with type 2 diabetes. Although there is a dose-dependent effect of RAASi with optimum protection when using maximal dose, little is known on actual use of maximal dosage RAASi in clinical practice. Here we investigate prevalence of maximal dosage RAASi, and contraindications for, optimizing RAASi dosage, in patients with complicated type 2 diabetes in a real-life clinical setting.
    Research design and methods: We performed a retrospective analysis in 668 patients included in the DIAbetes and LifEstyle Cohort Twente (DIALECT). We grouped patients according to no RAASi, submaximal RAASi and maximal RAASi use. All potassium and creatinine measurements between January 1st 2000 and date of inclusion in DIALECT were extracted from patients files. We identified determinants of maximal RAASi use vs. submaximal RAASi use with multivariate logistic regression analysis.
    Results: Mean age was 64 ± 10 years and 61% were men. In total, 460 patients (69%) used RAASi, and 30% used maximal RAASi. Maximal RAASi use was not statistically different between different indications for RAASi (i.e. hypertension, diabetic kidney disease, coronary heart disease and cerebrovascular disease; P > 0.05). Per patient, 2 [1-4] measurements of potassium and 20 [13-31] measurements of creatinine were retrieved, retrospective follow-up time was - 3.0 [-1.4 to -5.7] years. Pre-baseline hyperkalemia > 5.0 mmol/l and acute kidney injury were found in 151 (23%) patients and 119 patients (18%), respectively. Determinants of maximal RAASi were prior acute kidney injury (OR 0.51 (0.30-0.87)), increased albuminuria (OR 1.89 (1.17-3.08)) and total number of used antihypertensives (OR 1.66 (1.33-2.06)).
    Conclusions: Maximal dose RAASi is used in almost one third of complicated type 2 diabetes patients in a real-life setting. The prevalence of contraindications is considerable, but relative in nature, suggesting that it is worthwhile to explore strategies aimed at maximizing RAASi while circumventing the alleged contraindications.
    MeSH term(s) Male ; Humans ; Middle Aged ; Aged ; Female ; Renin-Angiotensin System ; Diabetes Mellitus, Type 2/complications ; Diabetes Mellitus, Type 2/drug therapy ; Diabetes Mellitus, Type 2/epidemiology ; Creatinine ; Retrospective Studies ; Diabetes Complications ; Acute Kidney Injury ; Contraindications ; Hypertension/drug therapy ; Hypertension/epidemiology
    Chemical Substances Creatinine (AYI8EX34EU)
    Language English
    Publishing date 2023-08-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2041348-8
    ISSN 1471-2369 ; 1471-2369
    ISSN (online) 1471-2369
    ISSN 1471-2369
    DOI 10.1186/s12882-023-03205-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: High Dietary Intake of Vegetable Protein Is Associated With Lower Prevalence of Renal Function Impairment

    Oosterwijk, Milou M. / Soedamah-Muthu, Sabita S. / Geleijnse, Johanna M. / Bakker, Stephan J.L. / Navis, Gerjan / Binnenmars, S.H. / Gant, Christina M. / Laverman, Gozewijn D.

    Kidney International Reports

    Results of the Dutch DIALECT-1 Cohort

    2019  Volume 4, Issue 5

    Abstract: Introduction: Dietary protein intake may influence development of renal function impairment in diabetes mellitus type 2 (T2DM). We assessed the association between sources of protein and prevalence of renal function impairment. Methods: Cross-sectional ... ...

    Abstract Introduction: Dietary protein intake may influence development of renal function impairment in diabetes mellitus type 2 (T2DM). We assessed the association between sources of protein and prevalence of renal function impairment. Methods: Cross-sectional analyses were performed in baseline data of 420 patients of the DIAbetes and LifEstyle Cohort Twente-1 (DIALECT-1)study. Protein intake was assessed using a Food Frequency Questionnaire, modified for accurate assessment of protein intake, including types and sources of protein. Renal function impairment was defined as estimated glomerular filtration rate (eGFR)<60 ml/min per 1.73 m 2 (Chronic Kidney Disease Epidemiology Collaboration formula). Results: Among 420 patients with T2DM, 99 renal function impairment cases were identified. Multivariate Cox proportional hazard models were used and adjusted for the main lifestyle and dietary factors. The prevalence ratios in the fully adjusted model were 1 (reference), 0.74 (95% confidence interval [CI]: 0.44–1.27; P = 0.28)and 0.47 (95% CI: 0.23–0.98; P = 0.04)according to increasing tertiles of vegetable protein intake. For animal protein intake the prevalence ratios were 1 (reference), 1.10 (95% CI: 0.64–1.88; P = 0.74)and 1.06 (95% CI: 0.56–1.99; P = 0.87)according to increasing tertiles of intake. Theoretical replacement models showed that replacing 3 energy percent from animal protein by vegetable protein lowered the prevalence ratio for the association with renal function impairment to 0.20 (95% CI: 0.06–0.63; P = 0.01). Conclusion: In conclusion, we found that higher intake of vegetable protein was associated with a lower prevalence of renal function impairment, and theoretical replacement of animal protein with vegetable protein was inversely associated with renal function impairment among patients with T2DM.
    Keywords diabetes mellitus type 2 ; diet ; kidney function ; lifestyle
    Subject code 616
    Language English
    Publishing country nl
    Document type Article ; Online
    ISSN 2468-0249
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Concordance of dietary sodium intake and concomitant phosphate load: Implications for sodium interventions.

    Humalda, J K / Keyzer, C A / Binnenmars, S H / Kwakernaak, A J / Slagman, M C J / Laverman, G D / Bakker, S J L / de Borst, M H / Navis, G J

    Nutrition, metabolism, and cardiovascular diseases : NMCD

    2016  Volume 26, Issue 8, Page(s) 689–696

    Abstract: Background and aims: Both a high dietary sodium and high phosphate load are associated with an increased cardiovascular risk in patients with chronic kidney disease (CKD), and possibly also in non-CKD populations. Sodium and phosphate are abundantly ... ...

    Abstract Background and aims: Both a high dietary sodium and high phosphate load are associated with an increased cardiovascular risk in patients with chronic kidney disease (CKD), and possibly also in non-CKD populations. Sodium and phosphate are abundantly present in processed food. We hypothesized that (modulation of) dietary sodium is accompanied by changes in phosphate load across populations with normal and impaired renal function.
    Methods and results: We first investigated the association between sodium and phosphate load in 24-h urine samples from healthy controls (n = 252), patients with type 2 diabetes mellitus (DM, n = 255) and renal transplant recipients (RTR, n = 705). Secondly, we assessed the effect of sodium restriction on phosphate excretion in a nondiabetic CKD cohort (ND-CKD: n = 43) and a diabetic CKD cohort (D-CKD: n = 39). Sodium excretion correlated with phosphate excretion in healthy controls (R = 0.386, P < 0.001), DM (R = 0.490, P < 0.001), and RTR (R = 0.519, P < 0.001). This correlation was also present during regular sodium intake in the intervention studies (ND-CKD: R = 0.491, P < 0.001; D-CKD: R = 0.729, P < 0.001). In multivariable regression analysis, sodium excretion remained significantly correlated with phosphate excretion after adjustment for age, gender, BMI, and eGFR in all observational cohorts. In ND-CKD and D-CKD moderate sodium restriction reduced phosphate excretion (31 ± 10 to 28 ± 10 mmol/d; P = 0.04 and 26 ± 11 to 23 ± 9 mmol/d; P = 0.02 respectively).
    Conclusions: Dietary exposure to sodium and phosphate are correlated across the spectrum of renal function impairment. The concomitant reduction in phosphate intake accompanying sodium restriction underlines the off-target effects on other nutritional components, which may contribute to the beneficial cardiovascular effects of sodium restriction. (f) Registration numbers: Dutch Trial Register NTR675, NTR2366.
    MeSH term(s) Adult ; Aged ; Case-Control Studies ; Diabetes Mellitus, Type 2/complications ; Diabetic Nephropathies/diet therapy ; Diabetic Nephropathies/etiology ; Diabetic Nephropathies/physiopathology ; Diabetic Nephropathies/urine ; Diet, Sodium-Restricted ; Fast Foods/adverse effects ; Female ; Humans ; Kidney/physiopathology ; Male ; Middle Aged ; Netherlands ; Phosphates/adverse effects ; Phosphates/urine ; Phosphorus, Dietary/adverse effects ; Phosphorus, Dietary/urine ; Prospective Studies ; Recommended Dietary Allowances ; Renal Elimination ; Renal Insufficiency, Chronic/diet therapy ; Renal Insufficiency, Chronic/etiology ; Renal Insufficiency, Chronic/physiopathology ; Renal Insufficiency, Chronic/urine ; Sodium, Dietary/adverse effects ; Sodium, Dietary/urine ; Time Factors ; Treatment Outcome
    Chemical Substances Phosphates ; Phosphorus, Dietary ; Sodium, Dietary
    Language English
    Publishing date 2016-08
    Publishing country Netherlands
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial
    ZDB-ID 1067704-5
    ISSN 1590-3729 ; 0939-4753
    ISSN (online) 1590-3729
    ISSN 0939-4753
    DOI 10.1016/j.numecd.2016.04.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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