9 results on '"Jongbloed, Monique R M"'
Search Results
2. Somatic growth in single ventricle patients: A systematic review and meta‐analysis.
- Author
-
Van den Eynde, Jef, Bartelse, Simone, Rijnberg, Friso M., Kutty, Shelby, Jongbloed, Monique R. M., de Bruin, Christiaan, Hazekamp, Mark G., Le Cessie, Saskia, and Roest, Arno A. W.
- Subjects
CARDIAC surgery ,RANDOM effects model ,PREVENTION of obesity ,BODY mass index - Abstract
Aim: To map somatic growth patterns throughout Fontan palliation and summarise evidence on its key modifiers. Methods: Databases were searched for relevant articles published from January 2000 to December 2021. Height and weight z scores at each time point (birth, Glenn procedure, Fontan procedure and >5 years after Fontan completion) were pooled using a random effects meta‐analysis. A random effects meta‐regression model was fitted to model the trend in z scores over time. Results: Nineteen studies fulfilled eligibility criteria, yielding a total of 2006 participants. The z scores for height and weight were markedly reduced from birth to the interstage period, but recovered by about 50% following the Glenn procedure. At >10 years after the Fontan procedure, the z scores for weight seemed to normalise despite persistent lower height, resulting in increased body mass index. The review revealed a number of modifiers of somatic growth, including aggressive nutritional management, timing of Glenn/Fontan, prompt resolution of complications and obesity prevention programmes in adolescence and adulthood. Conclusion: This review mapped the somatic growth of single ventricle patients and summarised key modifiers that may be amendable to improvement. These data provide guidance on strategies to further optimise somatic growth in this population and may serve as a benchmark for clinical follow‐up. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
3. The first experience with sodium-glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure.
- Author
-
Egorova, Anastasia D., Nederend, Marieke, Tops, Laurens F., Vliegen, Hubert W., Jongbloed, Monique R. M., and Kiès, Philippine
- Subjects
SODIUM-glucose cotransporter 2 inhibitors ,SODIUM-glucose cotransporters ,DAPAGLIFLOZIN ,TRANSPOSITION of great vessels ,HEART failure patients ,VENTRICULAR ejection fraction ,HEART failure - Abstract
In congenitally corrected transposition of the great arteries, the morphological right ventricle supports the systemic circulation. This chronic exposure to pressure overload ultimately leads to systemic right ventricular (sRV) dysfunction and heart failure. Pharmacological options for the treatment of sRV failure are poorly defined and no solid recommendations are made in the most recent guidelines. Sodium-glucose cotransporter 2 (SGLT-2) inhibitors are a new class of antihyperglycaemic drugs that have been demonstrated to significantly reduce the risk of worsening heart failure and death from cardiovascular causes in patients with chronic heart failure with reduced left ventricular ejection fraction, yet no data are available in sRV patients. We report on the treatment and clinical follow-up of a patient with advanced heart failure and poor sRV function in the context of congenitally corrected transposition of the great arteries, who did not tolerate sacubitril/valsartan and had a high burden of heart-failure-related hospitalizations. Treatment with dapagliflozin was well tolerated and resulted in (small) subjective and objective functional and echocardiographic improvement and a reduction in heart-failure-related hospitalizations. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
4. Autonomic control over myocardial function in vitro: Evaluation of current and future clinical therapies in a nonclinical setting.
- Author
-
Blok, Michiel, Jongbloed, Monique R. M., and Boukens, Bastiaan J. D.
- Subjects
- *
HEART failure , *ARRHYTHMIA , *AUTONOMIC nervous system , *MYOCARDIAL injury , *VAGUS nerve stimulation , *HEART diseases - Abstract
Although the study of either atrial or ventricular arrhythmias determines the cardiomyocyte subtype of choice by itself, it is here that also the subtype of neuron in coculture becomes of relevance. Many aspects of heart function, including heart rate and contractility, are under continuous influence of the autonomic nervous system. Employing patient-derived iPSCs would allow the study of functional consequences of their genetic background on neurocardiac interplay and how this relates to the effectiveness of therapies such as pharmaceutical therapy and CCM. [Extracted from the article]
- Published
- 2022
- Full Text
- View/download PDF
5. Assessment of human fetal cardiac autonomic nervous system development using color tissue Doppler imaging.
- Author
-
Zwanenburg, Fleur, Jongbloed, Monique R. M., Geloven, Nan, ten Harkel, Arend D. J., Lith, Jan M. M., and Haak, Monique C.
- Subjects
- *
FETAL heart rate , *AUTONOMIC nervous system , *COLOR Doppler ultrasonography , *FIRST trimester of pregnancy , *FETAL development , *HEART beat - Abstract
Objectives: Functional development of the fetal cardiac autonomic nervous system (cANS) plays a key role in fetal maturation and can be assessed through fetal heart rate variability (fHRV)‐analysis, with each HRV parameter representing different aspects of cANS activity. Current available techniques, however, are unable to assess the fHRV parameters accurately throughout the whole pregnancy. This study aims to test the feasibility of color tissue Doppler imaging (cTDI) as a new ultrasound technique for HRV analysis. Secondly, we explored time trends of fHRV parameters using this technique. Methods: 18 healthy singleton fetuses were examined sequentially every 8 weeks from 10 weeks GA onwards. From each examination, 3 cTDI recordings of the four‐chamber view of 10 seconds were retrieved to determine accurate beat‐to‐beat intervals. The fHRV parameters SDNN, RMSSD, SDNN/RMSSD, and pNN10, each representing different functional aspects of the cANS, were measured, and time trends during pregnancy were explored using spline functions within a linear mixed‐effects model. Results: In total, 77% (95% Cl 66–87%) of examinations were feasible for fHRV analysis from the first trimester onwards, which is a great improvement compared to other techniques. The technique is able to determine different maturation rates of the fHRV parameters, showing that cANS function, presumably parasympathetic activity, establishes around 20 weeks GA and matures rapidly until 30 weeks GA. Conclusions: This is the first study able to assess cANS function through fHRV analysis from the first trimester onwards. The use of cTDI to determine beat‐to‐beat intervals seems feasible in just 3 clips of 10 seconds, which holds promise for future clinical use in assessing fetal well‐being. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
6. Clinical Course Long After Atrial Switch: A Novel Risk Score for Major Clinical Events.
- Author
-
Woudstra, Odilia I., Zandstra, Tjitske E., Vogel, Rosanne F., van Dijk, Arie P. J., Vliegen, Hubert W., Kiès, Philippine, Jongbloed, Monique R. M., Egorova, Anastasia D., Doevendans, Pieter A. F. M., Konings, Thelma C., Mulder, Barbara J. M., Tanck, Michael W. T., Meijboom, Folkert J., and Bouma, Berto J.
- Published
- 2021
- Full Text
- View/download PDF
7. Disruption of RHOA‐ROCK Signaling Results in Atrioventricular Block and Disturbed Development of the Putative Atrioventricular Node.
- Author
-
Kelder, Tim P., Vicente‐Steijn, Rebecca, Poelmann, Robert E., Schalij, Martin J., Deruiter, Marco C., Jongbloed, Monique R. M., and Gittenberger‐de Groot, Adriana C.
- Published
- 2019
- Full Text
- View/download PDF
8. Echocardiographic Assessment of Embryonic and Fetal Mouse Heart Development: A Focus on Haemodynamics and Morphology.
- Author
-
Hahurij, Nathan D., Calkoen, Emmeline E., Jongbloed, Monique R. M., Roest, Arno A. W., Gittenberger-de Groot, Adriana C., Poelmann, Robert E., De Ruiter, Marco C., van Munsteren, Conny J., Steendijk, Paul, and Blom, Nico A.
- Subjects
ECHOCARDIOGRAPHY ,EMBRYOLOGY ,DEVELOPMENTAL biology ,LABORATORY mice ,HEMODYNAMICS - Abstract
Background. Heart development is a complex process, and abnormal development may result in congenital heart disease (CHD). Currently, studies on animal models mainly focus on cardiac morphology and the availability of hemodynamic data, especially of the right heart half, is limited. Here we aimed to assess the morphological and hemodynamic parameters of normal developing mouse embryos/fetuses by using a high-frequency ultrasound system. Methods. A timed breeding program was initiated with a WT mouse line (Swiss/129Sv background). All recordings were performed transabdominally, in isoflurane sedated pregnant mice, in hearts of sequential developmental stages: 12.5, 14.5, and 17.5 days after conception (n = 105). Results. Along development the heart rate increased significantly from 125 ± 9.5 to 219 ± 8.3 beats per minute. Reliable flow measurements could be performed across the developing mitral and tricuspid valves and outflow tract. M-mode measurements could be obtained of all cardiac compartments. An overall increase of cardiac systolic and diastolic function with embryonic/fetal development was observed. Conclusion. High-frequency echocardiography is a promising and useful imaging modality for structural and hemodynamic analysis of embryonic/fetal mouse hearts. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
9. The sinus venosus myocardium contributes to the atrioventricular canal: potential role during atrioventricular node development?
- Author
-
Kelder TP, Vicente-Steijn R, Harryvan TJ, Kosmidis G, Gittenberger-de Groot AC, Poelmann RE, Schalij MJ, DeRuiter MC, and Jongbloed MR
- Subjects
- Animals, Atrioventricular Node anatomy & histology, Atrioventricular Node embryology, Avian Proteins metabolism, Chick Embryo, Gene Expression Regulation, Developmental, Heart anatomy & histology, Heart embryology, Heart physiology, Homeodomain Proteins genetics, Homeodomain Proteins metabolism, Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels genetics, Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels metabolism, Imaging, Three-Dimensional, Immunohistochemistry, In Situ Hybridization, LIM-Homeodomain Proteins genetics, LIM-Homeodomain Proteins metabolism, Membrane Potentials, Microscopy, Fluorescence, Myocardium cytology, Myocytes, Cardiac metabolism, Myocytes, Cardiac physiology, Patch-Clamp Techniques, Reverse Transcriptase Polymerase Chain Reaction, Troponin I genetics, Troponin I metabolism, Atrioventricular Node metabolism, Avian Proteins genetics, Myocardium metabolism
- Abstract
The presence of distinct electrophysiological pathways within the atrioventricular node (AVN) is a prerequisite for atrioventricular nodal reentrant tachycardia to occur. In this study, the different cell contributions that may account for the anatomical and functional heterogeneity of the AVN were investigated. To study the temporal development of the AVN, the expression pattern of ISL1, expressed in cardiac progenitor cells, was studied in sequential stages performing co-staining with myocardial markers (TNNI2 and NKX2-5) and HCN4 (cardiac conduction system marker). An ISL1+/TNNI2+/HCN4+ continuity between the myocardium of the sinus venosus and atrioventricular canal was identified in the region of the putative AVN, which showed a pacemaker-like phenotype based on single cell patch-clamp experiments. Furthermore, qPCR analysis showed that even during early development, different cell populations can be identified in the region of the putative AVN. Fate mapping was performed by in ovo vital dye microinjection. Embryos were harvested and analysed 24 and 48 hrs post-injection. These experiments showed incorporation of sinus venosus myocardium in the posterior region of the atrioventricular canal. The myocardium of the sinus venosus contributes to the atrioventricular canal. It is postulated that the myocardium of the sinus venosus contributes to nodal extensions or transitional cells of the AVN since these cells are located in the posterior region of the AVN. This finding may help to understand the origin of atrioventricular nodal reentrant tachycardia., (© 2015 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.)
- Published
- 2015
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.