Factors associated with cardiovascular target organ damage in children after renal transplantation

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Factors associated with cardiovascular target organ damage in children after renal transplantation. / Borchert-Mörlins, Bianca; Thurn, Daniela; Schmidt, Bernhard M W; Büscher, Anja K; Oh, Jun; Kier, Tanja; Bauer, Elena; Baig, Sabrina; Kanzelmeyer, Nele; Kemper, Markus J; Büscher, Rainer; Melk, Anette.

in: PEDIATR NEPHROL, 13.08.2017.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Borchert-Mörlins, B, Thurn, D, Schmidt, BMW, Büscher, AK, Oh, J, Kier, T, Bauer, E, Baig, S, Kanzelmeyer, N, Kemper, MJ, Büscher, R & Melk, A 2017, 'Factors associated with cardiovascular target organ damage in children after renal transplantation', PEDIATR NEPHROL. https://doi.org/10.1007/s00467-017-3771-8

APA

Borchert-Mörlins, B., Thurn, D., Schmidt, B. M. W., Büscher, A. K., Oh, J., Kier, T., Bauer, E., Baig, S., Kanzelmeyer, N., Kemper, M. J., Büscher, R., & Melk, A. (2017). Factors associated with cardiovascular target organ damage in children after renal transplantation. PEDIATR NEPHROL. https://doi.org/10.1007/s00467-017-3771-8

Vancouver

Bibtex

@article{ea3691654dcb4c00b99f3f8bb7b67c9c,
title = "Factors associated with cardiovascular target organ damage in children after renal transplantation",
abstract = "BACKGROUND: Cardiovascular disease is the second-most common cause of death in pediatric renal transplant recipients. The aim of this study was to evaluate subclinical cardiovascular target organ damage defined as the presence of arterio- and atherosclerotic lesions and cardiac remodeling and to analyze contributing risk factors in a large cohort of children after renal transplantation (RT).METHODS: A total of 109 children aged 13.1 ± 3.3 years who had undergone RT at one of three German transplant centers were enrolled in this study. Patients had been transplanted a mean of 5.5 (±4.0) years prior to being enrolled in the study. Anthropometric data, laboratory values and office- and 24-h ambulatory blood pressure monitoring (ABPM) were evaluated. Cardiovascular target organ damage was determined through non-invasive measurements of aortic pulse wave velocity (PWV), carotid intima-media thickness (IMT) and left ventricular mass (LVM).RESULTS: Elevated PWV or IMT values were detected in 22 and 58% of patients, respectively. Left ventricular hypertrophy was found in as many as 43% of patients. The prevalence of uncontrolled or untreated hypertension was 41%, of which 16% of cases were only detected by ABPM measurements. In the multivariable analysis, higher diastolic blood pressure, everolimus intake and lower estimated glomerular filtration rate were independently associated with high PWV. Higher systolic blood pressure and body mass index were associated with elevated LVM.CONCLUSIONS: Our results showed an alarming burden of cardiovascular subclinical organ damage in children after RT. Hypertension, obesity, immunosuppressive regimen and renal function emerged as independent risk factors of organ damage. Whereas the latter is not modifiable, the results of our study strongly indicate that the management of children after RT should focus on the control of blood pressure and weight.",
keywords = "Journal Article",
author = "Bianca Borchert-M{\"o}rlins and Daniela Thurn and Schmidt, {Bernhard M W} and B{\"u}scher, {Anja K} and Jun Oh and Tanja Kier and Elena Bauer and Sabrina Baig and Nele Kanzelmeyer and Kemper, {Markus J} and Rainer B{\"u}scher and Anette Melk",
year = "2017",
month = aug,
day = "13",
doi = "10.1007/s00467-017-3771-8",
language = "English",
journal = "PEDIATR NEPHROL",
issn = "0931-041X",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Factors associated with cardiovascular target organ damage in children after renal transplantation

AU - Borchert-Mörlins, Bianca

AU - Thurn, Daniela

AU - Schmidt, Bernhard M W

AU - Büscher, Anja K

AU - Oh, Jun

AU - Kier, Tanja

AU - Bauer, Elena

AU - Baig, Sabrina

AU - Kanzelmeyer, Nele

AU - Kemper, Markus J

AU - Büscher, Rainer

AU - Melk, Anette

PY - 2017/8/13

Y1 - 2017/8/13

N2 - BACKGROUND: Cardiovascular disease is the second-most common cause of death in pediatric renal transplant recipients. The aim of this study was to evaluate subclinical cardiovascular target organ damage defined as the presence of arterio- and atherosclerotic lesions and cardiac remodeling and to analyze contributing risk factors in a large cohort of children after renal transplantation (RT).METHODS: A total of 109 children aged 13.1 ± 3.3 years who had undergone RT at one of three German transplant centers were enrolled in this study. Patients had been transplanted a mean of 5.5 (±4.0) years prior to being enrolled in the study. Anthropometric data, laboratory values and office- and 24-h ambulatory blood pressure monitoring (ABPM) were evaluated. Cardiovascular target organ damage was determined through non-invasive measurements of aortic pulse wave velocity (PWV), carotid intima-media thickness (IMT) and left ventricular mass (LVM).RESULTS: Elevated PWV or IMT values were detected in 22 and 58% of patients, respectively. Left ventricular hypertrophy was found in as many as 43% of patients. The prevalence of uncontrolled or untreated hypertension was 41%, of which 16% of cases were only detected by ABPM measurements. In the multivariable analysis, higher diastolic blood pressure, everolimus intake and lower estimated glomerular filtration rate were independently associated with high PWV. Higher systolic blood pressure and body mass index were associated with elevated LVM.CONCLUSIONS: Our results showed an alarming burden of cardiovascular subclinical organ damage in children after RT. Hypertension, obesity, immunosuppressive regimen and renal function emerged as independent risk factors of organ damage. Whereas the latter is not modifiable, the results of our study strongly indicate that the management of children after RT should focus on the control of blood pressure and weight.

AB - BACKGROUND: Cardiovascular disease is the second-most common cause of death in pediatric renal transplant recipients. The aim of this study was to evaluate subclinical cardiovascular target organ damage defined as the presence of arterio- and atherosclerotic lesions and cardiac remodeling and to analyze contributing risk factors in a large cohort of children after renal transplantation (RT).METHODS: A total of 109 children aged 13.1 ± 3.3 years who had undergone RT at one of three German transplant centers were enrolled in this study. Patients had been transplanted a mean of 5.5 (±4.0) years prior to being enrolled in the study. Anthropometric data, laboratory values and office- and 24-h ambulatory blood pressure monitoring (ABPM) were evaluated. Cardiovascular target organ damage was determined through non-invasive measurements of aortic pulse wave velocity (PWV), carotid intima-media thickness (IMT) and left ventricular mass (LVM).RESULTS: Elevated PWV or IMT values were detected in 22 and 58% of patients, respectively. Left ventricular hypertrophy was found in as many as 43% of patients. The prevalence of uncontrolled or untreated hypertension was 41%, of which 16% of cases were only detected by ABPM measurements. In the multivariable analysis, higher diastolic blood pressure, everolimus intake and lower estimated glomerular filtration rate were independently associated with high PWV. Higher systolic blood pressure and body mass index were associated with elevated LVM.CONCLUSIONS: Our results showed an alarming burden of cardiovascular subclinical organ damage in children after RT. Hypertension, obesity, immunosuppressive regimen and renal function emerged as independent risk factors of organ damage. Whereas the latter is not modifiable, the results of our study strongly indicate that the management of children after RT should focus on the control of blood pressure and weight.

KW - Journal Article

U2 - 10.1007/s00467-017-3771-8

DO - 10.1007/s00467-017-3771-8

M3 - SCORING: Journal article

C2 - 28804814

JO - PEDIATR NEPHROL

JF - PEDIATR NEPHROL

SN - 0931-041X

ER -