Greater Susceptibility for Metabolic Syndrome in Pediatric Solid Organ and Stem Cell Transplant Recipients.


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
11 2019
Historique:
pubmed: 26 2 2019
medline: 23 6 2020
entrez: 26 2 2019
Statut: ppublish

Résumé

Cardiovascular comorbidity is of increasing importance after transplantation. Metabolic syndrome (MS) contributes to the risk for cardiovascular sequelae. Our aim was to assess the risk for MS in pediatric solid organ and stem cell transplant recipients by comparing them with matched untransplanted peers in a multicenter study. We prospectively assessed MS in 295 pediatric transplant recipients and compared them with 1475 age- and sex-matched controls. Posttransplant metabolic syndrome (PTMS) was most frequent in lung (43%) and kidney (39%), followed by liver (16%) and stem cell (13%) recipients, compared with nontransplanted peers (4%; P < 0.01). The risk of displaying PTMS was almost 22-fold higher after lung (95% confidence interval, CI, 8.2-57.4), 16-fold higher after kidney (95% CI, 9.1-28.9), 5-fold higher after liver (95% CI, 2.1-10.1), and 4-fold higher after stem cell (95% CI, 1.4-9.5) transplantation. The contribution of individual components leading to MS differed depending on transplant type. In the combined analysis of all transplant groups, older age, less physical activity, calcineurin or mammalian target of rapamycin inhibitor-based immunosuppression, and hypovitaminosis D were associated with PTMS. By investigating a large group of patients, our study not only shows a high prevalence of PTMS but also identifies kidney and lung transplant patients as being at a particularly high risk. Moreover, knowledge on the factors associated with PTMS allows for individualized treatment approaches as well as potential preventive measures.

Sections du résumé

BACKGROUND
Cardiovascular comorbidity is of increasing importance after transplantation. Metabolic syndrome (MS) contributes to the risk for cardiovascular sequelae. Our aim was to assess the risk for MS in pediatric solid organ and stem cell transplant recipients by comparing them with matched untransplanted peers in a multicenter study.
METHODS
We prospectively assessed MS in 295 pediatric transplant recipients and compared them with 1475 age- and sex-matched controls.
RESULTS
Posttransplant metabolic syndrome (PTMS) was most frequent in lung (43%) and kidney (39%), followed by liver (16%) and stem cell (13%) recipients, compared with nontransplanted peers (4%; P < 0.01). The risk of displaying PTMS was almost 22-fold higher after lung (95% confidence interval, CI, 8.2-57.4), 16-fold higher after kidney (95% CI, 9.1-28.9), 5-fold higher after liver (95% CI, 2.1-10.1), and 4-fold higher after stem cell (95% CI, 1.4-9.5) transplantation. The contribution of individual components leading to MS differed depending on transplant type. In the combined analysis of all transplant groups, older age, less physical activity, calcineurin or mammalian target of rapamycin inhibitor-based immunosuppression, and hypovitaminosis D were associated with PTMS.
CONCLUSIONS
By investigating a large group of patients, our study not only shows a high prevalence of PTMS but also identifies kidney and lung transplant patients as being at a particularly high risk. Moreover, knowledge on the factors associated with PTMS allows for individualized treatment approaches as well as potential preventive measures.

Identifiants

pubmed: 30801541
doi: 10.1097/TP.0000000000002675
doi:

Substances chimiques

Immunosuppressive Agents 0
Lipids 0

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2423-2433

Auteurs

Ricarda Blöte (R)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Nima Memaran (N)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Bianca Borchert-Mörlins (B)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Daniela Thurn-Valsassina (D)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Imeke Goldschmidt (I)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Rita Beier (R)

Department of Pediatric Hematology and Oncology, Clinic for Pediatrics III, University Hospital Essen, Essen, Germany.

Martin Sauer (M)

Department of Pediatric Hematology and Oncology, Hannover Medical School, Hanover, Germany.

Carsten Müller (C)

Department of Pediatric Pulmonology, Allergology and Neonatology, Hannover Medical School, Hanover, Germany.

Giselle Sarganas (G)

Department of Epidemiology and Health Monitoring, Robert Koch Institute, Berlin, Germany.

Jun Oh (J)

Department of Pediatric Nephrology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Rainer Büscher (R)

Department of Pediatric Nephrology, University Hospital, Essen, Germany.

Markus J Kemper (MJ)

Department of Pediatrics, AK Hamburg Nord, Asklepios Medical School, Hamburg, Germany.

Rizky I Sugianto (RI)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

Jelena Epping (J)

Department of Medical Sociology, Hannover Medical School, Hanover, Germany.

Bernhard M W Schmidt (BMW)

Department of Nephrology, Hannover Medical School, Hanover, Germany.

Anette Melk (A)

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hanover, Germany.

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