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Risk factors and incidence for lipid abnormalities in kidney transplant patients.
Ichimaru, N; Yamanaka, K; Kato, T; Kakuta, Y; Abe, T; Imamura, R; Nonomura, N; Kaimori, J-Y; Takahara, S.
Afiliación
  • Ichimaru N; Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Japan. Electronic address: ichimaru@att.med.osaka-u.ac.jp.
  • Yamanaka K; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Kato T; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Kakuta Y; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Abe T; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Imamura R; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Nonomura N; Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Kaimori JY; Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Takahara S; Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Japan.
Transplant Proc ; 47(3): 672-4, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25891708
ABSTRACT

BACKGROUND:

Lipid abnormalities (LA) are related to an increased risk for cardiovascular diseases in kidney transplantation patients. PATIENTS AND

METHODS:

Multivariable logistic regression models were used to estimate the risk of LA associated with potential risk factors, including immunosuppressant use, patient background characteristics, and laboratory data.

RESULTS:

In total, 386 patients who were undergoing kidney transplantation were included in the study. Statins were prescribed to 43% of patients. The LA composite outcome was defined as statin use and/or low density lipoprotein cholesterol level ≥120 mg/dL, and 229 patients (59.3%) developed LA as a result. LA was significantly related to everolimus, corticosteroid, age, and estimated glomerular filtration ratio in the multiple logistic regression analysis. The odds ratios were 2.264, 3.119, 1.186, and 0.870, respectively. Mycophenolate mofetil, mizoribine, azathioprine, cyclosporine (CYA), tacrolimus, proteinuria, body mass index, and male sex were not related to LA.

DISCUSSION:

CYA influenced lipid metabolism but was not related to LA in our study. The mean post transplantation period was 8.4 years, and the CYA dose decreased over time. The CYA blood concentration was 70.0 ng/mL, which is relatively low, but it decreased the susceptibility to LA. Serum lipid levels were well controlled by statins, and the estimated glomerular filtration rate was maintained stably.

CONCLUSIONS:

Everolimus and corticosteroid use, as well as a lower estimated glomerular filtration rate and higher age, were significant risk factors for LA. CYA is known for its adverse LA effects, but it was not a significant risk factor for LA in patients undergoing maintenance phase kidney transplantation.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Dislipidemias / Inmunosupresores / Lípidos Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies Idioma: En Revista: Transplant Proc Año: 2015 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Dislipidemias / Inmunosupresores / Lípidos Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies Idioma: En Revista: Transplant Proc Año: 2015 Tipo del documento: Article