Back to Search Start Over

Risk factors for the metabolic syndrome components of hypertension, diabetes mellitus, and dyslipidemia after living donor liver transplantation.

Authors :
Toshima, Takeo
Yoshizumi, Tomoharu
Inokuchi, Shoichi
Kosai-Fujimoto, Yukiko
Kurihara, Takeshi
Yoshiya, Shohei
Mano, Yohei
Takeishi, Kazuki
Itoh, Shinji
Harada, Noboru
Ikegami, Toru
Soejima, Yuji
Shimokawa, Mototsugu
Maehara, Yoshihiko
Mori, Masaki
Source :
HPB. Apr2020, Vol. 22 Issue 4, p511-520. 10p.
Publication Year :
2020

Abstract

Metabolic syndrome (MS) is the most common long-term complication after liver transplantation, and it has been increasing in incidence. The aim of this study was to clarify the risk factors for each MS component -hypertension, diabetes mellitus, and dyslipidemia-after living-donor liver transplantation (LDLT), including characteristics of living-donors. Data related to clinicopathological parameters including MS components in 461 consecutive patients who underwent LDLT were analyzed retrospectively. Prevalence of all MS components (hypertension, diabetes mellitus, and dyslipidemia) increased from 9.3%, 16.5%, and 7.2% before LDLT to 44.9%, 45.3%, and 50.8% after LDLT, respectively. By multivariate logistic regression analysis, the three factors, cyclosporine use (OR 2.086, P = 0.001), recipient age (OR 1.036, P = 0.001), and BMI (OR 1.072, P = 0.026) were independent predictors for post-LDLT hypertension. Next, the three factors, male recipient (OR 2.471, P < 0.001), recipient age (OR 1.039, P = 0.002), and donor BMI (OR 1.124, P = 0.012) were independent for post-LDLT diabetes mellitus. The four factors, cyclosporine use (OR 2.015, P = 0.001), prolonged prednisolone use (OR 1.928, P = 0.002), recipient age (OR 1.019, P = 0.037), and GRWR (OR 0.316, P = 0.037) were independent for post-LDLT dyslipidemia as well. Not only recipient-related factors but also donor-related factors were independently associated with each targeted post-LDLT MS component. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1365182X
Volume :
22
Issue :
4
Database :
Academic Search Index
Journal :
HPB
Publication Type :
Academic Journal
Accession number :
142812899
Full Text :
https://doi.org/10.1016/j.hpb.2019.08.008