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. 2019 Oct 1;8(10):1576.
doi: 10.3390/jcm8101576.

Growth Differentiation Factor-15 (GDF-15) is a Biomarker of Muscle Wasting and Renal Dysfunction in Preoperative Cardiovascular Surgery Patients

Affiliations

Growth Differentiation Factor-15 (GDF-15) is a Biomarker of Muscle Wasting and Renal Dysfunction in Preoperative Cardiovascular Surgery Patients

Toshiaki Nakajima et al. J Clin Med. .

Abstract

Frailty and sarcopenia increase the risk of complications and mortality when invasive treatment such as cardiac surgery is performed. Growth differentiation factor-15 (GDF-15) involves various pathophysiological conditions including renal dysfunction, heart failure and cachexia. We investigated the pathophysiological roles of preoperative GDF-15 levels in cardiovascular surgery patients. Preoperative skeletal muscle index (SMI) determined by bioelectrical impedance analysis, hand-grip strength, 4 m gait speed, and anterior thigh muscle thickness (TMth) measured by echocardiography were assessed in 72 patients (average age 69.9 years) who underwent cardiovascular surgery. The preoperative serum GDF-15 concentration was determined by enzyme-linked immunosorbent assay. Circulating GDF-15 level was correlated with age, brain natriuretic peptide, and estimated glomerular filtration rate (eGFR). It was also negatively correlated with SMI, hand-grip strength, and anterior TMth. In multivariate analysis, eGFR and anterior TMth were the independent determinants of GDF-15 concentration even after adjusting for age, sex, and body mass index. Alternatively, the GDF-15 level was an independent determinant of eGFR and anterior TMth. We concluded that preoperative GDF-15 levels reflect muscle wasting as well as renal dysfunction in preoperative cardiovascular surgery patients. GDF-15 may be a novel biomarker for identify high-risk patients with muscle wasting and renal dysfunction before cardiovascular surgery.

Keywords: GDF-15; biomarkers; cardiovascular surgery; chronic kidney disease; muscle wasting; operative risk; renal dysfunction; sarcopenia.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Correlations between clinical data (age, eGFR) and serum concentrations of GDF-15, TNF-α, and IGF-1. Relationships between laboratory data (age (a), eGFR (b)) and serum concentrations of GDF-15 (Aa,Ab), TNF-α (Ba,Bb) and IGF-1 (Ca,Cb) in males and females. ** p < 0.01, *** p < 0.001.
Figure 2
Figure 2
Correlations between the physical data (anterior thigh muscle thickness, grip strength) and serum concentrations of GDF-15, TNF-α, and IGF-1. Relationships between the laboratory data (anterior thigh muscle thickness (TMth, supine) (a), grip strength (b) and serum concentrations of GDF-15 (Aa,Ab), TNF-α (Ba,Bb) and IGF-1 (Ca,Cb) in males * p < 0.05, ** p < 0.01, *** p < 0.001.
Figure 3
Figure 3
ROC curves to identify the optimal cut-off level of GDF-15, TNFα, and Hb for detecting eGFR < 60. In the ROC curves shown, different cut-off values of GDF-15, and TNFα, and Hb were used to predict eGFR < 60, with true positives plotted on the vertical axis (sensitivity) and Figure 1. plotted on the horizontal axis.

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