Reply to the Letter to the Editor: "GDF-15 - A matter of the heart or the kidney?".
Reply to the Letter to the Editor: "GDF-15 - A matter of the heart or the kidney?".
复制标题
回复给编辑的信:“GDF-15 - 心脏还是肾脏的问题?”。
DOI:
10.1016/j.ijcard.2020.04.008
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发表时间:
2020
影响因子:
3.5
通讯作者:
Book,Wendy
中科院分区:
文献类型:
--
作者:
Saraf,Anita;Book,Wendy
We thank Thorsteindottir et al.[2] for their insight into the influence of renal function on GDF-15 levels, as it is relevant to understanding the pathophysiology of systemically dysregulated biomarkers in our Fontan patients. In fact, we appreciate that some of the biomarkers that we investigated may originate in multiple organs or may be abnormal as a consequence of subclinical multiorgan dysregulation that is not appreciated by standard laboratory tests used in clinical practice.In our study [1], we considered GDF-15 to be an inflammatory marker (Table 3), as it plays a significant role in modulating chemokine expression in various instances of organ injury. In our Fontan cohort, however, there was no evidence of chronic kidney injury using parameters used by Thorsteindottir et al. As noted,(Table 2b) creatinine levels were normal both at baseline and follow up. GFR levels (not reported) were> 70 mL/min/1.73 m2 in the cohort as measured by standard laboratory tests. However, other markers of renal dysregulation such as Cystatin C and uPAR were abnormal in these patients, which further emphasizes the need to employ advanced biomarker testing in our complex patients. We expect that some biomarkers will correlate with each other,(Supplemental Fig. 1) as there is a positive correlation between GDF-15 and renal makers uPAR and Cystatin C, further validating that Fontan physiology has long term consequences on various organ systems, including the kidney, that precedes clinical deterioration.