Superiorita Of Cystatín C Over Kreatinín Pre Včasná Diagnóza Of Akútna Oblička Zranenie In Pediatrické Akútne Lymfoblastická Leukémia/ Lymfoblastic Lymfóm Ⅲ

Diskusia 

Our study revealed that every patient experienced AKI at least once during ALL/LBL treatment and AKI was diagnosed in 77% of the total chemotherapy courses using CysC-based eGFR. A study reported a 16.2% incidence in a cohort of 831 patients receiving chemotherapy for new-onset pediatric acute myeloid leukemia (Fisher et al. 2010). Another report demonstrated a 39% incidence of AKI in a study of 23 children with solid tumors (McMahon et al. 2018). To our knowledge, no study has evaluated the incidence of AKI among pediatric ALL/LBL patients. In the present study, the incidence of AKI during chemotherapy might be higher than the expectations of pediatric oncologylists or other previously reported incidence rates in pediatric cancer patients. This discrepancy in the incidence of AKI could be explained by several reasons. First, frequent assessment of renal function under the advice of pediatric nephrologists, conducting blood tests at least 3 times weekly, led to more attentive observations, and we were able to diagnose even very mild AKI. Second, different criteria have been used in previous studies. For the diagnosis of AKI, some studies have used the Kidney Disease: Improving Global Outcomes guidelines (Sutherland et al. 2015; Meersch et al. 2017) or the pRIFLE criteria (Sethi et al. 2015; Sutherland et al. 2015), while others have used the International Statistical Classification of Diseases and Related Health Problems codes (Ko et al. 2018). Third, the drugs used in different protocols may have influenced the results. Fourth, Cr-based eGFR was applied to assess renal function in most studies (McMahon et al. 2018), and CysC-based eGFR was rarely applied (Yong et al. 2017; Nakamura et al. 2018).

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Zlepšenia v diagnostike a liečbe of mať led na an nárast v počet z rakoviny avšak, veľa detstvo rakovina preživší rozvoj zdravie problémy roky neskôr as a výsledok ich rakovina liečba. Kooijmans et al. (2019) reviewed previous studies on renal dysfunction in childhood cancer survivors. They reported that the prevalence of CKD ranges from 2.4% to 32%. Another study reported that 0.5% of over 10,000 childhood cancer survivors treated in the 1970s and 1980s had developed renal failure or required dialysis by 18 years after the initial cancer diagnosis. They had a nine-fold higher risk than their siblings without cancer (Oeffinger et al. 2006). Chemotherapy-induced AKI is characterized by several pathological states such as podocytetauopathy, acute tubular injury, and crystal nephropathy (Perazella 2012). Although AKI recovery, maladaptive repair, and repetitive injury in most cases could lead to tubulointerstitial fibrosis and glomerulosclerosis resulting in CKD (Venkatachalam et al. 2015; Basile et al. 2016), our findings suggest that oncologists might have overlooked mild AKIs. Cancer patients usually undergo several courses of chemotherapy, which can lead to repeated kidney injury and an increased riziko z CKD. Preto, onkológovia spolu s nefrológovia musí opatrne detekovať dokonca mierne AKI počas chemoterapia. 

In the present study, during the 75 courses, AKI was diagnosed in 58 courses by CysC-based eGFR (77%) and 49 courses by Cr-based eGFR (65%). Of these cases, the diagnosis of AKI showed good agreement using the two assessment measures in 42 courses. By contrast, there was a discrepancy in the incidence of AKI diagnosed by CysC-based eGFR and Cr-based eGFR in 23 courses, although no significant difference was found in the incidence of AKI regardless of whether CysC-based eGFR or Cr-based eGFR was used for diagnosis (p=0.104). We suggest the following mechanisms contribute to this discrepancy: Among the seven courses diagnosed with AKI only by Cr-based eGFR, six patients (86%) received asparaginase immediately before the development of AKI. Since asparaginase may lower serum CysC levels by suppressing triiodothyronine blood levels, which promote CysC secretion from the smooth muscle via transforming growth factor-beta 1, AKI evaluated using CysC-based eGFR might be overlooked because of decreased serum CysC levels in patients receiving asparaginase (Ferster et al. 1992; Kotajima et al. 2010). Meanwhile, among the 16 courses diagnosed with AKI by using the CysC-based eGFR alone, most had a negative Z-score for body weight, suggesting that they had reduced muscle mass. Since serum Cr levels are largely influenced by muscle mass, this might have resulted in false-negative results in the diagnosis of AKI relying on Cr-based eGFR. Essentially, Rayar et al. (2013) reported that children with ALL had lower skeletal muscle mass (mean Z score of −0.18) than healthy children at the time of diagnosis

Sérum Cr je typicky použité v diagnóza AKI a monitorovanie renálna funkcia. However, its levels may not change until approximately 50% of the kidney function has been lost (Nguyen and Devarajan 2008). CysC is a low-molecular weight protein constantly produced and secreted by nucleated cells throughout the body. It is freely filtered by the glomerulus and is completely reabsorbed and metabolized by the renal proximal tubules; it has an inverse correlation with GFR as measured using radioisotopes (Coll et al. 2000). Because of these biological characteristics, CysC could potentially be more suitable for the assessment of renal function in children (Lankisch et al. 2006; NakhjavanShahraki et al. 2017). A recent meta-analysis showed the superiority of CysC over Cr in diagnosing AKI (Nakhjavan-Shahraki et al. 2017), which presents a suitable alternative to traditional diagnostic measures in nephrology. However, glucocorticoid administration in adult patients with asthma and solid tumors could increase serum CysC levels independent of renal function, even though the exact mechanism remains unknown (Bjarnadottir et al. 1995; Manetti et al. 2005). This may result in a falsely increased incidence of AKI if assessed by CysC-based eGFR. In contrast, there is controversy over whether glucocorticoids affect serum CysC levels in pediatric patients (Bokenkamp et al. 2002; Foster et al. 2006; Bokenkamp et al. 2007; Bardi et al. 2010; Slort et al. 2012). Therefore, in the present study, the incidence of AKI was compared separately by glucocorticoid therapy status. The results showed no significant difference between the two regimens in terms of AKI: the former was 77.4%, while the latter was 77.3% (Table 3). Furthermore, serial changes in the rate of CysC-based eGFR reduction during 42 courses of AKI, which included 28 courses with glucocorticoids, demonstrated improvement in renal function within 12 days despite continuous glucocorticoid administration over 2 weeks. Taken together, we believe that glucocorticoids have a negligible effect on serum CysC levels and CysC-based eGFR and that the results of our study suggest that CysC-based eGFR is more sensitive than Cr-based eGFR for assessing renal function in patients with ALL/LBL. We also compared AKI incidence by type of chemotherapy course. AKI occurred often during consolidation courses, possibly due to the use of high-dose methotrexate. Although not statistically significant, in all four types of courses, AKI was detected more often when defined using CysC-based eGFR versus Cr-based eGFR, which demonstrates the usefulness of CysC-based eGFR in diagnosing AKI during chemotherapy.

Aj keď oboje CysC- a Cr-based eGFR have výhody a nevýhody, we found definite zásluhy of založené na CysC eGFR nad Cr-based eGFR for the early diagnosis of AKI in pediatric patients with ALL/LBL podstupujúci chemoterapiu. Detekcia AKI at an early stage would allow appropriate protective measures to prevencia ďalších renal damage. Possible preventívne terapeutické možnosti vrátane liek dávkovanie zníženie, hydratácia, podávanie of diuretiká (Horie et al. 2018), a iné prostriedky na ochranu obličiek lieky môže prispievať k prevencii of future CKD. V toto štúdii, my sledované pacienti pre a medián of 29 mesiacov po opätovnej indukcii kurzy na potvrdenie vývoj of CKD; nie pacienti had znížený eGFR. Odvtedy pacienti kto skúsenosť AKI are at riziko of future CKD, we budeme pokračovať ďalej následné sledovanie.

This study has some limitations that should be considered. First, as all study patients recovered naturally, no intervention was implemented to address AKI. Further studies are needed to determine whether recovery can be accelerated with interventions, such as dose reduction of anti-cancer agents, large-volume fluid infusion, or alkalization. Moreover, future prospective studies are required to determine whether early intervention can reduce the risk of development of CKD. Second, drugs from preceding treatment courses may have a residual effect on subsequent courses. Nevertheless, because the median CysC-based eGFR at the start of each treatment course was 160 (IQR, 135 to 181), we believe that this possibility is quite low. Third, the sample size was small. However, the sample size was sufficient for evaluating the primary outcome of time to AKI diagnosis. The effect size in our study was 0.609, which is sufficient for non-parametric data. The small sample size restricted further detailed investigations regarding the effects of individual treatment protocols or drugs. More detailed studies with more patients are necessary

V záver, výsledky z naše štúdia zvýraznené dva dôležité aspekty súvisiace s AKI v pacientoch podstupujúcich chemoterapii pre pediatrických ALL/LBL. Prvý, my ukázal the možnosť z vysoká AKI výskyt medzi pacientmi. Hoci nefrotoxicita je dobre známe s chemoterapiou užívanie niektoré špecifické lieky, nie súčasnosť správa has vyhodnotené nefrotoxicita due to ALL/LBL liečba v deti. Časté pozorovania povolené nás detekcia rovnomerné mierne AKI. Second, CysC-based eGFR allowed allower diagnosis of AKI than Cr-based eGFR. Therefore, considering the merits and demerits of CysC-based eGFR and Cr-based eGFR in diagnostikovanie detstvo AKI during chemotherapy, we propose frequent renal function assessment by both measures.

Poďakovanie 

We would like to thank Editage (https://www.editage. com) for English language editing. 

Autor Príspevky S.A., S.T., and K.K. designed the study; T.Y., S.A., and Y.A. collected data; T.Y., S.A., Y.A., and S.Y. analyzed data; T.Y., S.A., M.R., and Y.A. wrote the rukopis; and S.Y., T.O., T.K., and S.T. gave technical support and kriticky recenzovaný the rukopis. K.K. supervidovaný the whole study process. All authors read and approved the final rukopis. Konflikt of Interest The authors deklarovať nie konflikt of záujmov.

Akcan-Arikan, A., Zappitelli, M., Loftis, L.L., Washburn, K.K., Jefferson, L.S. & Goldstein, S.L. (2007) Modifikovaný RIFLE kritériá in kriticky chorý deti s akútne obličky zranenie. Obličky int, 71, 1028-1035. Bardi, E., Dobos, E., Kappelmayer, J. & Kiss, C. (2010) Diferenciál účinok of kortikosteroidy na sérum cystatín C v trombocytovýtéma purpura a leukémia. Patol. Onkol. Res., 16, 453-456. 

Basile, D.P., Bonventre, J.V., Mehta, R., Nangaku, M., Unwin, R., Rosner, M.H., Kellum, J.A. & Ronco, C.; ADQI XIII Práca skupina (2016) Progresia po AKI: porozumenie maladaptedtive oprava procesy na predpovedať predpovedať a identifikovať terapeutická liečba. J. Am. Soc. Nefrol., 27, 687-697. 

Bjarnadottir, M., Grubb, A. & Olafsson, I. (1995) Promótor-sprostredkovaný, dexametazónom indukovaný zvýšenie in in cystatín C produkcia by HeLa bunky. Scand. J. Clin. Lab. Invest., 55, 617-623. Bokenkamp, A., Laarman, C.A., Braam, K.I., van Wijk, J.A., Kors, W.A., Kool, M., de Valk, J., Bouman, A.A., Spreeuwenberg, M.D. & Stoffel-Wagner, B. (2007) 

Účinok of kortikosteroid terapia na nízkomolekulárna-hmotnosť proteín markery of obličky funkcia. Klin. Chem., 53, 2219-2221. Bokenkamp, A., van Wijk, J.A., Lentze, M.J. & Stoffel-Wagner, B. (2002) Účinok of kortikosteroidy terapia na sérum cystatín C a beta2-mikroglobulín koncentrácie. 

Klin. Chem., 48, 1123-1126.d. Ciarimboli, G., Holle, S.K., Vollenbrocker, B., Hagos, Y., Reuter, S., Burckhardt, G., Bierer, S., Herrmann, E., Pavenstadt, H., Rossi, R., Kleta, R. & Schlatter, E. (2011) Nové stopy pre nefrotoxicita indukované by ifosfamid: preferenčné obličky vychytávanie via the human organic katión transport 2. Mol. Pharm., 8, 270-279.