- Research article
- Open Access
Impact of thyroid function on cystatin C in detecting acute kidney injury: a prospective, observational study
BMC Nephrology volume 20, Article number: 41 (2019)
Cystatin C (Cys C) used clinically for detecting early acute kidney injury (AKI) was reported to be associated with thyroid function. Therefore, whether the performance of Cys C is affected by thyroid hormones has raised concern in critically ill patients. This study aimed to investigate the impact of thyroid hormones on the diagnostic and predictive accuracy of Cys C for AKI, and hence optimize the clinical application of Cys C.
A prospective observational study was conducted in the general intensive care units (ICUs). Serum creatinine (SCr), Cys C, and thyroid function were documented for all patients at ICU admission. Patients were separated into five quintiles based on free triiodothyronine (FT3) and total triiodothyronine (TT3), and two categories according to the presence of low T3 syndrome or not. The impact of thyroid function on the performance of Cys C in diagnosing and predicting AKI was assessed by area under the receiver operating characteristic curve (AUC).
The AKI incidence was 30.0% (402/1339); 225 patients had AKI upon entry, and 177 patients developed AKI during the subsequent 7 days. The AUCs for Cys C in detecting total AKI, established AKI, and later-onset AKI was 0.753, 0.797, and 0.669, respectively. The multiple linear regression analysis demonstrated that TT3 and FT3 were independently associated with Cys C. Overall, although Cys C did not yield any significant difference in AUCs for detecting AKI among patients with different thyroid hormones, the optimal cut-off value of Cys C to detect AKI was markedly different between patients with and without low T3 syndrome.
The thyroid function had no significant impact on the diagnostic and predictive accuracy of Cys C in detecting AKI in ICU patients. However, the optimal cut-off value of Cys C to detect AKI could be affected by thyroid function.
The thyroid hormones at admission were negatively associated with Cys C, and only TT3 and FT3 were independent factors correlated with Cys C.
Thyroid function alteration, including low T3 syndrome, might not exert a statistically significant impact on the performance of Cys C in diagnosing and predicting AKI in ICU patients.
The optimal cut-off value of Cys C to detect AKI could be affected by thyroid function.
Acute kidney injury (AKI) is an increasingly prevalent problem in patients hospitalized in intensive care units (ICUs), with the incidence varied from 9% to more than 50% [1, 2]. Despite the development of renal replacement therapy (RRT), AKI remains a major cause of adverse outcomes, including high mortality, increased length of hospital and ICU stay, as well as the economic burden [3, 4]. Timely detection of AKI is important to prevent its progression and hence potentially improve the timeliness of intervention. Nevertheless, the diagnosis of AKI based on conventional surrogate markers, serum creatinine (SCr), and urine output lags far behind the reduction in kidney function [5, 6]. Although some novel biomarkers are clinically available, the application of these biomarkers still has limitations . In this regard, the optimal utilization of the available biomarker would be a tremendous advance in clinical medicine.
Serum cystatin C (Cys C) has been reported to be a clinically available marker for early detecting AKI, which is routinely used in some hospitals [7,8,9]. Cys C is a cysteine proteinase inhibitor produced at a constant rate in all nucleated cells and minimally bound to proteins. It is freely filtered by the glomerulus and completely reabsorbed by the proximal tubules [10, 11]. Compared with SCr, the concentration of serum Cys C appeared to be less affected by muscle mass, diet, age, and sex, allowing for the superiority of Cys C to be a reliable marker for detecting an early minimal reduction in the glomerular filtration rate (GFR) [12,13,14,15]. However, growing evidence has demonstrated that the production of Cys C could be stimulated by thyroid hormones, and it was sensitive to small changes in thyroid function [16,17,18]. Although other studies proved that the performance of Cys C in the diagnosis and risk prediction of AKI was not impacted by thyroid function [19, 20], these results have not been verified in larger studies.
Therefore, this prospective, observational study was conducted in a larger critically ill cohort to analyze the association between thyroid function and the diagnostic and predictive accuracy of Cys C in detecting AKI.
Study design and participants
This prospective observational study was conducted in the general ICUs in Guangdong General Hospital. All consecutive patients aged 18 years or elder admitted to ICUs from October 2014 to December 2016 were enrolled for the study. The exclusion criteria included refusal of consent, preexisting hyperthyroidism or hypothyroidism, medical history of hormone replacement therapy except insulin use, preexisting end-stage renal disease (ESRD) or renal dysfunction requiring RRT before admission, preexisting renal transplantation or nephrectomy, or missing admission data. The primary outcome of this study was the detection of AKI within 1 week after ICU admission, and the secondary outcome comprised length of ICU and hospital stay, RRT during ICU stay, as well as ICU and hospital mortality.
Data collection and definition
Each patient’s baseline characteristics, including age, gender, body mass index (BMI), preexisting clinical conditions, sepsis, admission type, baseline SCr, baseline estimated glomerular filtration rate (eGFR), acute physiology and chronic health evaluation (APACHE II) score, length of ICU stay, length of hospital stay, RRT during ICU stay, ICU mortality, and hospital mortality, were collected from the electronic medical system. The serum sample for measuring SCr, Cys C, total triiodothyronine (TT3, normal value range: 1.34–2.73 nmol/L), total thyroxine (TT4, normal value range: 78.40–158.40 nmol/L), free triiodothyronine (FT3, normal value range: 3.80–6.00 pmol/L), free thyroxine (FT4, normal value range: 7.50–21.10 pmol/L), thyroid-stimulating-hormone (TSH; normal value range: 0.34–5.60 μIU/mL), blood urea nitrogen (BUN), and albumin was collected at admission, and thereafter SCr was measured daily between 7 a.m. to 9 a.m. as a part of routine clinical care until ICU discharge. The eGFR was calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine equation .
A baseline SCr was determined using the following rules ranked in the descending order of preference : (1) the most recent pre-ICU value between 30 and 365 days before ICU admission (n = 143); (2) a stable pre-ICU value > 365 days for patients aged < 40 years (stable defined as within 15% of the lowest ICU measurement) before ICU admission (n = 6); (3) pre-ICU value > 365 days before ICU admission and less than the initial SCr at ICU admission (n = 51, 4) a pre-ICU value (between 3 and 39 days before ICU admission) less than or equal to the initial SCr on admission to ICU and not distinctly in AKI (n = 638); or (5) the lowest SCr upon initial admission to ICU (n = 173), the last ICU value (n = 216), or the minimum value at follow-up up to 365 days (n = 112). According to the KDIGO (Kidney Disease: Improving Global Outcomes) criteria, patients with an increase in SCr by ≥0.3 mg/dL (≥26.5 μmol/L) within 48 h, or increase in SCr to ≥1.5 times baseline within 1 week, or urine output < 0.5 mL/(kg ·h) for 6 h were diagnosed with AKI. However, since the urine output criteria has limited sensitivity when diuretics are administrated , the AKI diagnosis was based on serum creatinine in this study. Established AKI was defined as the diagnosis of AKI on entry, and later-onset AKI indicated no AKI diagnosis on entry but meeting the KDIGO criteria during the following 1 week after admission. Low T3 syndrome, also named non-thyroidal illness syndrome, is characterized by decreased serum T3 and, in severe illness, decreased serum T4, increased serum reverse T3 (rT3) concentrations, and normal or slightly decreased concentration of TSH [24, 25]. In this study, patients with an FT3 level below normal lower bound, and FT4 and TSH lower or within the normal range were diagnosed with low T3 syndrome according to the manufacturer’s standard value, as described in a previous study .
All samples were collected within 1 h after ICU admission and measured within 24 h after collection. SCr, serum Cys C, albumin, and BUN were measured using a UniCel DxC 800 Synchron System (Beckman Coulter, CA, USA). Cys C was assayed by immunoturbidimetry, the coefficients of interassay and intraassay variations for which were ≤ 5% and ≤ 10%, respectively. The thyroid function test was conducted via chemiluminescent immunoassay using Unicel DxI800 Synchron System (Beckman Coulter, CA, USA).
All statistical analyses were conducted using SPSS version 16.0 (SPSS, IL, USA; 2007), and MedCalc version 15.8 (MedCalc Software bvba, Ostend, Belgium; 2015) software programs. A two-tailed P value < 0.05 was considered statistically significant. The characteristics of patients with continuous and categorical data were presented with median (interquartile range, IQR) and absolute value (percentage), respectively. For continuous variables, normally distributed variables were compared using the t test and non-normally distributed variables were compared using the Wilcoxon rank-sum test. Categorical variables were compared using the chi-square test or Fisher’s exact test. The bivariate correlation analysis was used to evaluate the association between two variables. A multivariable linear regression analysis was conducted to identify the independent factors for Cys C and determine the representative index of thyroid function for further analysis. A receiver operating characteristic (ROC) curve analysis was performed, and the area under the curve (AUC) was calculated to demonstrate the diagnostic and predictive value of Cys C in detecting AKI. The difference between AUCs in each group was calculated using the Hanley–McNeil method , and the optimal cutoff value for AKI detection was determined with the Youden’s index using the MedCalc software.
Patient characteristics and outcomes
Figure 1 presents the protocol and flow diagram of screening process. Among 1463 critically ill adult patients enrolled for the study, 124 were excluded for the following reasons: refused to consent (n = 45), complicated with thyroid dysfunction (hyperthyroidism or hypothyroidism, n = 24), history of nephrectomy (n = 10) or renal transplantation (n = 5), and ESRD (n = 40) prior to ICU admission. Finally, 1339 patients got involved in the study; AKI occurred in 402 patients, of which 225 were diagnosed with AKI at admission and 177 developed AKI during the following 1 week.
Basic clinical data and outcomes of the patients were demonstrated in Table 1. Compared with non-AKI patients, the patients with AKI were elder and had a significantly higher rate of complications, including hypertension (HTN), diabetes mellitus (DM), chronic kidney disease (CKD), coronary artery disease (CAD), chronic heart failure (CHF), stoke, and chronic liver disease. Sepsis was significantly associated with AKI, with an occurrence rate of 33.1%. The thyroid hormones concentration was significantly lower in the AKI group than in the non-AKI group, and patients in AKI group tended to be complicated with low T3 syndrome. Emergency patients and medical patients admitted to ICU were predisposed to be complicated with AKI. Patients with AKI showed significantly higher hospital and ICU mortality, and longer hospital and ICU stay.
Factors associated with Cys C
As indicated in Table 2 showing the bivariate correlation analysis between Cys C and other factors, patients with a higher Cys C concentration were elder and had higher APACHE II score, SCr at admission, baseline SCr, and BUN. Moreover, albumin, and thyroid hormone concentrations, including FT3, TT3, and TT4 were negatively associated with Cys C. The multiple linear regression analysis shown in Table 3 indicated that among the abovementioned thyroid hormones, only FT3 (standardized β = − 0.100, P < 0.001) and TT3 (standardized β = 0.059, P = 0.007) were independently associated with Cys C. In addition, sex (standardized β = − 0.059, P < 0.001), age (standardized β = 0.136, P < 0.001), APACHE II score (standardized β = 0.087, P < 0.001), SCr at admission (standardized β = 0.578, P < 0.001), baseline SCr (standardized β = 0.066, P = 0.004), and BUN at admission (standardized β = 0.166, P < 0.001) were independent factors related to Cys C.
Detection of AKI using Cys C with respect to thyroid hormones stratification
Cys C was significantly higher in the AKI group than the non-AKI group (Table 1). Figure 2 demonstrated the ROC analysis for the diagnostic and predictive ability of Cys C in detecting AKI. The AUCs calculated for Cys C was 0.753, 0.797, and 0.669 in detecting total AKI, established AKI, and later-onset AKI, respectively.
The patients were divided into five quintiles based on FT3 (Table 4), TT3 (Table 5), and FT4 (Additional file 1: Table S1), and AUC-ROC analysis was conducted to evaluate the impact of thyroid hormones on Cys C in detecting AKI. In the stratification of FT3 (Table 4), AUCs for Cys C in detecting total AKI, established AKI, and later-onset AKI was 0.777, 0.786, and 0.667, respectively, in quintile I; 0.740, 0.799, and 0.658, respectively, in quintile II; 0.721, 0.774, and 0.617, respectively, in quintile III; 0.727, 0.751, and 0.694, respectively, in quintile IV; and 0.700, 0.733, and 0.661, respectively, in quintile V. For quintiles of TT3 (Table 5), Cys C demonstrated its diagnostic value as indicated by AUCs of 0.784, 0.738, 0.730, 0.708, and 0.707, respectively, to detect total AKI; 0.804, 0.781, 0.786, 0.706, and 0.757, respectively, to detect established AKI; and 0.651, 0.652, 0.657, 0.690, and 0.670, respectively, to detect later-onset AKI. In summary, despite a tendency of decreasing AUCs across the quintiles by FT3 and TT3 in total and established AKI, no significant difference between AUCs was observed in any two groups for total AKI, established AKI, and later-onset AKI in different stratification of thyroid hormones.
Impact of low T3 syndrome on detecting AKI using Cys C
Table 6 shows the subgroup analysis for the impact of low T3 syndrome on detecting AKI using Cys C. The patients were further separated into two categories: 650 with low T3 syndrome (FT3 < 3.8 pmol/L, and FT4 and TSH within or lower than the normal range), and 689 without low T3 syndrome. Compared with non-low T3 syndrome patients, the AUCs of Cys C in patients with low T3 syndrome were higher (0.762 vs 0.725, 0.789 vs 0.784, and 0.669 vs 0.663, respectively) in detecting total AKI, established AKI, and later-onset AKI. Furthermore, the optimal cut-off values of Cys C for AKI detection were markedly different between low T3 syndrome and non-low T3 syndrome patients. However, similar result was observed that AUCs for discrimination ability of AKI detection by Cys C did not differ significantly between groups.
This prospective, observational study assessed the influence of thyroid function on AKI detection by serum Cys C in heterogenous ICU cohort. The major finding was that there was no significant difference in the diagnostic and predictive performance of Cys C among patients with different thyroid hormone levels. However, the optimal cut-off value of Cys C to detect AKI could be affected by thyroid function alteration in ICU patients.
Serving as a clinical routine biomarker, Cys C has been postulated to be superior to SCr for early AKI identification and outcome prediction [7, 12,13,14]. In the diagnostic performance testing in this study, Cys C demonstrated a good diagnostic value to detect AKI, as indicated by the AUC-ROC analysis of 0.797 for established AKI. However, the predictive ability of Cys C for detecting AKI was poor with the AUC of 0.669. Furthermore, this study indicated that several factors, including age, sex, baseline SCr levels, BUN, albumin level, and thyroid hormones were related to the Cys C concentration. Therefore, whether the performance of Cys C in detecting AKI is affected by the abovementioned variables should be verified.
Increasing evidence has demonstrated that Cys C concentration could be influenced by the thyroid hormone level and was sensitive to small alterations of thyroid function [16,17,18]. Fricker et al. found that patients had higher concentrations of Cys C in the hyperthyroid state and lower Cys C concentrations in the hypothyroid state, thereby confirming that the thyroid function had a major impact on Cys C level . Similarly, another study involved 113 patients with Graves’ disease further proved that the eGFR by CysC levels significantly decreased with elevated FT3 and FT4 levels in patients with hyperthyroidism . Furthermore, Schmid et al. illustrated the mechanism by which T3 directly stimulated the production of Cys C in vitro . However, a recent prospective, observational study by Wang et al., including 446 critically ill patients hospitalized in the ICU, showed a negative relationship between Cys C and thyroid function . Likewise, in the present study, Cys C concentration was negatively associated with FT3, TT3, and TT4 levels. This might be explained by the significant association between low T3 syndrome and adverse outcomes in critical illness [25, 29,30,31], and the positive correlation between APACHE II score and Cys C. The multiple linear regression analysis showed that both TT3 and FT3 were independently correlated with Cys C. Moreover, it is acknowledged that T3 is the biologically active thyroid hormone [32, 33]. Consequently, TT3 and FT3 were selected as the representative variables to analyze the impact of thyroid function on the diagnostic and predictive value of Cys C in detecting AKI.
It was previously reported that patients with critical illness were predisposed to thyroid function derangement, of which low T3 syndrome was the most common [30, 31]. Although the presence of thyroid dysfunction seemed not to be associated with the clinical and prognostic implication of AKI in previous report , some other studies documented that Cys C concentration was sensitive to small change of thyroid hormones. Therefore, alterations of thyroid function should be considered when Cys C is used for AKI detection in critically ill patients [16,17,18]. In this regard, Schanz et al. confirmed that thyroid function had no relevant influence on clinical practice of Cys C in risk prediction of AKI in emergency department . Wang et al. also reported that thyroid function, as indicated by FT4, had no impact on the performance of Cys C in diagnosing AKI in ICU settings . However, one focused only on the newly AKI, and the later centered on the established AKI, using AKIN (Acute Kidney Injury Network) criteria. Based on the KDIGO criteria, the present study not only analyzed the impact of thyroid hormones, TT3 and FT3, on the diagnostic and predictive ability of Cys C in detecting AKI, but also tested the influence produced by FT4 on AKI detection by Cys C in a larger critically ill cohort. The thyroid hormones had no statistically significant effect on Cys C in diagnosing AKI on admission to ICU, in accordance with previous findings. Meanwhile, this study further confirmed that the predictive ability of Cys C in detecting AKI was also not interfered by thyroid function. In addition, the present study showed that Cys C did not yield any significant difference between patients with and without low T3 syndrome, either for established AKI, or later-onset AKI.
It was previously observed that the optimal cut-off value of Cys C in detecting AKI increased across thyroid hormone stratification . However, the similar result was not displayed in the present study. The optimal cut-off value was markedly higher in patients with low T3 syndrome, in this study, the possible reason for which might be the negative correlation between Cys C and thyroid hormone concentration. This result strongly suggested that the optimal cut-off value of Cys C to detect AKI was affected by low T3 syndrome. Therefore, the reasonable cut-off point should be established when Cys C is used to detect AKI in patients with thyroid function alteration.
The present study had some limitations. First, it assessed the impact of thyroid hormones on the ability of Cys C to detect AKI, rather than predict the stratification and outcome of AKI in the critically ill patients. However, the prognostic ability of Cys C in AKI was still uncertain. Second, it only detected the effect of the baseline thyroid function on the performance of Cys C. However, critical illness is closely associated with alteration in thyroid hormone concentration. The study could not exclude that the alteration of thyroid function after admission might have an influence on Cys C in detecting AKI.
This prospective, observational study found that thyroid function alteration, including low T3 syndrome, might not exert a statistically significant impact on the performance of Cys C in diagnosing and predicting AKI in ICU patients. However, the optimal cut-off value of Cys C to detect AKI could be affected by thyroid function.
- 95% CI:
95% confidence interval
Acute kidney injury
- APACHE II:
Acute physiology and chronic health evaluation II score
Area under the receiver operating characteristic curve
Body mass index
Blood urea nitrogen
Coronary artery disease
Chronic heart failure
Chronic Kidney Disease
- Cys C:
Estimated glomerular filtration rate
End-stage renal disease
Intensive care unit
Receiver operating characteristic curve
Renal replacement therapy
Urine production first 24 h after admission
Hoste EA, Bagshaw SM, Bellomo R, Cely CM, Colman R, Cruz DN, Edipidis K, Forni LG, Gomersall CD, Govil D, Honore PM, Joannes-Boyau O, Joannidis M, Korhonen AM, Lavrentieva A, Mehta RL, Palevsky P, Roessler E, Ronco C, Uchino S, Vazquez JA, Vidal Andrade E, Webb S, Kellum JA. Epidemiology of acute kidney injury in critically ill patients: the multinational AKI-EPI study. Intensive Care Med. 2015;41(8):1411–23.
Thakar CV, Christianson A, Freyberg R, Almenoff P, Render ML. Incidence and outcomes of acute kidney injury in intensive care units: a veterans administration study. Crit Care Med. 2009;37(9):2552–8.
Eachempati SR, Wang JC, Hydo LJ, Shou J, Barie PS. Acute renal failure in critically ill surgical patients: persistent lethality despite new modes of renal replacement therapy. J Trauma. 2007;63(5):987–93.
Vandijck DM, Oeyen S, Decruyenaere JM, Annemans L, Hoste EA. Acute kidney injury, length of stay, and costs in patients hospitalized in the intensive care unit. Acta Clin Belg. 2014;62(sup2):341–5.
American Society of Nephrology Renal Research Report. J Am Soc Nephrol. 2005;16(7):1886–903.
Wasung ME, Chawla LS, Madero M. Biomarkers of renal function, which and when? Clin Chim Acta. 2015;438:350–7.
Ostermann M, Joannidis M. Acute kidney injury 2016: diagnosis and diagnostic workup. Crit Care. 2016;20(1):299.
Deng Y, Chi R, Chen S, Ye H, Yuan J, Wang L, Zhai Y, Gao L, Zhang D, Hu L, Lv B, Long Y, Sun C, Yang X, Zou X, Chen C. Evaluation of clinically available renal biomarkers in critically ill adults: a prospective multicenter observational study. Crit Care. 2017;21(1):46.
Deng Y, Yuan J, Chi R, Ye H, Zhou D, Wang S, Mai C, Nie Z, Wang L, Zhai Y, Gao L, Zhang D, Hu L, Deng Y, Chen C. The incidence, risk factors and outcomes of postoperative acute kidney injury in neurosurgical critically ill patients. Sci Rep. 2017;7(1):4245.
Abrahamson M, Olafsson I, Palsdottir A, Ulvsbäck M, Lundwall A, Jensson O, Grubb A. Structure and expression of the human cystatin C gene. Biochem J. 1990;268(2):287–94.
Tenstad O, Roald AB, Grubb A, Aukland K. Renal handling of radiolabelled human cystatin C in the rat. Scand J Clin Lab Invest. 1996;56(5):409–14.
Coll E, Botey A, Alvarez L, Poch E, Quinto L, Saurina A, Vera M, Piera C, Darnell A. Serum cystatin C as a new marker for noninvasive estimation of glomerular filtration rate and as a marker for early renal impairment. Am J Kidney Dis. 2000;36(1):29–34.
Dharnidharka VR, Kwon C, Stevens G. Serum cystatin C is superior to serum creatinine as a marker of kidney function: a meta-analysis. Am J Kidney Dis. 2002;40(2):221–6.
Fouad M, Boraie M. Cystatin C as an early marker of acute kidney injury and predictor of mortality in the intensive care unit after acute myocardial infarction. Arab J Nephrol Transplant. 2013;6(1):21–6.
Nejat M, Pickering JW, Walker RJ, Endre ZH. Rapid detection of acute kidney injury by plasma cystatin C in the intensive care unit. Nephrol Dial Transplant. 2010;25(10):3283–9.
Fricker M, Wiesli P, Brandle M, Schwegler B, Schmid C. Impact of thyroid dysfunction on serum cystatin C. Kidney Int. 2003;63(5):1944–7.
Schmid C, Ghirlanda-Keller C, Zwimpfer C, Zoidis E. Triiodothyronine stimulates cystatin C production in bone cells. Biochem Biophys Res Commun. 2012;419(2):425–30.
Wiesli P, Schwegler B, Spinas GA, Schmid C. Serum cystatin C is sensitive to small changes in thyroid function. Clin Chim Acta. 2003;338(1–2):87–90.
Schanz M, Pannes D, Dippon J, Wasser C, Alscher MD, Kimmel M. The influence of thyroid function, inflammation, and obesity on risk prediction of acute kidney injury by cystatin C in the emergency department. Kidney Blood Press Res. 2016;41(5):604–13.
Wang F, Pan W, Wang H, Zhou Y, Wang S, Pan S. The impacts of thyroid function on the diagnostic accuracy of cystatin C to detect acute kidney injury in ICU patients: a prospective, observational study. Crit Care. 2014;18(1):R9.
Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF 3rd, Feldman HI, Kusek JW, Eggers P, Van Lente F, Greene T, Coresh J. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):604–12.
Endre ZH, Walker RJ, Pickering JW, Shaw GM, Frampton CM, Henderson SJ, Hutchison R, Mehrtens JE, Robinson JM, Schollum JB, Westhuyzen J, Celi LA, McGinley RJ, Campbell IJ, George PM. Early intervention with erythropoietin does not affect the outcome of acute kidney injury (the EARLYARF trial). Kidney Int. 2010;77(11):1020–30.
McCullough PA, Shaw AD, Haase M, Bouchard J, Waikar SS, Siew ED, Murray PT, Mehta RL, Ronco C. Diagnosis of acute kidney injury using functional and injury biomarkers: workgroup statements from the tenth acute Dialysis quality initiative consensus conference. Contrib Nephrol. 2013;182:13–29.
Boelen A, Kwakkel J, Fliers E. Beyond low plasma T3: local thyroid hormone metabolism during inflammation and infection. Endocr Rev. 2011;32(5):670–93.
Fliers E, Bianco AC, Langouche L, Boelen A. Thyroid function in critically ill patients. Lancet Diabetes Endocrinol. 2015;3(10):816–25.
Gao R, Liang JH, Wang L, Zhu HY, Wu W, Wu JZ, Xia Y, Cao L, Fan L, Yang T, Li JY, Xu W. Low T3 syndrome is a strong prognostic predictor in diffuse large B cell lymphoma. Br J Haematol. 2017;177(1):95–105.
Hanley JA. McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148(3):839–43.
Suzuki Y, Matsushita K, Seimiya M, Yoshida T, Sawabe Y, Ogawa M, Nomura F. Paradoxical effects of thyroid function on glomerular filtration rate estimated from serum creatinine or standardized cystatin C in patients with Japanese Graves' disease. Clin Chim Acta. 2015;451(Pt B):316–22.
Zaloga GP, Chernow B, Smallridge RC, Zajtchuk R, Hall-Boyer K, Hargraves R, Lake CR. Burman KD. A longitudinal evaluation of thyroid function in critically ill surgical patients. Ann Surg. 1985;201(4):456–64.
Golombek SG. Nonthyroidal illness syndrome and euthyroid sick syndrome in intensive care patients. Semin Perinatol. 2008;32(6):413–8.
Mebis L, Van den Berghe G. Thyroid axis function and dysfunction in critical illness. Best Pract Res Clin Endocrinol Metab. 2011;25(5):745–57.
Surks MI, Oppenheimer JH. Concentration of L-thyroxine and L-triiodothyronine specifically bound to nuclear receptors in rat liver and kidney. Quantitative evidence favoring a major role of T3 in thyroid hormone action. J Clin Invest. 1977;60(3):555–62.
Engler D, Burger AG. The deiodination of the iodothyronines and of their derivatives in man. Endocr Rev. 1984;5(2):151–84.
Iglesias P, Olea T, Vega-Cabrera C, Heras M, Bajo MA, del Peso G, Arias MJ, Selgas R, Diez JJ. Thyroid function tests in acute kidney injury. J Nephrol. 2013;26(1):164–72.
The authors are grateful to all doctors, nurses, and technicians for the collection and testing of the blood samples. They also thank the patients for their dedication in the study.
The study was supported by grants from the National Natural Science Foundation of China (81671963 to CC), the Science and Technology Planning Project of Guangdong Province (Key Program) (2014B020212023 to CC), the National Science and Technology Support Program (2015BAI12B07 to CC), and the Science and Technology Planning Project of Guangdong Province (2016A020215129 to YD).
Availability of data and materials
The datasets generated and/or analyzed during this study are not publicly available owing to currently ongoing research studies, but the data are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The Ethics committee of the Guangdong General Hospital supervised the study, including the study design, protocol, ethical issue, and data and sample collection. Written informed consent was obtained from each patient or from the appropriate guardian.
Consent for publication
Not applicable. No individual personal data were included in the study. All patients provided necessary consent to participate in the present study.
The authors declare that they have no competing interests.
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Zhang, D., Gao, L., Ye, H. et al. Impact of thyroid function on cystatin C in detecting acute kidney injury: a prospective, observational study. BMC Nephrol 20, 41 (2019). https://doi.org/10.1186/s12882-019-1201-9
- Acute kidney injury
- Cystatin C
- Intensive care unit
- Renal biomarker
- Thyroid function