[Full text] Increased Serum Cystatin C Levels Were Associated with Depressive Symp

Introduction

Diabetes mellitus (DM) has been strongly associated with an increased risk of developing depressive symptoms.^1–3 Existing studies have suggested that the risk of depression is higher in people with DM than in those without DM.^4–6 Although the current mechanisms are poorly understood, increased inflammation and oxidative stress in DM play important roles in an increased risk of depression.^7–9 Depressive symptoms are a major health problem and have been identified as strong prognostic factors of heavy medical burden and poor quality of life in patients with DM.¹⁰ Therefore, identifying relevant risk factors for depressive symptoms in patients with DM must be addressed.

Cystatin C is a low-molecular-weight protein (13.4 kDa) that is synthesized at a constant rate in all nucleated cells.¹¹ Cystatin C is freely filtered through the glomerulus and then reabsorbed and fully catabolized without secretion or subsequent reabsorption into the circulation.¹² Serum cystatin C is less likely to be influenced by individual characteristics, such as age, sex, ethnicity, muscle mass, and medication use, than serum creatinine.^13–15 thus, researchers have proposed cystatin C as a more reliable endogenous marker of early renal dysfunction.^15,16 However, the results of previous studies have also suggested that serum cystatin C may be an independent risk factor for all-cause mortality among elderly persons with cardiovascular diseases (CVDs).^17–19 It has also been reported that higher serum cystatin C may be associated with an increased risk of CVDs, such as stroke and coronary heart disease, and subsequent mortality, even in individuals without established chronic kidney disease (CKD).^13–15,19 The aim of our study was to evaluate whether serum cystatin C levels are an independent predictor of depressive symptoms in patients with DM.

To date, few studies have explored the association between serum cystatin C levels and depression in patients with DM. The aim of this study was to investigate whether increased serum levels of cystatin C contribute to an increased risk of depressive symptoms. This was also the first study to explore the prognostic value of serum cystatin C for predicting depression in patients with DM.

Materials and Methods

Study Population

We studied 254 hospitalized patients who were admitted to Chongqing University Three Gorges Hospital and the Chinese People’s Armed Police Force Zhejiang Corps Hospital in China because of DM between January 2013 and December 2015. All eligible DM patients had no other serious acute illnesses, including acute dysfunction of liver or kidney function or acute heart failure, and they and were stable for more than three months before admission. There are three diagnostic criteria for diabetes: typical symptoms of diabetes, such as polydipsia, polydipsia, polyuria and emaciation, or a random serum glucose level greater than or equal to 11.1 mmol/l; a fasting serum glucose level greater than or equal to 7.0 mmol/L; and blood glucose and serum glucose levels greater than or equal to 11.1 mmol/L two hours after glucose loading. The above diagnostic criteria must be repeated on different days before diagnosis.²⁰ The diagnosis of DM in the current study was performed by two endocrinologists who used the same diagnostic criteria for the included DM patients. Patients with DM were clinically stable during hospitalization and were prospectively followed up after discharge. Of these patients, 53 patients with DM were identified as having depressive symptoms in this study. Patients (N=19) with liver dysfunction, kidney dysfunction, neoplastic diseases, or other serious diseases were excluded.

The diagnosis of CVDs, including coronary heart disease, stroke, hypertension and others, was based on the patient’s current or previous medical records. Other data on clinical characteristics, including age, sex, body mass index (BMI), smoking, alcohol consumption, blood pressure (BP) and others, were collected from patient interviews or medical records. According to the Declaration of Helsinki guidelines, the Ethics Committee of Chongqing University Three Gorges Hospital and the Chinese People’s Armed Police Force Zhejiang Corps Hospital approved this study, and all patients gave written informed consent.

Blood Specimen Collection and Laboratory Analysis

Venous blood samples from patients with DM were collected within the first 24 hours after admission. The samples were prepared immediately by centrifugation and processed for determination of cystatin C. Serum levels of cystatin C were measured via particle-enhanced immunonephelometric assay using the Siemens ADVIA 2400 autoanalyzer (Siemens AG, Munich, Germany). Fasting venous blood samples from patients with DM were also tested for albumin (ALB), blood glucose (FBG), hemoglobin (Hb), fasting hs-CRP (hs-C reactive protein), HbA1c (glycosylated hemoglobin), high density lipoprotein (HDL) and LDL (low density lipoprotein) with the use of the Siemens ADVIA 2400 automatic biochemistry analyzer (Siemens AG). The estimated glomerular filtration rate (eGFR) was calculated by using the Chronic Kidney Disease Epidemiology Collaboration Group (CKD-EPI) equation.²¹

Depression Score

The Centre for Epidemiological Studies Depression (CES-D) scale was used to calculate depressive scores.^22,23 A cutoff score of 16 was considered indicative of depressive symptoms at baseline. During the follow-up period, a score ≥16 was considered indicative of depression events. The CES-D scale has been used widely in epidemiological studies and is appropriate for use in our studies.^22,23 In addition, the subjects were considered to have depression if they took antidepressant medications.

Follow-Up

All patients were followed prospectively after discharge for a median period of 35 months (range=3–37). Patients were followed by telephone or review of the medical record four times a year until the occurrence of depressive symptoms (depression event).

Statistical Analyses

The Kolmogorov–Smirnov test was used to analyze the normality of the data. A P value ≤ 0.05 was considered to be statistically significant. The data that were not normally distributed were analyzed by the Mann–Whitney U-test and then expressed as the median (interquartile range [IQR]). Data were analyzed by independent t-test and presented as the mean ± SD for normally distributed data. The chi-square test was used to analyze categorical variables and is expressed as n (%). A multivariate linear regression model was used to assess the independent relationship between serum cystatin C levels and CES-D scores in DM patients at baseline after controlling for age, sex, BMI, current smoking status, current alcohol consumption status, admission systolic and diastolic BP, CVD history and laboratory measurements. Then, Cox proportional hazard analysis was performed to assess the independent prognostic factors for depressive symptoms in patients with DM during the follow-up period after controlling for these same confounding factors. In these multivariate analyses, we adjusted for clinical data relevant to stroke and cognitive function even if the factors were not significantly associated with depressive symptoms in the univariate analysis because they are key clinical variables and may be associated with depressive symptoms in the multivariate but not univariate analyses. Additionally, sensitivity and stratification analyses were also performed to evaluate the independent association between serum cystatin C levels and depressive symptoms (depression event) by adding “antidepressant therapy” and “CKD history” as covariates. All of the analyses were performed by using SPSS 24.0.

Results

Clinical Characteristics of Study Subjects at Baseline

The clinical characteristics of the DM patients at baseline are presented in Table 1. The mean age of all included DM patients was 63.2±7.9 years, and there were 120 males (47.2%). The CES-D score was 10.7 ± 9.2, and the total number of patients with depressive symptoms was 53 (20.9%). The median value of serum cystatin C levels was 1.39 (mg/L).

Table 1 Clinical Characteristics in 254 Patients with DM at Baseline

Increased Serum Levels of Cystatin C Showed a Significant Association with CES-D Score in 254 Patients with DM

To assess the association of serum cystatin C levels in stroke patients with CES-D scores, a multivariate linear regression model was performed (Table 2). Model 1 showed that higher serum levels of cystatin C were significantly associated with CES-D score after no adjustment was made (Sβ=0.153, 95% CI 0.104–0.224, P<0.001). The results of Model 2 were similar to those of Model 1 (Sβ=0.143, 95% CI 0.095–0.200, P<0.001) after adjustments were made for age, sex, BMI, current smoking status, current drinking status, admission systolic and diastolic BP and CVD history. This relationship in Model 3 remained statistically significant and changed minimally after adding laboratory measurements to Model 2 (Sβ=0.127, 95% CI 0.083–0.185, P=0.002).

Table 2 Multivariate Linear Regression Analysis for the Association Between the Serum Cystatin C Levels and CESD Score in 254 Patients with DM at Baseline

Cox Proportional Hazard Analysis for Predicting Depressive Symptoms (Depression Events) in 254 DM Patients

All included DM patients (N=254) were prospectively followed up for a median period of 35 months (range=3–37). Depressive symptoms (depression events) occurred in 53 of the included DM patients. To assess the risk factors for depression events, a multivariate Cox proportional hazard regression model was used (Table 3). After adjustments were made for age, sex, BMI, current smoking status, current drinking status, admission systolic and diastolic BP, CVD history and laboratory measurements, multivariate Cox proportional hazard analysis suggested that serum cystatin C levels (HR=2.360, 95% CI 1.500–3.891, P-trend<0.001) were an independent prognostic factor for depression events. Kaplan–Meier analysis showed that DM patients with serum levels of cystatin C above the median had a significantly higher rate of depression events than patients with serum levels of cystatin C below the median value (Log rank test, P<0.001, Figure 1).

Table 3 Cox Proportional Hazard Analysis for the Association of Serum Cystatin C Levels and Depressive Symptoms

Figure 1 Kaplan–Meier analysis of depression events free stratified into 2 groups by the median levels of serum cystatin C.

Sensitivity and Stratification Analysis for Predicting Depressive Symptoms (Depression Events) in 254 DM Patients

We performed an additional sensitivity analysis to evaluate the association of serum cystatin C with depression events in DM patients by adding “antidepressant therapy” as a covariate (Table 4). The sensitivity analysis suggested that higher serum cystatin C levels were still independently associated with a higher risk of depression events during the follow-up of 3 years. Stratified analysis, performed by adding “CKD history” as a covariate, showed that the significant association between serum cystatin C levels and depression events in DM patients was affected by CKD history. A significant association existed in patients with a history of CKD but not in patients without a history of CKD (Table 5).

Table 4 Sensitivity Analysis for the Association of Serum Cystatin C Levels and Depressive Symptoms

Table 5 Stratified Analysis for the Association of Serum Cystatin C Levels and Depressive Symptoms

Discussion

In this study, we investigated whether serum cystatin C levels can serve as an independent predictive marker for the prognosis of depression events in patients with DM. Our results suggested that serum cystatin C levels were an independent prognostic factor for depression events in DM patients by multivariate Cox proportional hazard analysis.

It is currently unclear whether cystatin C has a close association with depression in patients with DM. Inflammation plays an important role in the pathogenesis and prognosis of DM and depression.24–26 The results of our study and other studies have suggested a close correlation between cystatin C and conventional inflammatory markers, such as hs-CRP.^27–29 Therefore, it is reasonable to suggest that the cystatin C level may be of value in predicting depressive symptoms by reflecting the amount of systemic inflammation. Indeed, examination of the relationship between serum cystatin C and frequent inflammatory responses in patients with DM has been reported in the literature,^30–32 which is consistent with our results. In our study, we first showed that patients with higher serum levels of cystatin C had an increased CES-D score at baseline and then had a higher risk of depression events after a follow-up of 3 years, which may be mostly or partly explained by the research on inflammatory mechanisms performed in previous studies.^28,30 These studies have suggested that chronic vascular inflammation caused by DM promotes the occurrence of depression events.^33–36 The early detection of depressive symptoms in these DM patients may provide us with a chance to develop strategies aiming to reduce the medical burden and improve prognosis. Our results seemed to imply that serum cystatin C might be a sensitive biomarker for the early recognition of depressive symptoms in patients with DM.

Our results have several obvious strengths. First, we are the first to find that serum cystatin C can be considered a valuable prognostic factor for depressive symptoms in DM patients. Second, we ensured comprehensive follow-up and rigorous adjudication of depression events, so our results are very reliable. Third, the serum cystatin C assay chosen for this study is both widely available and analytically stable (coefficient of variation of precision <5%). This serum index is convenient and reliable for clinical popularization.

Certainly, this study also has several limitations. The study sample was recruited from a single-center, and the sample size was fairly small. Additionally, cystatin C was only measured once in the morning of the first day after admission. The time courses of cystatin C levels were not evaluated. Information regarding the long-term prognosis throughout the hospitalization period was not available. Further investigation will be necessary to solidify the clinical significance of cystatin C in predicting depressive symptoms in patients with DM by evaluating the time course of cystatin C.

Conclusions

We demonstrated that serum cystatin C is an independent prognostic factor for depressive symptoms in patients with DM. These results suggest that serum cystatin C might be a useful biomarker for predicting depressive symptoms in patients with DM.