Development and validation of a prognostic model for patients with hepatorenal syndrome: A retrospective cohort study

Abstract

BACKGROUND

Hepatorenal syndrome (HRS) is a severe complication of cirrhosis with high mortality, which necessitates accurate clinical decision. However, studies on prognostic factors and scoring systems to predict overall survival of HRS are not enough. Meanwhile, a multicenter cohort study with a long span of time could be more convincing.

AIM

To develop a novel and effective prognostic model for patients with HRS and clarify new prognostic factors.

METHODS

We retrospectively enrolled 1667 patients from four hospitals, and 371 eligible patients were finally analyzed to develop and validate a novel prognostic model for patients with HRS. Characteristics were compared between survivors and non-survivors, and potential prognostic factors were selected according to the impact on 28-d mortality. Accuracy in predicting 28-d mortality was compared between the novel and other scoring systems, including Model for End-Stage Liver Disease (MELD), Chronic Liver Failure-Sequential Organ Failure Assessment (CLIF-SOFA), and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure (COSSH-ACLF).

RESULTS

Five prognostic factors, comprised of gender, international normalized ratio, mean corpuscular hemoglobin concentration, neutrophil percentage, and stage, were integrated into a new score, GIMNS; stage is a binary variable defined by the number of failed organs. GIMNS was positively correlated with MELD, CLIF-SOFA, and COSSH-ACLF. Additionally, it had better accuracy [area under the receiver operating characteristic curve (AUROC): 0.830] than MELD (AUROC: 0.759), CLIF-SOFA (AUROC: 0.767), and COSSH-ACLF (AUROC: 0.759) in the derivation cohort (P < 0.05). It performed better than MELD and CLIF-SOFA in the validation cohort (P < 0.050) and had a higher AUROC than COSSH-ACLF (P = 0.122).

CONCLUSION

We have developed a new scoring system, GIMNS, to predict 28-d mortality of HRS patients. Mean corpuscular hemoglobin concentration and stage were first proposed and found to be related to the mortality of HRS. Additionally, the GIMNS score showed better accuracy than MELD and CLIF-SOFA, and the AUROC was higher than that of COSSH-ACLF.

Key Words: Hepatorenal syndrome; Prognostic factor; Mean corpuscular hemoglobin concentration; Mortality; Scoring system; Cohort study

Core Tip: This multicenter retrospective cohort study investigated the prognostic factors for patients with hepatorenal syndrome and developed a novel prognostic model, named GIMNS. GIMNS contains five prognostic factors, comprised of gender, international normalized ratio, mean corpuscular hemoglobin concentration, neutrophil percentage, and stage, which had different expression levels between survivors and non-survivors. Stage, defined according to the number of organ failures and mean corpuscular hemoglobin concentration, was found to be an effective prognostic factor for the first time. The area under the operating characteristic curve reached 0.830 for 28-d mortality. The GIMNS score showed better accuracy than Model for End-Stage Liver Disease, Chronic Liver Failure-Sequential Organ Failure Assessment, and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure.

INTRODUCTION

Hepatorenal syndrome (HRS) is a severe complication of cirrhosis characterized by increased splanchnic blood flow and rapid kidney dysfunction excluding other reasons[1]. It has high mortality within 2 wk, and the most effective treatment is liver transplantation, either liver only or simultaneous liver–kidney transplantation. Although pharmacological therapy, mainly vasoconstrictive (terlipressin or norepinephrine) plus albumin, can improve kidney function, it may make no difference to the percentage of patients who die or develop serious complications or the percentage of complications of any severity[2]. A retrospective study demonstrated that with present medical tools, there is still significantly high mortality in HRS despite guideline-based treatment[3]. According to another, single center study, occurrence of HRS is associated with a significantly worse outcome after living donor liver transplantation[4]. The focus of current HRS research is mainly on diagnosis and treatment, and there has been only a small number of studies on the prognosis of HRS. Thus, it is critical to develop a predictive tool to predict the mortality of HRS and to manage liver graft allocation on waiting lists.

A prospective study has demonstrated that age, serum bilirubin, and no reversal of creatinine after volume expansion independently predict mortality[5]. Another study has claimed that factors associated with poor prognosis are baseline bilirubin, no reversibility of type-1 HRS, lack of resolution of the infection, and sepsis after diagnosis of type-1 HRS[6]. Acute-on-chronic liver failure (ACLF) grade is defined by the number of organ failures. A retrospective analysis from centers in Europe found that ACLF grade is the largest determinant of response and could affect the survival of HRS[7]. Among the predictors, the Model for End-stage Liver Disease (MELD) score has been widely applied for evaluating the severity of advanced liver diseases and liver graft allocation[8]. However, it has a limitation of failure to predict mortality after liver transplantation[9]. Therefore, a new effective model is urgently needed.

In this study, we aimed to construct a new prognostic model to predict mortality of HRS through a multicenter cohort study and retrospectively enrolled HRS patients from 2011 to 2019.

MATERIALS AND METHODS

Patient studies

Study population and data collection: In this retrospective cohort study we enrolled patients from four hospitals: First affiliated Hospital of Zhejiang University, Shulan Hospital, People’s Hospital of Zhejiang Province, and People’s Hospital of Shengzhou City. We studied a cohort with decompensated cirrhosis with acute renal injury from January 2011 to October 2019. Patients from the First Affiliated Hospital of Zhejiang University formed the derivation cohort and patients from the other three hospitals were the validation cohort. Demographic data (age and gender), history (vital signs and treatment), and laboratory parameters were available from medical records or the hospital database. The 28-d mortality was obtained from medical records or by directly contacting the patients or their families. All assays for serum biochemical parameters were routinely performed at the Central Clinical Laboratory of the four hospitals with the same type of testing equipment. The study was approved by the Ethics Committee of the First Affiliated Hospital, College of Medicine, Zhejiang University (No. 2019-1449-1), and complied with the ethical guidelines of the Declaration of Helsinki. The researchers only analyzed anonymous data, so informed consent was waived.

Inclusion and exclusion criteria: HRS was diagnosed based on criteria proposed by the International Club of Ascites in 2015. Acute kidney injury (AKI) was identified according to the standard Kidney Disease: Improving Global Outcomes criteria. The exclusion criteria were: (1) absence of ascites; (2) hepatocellular carcinoma; (3) other types of tumors; (4) chronic renal diseases; (5) liver transplantation; (6) age < 18 years; (7) thyroid diseases; (8) severe immunosuppression; (9) hospital stay < 1 wk; and (10) incomplete information. Finally, we excluded patients who were lost to follow-up (Figure 1).

Figure 1 Workflow. The eligible cohort selection process after applying the inclusion and exclusion criteria from four hospitals. HRS: Hepatorenal syndrome.

Scoring models: The MELD score was calculated by the following formula: MELD = 3.78 ln [Total bilirubin (mg/dL)] + 11.2 ln (INR) + ln [serum creatinine (mg/dL)] + 6.43 (INR is international normalized ratio). The Chronic Liver Failure-Sequential Organ Failure Assessment (CLIF-SOFA) score summed the severity grades of organ failures. Liver failure was defined as bilirubin ≥ 12 mg/dL, coagulation failure as INR ≥ 2.5, brain failure as hepatic encephalopathy grade ≥ 3 (West Haven criteria), respiratory failure as a pulse oximetric saturation/fraction of inspired oxygen ratio ≤ 214 or arterial partial pressure of oxygen/fraction of inspired oxygen ratio ≤ 200 or the need for mechanical ventilation, and circulatory failure as the need for vasopressor therapy to achieve an adequate mean arterial pressure (MAP)[10]. The Chinese Group on the Study of Severe Hepatitis B-ACLF (COSSH-ACLF) was calculated as 0.741 INR + 0.523 hepatitis B virus (HBV)-SOFA + 0.026 age + 0.003 Total bilirubin. Stage was defined according to the number of organ failures, except renal failure. Stage 0 contained patients with zero or one organ failure, while stage 1 contained patients with more than two organ failures.

Statistical analysis: Clinicopathological features were summarized using medians and interquartile ranges or frequencies with percentages for normally distributed factors while using means with standard deviation for skewed distributed factors. Continuous variables were compared using t test or Mann–Whitney U test, and categorical variables were compared using the χ² test or Fisher’s exact test. Patients were followed up from the day of diagnosis with HRS–AKI and ended at death or last follow–up at day 28. Univariate and multivariate Cox regression analyses were performed to establish the association between prognostic factors and overall survival of HRS. The Kaplan–Meier method was used to evaluate the survival probability of HRS, and a log–rank test was used to assess differences between groups. Hazard ratios were estimated using the Cox regression model. Statistical analyses were performed with R version 3.6.2 (R Foundation for Statistical Computing, Vienna, Austria). All tests were two-sided, and P < 0.05 was considered statistically significant. The statistical methods of this study were reviewed by a member of the Biostatistics Service from the First Affiliated Hospital, College of Medicine, Zhejiang University.

RESULTS

Clinical characteristics

We retrospectively enrolled 1667 patients from four large general hospitals in Zhejiang province between January 2011 and October 2019. After inclusion and exclusion criteria, we had 383 eligible patients. Twelve patients were lost to follow-up due to a lack of contact information or survival information. Finally, we had 371 HRS patients for analysis: 248 in the derivation cohort and 123 in the validation cohort.

There were no significant differences in characteristics including demographic and clinical information between the derivation and validation cohorts (P > 0.05) (Table 1). Until the end of follow-up, 278 (74.9%) patients died, comprising 188 in the derivation cohort and 90 in the validation cohort. Male patients made up 76.8% (285) of the cohort, with 76.6% (190) and 77.2% (95) male in the derivation and validation cohorts, respectively. MAP, INR, alanine aminotransferase, serum bilirubin, number of failed organs, and the MELD, CLIF-SOFA, and COSSH-ACLF scores differed significantly between non-survivors and survivors in both cohorts (all P < 0.05). Age, gender, cause of cirrhosis, neutrophil percentage, hemoglobin, mean corpuscular hemoglobin (MCH) and MCH concentration (MCHC) differed between non-survivors and survivors only in the derivation cohort. Cirrhosis caused by HBV or HBV plus other reasons accounted for most of the patients (63.7% in the derivation cohort and 52.0% in the validation cohort). MAP was significantly higher in survivors than in non-survivors. Non-survivors had higher levels of INR and alanine aminotransferase compared with survivors. The MELD, CLIF-SOFA, and COSSH-ACLF scores were significantly higher in non-survivors in both cohorts (P < 0.05). Regarding treatment, all the eligible patients accepted rehydration treatment with albumin. In total, 21.3% (79) of patients received terlipressin plus albumin, and treatment was the same among the four hospitals (P > 0.05).

Table 1 Characteristics of patients with hepatorenal syndrome, n (%).

Variables	Derivation cohort (n = 248)			Validation cohort (n = 123)			1P value
	Non-survivor (n = 188)	Survivor (n = 60)	P value	Non-survivor (n = 90)	Survivor (n = 33)	P value
Age (y)	59.11 ± 12.61	55.43 ± 12.04	0.048	56.94 ± 12.17	57.21 ± 11.81	0.913	0.379
Gender (male/female)	138/50	52/8	0.031	69/21	26/7	0.995	0.795
Causes of cirrhosis			0.046			0.741	0.096
HBV/HBV plus others	124 (66.0)	34 (56.7)		45 (50.0)	19 (57.6)
Alcoholic	27 (14.4)	17 (28.3)		21 (23.3)	7 (21.2)
Others	37 (19.7)	9 (15.0)		24 (26.7)	7 (21.2)
MAP (mmHg)	95.16 ± 16.42	100.31 ± 18.44	0.041	93.1 ± 15.01	100.58 ± 18.33	0.023	0.483
INR	1.90 (1.70-2.60)	1.60 (1.30-1.90)	< 0.001	1.96 (1.54-2.40)	1.50 (1.31-1.90)	< 0.001	0.305
Neutrophil	75.68 ± 11.99	71.21 ± 13.03	0.015	76.03 ± 10.98	72.95 ± 10.97	0.170	0.647
RBC (× 109/L)	3.15 ± 0.85	3.04 ± 0.85	0.404	3.16 ± 1.05	2.99 ± 0.78	0.388	0.950
Hemoglobin (g/L)	103.13 ± 25.48	95.14 ± 26.89	0.044	102.55 ± 29.63	95.41 ± 25.60	0.229	0.840
MCV (fl)	94.20 ± 9.16	92.21 ± 8.07	0.146	95.28 ± 11.72	94.00 ± 9.71	0.580	0.267
MCH (pg)	33.19 ± 3.78	31.45 ± 3.21	0.002	33.17 ± 3.93	32.21 ± 3.66	0.233	0.756
MCHC (g/L)	351.81 ± 18.15	341.77 ± 19.35	< 0.001	349.14 ± 19.13	342.83 ± 18.25	0.104	0.355
Platelet (× 109/L)	66.5 (42.0-97.5)	69.0 (45.5-98.0)	0.419	64.0 (36.0-103.0)	75.0 (46.0-118.0)	0.250	0.737
Albumin (g/L)	29.12 ± 5.48	28.77 ± 5.37	0.668	29.22 ± 5.41	30.99 ± 5.61	0.115	0.274
A/G	1.00 (0.78-1.40)	0.92 (0.73-1.30)	0.267	1.13 ± 0.56	1.19 ± 0.51	0.620	0.400
ALT	60.00 (31.00-137.00)	32.50 (18.25-66.00)	0.001	59.00 (26.50-135.00)	36.00 (16.00-104.00)	0.035	0.673
Serum bilirubin	15.00 (5.32-27.50)	3.92 (1.10-12.80)	< 0.001	18.30 (6.75-25.30)	2.30 (1.17-23.30)	0.003	0.779
Cholinesterase (U/L)	1963.00 (1399.00-2559.00)	2264.00 (1410.50-3081.50)	0.197	1937.50 (1585.75-2637.20)	2376.00 (1716.00-3903.00)	0.152	0.198
Creatinine (mg/dL)	1.60 (0.92-2.70)	1.84 (1.14-2.80)	0.206	1.43 (0.85-2.20)	2.10 (1.10-2.90)	0.046	0.291
Sodium (mmol/L)	133.74 ± 6.79	135.66 ± 6.34	0.053	132.88 ± 5.89	136.02 ± 4.90	0.009	0.499
Potassium (mmol/L)	4.35 ± 1.01	4.18 ± 0.74	0.217	4.16 ± 0.80	4.31 ± 0.65	0.352	0.288
Number of failed organs	1 (0.75-2.00)	0 (0-1.00)	< 0.001	1 (0-2.00)	0 (0-1.00)	< 0.001	0.433
One organ failed	65 (34.6)	19 (31.7)	0.797	28 (31.1)	11 (33.3)	0.987	0.764
Two organs failed	50 (26.6)	1 (1.7)	< 0.001	26 (28.9)	3 (9.1)	0.040	0.596
≥ Three organs failed	26 (13.8)	1 (1.7)	0.017	12 (13.3)	1 (3.0)	0.188	0.990
MELD	29.50 ± 9.06	22.97 ± 8.00	< 0.001	28.04 ± 8.74	23.46 ± 9.47	0.013	0.276
CLIF-SOFA	10.79 ± 3.29	8.18 ± 3.08	< 0.001	10.86 ± 3.75	8.09 ± 3.37	< 0.001	0.912
COSSH-ACLF	7.57 ± 1.84	6.05 ± 1.27	< 0.001	7.57 ± 1.86	6.14 ± 1.49	< 0.001	0.958
Treatment			0.261			0.842	0.125
Terlipressin plus albumin	41 (21.8)	18 (30.0)		15 (16.7)	5 (15.2)
Albumin only	147 (78.2)	42 (70.0)		75 (83.3)	28 (84.8)

P non-survivor vs survivor.

¹P derivation cohort vs validation cohort. A/G: Albumin/globulin; ALT: Alanine aminotransferase; CLIF-SOFA: Chronic Liver Failure-Sequential Organ Failure Assessment; COSSH-ACLF: Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure; HBV: Hepatitis B virus; INR: International normalized ratio; MAP: Mean arterial pressure; MCH: Mean cell hemoglobin; MCHC: Mean corpuscular hemoglobin concentration; MCV: Mean cell volume; MELD: Model for End-Stage Liver Disease; RBC: Red blood cells.

Univariate and multivariate Cox regression

In the derivation cohort, gender, MAP, INR, neutrophil percentage, hemoglobin, MCH, MCHC, albumin/globulin, serum bilirubin, sodium, stage (defined above), and the MELD, CLIF-SOFA, and COSSH-ACLF scores were significantly associated with overall survival by univariate Cox regression (Table 2). We incorporated the above variables into multivariate Cox regression and finally five prognostic factors, including gender, INR, neutrophil percentage, MCHC and stage, were independently associated with overall survival.

Table 2 Univariate and multivariate Cox regression.

Variables	Univariate Cox regression		Multivariate Cox regression
	HR (95%CI)	P value	HR (95%CI)	P value
Age	1.007 (0.995-1.019)	0.244
Gender	0.586 (0.425-0.807)	0.001	0.532 (0.384-0.737)	< 0.001
Causes of cirrhosis	0.946 (0.785-1.140)	0.557
MAP	0.990 (0.981-0.999)	0.024
INR	1.842 (1.599-2.122)	< 0.001	1.408 (1.173-1.691)	< 0.001
Neutrophil	1.028 (1.015-1.041)	< 0.001	1.031 (1.018-1.044)	< 0.001
RBC	1.137 (0.959-1.348)	0.139
Hemoglobin	1.007 (1.002-1.012)	0.012
MCV	1.004 (0.988-1.021)	0.599
MCH	1.066 (1.022-1.111)	0.003
MCHC	1.019 (1.010-1.027)	< 0.001	1.014 (1.005-1.022)	0.002
Platelet	0.997 (0.994-1.000)	0.090
Albumin	1.000 (0.973-1.028)	0.999
A/G	1.257 (1.093-1.445)	0.001
ALT	1.000 (1.000-1.001)	0.094
Serum bilirubin	1.002 (1.001-1.003)	< 0.001
Cholinesterase	1.000 (0.999-1.000)	0.160
Creatinine	1.000 (0.999-1.001)	0.704
Sodium	0.960 (0.939-0.982)	< 0.001
Potassium	1.215 (1.032-1.430)	0.019
Stage	3.805 (2.800-5.170)	< 0.001	2.724 (1.877-3.952)	< 0.001
MELD	1.077 (1.058-1.096)	< 0.001
CLIF-SOFA	1.221 (1.166-1.278)	< 0.001
COSSH-ACLF	1.467 (1.361-1.581)	< 0.001

A/G: Albumin/globulin; ALT: Alanine aminotransferase; CI: Confidence interval; CLIF-SOFA: Chronic liver failure-sequential organ failure assessment; COSSH-ACLF: Chinese Group on the study of severe hepatitis B-acute-on-chronic liver failure; HR: Hazard ratio; INR: International normalized ratio; MAP: Mean arterial pressure; MCH: Mean cell hemoglobin; MCHC: Mean corpuscular hemoglobin concentration; MCV: Mean cell volume; MELD: Model for end-stage liver disease; RBC: Red blood cells.

The hazard ratio of stage was 2.724 (95% confidence interval, 1.877–3.952), and the hazard ratios of gender, INR, neutrophil percentage, and MCHC were 0.532, 1.408, 1.031, and 1.014, respectively. The risk of death in female patients was approximately 1.5 times that of male patients. Patients with ≥ two organ failures had up to 2.7 times greater mortality risk compared with those with ≤ one organ failure. Creatinine was not associated with overall survival of HRS patients, although AKI stage was defined by creatinine level.

GIMNS score development

According to the multivariate logistic regression based on 28-d mortality, the GIMNS score was developed. The formula is:

GIMNS = -1.412 gender + 0.053 neutrophil percentage + 0.014 MCHC + 2.073 ln (INR) + 1.231 stage - 9.217.

Mortality at 28 d in stratified HRS patients showed that patients with GIMNS > 2 were all dead, while those with GIMNS < 0 had the lowest mortality (30.34%) (Table 3). The mortality rates of patients with score 1–2 and 0–1 were 73.81% and 57.14%, respectively. Figure 2A showed the importance of each prognostic factor based on the logistic regression, and stage was the most important factor. Cumulative percentage also demonstrated this.

Figure 2 Characteristics associated with survival. A: Importance of each characteristic of GIMNS; B: Mosaic plot. Survival status of patients with different causes of cirrhosis, gender, and stage. HBV: Hepatitis B virus; INR: International normalized ratio; MCHC: Mean corpuscular hemoglobin concentration.

Table 3 Mortality at 28 d in patients with hepatorenal syndrome stratified according to the GIMNS score.

GIMNS score	28-d mortality in HRS patients (%)
≥ 2	100.0
1-2	73.8
0-1	57.1
< 0	30.3

HRS: Hepatorenal syndrome.

Characteristics in the GIMNS score

The GIMNS score contains five variables: gender, INR, MCHC, neutrophil percentage, and stage. The mosaic plot acquired from the derivation cohort could intuitively sense the distribution of the patients’ survival statuses among different variables and establish the relationship between the variables (Figure 2B). From the mosaic plot, HBV-related cirrhosis accounted for the majority of the patients. For patients with HBV-related cirrhosis, male patients accounted for most, and 97.7% of the alcoholic HRS patients were male. As for patients with HRS of other causes, the proportion of female patients was larger than that of male patients. Although for every part of the whole mosaic plot, the number of patients with stage 1 disease was smaller than those with stage 0, the mortality was higher.

For the prognostic factors in the GIMNS score, we converted continuous variables into categorical variables by upper and lower quartiles (Figure 3A-C). INR was negatively correlated with survival probability. The survival probability of the upper quartile of INR was < 20%, which was lower compared with that of the others (P < 0.001). Similarly, patients with the lower quartile of neutrophil percentage had better overall survival compared with the others. Stratified MCHC also had different prognoses (P = 0.003).

Figure 3 Kaplan–Meier curves of variables of GIMNS. A: Stratified international normalized ratio; B: Stratified neutrophil percentage; C: Stratified mean corpuscular hemoglobin concentration; D: Stage; E. Gender. INR: International normalized ratio; MCHC: Mean corpuscular hemoglobin concentration.

Stage based on the number of organ failures (stage 0: 0–1, stage 1: ≥ 2) was the most important independent risk factor affecting overall survival of patients with HRS. The survival probability of stage 1 patients was < 10% while that of stage 0 patients was > 30%, which emphasized the essential role in predicting the prognosis of HRS (Figure 3D). Although female patients accounted for a small part of the whole cohort, they had a worse prognosis (P < 0.01) (Figure 3E).

GIMNS score and other scores

The GIMNS score was significantly higher in non-survivors in the derivation and validation cohorts (Figure 4A). The GIMNS score was divided into three parts according to the upper and lower quartiles. According to the Kaplan–Meier curves, mortality increased with GIMNS score (P < 0.001) (Figure 4B). The GIMNS score had a superior discrimination of risk of mortality of HRS patients. The GIMNS score was positively correlated with the MELD, CLIF-SOFA, and COSSH-ACLF scores (Figure 5A-C).

Figure 4 Distributions of the GIMNS score. A: The GIMNS score distribution between survivors and non-survivors in the derivation and validation cohorts; B: Kaplan–Meier curves of GIMNS.

Figure 5 Relationship between GIMNS and other scoring systems and receiver operating characteristic curve curves. A: GIMNS and Model for End-stage Liver Disease; B: GIMNS and Chronic Liver Failure-Sequential Organ Failure Assessment; C: GIMNS and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure; D: Receiver operating characteristic curve curves in derivation cohort; E: Receiver operating characteristic curve in validation cohort. CLIF-SOFA: Chronic Liver Failure-Sequential Organ Failure Assessment; COSSH-ACLF: Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure; MELD: Model for End-stage Liver Disease; AUC: Area under the curve.

Accuracy of the GIMNS score

The area under the receiver operating characteristic curve (AUROC) of the GIMNS score for 28-d mortality was 0.830, with a sensitivity of 0.735 and specificity of 0.787 at a cut-off value of 0.36 (Table 4). The mortality rate of the upper quartile GIMNS score group was significantly higher than that of the lower quartile GIMNS score group. In the derivation cohort, the GIMNS score had significantly higher predictive power for the outcome of HRS patients than did the MELD, CLIF-SOFA, and COSSH-ACLF scores (P < 0.05) (Figure 5D). The AUROCs of GIMNS and other scoring systems are compared in Table 4.

Table 4 Accuracy of different scoring systems in derivation and validation cohorts.

Models	Cut-off	Sensitivity (%)	Specificity (%)	Youden	AUROC (95%CI)	P value	P value
							compared with GIMNS
Derivation cohort (n = 248)
GIMNS	0.4	73.5	78.7	0.522	0.830 (0.778-0.882)	< 0.001	-
MELD	24.8	61.4	76.6	0.380	0.759 (0.670-0.821)	< 0.001	0.029
CLIF-SOFA	9.0	72.7	68.1	0.408	0.767 (0.706-0.827)	< 0.001	0.045
COSSH-ACLF	7.5	56.8	84.0	0.408	0.759 (0.696-0.821)	< 0.001	0.026
Validation cohort (n = 123)
GIMNS	0.7	57.8	79.6	0.374	0.732 (0.642-0.821)	< 0.001	-
MELD	26.6	65.6	63.0	0.286	0.623 (0.520-0.726)	< 0.050	0.013
CLIF-SOFA	11.0	29.7	94.4	0.241	0.661 (0.563-0.758)	< 0.010	0.049
COSSH-ACLF	7.9	51.6	81.5	0.331	0.674 (0.577-0.770)	< 0.001	0.122

AUROC: Area under the receiver operating characteristic curve; CLIF-SOFA: Chronic liver failure-sequential organ failure assessment; COSSH-ACLF: Chinese Group on the study of severe hepatitis B-acute-on-chronic liver failure; MELD: Model for end-stage liver disease; CI: Confidence interval.

Validation of performance of GIMNS score

The clinical and laboratory characteristics of the derivation and validation cohorts are shown in Table 1, which verified that there was no difference in the distribution of the characteristics between the cohorts. The mortality rate of the upper quartile GIMNS score group was significantly higher than that of the lower quartile GIMNS score group (P < 0.001). The AUROC of the GIMNS score model for 28-d mortality was 0.732, which was significantly better than that of the MELD (P = 0.038) and CLIF-SOFA (P = 0.049) scores and tended to be better than that of the COSSH-ACLF score (P = 0.122) (Figure 5E). The AUROCs of GIMNS and the other scoring systems were compared in Table 4.

DISCUSSION

In this study, we developed a novel model for prediction of prognosis of HRS called GIMNS, which had better accuracy than the traditional scoring systems MELD and CLIF-SOFA and a larger AUROC than COSSH-ACLF. GIMNS contains five prognostic factors: gender, INR, MCHC, neutrophil percentage, and stage.

INR is normally used in scoring systems to evaluate the severity of advanced liver diseases. In our study, different quartiles of INR indeed resulted in significantly different survival rates. Patients with higher INR have problems with blood coagulation and have a worse outcome. There was an obvious survival benefit in male patients, although the proportion of female patients was smaller, accounting for only 23.2% of the whole cohort. This suggests that female HRS patients should be given more attention than usual[11].

MCHC has traditionally been a subordinate process to diagnose the type of anemia combined with MCH and mean corpuscular volume. However, the association between MCHC and outcome of HRS, especially the role of MCHC in predicting survival, has been ignored. We found that when adjusted by other confounding factors in multivariate Cox analysis, the mortality risk of patients in the lower quartile of MCHC was nearly twice that of patients in the upper quartile (data not shown).

It has been shown that advanced cirrhosis is linked to increased serum levels of proinflammatory cytokines, which are common triggers of HRS[12,13]. These cytokines somehow cause kidney dysfunction. Neutrophil percentage reflects inflammatory state. Also, different neutrophil percentages divided by upper and lower quartiles resulted in different outcomes, meaning that patients with lower neutrophil percentage achieved a survival benefit.

For the first time, we incorporated the number of organ failures into the prognostic scoring system and divided the entire cohort into two, stage 0 with zero or one organ failure, except renal failure, and stage 1 with ≥ two organ failures. From the multivariate Cox analysis, we found that the 28-d mortality was significantly higher in stage 1 HRS, and the risk of stage 1 was almost three times that of stage 0 HRS. Organ failures have been used in the CLIF-SOFA score to evaluate the severity of advanced liver diseases[14]. Studies on the relationship between organ failure and prognosis of HRS are rare. It is essential to take this into consideration when developing a prognostic tool, either predicting the mortality or managing the liver transplantation waiting list.

The GIMNS score considered five prognostic factors and had better accuracy than the MELD and CLIF-SOFA scores in the derivation and validation cohorts. It also had a trend toward greater accuracy than the COSSH-ACLF had. The MELD score has been widely used in advanced liver diseases and plays an important role in liver graft allocation policy[15]. The MELD score is associated with 3-mo survival and can alter overall graft and outcome of HRS after transplantation. There is no doubt that the MELD score has been the first choice when evaluating prognosis of HRS and managing waiting lists for liver transplantation. However, with deeper understanding of HRS, more prognostic factors associated with HRS have been included, and a new score for predicting the mortality of HRS should be developed.

Preceding studies have found that gender is not associated with AKI, including HRS. However, we found that female patients were in more danger compared with male patients. Previous research has shown that predictors of AKI improvement are absence of alcoholic hepatitis, baseline creatinine, and male gender[11]. Male patients performed better in AKI, including HRS. In the derivation cohort, 72.2% of male patients and 86.8% of female patients died. The mortality risk in female patients was almost twice that in male patients. Thus, female patients have been ignored for a long time and more attention should be paid to this group.

INR has long been used as an indicator to evaluate advanced liver diseases, and it is widely used in different scoring systems, such as MELD, CLIF-SOFA, and COSSH-ACLF. INR can reflect coagulation function, and according to the Kaplan–Meier curves, patients with higher INR can have poor outcome. If the INR level is > 2.50, mortality is 95.0%, while if it is < 1.84, mortality can decrease to 64.0%. MCHC can also predict 28-d mortality of HRS partly because of kidney and liver dysfunction. Although the underlying pathological mechanism of MCHC remains unclear, it is associated with outcome of HRS and thus can act as a prognostic factor. Erythrocyte indices contain MCHC, MCH, and mean corpuscular volume. MCH and mean corpuscular volume have no relationship with the prognosis of HRS. A previous retrospective study proposed that MCHC is independently associated with occurrence of HRS[16]. However, study on the association between MCHC and prognosis of HRS has not continued.

The GIMNS score is the first system to incorporate organ failure. It has been utilized in the ACLF score to stratify patients. It is classed as ACLF-1, ACLF-2, and ACLF-3 according to the number of organ failures, and this grade is significantly associated with outcome of ACLF. As HRS is a severe complication of end-stage cirrhosis, we previously proposed that stratification by the number of organ failures, like ACLF grade, could be useful for predicting prognosis of HRS. Finally, stage was found to be an important prognostic factor.

There have been some studies on factors associated with outcome of HRS, mainly mortality or reversal of HRS. One retrospective study has shown a death risk prediction score model included four independent risk factors: liver cancer, neutrophil > 70%, alanine aminotransferase > 40 U/L, and creatinine > 127 mmol/L[17]. It confirmed the essential role of neutrophil percentage in predicting mortality of HRS, although liver cancer should be excluded as it could be a competitive factor for mortality. We compared the creatinine levels between non-survivors and survivors in the derivation and validation cohorts, and there was no significant difference. Consistently, creatinine level was not associated with 28-d mortality. Another study showed that serum creatinine and urinary sodium at the time of diagnosis were associated with survival in univariate Cox analysis, but when adjusted by other confounding factors, serum creatinine had no relationship with outcome of HRS[18]. All the above results confirm that, although creatinine level defines the severity of AKI, it cannot help to predict the prognosis of HRS.

A retrospective study from a tertiary center created a new score that was an extension of the MELD score, including changes in serum bilirubin, creatinine, and albumin level during admission, to predict prognosis of type-1 HRS[19]. Although the concept of HRS-1 has been abandoned, it still helps to construct better prediction models. The MELD score has been widely used to evaluate advanced liver diseases, especially for liver graft allocation policy. However, it fails to predict outcomes of HRS after transplantation and could be a little outdated considering more prognostic factors have been found[20]. The new score derived from MELD proves this point.

Prognostic models for the short-term prognosis of HRS are not enough. Some commonly used prognostic models for end-stage liver disease, such as MELD, MELD-Na, COSSH-ACLF, and CLIF-SOFA, are developed for all end-stage liver diseases including severe hepatitis and cirrhosis. The novel model, GIMNS, takes HRS as the target disease. Moreover, our HRS patients were enrolled according to the latest diagnostic criteria of the International Club of Ascites in 2015, and the sample size is larger than other studies, which can increase the credibility of the results. We operated external validation in three other hospitals to prevent overfitting. Finally, GIMNS performed better in both the derivation and validation cohorts. As its prognostic efficacy is better than MELD, COSSH-ACLF, and CLIF-SOFA, it has the value of clinical application.

Our new GIMNS score was based on all previous studies and showed better accuracy than MELD and the other commonly used scoring systems. Also, it is inexpensive and convenient to use, and MCHC and stage are given more attention. Our study had some limitations. First, this was a retrospective study, and therefore had a lower level of evidence compared with randomized controlled trials. We tried to balance the bias through external validation in three hospitals throughout Zhejiang Province, while developing the GIMNS score in one hospital. This could increase the credibility of our study. Second, it was hard to distinguish between HRS and other complications of AKI with cirrhosis, especially acute tubular necrosis. Thus, our cohort may have contained acute tubular necrosis patients, which could have interfered with our model development. Pathological sections are needed to separate HRS from acute tubular necrosis. Finally, this study did not include urine output in the AKI diagnosis, which may have missed some eligible patients.

In summary, we developed a new scoring system, GIMNS, to predict 28-d mortality of HRS patients. The GIMNS score contains five elements: Gender, INR, MCHC, neutrophil percentage, and stage. Some of these elements have been widely used and others are recent additions. The GIMNS score has better accuracy than MELD and CLIF-SOFA, and the AUROC is larger than that of COSSH-ACLF. Prospective studies are needed for confirmation.

CONCLUSION

We developed a new scoring system, GIMNS, to predict 28-d mortality of HRS patients. Two of the five prognostic indicators, MCHC and stage, were proposed and found to be related to the mortality of HRS for the first time. Additionally, the GIMNS score showed better accuracy than MELD and CLIF-SOFA, and the AUROC was higher than that of COSSH-ACLF.

ARTICLE HIGHLIGHTS

Research background

Hepatorenal syndrome (HRS) is a severe complication of cirrhosis with high mortality. It has a unique in vivo pathological environment compared with other end-stage liver diseases. Meanwhile, prognostic factors associated with prognosis of HRS are not rich enough, and current prognostic scoring systems for end-stage liver diseases need to be updated to fit the application in HRS.

Research motivation

As the diagnostic criteria for HRS were confusing before 2015, a multicenter retrospective study, strictly following the criteria proposed by the International Club of Ascites in 2015, was designed to systematically evaluate the evolution of HRS over the past decade at our institution and to figure out what affects the prognosis of HRS.

Research objectives

Our goal was to develop a novel scoring system to predict 28-d mortality of HRS and evaluate the accuracy, sensitivity, and specificity compared with other scoring systems, including Model for End-stage Liver Disease, Chronic Liver Failure-Sequential Organ Failure Assessment, and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure.

Research methods

Demographic/clinical variables and medical records of HRS patients from January 2011 to October 2019 were collected from four tertiary medical centers, and strict eligibility criteria were applied. The final analysis included 371 patients with HRS. Univariate and multivariate Cox regression analyses were performed for prediction modeling of HRS.

Research results

We found that five indicators can be used as prognostic factors for HRS, including gender, international normalized ratio, mean corpuscular hemoglobin concentration, neutrophil percentage, and stage (defined as a binary variable by the number of failed organs). They formed a new score, GIMNS, based on the weight coefficient. As the GIMNS increases, the risk of mortality gets higher. The sensitivity and specificity of GIMNS were much higher than those of Model for End-stage Liver Disease, Chronic Liver Failure-Sequential Organ Failure Assessment, and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure in both the derivation and validation cohorts.

Research conclusions

We innovatively defined a new variable, stage (based on the number of failed organs), to predict the prognosis of HRS. Importantly, we developed a new scoring system, GIMNS, which was specifically for patients with HRS and performed better than Model for End-stage Liver Disease, Chronic Liver Failure-Sequential Organ Failure Assessment, and Chinese Group on the Study of Severe Hepatitis B-Acute-on-Chronic Liver Failure in accuracy, sensitivity, and specificity. As the five prognostic factors in GIMNS are easily available, clinical application of GIMNS could be more convenient.

Research perspectives

The GIMNS scoring system should be validated in future prospective studies to get a more complete assessment.

ACKNOWLEDGEMENTS

We thank The First Affiliated Hospital of Zhejiang University, Shulan Hospital, People’s Hospital of Zhejiang Province, and People’s Hospital of Shengzhou City for providing data.