Abstract
Background:
Graft and patient survival are of great importance after transplantation. This study aimed to determine the long-term survival rate of kidney transplantation and its effective factors among transplanted patients in Mashhad transplantation centers in northeastern Iran.
Methods:
Overall, 618 kidney transplant recipients were examined in different transplantation centers during the years from 2000 to 2015 in a historical cohort study. The Kaplan-Meier method and the Log-rank test were used to calculate the survival rate of the kidney transplant, and to check the difference between survival curves respectively. Modeling of effective factors in survival rate was performed using Cox regression model.
Results:
Overall, 1, 3, 5, 7, 10, and 15-year survival rate of kidney transplantation were 99%, 98%, 97%, 93%, 88 and 70% respectively. The adjusted hazard ratio indicated that variables such as recipient age >40 yr [HR=0.22, 95% CI=(0.071,0.691)], serum creatinine after transplantation >1.6 Mg/dl [HR=3.03, 95% CI=(1.284,7.125)], history of hypertension [HR=6.70, 95% CI=(2.746,16.348)], and BMI [HR (normal weight versus underweight)=0.26, 95% CI=(0.088,0.761), HR (over weight versus underweight)=0.13,95% CI=(0.038,0.442)] were significant factors on kidney transplant survival rate.
Conclusion:
The short-term transplant survival rate was good in transplant patients. What’s more, through a consideration of variables such as age, creatinine serum after transplantation, history hypertension and body mass index, as well as proper planning to control their effect, it is possible to improve the long-term graft survival rate.
Keywords: Kidney transplantation, Graft survival, Proportional hazards models, Kidney failure, Chronic, Survival rate
Introduction
One of the consequences of chronic kidney disease (CKD) is leading to end-stage renal disease. The number of such patients has been increasing in recent years (1, 2). Prevalence of end-stage renal disease (ESRD) in Iran was 137 per million populations (pmp) in 1997, 274 pmp in 2004, 357 pmp in 2006, and 531.7 pmp in 2011(1, 3, 4). Renal transplantation is the most effective treatment for patients with this condition, because it is more economical than dialysis, and while it reduces the risk of mortality in patients in ESRD, it also improves their life quality (5–7). Apart from mortality rate in transplant patients, another major source of concern has to do with allograft failure, as graft loss increases mortality and health care in the community (8).
Over the past two decades, application of new therapeutic systems has been associated with a reduction in the prevalence of acute graft rejection and an approximately one-year improvement in graft survival (9, 10). However, despite successful renal transplantation surgeries, long-term graft survival has not been consistent with recovery expectations as opposed to short-term survival rates (11, 12).
Since new renal transplantation is carried out under certain conditions, it is important to know risk factors associated with kidney survival, which are mostly predictable and preventable. An analysis of kidney transplant data can contribute to the effectiveness of transplantation activities, as well as the assessment of the expenditure in the health care system in the future (13).
Although several studies have been conducted in different transplantation centers in Iran to estimate the survival rate of kidney transplantation, there are still differences in the causes of reversible rejection in renal transplantation in these studies (14–17). Therefore, it is essential to determine the effective factors in improving the survival rate of the first transplant in different transplantation centers in Mashhad as a major transplantation center in Northeast Iran.
We aimed to evaluate the long-term survival of renal transplantation as well as the known prognostic factors for graft survival.
Methods
In this historical cohort study, the medical records of 731 renal transplant patients in transplantation centers were examined across15 years, from Jul 2000 to Dec 2015. Patients who followed for less than three months and had undergone renal transplantation more than once were excluded. Recipients with other kinds of organ transplants, such as liver, pancreas, or heart, were also excluded. The exact time of transplant was regarded as the initial event and reversible rejection in renal transplantation leading to the individual’s return to dialysis, and in some cases to death, counted as the final event. The cases with the end event due to the end of the study, the loss of follow-up, or the patient’s death for reasons other than transplant rejection were used as censored data. Allograft failure was defined as creatinine greater than 6 mg/dL for more than 3 months or clinical diagnosis and the need for peritoneal dialysis or hemodialysis (18). To obtain accurate estimates of graft survival, the end time of the study was 2 years after the last transplant (Dec 2015).
Survival rates were estimated using lifetime tables, calculated using the Kaplan-Meier method and compared in subgroups using the Log-rank test. To determine the effective factors affecting graft survival, the significant variables with a significant level of less than 0.2 in the univariate analysis with the assumption that the risk ratio is fixed underwent Cox multivariate model. Adjusted hazard ratios were calculated using Cox stepwise relative risk model and were reported with a 95% confidence interval. The analyses were performed using the survival package with R software (ver. 2.15.1) (the R Foundation for statistical calculations, Vienna, Austria). The significant level for all the analyses was 0.05.
The following risk factors were examined in Cox regression model based on patients records: age of recipients (less than 40 yr versus above 40), recipient gender (male and female), delivery type (live, cadaver), hypertension (systolic hypertension greater than 140 or diastolic hypertension greater than 90), serum creatinine level within one month after transplantation (greater than 1.6 versus less than 1.6 mg/dL), duration of dialysis (less than 2 yr versus more than 2 yr), type of immunosuppressant drugs (patients receiving prednisolone, Cellcept and cyclosporine were marked with “1”, and patients who received prednisone, cyclosporine and Imuran were indicated by “2”). Categorization of the variables is based on similar research (19, 20). Moreover, the body mass index (BMI) on the last visit (bodyweight by per kilogram to height per square meter [kg/m2]) was recorded. Individuals with a BMI less than 18.5 were considered as under-weight, from 18.5 to 24.9 as normal, and those over 24.9 as overweight (21).
The proposed study was approved by the Ethics Committee of the Vice-Chancellor of Research of [deleted by editor] University of Medical Sciences under code of IR.MUMS.REC.1395.232.
Results
The survival rate of 618 cases out of 731(84.5%) was successfully followed up during the time. Among the follow-up patients, 35 (5.7%) of cases of irreversible rejected graft resulted in dialysis, and 7 others (1.1%) in death. The median follow-up time (interquartile range) was 6.36 (4.97) years. The mean age of the patients at the time of transplantation was 34.8 ± 12.6 yr and most of them (67.5%) were under 40 years. In 94.2% of cases, the drug of group 1 (cyclosporine, Cellcept and prednisolone) was used. The rest of information concerning the research variables is presented in Table 1.
Table 1:
Graft survival rates at different times after kidney transplantation relative to studied variables
| Variables | No. (%) | Survival rates | P-value (log-rank test) | ||||||
|---|---|---|---|---|---|---|---|---|---|
|
| |||||||||
| 1 yr | 3 yr | 5 yr | 7 yr | 10 yr | 15 yr | ||||
| Sex of recipients | Male | 341 (55.2) | 1.00 | 0.98 | 0.96 | 0.93 | 0.87 | 0.72 | 0.400 |
| Female | 277 (44.8) | 1.00 | 0.99 | 0.98 | 0.94 | 0.90 | 0.64 | ||
| Age of recipients | <40 | 409 (67.5) | 0.99 | 0.98 | 0.97 | 0.91 | 0.85 | 0.62 | 0.011 |
| >40 | 197 (32.5) | 1.00 | 0.99 | 0.99 | 0.98 | 0.95 | 0.92 | ||
| Serum creatinine within one month after transplant | <1.6 | 503 (81.4) | 1.00 | 0.99 | 0.98 | 0.95 | 0.92 | 0.89 | <0.001 |
| >1.6 | 115 (18.6) | 0.99 | 0.97 | 0.96 | 0.87 | 0.74 | 0.32 | ||
| Hypertension | Yes | 269 (43.5) | 0.99 | 0.97 | 0.95 | 0.89 | 0.84 | 0.51 | 0.001 |
| No | 349 (56.5) | 1.00 | 1.00 | 0.99 | 0.96 | 0.91 | 0.78 | ||
| Delivery type | Live | 420 (70.8) | 1.00 | 0.99 | 0.98 | 0.95 | 0.91 | 0.87 | 0.077 |
| Cadaver | 173 (29.2) | 0.99 | 0.98 | 0.97 | 0.90 | 0.84 | 0.84 | ||
| BMI at last visit | Under-weight | 33 (8.3) | 1.00 | 0.97 | 0.90 | 0.80 | 0.66 | 0.66 | 0.006 |
| Normal | 197 (49.5) | 1.00 | 0.98 | 0.96 | 0.95 | 0.89 | 0.62 | ||
| Overweight | 168 (42.2) | 1.00 | 0.99 | 0.99 | 0.97 | 0.93 | 0.93 | ||
| Time of dialysis at pretransplantation | <24 | 447 (76.7) | 0.99 | 0.98 | 0.97 | 0.94 | 0.89 | 0.68 | 0.702 |
| >24 | 136 (23.3) | 1.00 | 1.00 | 0.98 | 0.93 | 0.89 | 0.89 | ||
| Living area | Mashhad | 316 (54.5) | 1.00 | 0.99 | 0.98 | 0.94 | 0.88 | 0.69 | 0.838 |
| Other cities | 264 (45.5) | 0.99 | 0.97 | 0.96 | 0.94 | 0.88 | 0.70 | ||
| Type of immunosuppressant’s drugs1 | 1 | 582 (94.2) | 0.99 | 0.98 | 0.97 | 0.94 | 0.89 | 0.70 | 0.082 |
| 2 | 36 (5.8) | 1.00 | 1.00 | 0.97 | 0.85 | 0.79 | 0.71 | ||
| Total | 0.99 | 0.98 | 0.97 | 0.93 | 0.88 | 0.70 | |||
Patients who received prednisone, Cellcept and cyclosporine are marked with the code “1” and patients who received prednisone, cyclosporine and Imuran, are marked with the code “2”
Only in 86 (13.9%) of patients’ files had been recorded the cause of ESRD, which was hypertension (47 cases) and diabetes (13 cases), as well as some other causes, such as urinary tract infections, glomerulonephritis, and urolithiasis. For this reason, that is, because of the unspecification of a large number of items, the information concerning this factor was not included in the modeling.
As shown in Fig. 1, survival rates of 1, 3, 5, 7, 10 and 15 yr were 99, 98, 97, 93, 88 and 70 percent, respectively. Given the chart, graft survival is almost constant over the first 5 years, but then it falls into a steady decline.
Fig. 1:

The survival rate of kidney transplantation from the time of surgery to the time of rejection using the Kaplan-Meier curve with 95% confidence interval
As presented in Table 1, based on the results of the Log-rank test, the cumulative survival rate during the study was significantly higher in patients over 40 yr than those under 40 (P=0.001). The survival rate for recipients with serum creatinine levels below 1.6 was significantly higher than those with serum creatinine higher than 1.6 (P<0.001). The survival rates were significantly lower in recipients with a history of hypertension compared to the rest of recipients (P=0.001). The cumulative survival rate in recipients with a BMI less than 18.9 (underweight) was significantly lower than recipients with a BMI greater than 18.9 (normal and overweight) (P<0.05).
In the present study, the cumulative survival rate of renal transplantation indicated no significant difference in the following cases: gender of recipients (P=0.400), delivery type (P=0.077), duration of dialysis before transplantation (P=0.702), living place of transplant recipients (P=0.838) and the type of immunosuppressive drugs (P=0.082).
Univariate analysis showed that the recipient age, serum creatinine in the transplant, hypertension, and BMI are among the risk factors associated with transplant rejection.
Adjusted results of Cox multiple regression showed that the factors affecting transplant rejection are as follows: The rejection rate in the 40-year-old age group was about 80% lower than the age group younger than 40 yr old [risk ratio (HR)=0.22, 95% CI=(0.071,0.691)]. Regarding serum creatinine levels after transplantation, the risk of transplant rejection is about 3 times higher for patients with serum creatinine levels greater than 1.6 mg/dL [HR=3.03, 95% CI=(1.284,7.125)]. The rate of irreversible kidney transplantation in individuals with a history of hypertension is about 6 times higher than those without it [HR=6.70, 95% CI= (2.746, 16.348)]. In the case of BMI, multivariate results indicated that the survival rate of the transplant was higher in subjects with normal weight [HR (normal weight versus underweight) =0.26, 95% CI= (0.088, 0.761)] and overweight [HR (overweight versus underweight) =0.13,95%CI=(0.038,0.442)] than underbody subjects (Table 2).
Table 2:
Demographic and clinical characteristics associated with graft failure in kidney transplantation patients using univariate and multivariate Cox proportional hazard model (n=618)
| Variable | Univariate analysis | Multiple analysisa | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Crude HR | 95% CI | P-value | Adjusted HR | 95% CI | P-value | |||||
| Sex of recipients (male versus female) | 1.30 | 0.701–2.411 | 0.405 | |||||||
| Age of recipients (≥40 versus <40) | 0.34 | 0.143–0.810 | 0.015 | 0.22 | 0.071–0.691 | 0.009 | ||||
| Serum creatinine at transplant (≥1.6 versus <1.6) | 3.53 | 1.911–6.517 | <0.001 | 3.03 | 1.284–7.125 | 0.011 | ||||
| Hypertension (yes versus no) | 2.70 | 1.441–5.049 | 0.002 | 6.70 | 2.746–16.348 | <0.001 | ||||
| Delivery type (cadaver versus live) | 1.82 | 0.928–3.587 | 0.082 | 0.77 | 0.288–2.066 | 0.606 | ||||
| BMI | ||||||||||
| (normal weight versus underweight) | 0.40 | 0.154–1.030 | 0.058 | 0.26 | 0.088–0.761 | 0.014 | ||||
| (over weight versus underweight) | 0.18 | 0.059–0.568 | 0.003 | 0.13 | 0.038–0.442 | 0.001 | ||||
| Time of dialysis before transplantation (>24 months versus ≤24 months) | 0.85 | 0.376–1.929 | 0.721 | |||||||
| Living area (Other cities versus Mashhad) | 1.07 | 0.571–2.000 | 0.838 | |||||||
| Type of immunosuppressant’s drugs | 2.11 | 0.887–5.010 | 0.091 | 1.13 | 0.333–3.859 | 0.841 | ||||
multivariate analysis with the forward selection method
Discussion
In this historical cohort study, the survival rate of graft after 1, 3, 5, 7, 10 and 15 years of transplantation was estimated to be 99, 98, 97, 93, 88 and 70 percent respectively during a 15-year timespan. Graft survival is very high in the first 5 years after the transplant. After that time, a sustained decrease is observable in the graft survival rate.
In a similar study conducted between 1994 and 2011 in western Iran, the graft survival rate after 1, 5, 10, and 15 years of transplantation was estimated to be 97.9, 92.3, 86.2, and 77.6 percent respectively (17).
Based on the results of the largest graft survival analysis in the country between 1984 and 2005, the survival rate after 1, 3, 5, and 10 years was reported to be 85, 76.4, 68.3, 46.4 and 23.8 percent respectively (18). In a similar study in South Korea on 620 patients who received transplants from live donors between 1979 and 2002, the survival rate at 1, 5 and 10 years was reported to be 92.6, 82.4 and 76.1 percent respectively (22). Overall, 1308 Spanish patients were examined between 1981 and 2008, and the 6-year survival rate of kidney transplantation was reported to be 89% (23). In general, the differences may be due to the lack of concurrence of these studies and changes in the methods of transplantation or prescribed drugs and the type of immunosuppressant drugs over time (17).
Type 2 diabetic nephropathy and hypertension constitute two major causes of ESRD in developed countries (24, 25). A few studies have been conducted to determine the initial causes of ESRD in Iran, indicating that DM and HTN are the major ones (1, 26). Compared to the United States and other developed countries, the cause of ESRD in most patients in Iran is due to unknown factors (13). In Iran as well as many other developing countries, patients with chronic kidney disease are referred to hospital when they suffer severe symptoms, a time that it is not possible to determine the initial cause of ESRD at (27).
The probability of kidney transplant rejection in older recipient age groups is lower than the younger recipient age groups. This result has also been reported by previous studies, some being following the results of ours (28, 29). However, there was no significant relationship between recipient age and graft survival (27, 30), which can be due to the lower age range of transplant recipients.
The amount of Creatinine at the time of discharge from hospital is another important factor in the graft survival rates, known as a predictor of graft survival (14, 17, 20, 31) in most important studies.
The risk of rejection in subjects with BMI lower than the normal was higher than others. Some studies are confirming the finding that receptor weight affects graft failure (19, 32). It has been shown in a meta-analysis study examining the effect of BMI on transplantation survival that BMI of more than 30 in the recipient causes a graft failure (33). In this study, the number of individuals with a BMI greater than 30 was very low, with the individuals being included in the overweight group. No significant correlation was observed between BMI and graft failure in some studies (17, 20).
The duration of dialysis before transplantation was not significantly related to the graft survival rate, a result confirmed by several other studies (14, 17, 27). However, longer duration of dialysis before transplantation had a significant relationship with a lower survival rate (19, 34).
In this study, there was no significant relationship between the graft survival rate and donor type. This is in accordance with a few studies (15, 35). However, in a few other studies, the percentage of irreversible rejection of the transplant that led to the initiation of dialysis was greater in recipients from a Cadaver (17, 36). This may be either due to differences in the transplant system, or the ischemic time of the kidney, as increased ischemic time reduces graft survival (16).
In recent decades, with the advancement in immunosuppressant drugs, the survival rate has increased. In general, there is no relationship between the type of immunosuppressant drug used and the survival rate (14, 37, 38). However, there was a significant relationship between rejection and use of immunosuppressant drugs, the difference between which was not significant according to the multivariate Cox model (17). In this study, the long-term survival of the second treatment group is better than that of the first treatment group. However, a well-designed controlled clinical trial is needed to measure the effectiveness of these two drug therapies.
The ineffectiveness of gender for kidney transplants was observed in our study. This is also known as an ineffective factor in transplant survival rates in most studies (28, 29). At the same time, the recipient’s gender had to do with graft survival (8, 19, 39). However, most studies have reported univariate estimates (CRUDE) compared to ADJUSTED values, which may explain the inconsistency between the results of various studies.
Using the results of multivariate modeling, hypertension as one of the major causes of ESRD has been shown to increase the risk of transplant rejection, which contrary to another study (40), was consistent with other studies (31, 41).
This study had some limitations. First, estimates of survival and its prognostic factors require reliable sources from a prospective plan, but our study was a historical cohort study and medical records were used in it instead. Secondly, some patients were excluded from the study during a long follow-up, and thus the occurrence of a favorite event (rejection of the transplant) was not clear in their case of them, which may affect our results. Other limitations of this study are as follows: lack of record or incomplete recording of other important variables such as ischemic time, age, cause of ESRD, failure to record HLA typing of patients and impossibility to assess their effect on the graft survival rate.
Conclusion
The short-term transplant survival rate was good in transplant patients. What’s more, through a consideration of the variables of age, creatinine serum after transplantation, history of hypertension and body mass index, and proper planning for controlling their effect, it is possible to improve long-term graft survival.
Ethical considerations
Ethical issues (Including plagiarism, informed consent, misconduct, data fabrication and/or falsification, double publication and/or submission, redundancy, etc.) have been completely observed by the authors.
Acknowledgements
This study is a result of the author’s doctoral dissertation at Tehran University of Medical Sciences. It has been funded under research project No. 941835 approved by the Graduate Council of Mashhad University of Medical Sciences. We hereby express our gratitude to Mashhad University of Medical Sciences.
Footnotes
Conflict of interest
The authors state that there are no conflicts of interest.
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