The association between transferrin saturation and all-cause mortality in chronic kidney disease: findings from Korean Cohort Study for Outcome in Patients with Chronic Kidney Disease

Article information

Korean J Nephrol. 2024;.j.krcp.23.278

Publication date (electronic) : 2024 May 3

doi : https://doi.org/10.23876/j.krcp.23.278

Eunmi Jo^1,*, Hyo Jin Kim^1,2,*, Jayoun Kim³, Tae-Hyun Yoo⁴, Yaeni Kim⁵, Soo Wan Kim⁶, Kook-Hwan Oh^7,8, Eun Young Seong^,1,2,†, Sang Heon Song^,1,2,†

¹Department of Internal Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea

²Department of Internal Medicine, Pusan National University School of Medicine, Yangsan, Korea

³Medical Research Collaborating Center, Seoul National University Hospital, Seoul, Republic of Korea

⁴Department of Internal Medicine, College of Medicine, Institute of Kidney Disease Research, Yonsei University, Seoul, Republic of Korea

⁵Department of Internal Medicine, Seoul St Mary‘s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea

⁶Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea

⁷Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea

⁸Kidney Research Institute, Seoul National University Medical Research Center, Seoul, Korea

Correspondence: Eun Young Seong Department of Internal Medicine, Pusan National University Hospital, 179 Gudeok-ro, Seo-gu, Busan 49241, Republic of Korea. E-mail: sey0220@pusan.ac.kr

Sang Heon Song Department of Internal Medicine, Pusan National University Hospital, 179 Gudeok-ro, Seo-gu, Busan 49241, Republic of Korea. E-mail: shsong0209@gmail.com

*Eunmi Jo and Hyo Jin Kim contributed equally to this study as co-first authors.†Eun Young Seong and Sang Heon Song contributed equally to this study as co-corresponding authors.

Received 2023 September 1; Revised 2023 December 18; Accepted 2024 January 6.

Abstract

Introduction

In patients with chronic kidney disease (CKD), anemia is a common complication that plays a major role in determining the prognosis. The lower the hemoglobin concentration, the higher the mortality, the faster the decline in renal function, the more severe the associated symptoms, and the lower the productivity of daily life [1–4].

Iron deficiency anemia is a leading cause of anemia, and the importance of iron deficiency (ID) itself is increasing regardless of the occurrence of anemia [5–7]. Serum ferritin and transferrin saturation (TSAT) are the most common tools used to evaluate ID. Ferritin is a marker of stored iron and TSAT is a marker of circulating iron, indicating iron availability to the tissue [8]. However, serum ferritin has limitations in diagnosing functional ID (FID) because it can be increased in the inflammatory state as an acute-phase reactant, independent of iron metabolism [9]. In CKD, where both absolute and FID are important, TSAT can be a useful marker for assessing low iron availability [5,7].

However, the exact ranges of serum biomarkers for iron supply are inconsistent. The 2012 Kidney Disease–Improving Global Outcomes (KDIGO) guidelines recommend iron supplementation when ferritin is less than 500 ng/mL and TSAT is less than 30% in both dialysis and non-dialysis CKD (NDCKD) patients [10]. However, subsequent studies have shown a better prognosis in a higher range than the current guidelines, with mortality rising again above a certain level of TSAT [11–14].

Serum iron is reduced in ID, even in the setting of inflammation, and its usefulness in evaluating ID is emerging [7,15]. However, in the progression of anemia serum iron begins to decrease later than stored iron and alone its concentrations do not indicate ID [7]. It may be helpful to evaluate the prognosis through the relationship between serum iron and ferritin as well as TSAT.

Therefore, we aimed to analyze the effect of TSAT on the prognosis of patients with NDCKD through all-cause mortality, cardiovascular outcomes, and its association with other iron biomarkers.

Methods

Results

Baseline characteristics

Of the 2,157 patients, 644 patients were in the TSAT <25% group, 1,240 were in the TSAT ≥25% and <45% group (reference), and 273 were in the TSAT ≥45% group (Supplementary Fig. 1, available online). The baseline demographic and clinical characteristics of the patients are shown in Table 1. The mean age was 53.7 ± 12.2 years and the mean eGFR was 53.0 ± 30.7 mL/min per 1.73 m². The mean value of TSAT was 31.7% ± 12.1% and the median value of ferritin was 99.9 ng/mL (IQR, 54.1–176.6 ng/mL). The incidence of DM (p < 0.001) and cardiovascular disease (p = 0.03) was higher in the lower TSAT group. There were no differences in the prescriptions of ESA and supplementary iron between the TSAT groups.

Table 1.

Baseline characteristics

Primary outcome

During a mean follow-up duration of 7.1 ± 2.9 years, 182 patients (8.4%) died. The causes of death were evaluated in 120 patients, with 41 (deaths 34.2%) attributed to infection, 25 (20.8%) to malignancy, 23 (19.2%) to cardiovascular disease, and 31 (25.8%) to other causes. For patients with TSAT categories of <25%, ≥25% and <45%, and ≥45%, the mortality rate was 11.0%, 7.7%, and 5.5%, respectively. Cardiovascular death was more common in the TSAT <25% group than in other groups (Supplementary Fig. 3, available online). Kaplan-Meier analysis showed higher all-cause mortality in the TSAT <25% group than in the other groups and a decrease with higher TSAT (log-rank p = 0.005) (Fig. 1). Four models of multivariable Cox analysis revealed that the TSAT <25% was associated with higher mortality risk, even after adjustment for hemoglobin, ferritin, ESA use, and iron supplementation (HR, 1.44; 95% CI, 1.00–2.03; p = 0.04) (Table 2). The all-cause mortality showed a trend toward decrease with higher TSAT, but no statistically significant difference at TSAT ≥45% (HR, 0.90; 95% CI, 0.50–1.64; p = 0.73). Supplementary Fig. 3 (available online) shows the restricted cubic spline curve for the multivariable Cox regression analysis of all-cause mortality according to TSAT. The results of the subgroup analyses are shown in Supplementary Table 1 (available online). In the subgroup analysis of patients with BMI <25 kg/m², serum ferritin <100 ng/mL, eGFR ≥30 mL/min per 1.73 m², and hepcidin <15 ng/mL, the HRs of the TSAT <25% group showed significantly increased mortality compared with the TSAT ≥25% and <45% group.

Figure 1.

Kaplan-Meier survival curve for all-cause mortality according to baseline TSAT value.

TSAT, transferrin saturation.

Table 2.

HRs for all-cause mortality by TSAT levels

Secondary outcome

For patients with TSAT categories of <25%, ≥25% and <45%, and ≥45%, the incidence of 4-point MACE was 12.9%, 9.7%, and 5.9%, respectively. Similar to the all-cause mortality outcomes, 4-point MACE decreased in the higher TSAT group (log-rank p = 0.03) (Fig. 2). In the Cox regression analysis, the TSAT <25% group had increased MACE compared with the TSAT ≥25% and <45% group in univariable analysis (HR, 1.48; 95% CI, 1.02–2.15; p = 0.04). However, this was not significant in the multivariable analysis (HR, 1.38; 95% CI, 0.89–2.15; p = 0.15). The TSAT ≥45% group also showed no significant difference in MACE compared with the TSAT ≥25% and <45% group (HR, 0.72; 95% CI, 0.32–1.60; p = 0.42) (Table 3).

Figure 2.

Cumulative incidence of 4-point MACE by baseline TSAT value.

MACE, major adverse cardiovascular event; TSAT, transferrin saturation.

Table 3.

HRs for 4-point MACE by TSAT levels

Association of transferrin saturation with other iron biomarkers: ferritin and iron levels

Differences in all-cause mortality were analyzed for the combination of TSAT and serum ferritin and TSAT and serum iron. Supplementary Fig. 4 (available online) shows the HR of all-cause mortality according to serum ferritin and iron levels using a restricted cubic spline plot. The serum ferritin level was divided by 100 ng/mL, which is the current general reference value for ID in NDCKD, and the iron level was divided by 80 μg/dL based on the restricted cubic spline of the HR. Kaplan-Meier analysis showed that mortality was highest in the group with TSAT <25% and ferritin <100 ng/mL (Fig. 3A). In a multivariable Cox analysis with the TSAT ≥25% and ferritin ≥100 ng/mL group as the reference, the adjusted HR was highest when TSAT <25% and ferritin <100 ng/mL (HR, 1.69; 95% CI, 1.12–2.56; p = 0.01) (Fig. 3B). The TSAT <25% and ferritin ≥100 ng/mL group was the next highest, but it was not statistically significant. For TSAT and iron, the Kaplan-Meier analysis showed higher mortality in the two iron <80 μg/dL groups (Fig. 3C). In Cox analysis with the TSAT ≥25% and iron ≥80 μg/dL group as the reference, the adjusted HR was highest in the TSAT <25% and iron <80 μg/dL group (HR, 1.67; 95% CI, 1.13–2.46; p = 0.009) (Fig. 3D). The TSAT ≥25% and iron <80 μg/dL group had the next highest, but this was not statistically significant.

Figure 3.

Kaplan-Meier survival curve and Cox analysis for all-cause mortality according to iron biomarkers: serum ferritin and iron.

Kaplan-Meier survival curve according to TSAT and ferritin (A) and TSAT and iron (C). Unadjusted and adjusted hazard ratio for TSAT and ferritin (B) and TSAT and iron (D). In the Cox analysis, adjustment for TSAT and ferritin groups included age, sex, BMI, MBP, underlying comorbidities, estimated glomerular filtration rate (eGFR), albumin, uric acid, phosphate, corrected calcium, low-density lipoprotein cholesterol (LDL-C), log high-sensitivity C-reactive protein (log-hsCRP), log urine albumin-to-creatinine ratio (log-UACR), hemoglobin, total iron-binding capacity (TIBC), erythropoietin-stimulating agent (ESA) use, and iron supplementation. Adjustments for the TSAT and iron groups included age, sex, body mass index, mean blood pressure, underlying comorbidities, eGFR, albumin, uric acid, phosphate, corrected calcium, LDL-C, log-hsCRP, log-UACR, hemoglobin, TIBC, log-ferritin, ESA use, and iron supplementation.

TSAT, transferrin saturation.

Iron-to-log-ferritin ratio

Cox regression analysis of the iron-to-log-ferritin ratio showed a U-shaped distribution, with the lowest mortality in the second tertile group (T2) (Fig. 4A). The HR of the first tertile group (T1) was significantly increased compared with T2 as the reference group (HR, 1.71; 95% CI, 1.16–2.51; p = 0.007) (Fig. 4B). There was also an increase in mortality in the third tertile (T3), but this was not statistically significant. The median values of the iron biomarkers in the T2 range were as follows: TSAT, 30% (IQR, 25%–35%); iron, 90 μg/dL (IQR, 79–101 μg/dL); and ferritin, 108 ng/mL (IQR, 60–176 ng/mL).

Figure 4.

Adjusted hazard ratio of all-cause mortality by iron-to-log-ferritin ratio.

(A) Restricted cubic spline curve for the hazard ratio for iron-to-log-ferritin ratio using multivariable Cox regression analysis. (B) Hazard ratio and values of iron biomarkers by iron-to-log-ferritin ratio tertiles. Iron-to-log-ferritin ratio was divided into tertiles (T1, T2, and T3, respectively) and compared with T2 as the reference group. The median value (interquartile range) of TSAT, serum iron, and ferritin according to each tertile section are indicated under the column.

TSAT, transferrin saturation.

Discussion

In our study, the TSAT <25% group had a significantly higher mortality rate than the ≥25% and <45% group. Overall, all-cause mortality decreased with increasing TSAT, but there was no significance at TSAT 45% or higher. The incidence of 4-point MACE was significantly increased in the univariable analysis in the TSAT <25% group, but the significance was lost after multivariable adjustment. The 4-point MACE incidence tended to decrease as TSAT increased, but the difference was not statistically significant.

Various studies on TSAT have been published since the 2012 KDIGO guidelines. The PIVOTAL trial, a randomized controlled trial (RCT) in patients with CKD on dialysis (HDCKD), showed that high-dose intravenous (IV) iron administered proactively (with a ferritin cutoff of 700 ng/mL or TSAT 40%) was superior to low-dose IV iron administered reactively (administered to maintain ferritin 200 ng/mL and TSAT 20%) [14]. Observational studies have suggested relatively clear optimal ranges. In patients with NDCKD, mortality has been shown to be higher in TSAT <10%–17% [12,18–20], with increased mortality above 45%–55% [12,21]. In the 2021 CKDopps study, all-cause mortality and MACE were the lowest in the TSAT 35%–45% range and increased again above 46% [12]. In patients with HDCKD, TSAT <20% was associated with higher mortality and was a predictor of Coronary Artery Calcium Scoring >400 [22–24], with the best survival at 30%–50% [2].

Our results are consistent with those of the CKDopps study, which showed an increase in all-cause mortality below 25% when the TSAT 25%–35% group was used as a reference [12]. However, there was no upper cutoff for TSAT, and the HR continued to decrease. Nevertheless, caution is required in concluding that the higher the TSAT, the lower the mortality rate. Malignancy accounted for half of the deaths in the TSAT ≥45% group, and high TSAT and iron supply may contribute to increase oxidative stress and the risk of malignancy [25,26]. The average age of our participants was 53 years old, and in particular, the TSAT ≥45% group averaged 51 years old, which is younger than the average ages of 69 years [12] and 61 years [2] in previous studies. Therefore, if the incidence of malignancy increases with age due to longer follow-up periods, all-cause mortality in the high TSAT range may increase. In the subgroup analysis, the TSAT <25% group had a higher HR in the nonobese subgroup, relatively preserved renal function, and lower serum ferritin and hepcidin levels. This suggests that the impact of a low TSAT is more pronounced in patients with better overall health. Under inflammatory conditions, such as CKD or obesity, cytokines increase ferritin and hepcidin expression [27]. In a controlled environment of chronic inflammation, which may contribute to mortality, the impact of low TSAT levels may be more apparent.

Of the 182 deaths, only 35 patients (1.6%) were confirmed as cardiovascular deaths, making comparisons between groups difficult. Supplementary Table 2 (available online) shows the echocardiographic parameters. Lower TSAT has been shown to be associated with increased left ventricular geometric abnormalities, and increased E/E’ although in the normal range. This is consistent with previous findings that ID and anemia are associated with diastolic dysfunction and increased left ventricular mass [28,29]. Although there was no significant difference in 4-MACE incidence, avoiding TSAT <25% may be beneficial in preventing cardiac dysfunction.

ID can be classified as absolute ID (AID) or FID. AID is a condition in which iron stores in the whole body are insufficient and iron is reduced. In contrast, FID refers to a condition in which the body is not deficient in iron but cannot use iron for hematopoiesis and is mainly related to chronic inflammation [7]. In CKD, the use of ESAs increases iron demand by stimulating hematopoiesis; however, insufficient iron mobilization worsens FID [30–33]. At the KDIGO conference in 2019, AID was defined as TSAT <20% and ferritin <100 ng/mL, and FID was defined as TSAT <20% and ferritin >100 ng/mL in NDCKD. However, the definition of ID in CKD patients is still not consistently used [8]. Previous studies have also been conducted on serum ferritin levels. The FIND-CKD RCT indicated that IV iron targeting higher ferritin (400–600 ng/mL) delayed the need for other anemia management than low ferritin (100–200 ng/mL). Other observational studies have shown no directional association, but mortality increased at levels above 250 [19], 300 [12], or 500 [34].

In our study, regardless of the ferritin level, the group with low TSAT had a poor prognosis, and the AID group had a higher mortality rate than the FID group. For TSAT ≥25%, the prognosis was better with ferritin <100 than ≥100 ng/mL, and a similar result was found in a heart failure study [35]. This may be related to the implications of high ferritin because ferritin is always low in AID; however, when minimal iron is available, ferritin is regulated by non-iron-dependent factors, such as inflammation [36]. Therefore, when TSAT ≥25%, that is, when there is no shortage of iron supply, the prognosis may be better if the ferritin is low.

Under inflammatory conditions, cytokines upregulate ferritin and hepcidin and downregulate ferroportin, a transmembrane exporter of iron. Iron absorption in the gastrointestinal tract and its dissociation from macrophages and hepatocytes is impaired, limiting its supply to plasma and causing FID [7,27,32,37]. Because of this pathophysiology, even if ferritin levels are high in CKD, the possibility of FID cannot be ruled out [32,38]. In contrast, TSAT is more useful for identifying low plasma iron availability in both AID and FID [5,7]. In a study evaluating bone marrow aspiration in patients with heart failure, a low TSAT alone showed the best performance in diagnosing ID [39]. However, because TSAT can also be affected by inflammatory conditions, its limitations and the usefulness of serum iron have been noted [15,32,40]. In our study, the two groups with low iron levels, regardless of TSAT, had the worst prognoses. In patients with CKD, the value of TSAT required to achieve a serum iron level increases as a result of decreased TIBC [15]. Therefore, high TSAT levels have limitations as a stand-alone marker to exclude ID, and should also be considered a marker of inflammation in CKD [41]. In contrast, a low TSAT can be associated with low iron or high TIBC, both of which reflect the pathophysiology of ID.

As serum iron begins to deplete later than stored iron during the progression of anemia [7], the prognosis of ID was also analyzed using the iron-to-log-ferritin ratio, including ferritin, in our study. It showed a U-shape with the T2 range as a reference and a statistically significant increase in mortality in the T1 range. This can be interpreted as a poor prognosis in inflammatory conditions with decreased iron and high ferritin levels. In the T2 segment, each biomarker ranged from TSAT 25% to 35%, ferritin 60 to 176 ng/mL, and iron 79 to 101 μg/dL. These ranges were within the low mortality interval in our study. Based on the above results, serum iron and iron-to-log-ferritin ratios would be helpful in addition to TSAT when evaluating ID in patients with CKD.

Our study has several strengths. A long-term analysis was conducted on a large cohort of patients with CKD, and the relationship between TSAT and other iron biomarkers provided an overall insight into ID and its effects. However, this study also has its limitations. The relatively small number of patients with TSAT ≥45% may have contributed to the low incidence of the outcomes. In addition, iron status may vary according to ethnicity [42], but this study may have limitations in that it was conducted in a single ethnic group. Another limitation is that although we adjusted for multiple factors, this was an observational study, and confounding factors may remain.

In conclusion, TSAT <25% was an independent risk factor for all-cause mortality in patients with NDCKD compared to the TSAT ≥25% and <45% group. Care should be taken to prevent TSAT values of <25%. In the treatment of ID in patients with CKD, other indicators, such as serum iron and iron-to-log-ferritin ratio, may also be used to assess ID.

Supplementary Materials

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