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Original Research

Role of alpha-lipoic acid in the management of anemia in patients with chronic renal failure undergoing hemodialysis

, , , , &
Pages 161-168 | Published online: 27 Aug 2013

Abstract

Introduction

Anemia associated with chronic kidney disease is a serious complication necessitating expenditure of huge medical efforts and resources. This study investigates the role of alpha-lipoic acid (ALA) in end stage renal disease patients undergoing hemodialysis. By the virtue of its antioxidative effects, ALA is expected to act as an erythropoietin (EPO) adjuvant, and also has extended beneficial effects on endothelial dysfunction.

Methods

Forty-four patients undergoing hemodialysis and receiving EPO were randomized into two groups: the first group received ALA 600 mg once daily for 3 months; while the other group represented the control group. Parameters measured at baseline and at end of study were hemoglobin, EPO doses, EPO resistance index (ERI), iron store indices, malondialdehyde, oxidized low-density lipoprotein (ox-LDL), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and asymmetric dimethylarginine (ADMA), as well as routine laboratory follow-up.

Results

EPO doses and ERI were significantly decreased in the treatment group, while they did not change in the control group. Hemoglobin, iron store indices, malondialdehyde, oxidized ox-LDL, IL-6, TNF-α, and ADMA were similar in both treatment and control groups at baseline, and did not change by the end of study period. Likewise, routine laboratory measures were not affected by the treatment.

Conclusion

ALA could be used in hemodialysis patients to reduce requirements for EPO. However, larger and longer term studies are required to clarify the exact role of ALA in hemodialysis as well as in pre-hemodialysis patients.

Introduction

Anemia is a universal condition of end stage renal disease that is associated with poor outcome; it demands devoting a remarkable amount of resources and continuous effort to attain and maintain hemoglobin within guideline targets. Correction of anemia impacts essential outcomes such as quality of life,Citation1 cardiovascular function,Citation2,Citation3 and survival.Citation4 Erythropoietin (EPO) therapy has become the cornerstone of standard care when treating anemia in chronic kidney disease. However, implementation of anemia management guidelinesCitation5,Citation6 in real practice is hardly ever achieved, due mainly to complexity of complications accompanying end stage renal disease. This is noted particularly in developing countries, where economics greatly impact healthcare decisions. Another serious issue is the suggested association between administration of large EPO doses and an increased risk of cardiovascular complications and/or mortality.Citation7,Citation8

Reports studying EPO adjuvants being continuously compiled and published; however, no conclusive role for EPO adjuvants has until now been stated. Antioxidants have been attracting attention by virtue of their role in targeting oxidative stress, acting both as effector and consequence, and linking various risk factors of anemia and subsequent cardiovascular risk; additionally, they are of interest due to their leading role in EPO hyporesponsiveness. Antioxidants like Vitamin E, supplied orally or bound to the hemodialysis membrane, have been studied extensively; these studies have produced conflicting results on EPO responsiveness and dose reduction, as well as on other parameters such as oxidative-inflammatory markers and cardiovascular outcome.Citation9Citation11 Conflicting results have also been mentioned for other antioxidants such as ascorbic acid,Citation12,Citation13 N-acetylcysteine,Citation14,Citation15 and antioxidant combinations.Citation16 In addition, negative side effects have increased concern about their use, such as oxalosis with ascorbic acid,Citation17 toxicity, or even increased mortality with vitamin E.Citation18 In spite of its benefits, the impracticalities of electrolyzed-reduced water use has prevented its widespread use.Citation19

Alpha-lipoic acid (ALA) is a naturally occurring compound that is de novo synthesized in mitochondria and is an essential cofactor for certain dehydrogenase enzymes during mitochondrial energy metabolism. It acts as a potent antioxidant through multiple mechanisms. It scavenges reactive oxygen and nitrogen species, regenerates other antioxidants such as ascorbic acid, glutathione, alpha-tocopherol and coenzyme Q10, and chelates reactive free metal ions. Regarding its safety, it has been reported that doses of up to 1800–2400 mg/day can be tolerated safely in humans without reported toxicity or significant adverse side effects.Citation20,Citation21 Growing evidence has demonstrated a nephroprotective role for ALA; it improved histological lesions, ameliorated renal oxidative stress and inflammatory markers, and lowered the increase in serum creatinine and urea in rats induced by different insults.Citation22Citation25

The present study investigates the role of ALA as an EPO adjuvant in end stage renal disease patients undergoing hemodialysis. It also examines its antioxidative, anti-inflammatory effects, and its role in endothelial dysfunction. To our knowledge, this is the first study investigating ALA effect on anemia management.

Patient and methods

This study was conducted at the outpatient dialysis unit of Mansoura University’s Urology and Nephrology Centre. Forty-four end stage renal disease patients undergoing maintenance hemodialysis were randomly assigned to two groups of 22 patients each. Twenty-two patients comprised the treatment group and were given ALA (Thiotacid; EVA Pharma, Cairo, Egypt) 600 mg once daily (after hemodialysis sessions in days of dialysis), whereas the other 22 patients served as the control group. The clinical study was in accordance with the principles of the Declaration of Helsinki. It was approved by Mansoura University’s Medical Research Ethics Committee, and the patients gave their consent after being informed about the nature of the study.

Patients were anemic, were administered alpha recombinant human EPO (Epoetin; Sedico, Cairo, Egypt) as scheduled according to their needs, underwent hemodialysis three times weekly, and had adequate hemodialysis for at least 6 months using bicarbonate-based dialysate and polysulfone membrane dialyzers. Patients with symptoms of active infections or acute inflammation, malignancy, active Hepatitis C virus infection (HCV) (as evidenced by elevated liver enzymes), or a history of recent surgery or significant blood loss were excluded. Complete disease and drug histories and other relevant biodata were taken for all the patients. A summary of baseline data is presented in .

Table 1 Baseline characteristics of the treatment and control groups

Blood samples used for determination of study parameters were collected during appointments that were scheduled by the dialysis unit for routine patients’ examinations. They were collected prior to the second session of the week at the start and at the end of the 3-month study period. Non lipemic or hemolytic samples were immediately placed on ice. Plasma samples were mixed with (ethylenediaminetetraacetic acid) EDTA, centrifuged at 1000 g for 15 minutes, and aliquots were stored at −80°C till assay. They were used for determination of asymmetric dimethylarginine (ADMA), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), and oxidized low-density lipoprotein (ox-LDL). Serum samples were also stored at −80ºC for determination of malondialdehyde (MDA) and ferritin; other serum samples were used for the remaining assays and kept at 2°C–8°C and used instantly.

ADMA was determined by the use of enzyme linked immunoassays (Immunodiagnostik AG, Bensheim, Germany) according to manufacturer directions; the same was done for ox-LDL (Immunodiagnostik AG), IL-6 (R&D Systems, Minneapolis, MN, USA), TNF-α (R&D Systems, USA), and ferritin (Monobind Inc, Lake Forest, CA, USA). A Biotek ELx800 (BioTek Instruments, Inc, Winooski, VT, USA) was used to read ELISA assays. MDA was determined using the thiobarbituric acid reactive substances method; 0.5 mL of serum was mixed with 2.5 mL 20% trichloroacetic acid and 1 mL of 0.67% thiobarbituric acid. The mixture was incubated in a boiling water bath for 45 minutes, followed by cooling in tap water. Samples were mixed, shaken with 4 mL butanol and centrifuged to facilitate separation of layers. The upper red-colored butanol phase was separated and quantified spectrophotometrically at 535 nm. Malonaldehyde bis(diethylacetal) (1,1,3,3 tetraethoxypropane) was used as standard (all reagents supplied by Sigma-Aldrich [St Louis, MO, USA]).Citation26 Hemoglobin concentration was determined using Sysmex KX-21N hematology analyzer (Sysmex Corporation, Kobe, Japan). The EPO dose was estimated as the weekly dose requirements per patient, and EPO resistance index (ERI) was calculated as the ratio of the dose adjusted for body weight after a hemodialysis session, to hemoglobin concentration.Citation27 Iron was determined by the chromazurol B method. Transferrin saturation (TSAT%) was calculated by dividing the serum iron concentration by the total iron binding capacity and multiplying the result by 100, to obtain a percentage. Other laboratory parameters were measured via their routine methods.

Statistics

The data was presented as mean ± standard deviation (SD). The Kolmogorov–Smirnov test was used to test normality of data distribution. Groups at baseline were compared using Student’s t-test or Mann–Whitney U-test as appropriate. Paired t-test or Wilcoxon signed-ranks test was used to compare values within each group at baseline and at the end of the 3-month study. Chi-square test was used for comparing categorical values. Univariate analysis using Spearman’s correlation test and analysis of covariance were performed to test possible baseline factors that could confound ERI results. Statistical Package for Social Sciences (SPSS version 20; IBM Corporation, Armonk, NY, USA) for Windows was used. P < 0.05 was considered statistically significant.

Results

Nine patients were withdrawn from the original randomized sample of 53 patients; four patients from the treatment group and five from the control group. Two patients were in the treatment group and withdrawn due to gastrointestinal side effects, one patient suffered from hemorrhoids, and another patient underwent surgery to fix a fracture in her lumbar spine; additionally, two patients received transplants and three others were hospitalized for recurrent infections. Treatment group patients who completed the assigned treatment periods displayed 85% compliance.

There was no significant difference between the treatment and control groups regarding baseline characteristics () and laboratory parameters. Additionally, there were no changes in laboratory parameters by the end of the study in both treatment and control groups (). The changes in hemoglobin concentration, EPO doses, ERI, and iron indices are summarized in . There was no significant difference in the baseline values between the treatment and control groups. There were significant changes in the treatment group by the end of the study in EPO doses and ERI, whereas there were no significant changes in these values for the control group. There was no significant change between baseline and end of study in both treatment and control groups for hemoglobin concentration, serum iron, total iron binding capacity (TIBC), TSAT%, and ferritin.

Table 2 Changes in laboratory markers in treatment and control groups

Table 3 Changes in anemia control measures in treatment and control groups

The changes in MDA, ox-LDL, IL-6, TNF-α, and ADMA are summarized in . There was no significant difference in the baseline parameters between the treatment and control groups. There was no significant change between baseline and end of study in both treatment and control groups in MDA, ox-LDL, IL-6, TNF-α, and ADMA.

Table 4 Changes in biochemical parameters in treatment and control groups

An analysis for a number of parameters was done for the sub-group of patients with no HCV (12 patients, six in each group). The findings of these selected parameters were that there was no significant difference in baseline parameters between the treatment and control groups. The change in hemoglobin concentration by the end of the study was not significant in both treatment and control groups, from 10.58 ± 1.26 to 11.43 ± 0.91 g/dL and 11.08 ± 0.78 to 11.27 ± 1.11 g/dL, respectively. The changes in EPO doses and ERI in the treated group were from 7000 ± 3033.15 to 5000 ± 4335.9 IU/week (P = 0.06) and 11.32 ± 8.49 to 7.45 ± 7.48 (P < 0.05), respectively. In contrast, the changes in EPO doses and ERI in the control group were not significant (6000 ± 4000 to 5000 ± 3033.15 IU/week and 9.67 ± 7.71 to 7.64 ± 5.34 IU/kg per week per g/dL, respectively).

Univariate analysis revealed no correlation between ERI results and age, sex, smoking status, time on dialysis, intact parathyroid hormone (iPTH) values, presence of diabetes mellitus (DM), presence of HCV, and Kt/V Only baseline ERI values were correlated with ERI results (r = 0.79, P < 0.001). Analysis of covariance found no effect for all these covariates.

Discussion

The present study showed no effects of ALA either on markers of oxidative stress MDA and ox-LDL, or inflammatory markers IL-6 and TNF-α. This was in line with a previous study in which ALA did not affect the inflammatory marker high-sensitivity C-reactive protein (HsCRP), nor did it reduce ox-LDL in hemodialysis patients.Citation28

Lack of measurable effect in hemodialysis patients may be attributed to the fact that ALA acts indirectly to augment other endogenous antioxidants; it improves levels of ascorbic acid, glutathione, alpha-tocopherol, and coenzyme Q10, enhancing uptake from the blood, by inducing their synthesis, or by regenerating the reduced form.Citation20,Citation21 Hemodialysis is a case of excessively depleted antioxidant status, limiting ALA’s ability to perform its complete antioxidative role; in line with this is the suggestion raised in the SPACE study – one of the very few studies with positive effect upon oral administration of vitamin E in hemodialysis patients – that this positive effect may be due to the coadministration of ascorbic acid, which is capable of maintaining vitamin E in a reduced state.Citation10

The relatively small sample size of the study may hinder beneficial effects in this complicated population; the study group had multiple different confounding conditions, including smoking, inability to rule out low/high hemoglobin or iron deficiency/overload in the patients at all the time points, and comorbidities such as DM and HCV. A large-scale study could reveal beneficial differences or at least allow controlling for some of these confounders.

One of the most important nontraditional cardiovascular risk factors that explains the high prevalence of cardiovascular complications in patients with chronic renal failure is elevated ADMA. ADMA is the one of the most endogenous inhibitors of nitric oxide synthase (NOS), which produces nitric oxide (NO), thus resulting in endothelial complications. ADMA is not only an active mediator of various cardiovascular complications,Citation29,Citation30 it has also been found to predict progressive deterioration of renal function and cardiovascular events in different stages of chronic kidney disease.Citation31,Citation32

In cultured endothelial cells, ALA decreased ADMA concentration; it enhances activity of the ADMA-metabolizing enzyme dimethylarginine dimethylaminohydrolase (DDHA) and gene expression.Citation33 However, in the present study ALA did not exert an effect on ADMA. This contrasts with other studies of type 2 DM patientsCitation34 and hemodialysis patients.Citation28 Patients in these studies were all diabetics, whereas in the present study only a segment of the study population were diabetics. ALA may act selectively on those patients through antidiabetic mechanisms. ALA mimics insulin-induced glucose handling at the cellular level.Citation35 It improves glycemic control in type 2 diabetic patients.Citation36 This may be why ALA has enhanced efficacy in a wide array of clinical effects in the diabetes field. In diabetic rat kidney, ALA attenuated albuminuria, glomerulosclerosis, and tubulointerstitial fibrosis, and lowered renal expression of transforming growth factor-β1 (TGF-β1) and inducible NOS (iNOS).Citation24,Citation25 It attenuated markers of oxidative stress and inflammation in patients with diabetic overt nephropathy.Citation37 It improved endothelial dysfunction in subjects with impaired fasting glucoseCitation38 and in patients with type 2 diabetes,Citation39 and preserved their renal function by inhibiting progressive increase of urinary albumin excretion.Citation40 ALA also has a well-established role in management of diabetic neuropathy, a role which is based on compiled studies and which has been proven to be a safe and effective practice.Citation41

In vivo studies have shown that EPO provides endothelial protection, which is found to be mediated via activation of NOS,Citation42 thus antagonizing the effects of ADMA. In addition, EPO is known to have both a direct and indirect antioxidative role through recruitment of iron in red blood cell production (thus depleting body iron) and by increasing the number of new erythrocytes which are loaded with antioxidants.Citation43 The reduction in EPO doses noticed by the end of the present study in the ALA-treated group may have attenuated the beneficial effect on ADMA level and oxidative stress markers, and, as a result, inflammatory markers.

Patients in the present study were in general considered iron replete and did not show iron deficiency as revealed by their iron indices. ALA resulted in no effect on iron, ferritin, and TSAT%. In general, patients were considered non-anemic, with few hemoglobin readings below 10.5 g/dL. ALA resulted in no effect on hemoglobin and hematocrit values; in contrast, it significantly reduced required EPO doses and ERI.

ERI response was not found to be related to age, sex, smoking status, time on dialysis, iPTH values, presence of DM, presence of HCV, and Kt/V; it was found to be related to only baseline ERI values. Analysis of covariance found no effect for all these covariates. These findings, however, should be expressed cautiously due to the small sample size.

One of the limitations of the present study is that it did not provide evidence of either the antioxidative or the anti-inflammatory effects of ALA; thus, the mechanism by which it improved anemia remains speculative. At first, it is worth noting that there is no evidence to support the use of a definitive biomarker, and a panel of different oxidative stress markers may be required to adequately assess the antioxidative effect of ALA. Trials investigating the antioxidants in hemodialysis patients have yielded contradictive outcomes. Moreover, the use of some antioxidants affected biomarkers differentially in the same study. For example, coenzyme Q10 suppressed advanced oxidation protein products, whereas it had no effect on MDA.Citation44 Secondly, factors related to red blood cells have been suggested to contribute to the underlying mechanisms by which anemia occurs. The main erythrocyte metabolic pathway “hexosemonophosphate (HMP)” cycle and glucose-6-phosphate dehydrogenase (G-6-PDH), a key enzyme of the HMP cycle, show decreased activity in patients undergoing regular hemodialysis. The HMP cycle plays a significant role in red blood cell antioxidant reactions because it is the only source of NADPH (reduced nicotinamide adenine dinucleotide phosphate). This compound is indispensable in the process of restoring reduced glutathione (GSH). The GSH system is one of the major scavengers of activated oxygen species in erythrocytes. Reduced antioxidant defense mechanisms in the erythrocyte leads to increased peroxidation of the polyunsaturated fatty acids (PUFA) in red blood cell membranes and increased susceptibility to damage, resulting in hemolysis and a reduction of erythrocyte life span.Citation45,Citation46 Hemodialysis patients have been found to have low levels of erythrocyte GSH, which is correlated to low G-6-PDH activities,Citation47 and administration of exogenous glutathione to hemodialysis patients increased red blood cell GSH content, increased red blood cell survival, and reduced EPO need. This improvement was not accompanied by decreased oxidative stress indicator MDA.Citation48 ALA is capable of regenerating other endogenous antioxidants such as GSH. Investigating erythrocyte G-6-PDH and GSH may provide the exact targets of ALA effects. This has been proven in diabetic rats, where ALA administration preserved the structural and functional integrity of red blood cells by increasing the red blood cell activities of antioxidant enzymes and of reduced GSH.Citation49 Thirdly, the use of the nonspecific inflammatory marker HsCRP may yield positive results as found in a previous study.Citation50 Lastly, one could not rule out the presence of other mechanisms mediating ALA lowering effect of EPO.

Some studies have reported lowered levels of anemia in hemodialysis patients with HCV when compared with no HCV. They found that HCV patients had better hemoglobin values and demanded less EPO doses than age-, gender- and race-matched HCV-free patients.Citation51,Citation52 Bearing in mind that minor production of endogenous EPO comes from a healthy liver,Citation53 it was hypothesized that the chronic inflammation as a result of HCV infection or regenerating liver cells cause increased circulation of EPO released from hepatocytes. HCV patients constituted a high proportion of the present study population, and hence may impact the outcome results (HCV has a high prevalence in the general population in Egypt, which is increased further in susceptible groups such as hemodialysis patients). If the previous observation applies, then these patients already have an inherently improved response to exogenous EPO, and any beneficial change, even mild and unnoticed (provided by the antioxidant effect of ALA), would have amplified responses. To examine such an assumption, an analysis for the subgroup of patients with no HCV was done. In the treated group, the reduction in EPO doses showed a trend toward significance and the reduction in ERI was significant; in contrast, in the control group both parameters showed insignificant changes. Although small, this subgroup revealed favorable outcomes that clearly confirmed the role of ALA in anemia management, in both HCV-positive and HCV-negative hemodialysis patients. This was also demonstrated by the lack of effect HCV had on ERI results when analyzed as a covariate.

Conclusion

The study provided evidence for the use of ALA as an EPO adjuvant, reducing the requirement for EPO; this reduction not only offers economic advantages, it more importantly would protect against the proposed harmful effect of high EPO doses.

Disclosure

The authors report no conflicts of interest in this work.

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