ISSN: 2581-3870
Archives of Clinical Nephrology
Research Article       Open Access      Peer-Reviewed

Tubular dysfunction in patients with rheumatoid arthritis

Dejan Spasovski*

Clinic of Rheumatology, Clinical Center “Mother Therese”, Skopje, Republic of North Macedonia
*Corresponding author: Dejan Spasovski, Clinic of Rheumatology, Clinical Center “Mother Therese”, Skopje, Republic of North Macedonia, Tel: +389023147-668; E-mail:drspasovski@yahoo.co.uk
Published: 04 December, 2020 | Accepted: 24 December, 2020 | Received: 26 December, 2020
Keywords: N-acetyl-β-D-glucosaminidase; Microalbuminuria; Rheumatoid arthritis; Etoricoxib; Diclofenac

Cite this as

Spasovski D (2020) Tubular dysfunction in patients with rheumatoid arthritis. Arch Clin Nephrol 6(1): 038-041. DOI: 10.17352/acn.000047

Introduction: As an indicator of proximal tubular damage is used urinary excretion N-Acetyl-β-D-glucosaminidase (NAG), while Microalbuminuria is used as a tracer for glomerular damage.

Aim: The aim of the study is to determined effect of toxicity of these medicals by affecting the enzymuria that correlate with the damage of the epithelium of proximal tubular. To quantifice effects of the treatment with Etoricoxib and Diclofenac on renal proximal tubular in patients with Rheumatoid Arthritis (RA).

Methods: NAG is detected with colorimetric method. Microalbuminuria is detected with method od immunoturbidimetric. Tests were performed on 70 participants (35 RA treated with Etoricoxib, 35 RA patients with Diclofenac) in four time intervals in the eight weeks.

Results: Correlation between NAG and microalbuminuria (r = 0.21) in the group of patients treated with Etoricoxib is moderate, while correlation (r = 0.28) in the group with Diclofenac was significant. NAG enzymuria, in volume, number of participants in whom it was registered and at the time of its occurrence was much faster during the use of Diclofenac in relation to Etoricoxib.

Conclusion: Diclofenac is a potent NAG-inductor and gives a larger tubular enzymuria in comparison with Etoricoxib.

Introduction

Microalbuminuria is used as a marker for glomerular damage and urinary excretion of N-Acetyl-β-D-glucosaminidase (NAG) as an indicator of proximal tubular damage. These tests indicate that, there is no specific indicator, tracer, marker, which detects nephrotoxicity that occurs in the course of the therapy.

Many uses of certain groups of drugs for therapeutic purposes (NSAIDs, drugs that modify disease activity (DMRADs and immunosuppressive cytotoxic drugs), may have a specific nephrotoxic effect. The given dose is often not suitable for the patient’s condition, it can cause side effects, ie it can lead to reduction of the kidney function, as a result of accumulation in the kidneys’ cells. This is usually found in long-term therapy as in Rheumatoid arthritis.

Urinary enzymes to assess nephrotoxicity

Albumin in urine, (Microalbuminuria). Albumin (molecular weight of 66 KDa) is the most important protein in plasma, as well in urine. Approximately 30% of the protein in the urine belongs to it and presents a good indicator for assessing the change in glomerular permeability. Urinary albumin excretion has a high individual variability and depends on physical activity or food variations [1,2].

From all the urinary enzymes the most examined is U-NAG (urinary). This enzyme from the hydrolase class is abundantly present in lysosomes in proximal tubular cells. In human tissue and biological liquids there are two main enzyme forms: A (Acid) and B (Basic) (3-5). The percentage of isoform A (U-NAG-A) is the highest in normal urine [3,4]. Therefore, its excretion is related to the exfolliative turnover and is known as a functional enzymuria [5-14].

Materials and methods

Patients diagnosis is mades from on the diagnostic criteria for classification of Rheumatoid arthritis from American Association for Rheumatism (ARA) [15]. Criteria from 1 to 4 were present for at least 6 months. The study included 35 patients with RA (women 20, males 15) treated with Etoricozhib, as well as 35 patients with RA (women 22, males 13) treated with Diclofenac. The ages, means was 50.43 years (± 6.42) (38-65 years) in the treated group with Etoricohib, while 50.13 years (± 8.36) (39-65 years) in the group treated with Diclofenac. None of the patients used previously NSAID. The others did not use other drugs before taking the test, especially gold salts or antibiotics or diuretics. The samples were collected in period of 8 weeks.

Including criteria

Patients with RA was included in this research, in the age 18-65 years

All patients were not previously treated with NSAIDs or DMARDs.

Excluding criteria

1. Patients with a history of gonorrhea, mild to moderate hepatic, renal, hematologic, cardiovascular, neurological diseases, nausea, vomiting, autoimmune disease.

2. Patients with, diabetes mellitus, neoplasms mixed connective tissue disease

3. Patients with urinary tract arthritis, vasculitis.

4. Patients with a history of blood transfusion, and excessive body weight. febrile condition SLE

5. Excluded from the study was patients who receive baseline therapy for RA

6. Patient with a history of glycemia or increased levels of product degradation in the 0-th range: serum creatine and urine, serum urea, hypertension, arterial hypertension, and hematological and enzyme status. urinary tract infections

7. Patients previously treated with salicylates, antibiotics, gold salts, or diuretics, acute infections.

All participants voluntarily took part in this study, so that the criteria to do it are met.

Clinical assessment with disease activity score (DAS 28) index

Clinical assessment was made by sub specialist in the given area Disease Activity Score (DAS 28) index [16-18].

Score below 3.2 qualifies the disease as low active. DAS 28 indexes range from 0 to 10.

Laboratory assessment

For clinical assessment of disease, it is necessary to consider the following laboratory variables: aspartate aminotransferase (AST), urea / serum, creatinine / serum. Erytrocite Sedimentation Rate (ESR), C-Reactive Protein (CRP), ACPA antibodies, Alanine Aminotransferase (ALT), Complete Blood Count (CBC) and differential, Creatine Kinase (CK), Rheumatoid Factor (RF), Lactate Dehydrogenase (LDH), Acute Phase Reactants, Alkaline Phosphatase (AF).

Determination of microalbuminuria by immunoturbidimetric method (randox laboratories limited)

Reference values: Microalbuminuria 2.0-20.0 mg / L.

Determination of N-acetyl-α-D-glucosaminidase (NAG) activity: colorimetric method (Roche)

Principle: 3-Cresolsulfonphthaleinyl-N-Acetyl-α-D-glucosaminide, as sodium salt, is hydrolyzed by NAG to release 3-cresol-sulfonphthalein, sodium salt (3-cresol purple) which photometrically is measured at 5 nm (Roche mancheim kits). The urine that is examined previously is centrifuged and supernatants separated.

Reference values: NAG in urine 0.27-1.18 U / mmol creatine.

Statistical analysis

Two arithmetic means is testing of the differences between i.e. the corresponding proportions, the Student t-test is used, when comparing the mean values of the given number of parameters between two groups, such as Wilcoxon- matched test for independent samples. predictivity and sensitivity for negative and negative tests of the examined markers is determined with tests for sensitivity and specificity. Statistically significant is the P value of between 0.05 and 0.1 is considered. Statistical package Statistica 7.0 is used for data preceding.

Results

Between NAG and microalbuminuria, Pearson’s analysis of χ2 test showed that there was correlation, which was moderate (r=0.21) in the four samples tested during the period of 8 weeks in patient’s group treated only with Etoricoxib, while there was statistically significant correlation (r=0.28) between increase in NAG and microalbuminuria values ​​in the four samples in the period of 8 weeks in the group Diklofenak (Figure 1).

There is significance of the differences in the two groups in the group of treated with Etoricoxib, where the value mean of the microalbuminuria was (0.46 ± 0.37), while in the patients group treated with Diclofenac was (0.56 ± 0.41). This explains why Etoricoxib gives almost identical value to microalbuminuria in relation to Diclofenac.

Group of patients treated with Etoricoxib in relation to the distribution of patients according to the values ​​of NAG in the four groups, it was concluded that the values of NAG were registered in 4 patients in the 3rd week, when the mean value of NAG urinary induction was highest (1.12 ± 0.13).

It was concluded that NAG values ​​were registered in 6 patients in the 3rd week, when the mean value of NAG urinary induction was highest (1.41 ± 0.31). Analyzing patient’s distributions according to NAG values in the four probes in the group of patients treated only with Diclofenac.

Discussion

Approaches for the assessment of nephrotoxicity of drugs are possible only with drugs or medications that have a dominant proximal tubular excretion, such as Methotrexate, Etoricoxib, Diclofenac, Acetaminophen and gold salts. This approach for the assessment of nephrotoxicity of drugs is not possible with other medications or drugs from the baseline which are used in the treatment of RA, such as resorhin, sulfazalazine and leflunomide, due to predominantly hepatic excretion. For these preparations there are no literarature data on the occurrence of proximal tubular dysfunction.

Methotrexate in the low-dose regimen is the most commonly used drug from the DMARDs group, while from the NSAIL group the most commonly used drug is Diclofenum (DiklofenakR), as well as Etoricoxib (ArcoxiaR).

In the non-treated RA primarily is damaged tubular and to a very small extent the glomerular apparatus [19]. Significant increase in the activity is due to changes in cellular synthesis and not always the enzymuria may result in lytic or necrotic processes.

Etoricohib does not cause significant damage to the renal proximal tubules in the most of monitored patients. The nephrotoxicity during the use of Diclofenac is greater in relation to Etoricohib. Diclofenac is discretely more potent NAG inductor in relation to Etoricohib. These observations correspond with other authors [20,21].

Early detection of increased NAG enzymuria or occurrence of microalbuminuria before exposure to drugs may be used for prediction of possible toxicity associated with renal impairment.

There was not any change in clinical findings of renal function in relation to degradation products of nitrogen metabolism (serum creatine, urea / serum, GFR) during the follow-up.

Conclusion

Enzymura detected with urinary NAG, together with degradation product with urinary creatinine excretion may be considered as a complementary diagnostic tool.

The results obtained in some studies confirmed the safety of Etoricoxib and Diclofenac in the treatment of RA.

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