Gender Is a Risk Factor for Annual Decline in Estimated Glomerular Filtration Rate in Patients Treated with Biological DMARDs in Rheumatoid Arthritis and Ankylosing Spondylitis: a Retrospective Observational Study

Seong-Kyu Kim; Jung-Yoon Choe

doi:10.3346/jkms.2018.33.e188

Journal List > J Korean Med Sci > v.33(30) > 1107866

Go to TopGo to Top Go to BottomGo to Bottom

TOOLS

Kim and Choe: Gender Is a Risk Factor for Annual Decline in Estimated Glomerular Filtration Rate in Patients Treated with Biological DMARDs in Rheumatoid Arthritis and Ankylosing Spondylitis: a Retrospective Observational Study

Original Article

Immunology, Allergic Disorders & Rheumatology

Journal of Korean Medical Science 2018; 33(30): e188.

Published online: 28 May 2018

DOI: https://doi.org/10.3346/jkms.2018.33.e188

Gender Is a Risk Factor for Annual Decline in Estimated Glomerular Filtration Rate in Patients Treated with Biological DMARDs in Rheumatoid Arthritis and Ankylosing Spondylitis: a Retrospective Observational Study

Seong-Kyu Kim

, Jung-Yoon Choe

Division of Rheumatology, Department of Internal Medicine, Arthritis and Autoimmunity Research Center, Daegu Catholic University School of Medicine, Daegu, Korea.

Address for Correspondence: Seong-Kyu Kim, MD, PhD. Division of Rheumatology, Department of Internal Medicine, Arthritis and Autoimmunity Research Center, Daegu Catholic University School of Medicine, 33 Duryugongwon-ro 17-gil, Nam-gu, Daegu 42472, Republic of Korea. kimsk714@cu.ac.kr

Received 5 April 2018 Accepted 8 May 2018

The Korean Academy of Medical Sciences

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

This study identified the risk factors of changes in renal function in patients with rheumatoid arthritis (RA) and ankylosing spondylitis (AS) treated with biological disease-modifying anti-rheumatic drugs (bDMARDs).

Methods

We retrospectively enrolled patients with RA (n = 293) and AS (n = 125) treated with bDMARDs. The estimated glomerular filter rate (eGFR) using the Modification of Diet in Renal Disease equation was applied for assessment of annual changes in renal function between initiation and last visit after bDMARD therapy. The annual change in eGFR was used as an indicator for change in renal function. Statistical significance was assessed by Mann-Whitney test, Spearman's correlation coefficient, and multivariate linear regression analysis.

Results

The positive annual change in eGFR in women was significantly noted, compared to that in men (P = 0.004). The annual change in eGFR was different between men and women (P = 0.038) in RA, but not in AS patients (P = 0.126). In multivariate linear regression analysis, women patients and increased serum creatinine at baseline were closely associated with positive annual change in eGFR in both RA and AS patients. In RA patients, younger age and lower ESR level were considered risk factors of positive annual change in eGFR (P = 0.013 and P = 0.022, respectively). However, disease duration and duration of bDMARD use were not associated with annual change in eGFR.

Conclusion

This study found that gender, especially men, might be responsible for annual decline in eGFR in RA and AS patients treated with bDMARDs.

Graphical Abstract

Keywords: Rheumatoid Arthritis, Ankylosing Spondylitis, bDMARDs, Renal Function, eGFR

INTRODUCTION

Biological disease-modifying anti-rheumatic drugs (bDMARDs) have emerged as an available therapeutic option to treat inflammatory rheumatic diseases including rheumatoid arthritis (RA) and axial spondyloarthritis including ankylosing spondylitis (AS),1 2 combined with and without conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs). The profiles of safety and tolerability of bDMARDs frequently used in RA and AS have been approved to be generally acceptable in clinical studies during the past several decades, although the frequency of some adverse effects including injection site reaction, infection, cardiovascular disease, and hematologic diseases has been gradually increasing.3 4

Some evidence has suggested that the use of bDMARDs might be related to a beneficial or adverse effect on renal function. Although there is a small number of renal abnormalities caused by bDMARDs, autoimmune renal parenchymal diseases have been reported after therapeutic uses of bDMARDs such as tumor necrosis factor (TNF) inhibitors, cytotoxic T lymphocyte antigen 4 (CTLA4)-immunoglobulin, and interleukin-6 (IL-6) receptor antagonist.5 6 7 8 9 In contrast, some studies have shown that TNF inhibitors were not associated with worsening renal function even in patients with impaired renal function.10 11 In another study, TNF inhibitors improved the annual change of estimated glomerular filter rate (eGFR) in RA patients with chronic renal disease.12 Nevertheless, debate about the effect of bDMARDs on renal function continues. There is still the possibility that bDMARDs cause the change of renal function before the occurrence of overt renal diseases in subjects with normal renal function.

In our previous analysis, bDMARDs did not influence renal function based on analysis of the interaction between TNF inhibitors and renal function in patients with RA from the Korean College of Rheumatology Biologics (KOBIO) registry from 2012 to 2016.13 However, eGFR in RA patients treated with bDMARDs gradually declined over time. Until now, there has been a lack of data related to risk factors for the change in renal function in patients after initiation of bDMARDs. Here, we retrospectively assessed the risk factors related with the change in renal function using eGFR in RA and AS patients treated with diverse kinds of bDMARDs.

METHODS

Subjects

This study retrospectively enrolled 373 patients who met the 1987 American College of Rheumatology revised classification criteria for RA14 and 139 patients who met the modified New York criteria for AS15 and who were treated with bDMARDs such as TNF inhibitors (infliximab, etanercept, adalimumab, and golimumab) or non-TNF inhibitors (abatacept and tocilizumab) from January 2007 to November 2017. At the time of initiation of bDMARDs, patients with renal insufficiency (< 60 mL/min/1.73 m² of eGFR) or overt chronic kidney disease (CKD) with/without glomerulonephritis were not enrolled in this study. Among initially enrolled patients, 49 patients with RA were excluded in this study due to discontinuation by adverse effects or clinical improvement (n = 13), follow-up loss (n = 21), and uses of tofacitinib (Janus kinase inhibitor) or rituximab (monoclonal anti-CD20 antibody; n = 15) (Fig. 1). In addition, 31 RA patients who experienced switching between TNF inhibitors and non-TNF inhibitors were also excluded. In patients with AS, 14 patients were also not included due to discontinuation and follow-up loss. Among patients treated with bDMARDs during the same period. Patients with other rheumatic diseases including systemic lupus erythematosus, Sjogren's syndrome, psoriatic arthritis, systemic sclerosis, adult-onset Still disease, inflammatory myositis, and Behcet's disease were excluded. During bDMARDs therapy, participation of patients who experienced switching between TNF inhibitors or between non-TNF inhibitors was allowed. However, patients performed switching between TNF inhibitors and non-TNF inhibitors were also excluded.

Fig. 1

Flow chart illustrating study design and recruitment of study population.

bDMARDs = biological disease modifying anti-rheumatic drugs.

Collection of clinical information

The study used the standardized case record form. The form was recorded by an experienced research nurse to minimize the errors and bias of the data and also verified by two researchers (Kim SK and Choe JY). The case form collected information regarding clinical and laboratory data from patients with RA and AS at the time of initiation of bDMARDs or last visit such as age, gender, disease duration, duration of bDMARD use, blood urea nitrogen (BUN), creatinine, erythrocyte sediment rate (ESR), and C-reactive protein (CRP). In RA, rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibody and disease activity score 28-ESR (DAS28-ESR) were identified at the time of initiation of bDMARDs and last visit. The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and HLA-B27 positivity was also recorded in patients with AS. csDMARDs including methotrexate, hydroxychloroquine, sulfasalazine, and leflunomide used at the time of initiation of bDMARDs were identified. We also recorded the use of corticosteroid and nonsteroidal anti-inflammatory drugs (NSAIDs).

Estimation of renal function

Renal function was estimated by the MDRD equation using the variables serum creatinine, age, and gender. The equation was as follows: eGFR (mL/min/1.73 m²) = 175 × (serum creatinine)^−1.154 × (age)^−0.203 × (0.742 if women).16 17 The annual change of eGFR was calculated as (eGFR at last visit −eGFR at initial visit)/(time elapsed between initial and last visits).12 In this study, positive annual change in eGFR is defined as improvement of eGFR in renal function during bDMARDs treatment.

Sample size

The design of this study was to analyze the difference of dependent variable (annual change of eGFR) in a single study population with inflammatory rheumatic diseases such as RA and AS treated with bDMARDs. To explore sample size estimations in this study using the formula below, we applied 0.025 of α/2 (significance level), 0.200 of β (power), 20.000 of standard deviation and 2.500 of δ Estimated sample size was 502.3 patients. If 0.010 of drop rate in estimated sample size is applied, total sample size is 558.1 patients.

$n = {\{\frac{(Z_{α / 2} + Z_{β}) \cdot \hat{σ}}{δ}\}}^{2}$ jkms-33-e188-e001

Statistical analysis

Kolmogorov-Smirnov and Shapiro-Wilk tests were used to assess the normal distribution for all clinical and experimental data, which revealed non-normal distribution of all assessed parameters. The data were described as median ± interquartile range (IQR) for continuous variables and number and percentage (%) for non-continuous variables.

The correlations between clinical variables and change in eGFR were assessed by Spearman's correlation coefficient method. Independent-sample Mann-Whitney test was used to assess the difference in the change of eGFR between two groups (men vs. women, RA vs. AS, and TNF inhibitors vs. non-TNF inhibitors). An independent-sample Kruskal-Wallis test was used to compare the change in eGFR among all bDMARDs. To determine the risk factors associated with positive annual change of eGFR, univariate linear regression was applied between clinical and laboratory parameters and change of eGFR. To the next step, multivariate linear regression analysis was performed to identify candidate variables for positive annual change of eGFR using covariates such as age, gender, disease duration, duration of bDMARDs use, BUN, creatinine, or ESR. A P value less than 0.05 was considered statistically significant. Statistical analysis was performed using IBM SPSS Statistics 25.0 (IBM Corp., Armonk, NY, USA).

Ethics statement

This study was ethically approved by the Institutional Review Board at Daegu Catholic University Medical Center (CR-18-044). Informed consent was exempted because the data were examined retrospectively from medical records.

RESULTS

Baseline characteristics of enrolled subjects

The baseline characteristics of enrolled patients are illustrated in Table 1. There was a total of 418 patients (283 women, 67.7%) including 293 RA (261 women, 89.1%) and 125 AS (22 women, 17.6%) patients. The disease duration and duration of bDMARD use in enrolled subjects were a median of 11 years (IQR 7.0, 16.3) and 4 years (IQR 2.0, 6.0), respectively. Laboratory markers of BUN, creatinine, ESR, and CRP and disease activity indexes pf DAS28-ERS for RA and BASDAI for AS were recorded at the time of initiation of bDMARDs. Any medications currently used were also identified. TNF inhibitors including infliximab, etanercept, adalimumab, and golimumab accounted for 69.4% (n = 290) of medications. Across all patients, 56.3% of RA (n = 165) patients and 100% of AS patients (n = 125) were treated with TNF inhibitors.

Table 1

Baseline characteristics in enrolled patients treated with bDMARDs

Clinical variables		Total (n = 418)	RA (n = 293)	AS (n = 125)
Age, yr		52.0 (40.0, 61.0)	57.0 (48.0, 64.0)	39.0 (31.0, 47.0)
Gender, women, No. (%)		283 (67.7)	261 (89.1)	22 (17.6)
Disease duration, yr		11.0 (7.0, 16.3)	10.0 (6.5, 16.5)	11.0 (7.0, 16.5)
RF positivity, No. (%)			243 (82.9)
Anti-CCP antibody positivity, No. (%)^a			239 (81.8)
HLA-B27 positivity, No. (%)				117 (93.6)
Duration of bDMARDs use, yr		4.0 (2.0, 6.0)	3.0 (2.0, 5.0)	5.0 (3.0, 8.0)
BUN, mg/dL		13.8 (11.4, 16.8)	14.2 (11.4, 17.5)	13.2 (11.3, 16.1)
Creatinine, mg/dL		0.7 (0.6, 0.8)	0.7 (0.6, 0.7)	0.8 (0.7, 0.9)
eGFR, mL/min/1.73 m²		99.9 (84.7, 111.3)	99.1 (84.2, 108.4)	101.9 (89.1, 119.1)
ESR, mm/hr		43.0 (28.0, 64.8)	47.0 (31.5, 67.0)	32.0 (17.0, 55.0)
CRP, mg/L		16.6 (7.4, 32.7)	17.2 (8.4, 35.2)	14.8 (5.4, 29.3)
DAS28-ESR			6.5 (6.2, 7.0)
BASDAI				6.9 (6.0, 7.6)
Current medications
csDMARDs, No. (%)
	Methotrexate	332 (79.4)	272 (92.8)	60 (48.0)
	Hydrochloroquine	156 (52.9)	156 (53.2)	0 (0.0)
	Sulfasalazine	197 (47.1)	105 (35.8)	92 (73.6)
	Leflunomide	44 (10.5)	42 (14.3)	2 (1.6)
Corticosteroid, No. (%)		363 (86.8)	278 (94.9)	85 (68.0)
NSAIDs, No. (%)		407 (97.4)	287 (98.0)	120 (96.0)
bDMARDs, No. (%)
	Infliximab	46 (11.0)	8 (2.7)	38 (30.4)
	Etanercept	107 (25.6)	73 (24.9)	34 (27.2)
	Adalimumab	124 (29.7)	81 (27.6)	43 (34.4)
	Golimumab	13 (3.1)	3 (1.0)	10 (8.0)
	Abatacept	59 (14.1)	59 (20.1)	0 (0.0)
	Tocilizumab	69 (16.5)	69 (23.5)	0 (0.0)

Data are described as median ± interquartile range or number (%) and calculated by Student's t-test for continuous variables and χ² test for categorical variables.

bDMARDs = biological disease modifying anti-rheumatic drugs, RA = rheumatoid arthritis, AS = ankylosing spondylitiss, RF = rheumatoid factor, CCP = cyclic citrullinated peptide, BUN = blood urea nitrogen, eGFR = estimated glomerular filtration rate, ESR = erythrocyte sedimentation rate, CRP = C-reactive protein, DAS = disease activity score, BASDAI = bath ankylosing spondylitis disease activity index, csDMARDs = conventional synthetic disease modifying anti-rheumatic drugs, NSAIDs = non-steroidal anti-inflammatory drugs.

^aOne patient did not assess anti-CCP antibody.

Comparison of annual changes in renal function

First, the annual change in eGFR among bDMARDs in total patients irrespective of disease entity was compared (Fig. 2A). We found no significant difference in annual change in eGFR among all patients (P = 0.634). In addition, there was a similar annual change in eGFR between patients treated with TNF inhibitors and those treated with non-TNF inhibitors (−0.415 [IQR −5.378, 3.848] vs. −0.352 [IQR −8.715, 5.733], P = 0.946; Fig. 2B). In patients with RA, the change in eGFR from TNF inhibitors (n = 165) was not different from that induced by non-TNF inhibitors (n = 128) (−0.335 [IQR −4.538, 3.850] vs. −0.352 [IQR −8.715, 5.733], P = 0.475).

Fig. 2

Comparison for annual change of eGFR according to kinds of bDMARDs.

eGFR = estimated glomerular filtration rate, bDMARDs = biological disease-modifying anti-rheumatic drug, TNFi = tumor necrosis factor inhibitor.

The annual change in eGFR in RA patients treated with bDMARDs was similar to that in AS patients (−0.343 [IQR −6.475, 5.173] vs. −0.654 [IQR −5.784, 3.537], P = 0.127; Fig. 3A). Fig. 3B shows that a smaller annual change in eGFR was noted in woman patients compared to man patients (−0.342, [IQR −5.745, 5.501] vs. −0.700, [IQR −8.019, 1.708], P = 0.004). In RA patients, change in renal function in women was significantly less than that in man patients (−0.335 [IQR −5.785, 5.431) vs. −2.411 [IQR −9.179, −0.252], P = 0.038; Fig. 3C). However, there was no difference in change in eGFR between man and woman AS patients (P = 0.126; Fig. 3D).

Fig. 3

Comparison of annual change of eGFR according to disease entity and gender.

eGFR = estimated glomerular filtration rate, RA = rheumatoid arthritis, AS = ankylosing spondylitis.

Determination of risk factor for annual change in renal function

In the assessment of association between clinical variables and change in renal function, disease duration, duration of bDMARD use, BUN, creatinine, and ESR were significantly associated with positive annual change in eGFR in the total patients (Table 2). RA patients with high BUN and creatinine levels and lower ESR level showed an increasing trend for annual change in eGFR (P = 0.010, P < 0.001 and P = 0.030, respectively). Longer disease duration and duration of bDMARD use and high creatinine level were associated with positive annual change in eGFR in AS patients (P < 0.001 of all).

Table 2

Correlation analysis between variables and positive annual change in eGFR

Variables^a	Annual change of eGFR
Variables^a	Total (n = 418)	RA (n = 293)	AS (n = 125)
Age	r = 0.032, P = 0.517	r = −0.010, P = 0.862	r = 0.034, P = 0.707
Disease duration	r = 0.141, P = 0.004	r = 0.072, P = 0.219	r = 0.316, P < 0.001
Duration of bDMARDs use	r = 0.110, P = 0.024	r = 0.076, P = 0.193	r = 0.321, P < 0.001
BUN	r = 0.139, P = 0.004	r = 0.150, P = 0.010	r = 0.113, P = 0.208
Creatinine	r = 0.275, P < 0.001	r = 0.341, P < 0.001	r = 0.464, P < 0.001
RF		r = −0.012, P = 0.837
Anti-CCP antibody		r = −0.011, P = 0.856
CRP	r = −0.062, P = 0.206	r = −0.113, P = 0.053	r = 0.054, P = 0.561
ESR	r = −0.103, P = 0.036	r = −0.126, P = 0.030	r = −0.113, P = 0.223
DAS28-ESR		r = −0.111, P = 0.067
BASDAI			r = −0.142, P = 0.124

The statistical analysis was performed by Spearman's correlation analysis.

eGFR = estimated glomerular filter rate, RA = rheumatoid arthritis, AS = ankylosing spondylitis, bDMARDs = biological disease modifying anti-rheumatic drugs, BUN = blood urea nitrogen, RF = rheumatoid factor, CCP = cyclic citrullinated peptide, CRP = C-reactive protein, ESR = erythrocyte sedimentation rate, DAS = disease activity score, BASDAI = bath ankylosing spondylitis disease activity index.

^aVariables are the baseline values at the initiation of bDMARDs except for disease duration and duration of bDMADs use.

In the determination of risk factors related to annual change of eGFR by multivariate linear regression analysis, gender, age, serum creatinine, and ESR level at baseline in total patients were considered risk factors for positive annual change in eGFR (Table 3). RA patients with younger age and lower ESR level showed an increasing tendency for annual change in eGFR (P = 0.013 and P = 0.022, respectively). Women and increased creatinine in patients with RA and AS was associated with positive annual change in eGFR.

Table 3

Determination of the risk factors for positive annual change in eGFR

Variables^a	Total (n = 418)		RA (n = 293)		AS (n = 125)
Variables^a	β, 95% CI for β	P value	β, 95% CI for β	P value	β, 95% CI for β	P value
Gender, men	−10.800 (−14.123, −7.478)	< 0.001	−8.741 (−13.951, −3.530)	0.001	−12.394 (−18.624, −6.165)	< 0.001
Age	−0.132 (−0.239, −0.025)	0.016	−0.171 (−0.306, −0.036)	0.013	−0.119 (−0.320, 0.083)	0.246
Disease duration	0.061 (−0.131, 0.253)	0.534			0.220 (−0.207, 0.647)	0.309
Duration of bDMARDs use	0.135 (−0.427, 0.698)	0.636			0.170 (−0.651, 0.990)	0.683
BUN	0.224 (−0.099, 0.547)	0.174	0.259 (−0.130, 0.648)	0.191
Creatinine	29.916 (21.483, 38.350)	< 0.001	28.718 (18.046, 39.389)	< 0.001	34.489 (21.466, 47.513)	< 0.001
ESR	−0.059 (−0.106, −0.011)	0.015	−0.067 (−0.124, −0.010)	0.022

The statistical analysis was performed by multivariate linear regression analysis. Data were expressed as correlation coefficient (β) and P values for selected clinical variables.

eGFR = estimated glomerular filter rate, RA = rheumatoid arthritis, AS = ankylosing spondylitis, CI = confidence interval, bDMARDs = biological disease modifying anti-rheumatic drugs, BUN = blood urea nitrogen,ESR = erythrocyte sedimentation rate.

^aVariables are the baseline values at the initiation of bDMARDs except for disease duration and duration of bDMADs use.

DISCUSSION

There is growing interest in determining whether bDMARDs used in patients with RA and AS affect renal function or the development of renal diseases. One study of RA patients with CKD demonstrated that bDMARDs contributed to improvement in annual change of eGFR.12 However, it was noted that the trend toward eGFR decline is persistent over time even after administration of bDMARDs in patients with RA.13 18 In other way, there is a lack of data on the effect of bDMARD therapy on change in renal function in patients with AS. In the present study, we confirmed the statistical tendency of eGFR decline in RA patients treated with bDMARDs, although bDMARD therapy has a beneficial effect on renal function in some patients. Similar to RA, this study found decreased eGFR in AS patients before and after administration of TNF inhibitors, which showed a worse change in eGFR from bDMARDs in AS than RA. Although it does not provide sufficient information on the interrelationships between bDMARDs and the change of eGFR, it may suggest that bDMARDs have at least a partial effect on renal function.

The prevalence of renal disorders or impaired renal function in RA and AS was not accurately identified. Renal diseases in 5%–50% of RA patients were variably reported dependent on study population and design,19 whereas prevalence of renal disorders in AS was lower than 10%.20 21 The main causes of renal diseases have been found to be related with analgesic-induced nephropathy, chronic inflammation, secondary renal amyloidosis, and immune-mediated glomerulonephritis in patients with RA19 22 23 and AS.20 21 24 It was found that the use of bDMARDs irrespective of therapeutic target molecules (e.g., TNF, CTLA4, and IL-6) was associated with development of overt renal disorders in patients with various rheumatic diseases including RA, AS, Sjogren's syndrome, and psoriatic arthritis.5 6 7 8 9 Although development of these autoimmune-mediated renal diseases after use of bDMARDs is rare, most events occurred in patients treated with TNF inhibitors. The pathogenic mechanisms for bDMARD-induced renal disorders have not been identified. But, some have suggested the hypothesis that immune complex deposition or upregulation of autoantibody and inflammatory cytokine production can produce renal tissue damage.5 Especially, it has been proposed that there is an increase in TNF inhibitors due to autoantibodies such as ANA and anti-dsDNA produced as part of the shift to the Th-2 immune system.25 Molecular mimicry by increased susceptibility to infection after TNF inhibitors was also suggested as a causative mechanism.26 In addition, development of biologics-related renal disorders has rarely been reported in relatively new bDMARDs (non-TNF inhibitors) such as abatacept and tocillizumab.8 9 Non-TNF inhibitors may be more favorable with regard to change in renal function than TNF inhibitors. However, a previous study demonstrated that the change in eGFR between TNF inhibitors and non-TNF inhibitors was not different in the KOBIO data from 2012 to 2016.13 In our present study, the annual change in eGFR in all patients or all RA patients was also similar among bDMARDs. In contrast, some studies have demonstrated that TNF inhibitor therapy improves renal abnormalities including proteinuria and AA amyloidosis in RA and AS.21 27 28 Further research is needed to determine whether the type of bDMARDs affects the phenotype or severity of renal diseases.

In the present study, we estimated the risk factors affecting annual change in eGFR in patients with RA and AS. Interestingly, this study showed more eGFR decline in man patients than woman patients after bDMRAD therapy. In general, renal diseases in man subjects were more prevalent than in woman subjects.29 It is known that gender can influence the progression of renal disease including CKD.30 Sex hormones are involved in gender-specific differentiation and homeostasis of various organs including kidney, resulting in differences in renal function.31 The precise mechanism for gender-related nephrotoxicity has not been elucidated. TNF and TNF receptors may be relevant to inflammatory injury and immune regulation of kidneys, supporting a rationale for TNF blocking therapy in some nephropathy.32 Estrogen-depleted female mice significantly increased expression of the renal inflammatory cytokines including TNF and monocyte chemotactic protein-1 and tubular injury compared to estrogen-supplemented ovariectomized mice.33 Cyclosporin A was noted to result in renal TNF expression that was attenuated in female rats, but not in male rats.34 This result might suggest that the renal effect of bDMARDs might be associated with gender-specific nephrotoxicity.

In the present study, positive annual change in eGFR was observed in patients with younger age and lower ESR level at the time of initiation of bDMARDs. Aging is a crucial determinant for progressive structural change and functional decline of kidney.35 With aging, decreased production of nitric oxide (NO) and enhanced oxidative stress through decreased endothelial NO synthase was noted, suggesting that bDMARDs in patients with lower grade inflammation at younger age rather than older age are more likely to have improvement in renal function. Oxidative stress has been considered a potent therapeutic target in chronic inflammatory arthritis including RA and AS. Infliximab markedly suppressed oxidative molecule markers such as malondialdehyde + 4-hydroxyalkenals and protein carbonyls in patients with RA, AS, and psoriatic arthritis.36 Another risk factor related to annual change of eGFR in our present study was serum creatinine level at baseline. Interestingly, patients with increased creatinine level at baseline showed improvement in renal function with an increase in annual eGFR. This finding suggests the possibility of recovery of renal function after treatment with bDMARDs. Treatment with TNF inhibitors in RA with CKD was found to be associated with positive annual change in eGFR.12 In contrast, another study showed no significant difference in change in eGFR in RA with renal insufficiency.13 Considering this evidence, we suggest that bDMARDs contribute to protective effects on renal function.

There were some limitations in this study. First, this study was retrospectively performed, because regular follow-up of changes in renal function may give more confidence to the results. In this study, the use of data only from the initiation of bDMARDs to the beginning of the study can be evaluated as a weak point. However, this is thought to be overcome by using data for a relatively large number of patients. Second, the covariates related with renal function included comorbidities such as hypertension, hyperglycemia, dyslipidemia, body mass index, and lifestyle factors. These confounding factors were not considered in the analysis of this study. To overcome these issues, further prospective study including all covariates that can affect renal function will be needed in a larger study population.

Until now, there has been a lack of data about crucial risk factors for annual change in eGFR in the course of bDMARD administration. The main finding of this study is that gender might be associated with annual change in eGFR in patients treated with bDMARDs, and man patients treated with bDMARDs were found to be more susceptible to worse renal function. Further study is needed to determine if gender-specific nephrotoxicity might contribute to renal outcome in patients treated with bDMARDs.

ACKNOWLEDGMENTS

We thank to the research nurse (Hyo-Jeong Lee, RN) who helped organize the data. The editing service for this manuscript was provided by eWorldEditing, Inc. (Eugene, OR, USA).

Notes

^Disclosure The authors have no potential conflicts of interest to disclose.

^{Author Contributions}

Conceptualization: Kim SK.
Data curation: Kim SK, Choe JY.
Formal analysis: Kim SK.
Investigation: Kim SK.
Validation: Kim SK, Choe JY.
Writing - original draft: Kim SK.
Writing - review & editing: Kim SK, Choe JY.

References

1. Burmester GR, Pope JE. Novel treatment strategies in rheumatoid arthritis. Lancet. 2017; 389(10086):2338–2348.

2. Sieper J, Poddubnyy D. Axial spondyloarthritis. Lancet. 2017; 390(10089):73–84.

3. Ramiro S, Sepriano A, Chatzidionysiou K, Nam JL, Smolen JS, van der Heijde D, et al. Safety of synthetic and biological DMARDs: a systematic literature review informing the 2016 update of the EULAR recommendations for management of rheumatoid arthritis. Ann Rheum Dis. 2017; 76(6):1101–1136.

4. Sepriano A, Regel A, van der Heijde D, Braun J, Baraliakos X, Landewé R, et al. Efficacy and safety of biological and targeted-synthetic DMARDs: a systematic literature review informing the 2016 update of the ASAS/EULAR recommendations for the management of axial spondyloarthritis. RMD Open. 2017; 3(1):e000396.

5. Piga M, Chessa E, Ibba V, Mura V, Floris A, Cauli A, et al. Biologics-induced autoimmune renal disorders in chronic inflammatory rheumatic diseases: systematic literature review and analysis of a monocentric cohort. Autoimmun Rev. 2014; 13(8):873–879.

6. Stokes MB, Foster K, Markowitz GS, Ebrahimi F, Hines W, Kaufman D, et al. Development of glomerulonephritis during anti-TNF-alpha therapy for rheumatoid arthritis. Nephrol Dial Transplant. 2005; 20(7):1400–1406.

7. Hanzu-Pazara L, Muflic L, Dusa D, Pana C, Tudorache M, Suta M, et al. Renal disease in patients with rheumatoid arthritis related with biological therapy. ARS Medica Tomitana. 2016; 22(1):50–55.

8. Michel M, Henri P, Vincent FB, Leon N, Marcelli C. Mesangial immunoglobulin (Ig)A glomerulonephritis in a patient with rheumatoid arthritis treated with abatacept. Joint Bone Spine. 2013; 80(6):660–663.

9. Matsuo Y, Mizoguchi F, Kohsaka H, Ito E, Eishi Y, Miyasaka N. Tocilizumab-induced immune complex glomerulonephritis in a patient with rheumatoid arthritis. Rheumatology (Oxford). 2013; 52(7):1341–1343.

10. Hueber AJ, Tunc A, Schett G, Manger B. Anti-tumour necrosis factor alpha therapy in patients with impaired renal function. Ann Rheum Dis. 2007; 66(7):981–982.

11. Sumida K, Ubara Y, Suwabe T, Hayami N, Hiramatsu R, Hasegawa E, et al. Adalimumab treatment in patients with rheumatoid arthritis with renal insufficiency. Arthritis Care Res (Hoboken). 2013; 65(3):471–475.

12. Kim HW, Lee CK, Cha HS, Choe JY, Park EJ, Kim J. Effect of anti-tumor necrosis factor alpha treatment of rheumatoid arthritis and chronic kidney disease. Rheumatol Int. 2015; 35(4):727–734.

13. Kim SK, Choe JY, Kwak SG, Bae J, Park SH, Lee H. Effect of tumor necrosis factor-α inhibitors on renal function in patients with rheumatoid arthritis from KOBIO registry from 2012 to 2016. Clin Exp Rheumatol. Forthcoming. 2018.

14. Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988; 31(3):315–324.

15. van der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. A proposal for modification of the New York criteria. Arthritis Rheum. 1984; 27(4):361–368.

16. Levey AS, Coresh J, Greene T, Stevens LA, Zhang YL, Hendriksen S, et al. Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate. Ann Intern Med. 2006; 145(4):247–254.

17. Levey AS, Coresh J, Greene T, Marsh J, Stevens LA, Kusek JW, et al. Expressing the modification of diet in renal disease study equation for estimating glomerular filtration rate with standardized serum creatinine values. Clin Chem. 2007; 53(4):766–772.

18. Sumida K, Molnar MZ, Potukuchi PK, Hassan F, Thomas F, Yamagata K, et al. Treatment of rheumatoid arthritis with biologic agents lowers the risk of incident chronic kidney disease. Kidney Int. 2018; 93(5):1207–1216.

19. Karie S, Gandjbakhch F, Janus N, Launay-Vacher V, Rozenberg S, Mai Ba CU, et al. Kidney disease in RA patients: prevalence and implication on RA-related drugs management: the MATRIX study. Rheumatology (Oxford). 2008; 47(3):350–354.

20. Lange U, Stapfer G, Ditting T, Geiger H, Teichmann J, Müller-Ladner U, et al. Pathologic alterations of the heart and the kidney in patients with ankylosing spondylitis. Eur J Med Res. 2007; 12(12):573–581.

21. Lee SH, Lee EJ, Chung SW, Song R, Moon JY, Lee SH, et al. Renal involvement in ankylosing spondylitis: prevalence, pathology, response to TNF-alpha blocker. Rheumatol Int. 2013; 33(7):1689–1692.

22. Koseki Y, Terai C, Moriguchi M, Uesato M, Kamatani N. A prospective study of renal disease in patients with early rheumatoid arthritis. Ann Rheum Dis. 2001; 60(4):327–331.

23. Hickson LJ, Crowson CS, Gabriel SE, McCarthy JT, Matteson EL. Development of reduced kidney function in rheumatoid arthritis. Am J Kidney Dis. 2014; 63(2):206–213.

24. Strobel ES, Fritschka E. Renal diseases in ankylosing spondylitis: review of the literature illustrated by case reports. Clin Rheumatol. 1998; 17(6):524–530.

25. Becher B, Blain M, Giacomini PS, Antel JP. Inhibition of Th1 polarization by soluble TNF receptor is dependent on antigen-presenting cell-derived IL-12. J Immunol. 1999; 162(2):684–688.

26. Prinz JC. Autoimmune-like syndromes during TNF blockade: does infection have a role? Nat Rev Rheumatol. 2011; 7(7):429–434.

27. Kobak S, Oksel F, Kabasakal Y, Doganavsargil E. Ankylosing spondylitis-related secondary amyloidosis responded well to etanercept: a report of three patients. Clin Rheumatol. 2007; 26(12):2191–2194.

28. Esatoglu SN, Hatemi G, Ugurlu S, Gokturk A, Tascilar K, Ozdogan H. Long-term follow-up of secondary amyloidosis patients treated with tumor necrosis factor inhibitor therapy: A STROBE-compliant observational study. Medicine (Baltimore). 2017; 96(34):e7859.

29. Yang W, Xie D, Anderson AH, Joffe MM, Greene T, Teal V, CRIC Study Investigators, et al. Association of kidney disease outcomes with risk factors for CKD: findings from the Chronic Renal Insufficiency Cohort (CRIC) study. Am J Kidney Dis. 2014; 63(2):236–243.

30. Carrero JJ. Gender differences in chronic kidney disease: underpinnings and therapeutic implications. Kidney Blood Press Res. 2010; 33(5):383–392.

31. Sabolić I, Asif AR, Budach WE, Wanke C, Bahn A, Burckhardt G. Gender differences in kidney function. Pflugers Arch. 2007; 455(3):397–429.

32. Vielhauer V, Mayadas TN. Functions of TNF and its receptors in renal disease: distinct roles in inflammatory tissue injury and immune regulation. Semin Nephrol. 2007; 27(3):286–308.

33. Kang KP, Lee JE, Lee AS, Jung YJ, Kim D, Lee S, et al. Effect of gender differences on the regulation of renal ischemia-reperfusion-induced inflammation in mice. Mol Med Rep. 2014; 9(6):2061–2068.

34. El-Bassossy HM, Eid BG. Cyclosporine A exhibits gender-specific nephrotoxicity in rats: effect on renal tissue inflammation. Biochem Biophys Res Commun. 2018; 495(1):468–472.

35. Weinstein JR, Anderson S. The aging kidney: physiological changes. Adv Chronic Kidney Dis. 2010; 17(4):302–307.

36. Túnez I, Feijóo M, Huerta G, Montilla P, Muñoz E, Ruíz A, et al. The effect of infliximab on oxidative stress in chronic inflammatory joint disease. Curr Med Res Opin. 2007; 23(6):1259–1267.

TOOLS

ORCID iDs

Seong-Kyu Kim
https://orcid.org/0000-0002-7780-0167

Jung-Yoon Choe
https://orcid.org/0000-0003-0957-0395

Similar articles