Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Relationship between renal tissues phospholipase A2 receptor and its serum antibody and clinical condition and prognosis of idiopathic membranous nephropathy: a meta-analysis

BMC Nephrology volume 20, Article number: 444 (2019) Cite this article

Abstract

Objective

To investigate the correlation of M-type phospholipase A2 receptor (PLA2R) expression and serum anti-PLA2R antibody with the clinical parameters and prognosis of patients with idiopathic membranous nephropathy (IMN).

Methods

A literature search for relevant original articles published between January 2009 and October 2019 was conducted on domestic and foreign databases. RevMan 5.3 software was used for meta-analysis.

Results

Eighteen studies were included in this meta-analysis. There were 1235 anti-PLA2R antibody-positive and PLA2R-positive patients, and 407 serum anti-PLA2R antibody-negative and PLA2R-negative patients. Compared with negative group, patients in the serum PLA2R antibody -positive group had lower serum albumin [SMD = -1.11, 95% CI (− 1.82, − 0.40), P < 0.00001], higher age [MD = 2.71, 95% CI (1.94, 3.48), P < 0.00001], and lower estimated glomerular filtration rate (eGFR) [MD = -10.34, 95% CI (− 12.09, − 8.60), P < 0.00001]; no significant between-group difference was observed with respect to 24-h urine protein and serum creatinine. However, no significant difference was observed between renal tissues PLA2R -positive and -negative groups with respect to serum albumin, eGFR, serum creatinine, and 24-h urine protein. Remission rate in the serum anti-PLA2R antibody -positive group was lower than that in the -negative group [OR = 0.41, 95% CI (0.28, 0.61),P < 0.00001]; however, no significant between-group difference in this respect was observed between the renal tissue PLA2R-positive and -negative groups. In the serum anti-PLA2R antibody -positive group, the higher titer subgroup had lower remission rate [OR = 0.19, 95% CI (0.07, 0.55),P = 0.002]. No significant difference was observed between anti-PLA2R antibody -positive and -negative groups with respect to adverse events. Serum anti-PLA2R antibody titer did not affect the adverse event rate.

Conclusion

As compared to PLA2R, serum anti-PLA2R antibody is more closely related with IMN disease progression.

Peer Review reports

Background

Membranous nephropathy (MN) refers to a group of kidney diseases characterized by thickened glomerular basement membrane (GBM) and deposition of immune complexes on the GBM. According to the etiology, MN is classified into two types: idiopathic membranous nephropathy (IMN) and secondary membranous nephropathy (SMN) [1]. Studies have shown that about 40% of patients with IMN eventually develop end-stage renal disease (ESRD) [2]. Phospholipase A2 receptor (PLA2R) is a protein with a relative molecular weight of 180–200 kD. It is expressed on the membrane of human podocytes and belongs to the family of mannose receptors [3]. Till date, two subtypes of PLA2R have been found, namely M-type and N-type [4]. PLA2R is widely distributed in various organs of the human body, such as lung, kidney, and placenta [5]. In the kidney, M-type PLA2R is mainly expressed in the cytoplasm and membrane of the podocytes [6]. In 2009, Beck et al. detected the anti-PLA2R antibody (anti-PLA2R Ab) in the serum of adult IMN patients and used it as a specific marker of IMN [7]. Since then, a series of studies [8,9,10,11,12] have demonstrated that renal expression of PLA2R and serum anti-PLA2R antibodies can be used for diagnosis, and prognostic assessment of patients with IMN. However, no systematic review has evaluated the relationship of PLA2R and serum anti-PLA2R antibodies with IMN disease. In the present study, we performed a meta-analysis of data from relevant published clinical studies to evaluate this relationship.

Methods

Eligibility criteria

Studies that qualified the following criteria were included: (1) study type: cohort study; (2) Patients were diagnosed as idiopathic membranous nephropathy by renal biopsy; (3) The exposure factors: the study group was positive for serum PLA2R antibody or kidney tissues were PLA2R -positive, and the control group was serum PLA2R antibody -negative or renal tissues PLA2R -negative. (4) primary endpoint was complete remission (as defined in the included study) or partial remission (as defined in the included study) at the end of follow-up; secondary endpoint was adverse events such as renal injury, continuous proteinuria, progression to ESRD, disease palindromia, and death.

The exclusion criteria were: (1) patients with SMN; (2) duplicate publications; (3) literature reviews and animal experiments; (4) studies that had a follow-up time of < 6 months.

Data sources and search strategy

Relevant studies published between January 2009 and October 2019 which investigated the relationship of PLA2R and its antibodies with the clinical parameters and prognosis of IMN were retrieved from Pubmed, EMBASE, MEDLINE, China Biomedical Literature Database, Chinese Journal Full-text Database, and Wanfang Database. We adopted joint search of free words and subject words. Chinese search terms included: glomerulonephritis, membranous nephropathy, M-type phospholipase A2, and cohort studies. English search terms included: “Glomerulonephritis, Membranous” [Mesh], “Receptors, Phospholipase A2” [Mesh], “Cohort Studies” [Mesh].

Document retrieval process and results

A total of 683 documents were retrieved on initial literature search. The title and abstracts were screened independently by two reviewers to eliminate irrelevant articles. Full text of the remaining documents was reviewed against the inclusion and exclusion criteria. In case of any disagreement between the two reviewers, the decision was taken by consensus or by a third reviewer.

Finally, only 18 relevant publications were selected for this meta-analysis [8, 10, 11, 13,14,15,16,17,18,19,20,21,22,23,24,25,26,27]. These studies included 1235 PLA2R-positive and serum anti-PLA2R antibody-positive patients and 407 PLA2R-negative and serum PLA2R antibody-negative patients. A schematic illustration of literature search and results is shown in Fig. 1. The basic characteristics and results of quality assessment of the included studies are shown in Table 1. We measured serum creatinine, serum albumin, 24 h urine protein, eGFR to reflect the impairment of renal function in patients before treatment in anti-PLA2R antibody-positive, anti-PLA2R antibody-negative, kidney tissues PLA2R -positive and -negative groups. The remission rate and adverse prognosis was used to reflect the prognosis after treatment in anti-PLA2R antibody, renal tissue PLA2R -positive and -negative groups.

Fig. 1
figure 1

Schematic illustration of the literature search and study selection criteria

Full size image
Table 1 Baseline characteristics of cohorts in all included studies
Full size table

Quality assessment

The Newcastle-Ottawa Scale (NOS) for quality assessment of non-randomized controlled studies was used to evaluate the quality of the included studies, including aspects such as selection of subjects, comparability between groups and measurement of results. The full score is 9, and a study received more than 5 was quality assessed. The quality assessment was performed independently by two reviewers; disagreements, if any, were resolved by consensus or by involvement of a third reviewer.

Statistical analysis

Meta-analysis was performed using RevMan 5.3 software. Mean difference (MD) and standardized mean difference (SMD) were used for continuous variables, while relative risk (RR) or odds ratio (OR) was used as effect size for categorical variables; 95% confidence intervals were calculated for both. Heterogeneity among the included studies was assessed using I2 statistic. In the absence of significant heterogeneity among the included studies (P > 0.1, I2 < 50%), a fixed effect model was used for meta-analysis; in case of significant heterogeneity (P < 0.1, I2 > 50%), a random effect model was used for meta-analysis. Publication bias was assessed by Egger’s test and Begg‘s test using Stata13.0 software.

Results

Comparison of serum albumin levels in anti-PLA2R antibody-positive, kidney tissues PLA2R -positive and -negative groups

Eight studies had reported serum albumin levels in IMN patients disaggregated by serum anti-PLA2R antibody-positive (n = 748) and -negative groups (n = 268). Owing to significant heterogeneity among the studies (P < 0.00001, I2 = 95%), a random effect model was used for the meta-analysis. Serum albumin level in anti-PLA2R antibody-positive patients was significantly lower than that in anti-PLA2R antibody-negative patients [SMD = -1.11, 95% CI (− 1.82, − 0.40), P = 0.002] (Fig. 2).

Fig. 2
figure 2

Meta-analysis of serum albumin levels: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Three studies had reported serum albumin levels in IMN patients disaggregated by renal tissue PLA2R-positive and -negative groups. Owing to the lack of significant heterogeneity among the studies (P = 0.95, I2 = 0%), the fixed effect model was used for the analysis. The results showed no significant between-group difference with respect to serum albumin levels [MD = -1.50, 95% CI (− 4.03, − 1.02), P = 0.24] (Fig. 3).

Fig. 3
figure 3

Meta-analysis of serum albumin levels: renal tissue PLA2R-positive group versus -negative group

Full size image

Comparison of age between renal tissue PLA2R-positive, anti-PLA2R antibody-positive and -negative groups

Eight studies reported the age of IMN patients disaggregated by anti-PLA2R antibody-positive (n = 596) and -negative (n = 205) groups. Owing to the lack of significant heterogeneity (P = 0.23, I2 = 25%), the fixed effect model was used for analysis. The results showed that age of patients in the anti-PLA2R antibody-positive group was significantly higher than that in the anti-PLA2R antibody-negative group [MD = 2.71, 95% CI (1.94, 3.48), P < 0.00001] (Fig. 4).

Fig. 4
figure 4

Meta-analysis of age: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Three studies reported the age of IMN patients disaggregated by renal tissue PLA2R-positive and -negative groups. Owing to the lack of significant heterogeneity among the studies (P = 0.93, I2 = 0%), the fixed effect model was used. The results showed no significant difference between the age of patients in the two groups [MD = -1.35, 95% CI (− 6.51, 3.80), P = 0.61] (Fig. 5).

Fig. 5
figure 5

Meta-analysis of age: renal tissue PLA2R-positive group versus -negative group

Full size image

Comparison of serum creatinine level between anti-PLA2R antibody -positive and -negative groups

Seven studies reported serum creatinine level in IMN patients disaggregated by serum anti-PLA2R antibody -positive (n = 610) and -negative (n = 230) groups. Owing to the lack of significant heterogeneity (P < 0.0001, I2 = 90%), the fixed-effect model was used for analysis. There was no significant difference between the two groups [SMD = 0.43, 95%CI (− 0.10, 0.97), P = 0.11] (Fig. 6).

Fig. 6
figure 6

Meta-analysis of serum creatinine: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Comparison of estimated glomerular filtration rate between anti-PLA2R antibody -positive and -negative groups

Five studies reported the estimated glomerular filtration rate (eGFR) of IMN patients disaggregated by serum anti-PLA2R antibody -positive (n = 381) and -negative (n = 149) groups. Owing to the lack of significant heterogeneity (P = 0.17, I2 = 38%), the fixed effect model was used. eGFR of patients in the serum anti-PLA2R antibody -positive group was significantly lower than that in the serum anti-PLA2R antibody-negative group [MD = -10.34, 95% CI(− 12.09, − 8.60), P < 0.00001] (Fig. 7).

Fig. 7
figure 7

Meta-analysis of eGFR: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Comparison of 24-h urine protein between serum anti-PLA2R antibody -positive and -negative groups

Four studies had reported 24-h urinary protein of IMN patients disaggregated by serum anti-PLA2R antibody -positive (n = 460) and -negative (n = 131) groups. Owing to significant heterogeneity among the studies (P = 0.06, I2 = 59%), the random effect model was used for analysis. The results showed no significant between-group difference in this respect [SMD = 0.27, 95% CI (− 0.07, 0.61), P = 0.12] (Fig. 8).

Fig. 8
figure 8

Meta-analysis of 24-h urine protein: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Comparison of clinical parameters between renal tissue PLA2R -positive and -negative groups

We also performed a meta-analysis of serum creatinine, 24-h urine protein, and eGFR in the renal tissue PLA2R-positive and -negative groups. The 95% confidence interval included 0, and P > 0.05. No significant between-group differences were observed in this respect (Table 2).

Table 2 Comparison of clinical parameters in renal tissues PLA2R-positive and -negative groups
Full size table

Comparison of remission rate between anti-PLA2R antibody, renal tissue PLA2R -positive and -negative groups

Ten studies reported the remission rate of IMN patients disaggregated by serum anti-PLA2R antibody -positive (n = 675) and -negative (n = 226) groups. Owing to the lack of significant heterogeneity among the studies (P = 0.23, I2 = 23%), the fixed effect model was used. The results of the meta-analysis were z = 4.47, P < 0.00001, and the difference was statistically significant (Fig. 9). The combined effect of OR was 0.41, 95% CI: (0.28, 0.61). When OR = 1.00, it indicated that serum anti-PLA2R antibody -positive status was not related to the rate of remission in IMN patients. When OR > 1.00, it indicated that anti-PLA2R antibody -positive status was related to the remission rate of IMN patients, and the remission rate was high for these patients. When OR < 1.00, it indicated that anti-PLA2R antibody -positive status was related to the remission rate, but had low remission rate. When OR was more distant from 1.00, it indicated greater strength of correlation. If the invalid value (1.00) is within 95% CI, it indicated the lack of statistical significance. In this analysis, the invalid value was not within 95% CI, but was farther away from the original value, which suggested that the expression of serum anti-PLA2R antibody reduced the remission rate of IMN patients with increase in the strength of correlation.

Fig. 9
figure 9

Meta-analysis of remission rate: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Three studies reported the complete remission rate of IMN patients disaggregated by renal tissue PLA2R -positive and -negative groups. Owing to the lack of significant heterogeneity among the studies (P = 0.002, I2 = 84%), the fixed effect model was used. The results showed no significant difference in the remission rate between the two groups [OR = 0.42, 95% CI (0.02, 8.02), P = 0.56] (Fig. 10).

Fig. 10
figure 10

Meta-analysis of the remission rate: renal tissue PLA2R-positive group versus -negative group

Full size image

Relationship of remission rate and titre levels of serum anti-PLA2R antibody

Five studies reported remission rates of serum anti-PLA2R antibody-positive IMN patients disaggregated by high-titer (n = 183) and low-titer (n = 120) groups. Owing to significant heterogeneity among the studies (P = 0.02, I2 = 66%), the random effect model was used. The results of the meta-analysis were z = 3.08, P = 0.002 < 0.05, and the difference was statistically significant (Fig. 11). The combined effects were OR = 0.19 (95% CI: 0.07, 0.55). The invalid value was not within the 95% CI, and the difference was statistically significant. Away from 1.00, suggesting that the high expression of serum anti-PLA2R antibody reduced the remission rate of IMN patients and the strength of correlation was greater.

Fig. 11
figure 11

Meta-analysis of remission rate: high-titer versus low-titer subgroups of the serum anti-PLA2R antibody -positive group

Full size image

Comparison of adverse prognosis of IMN patients with serum anti-PLA2R antibody positive and negative groups

Seven studies reported the occurrence of adverse prognosis in 590 IMN patients with serum anti-PLA2R antibody positive (n = 478) and negative (n = 112) groups. Owing to the lack of significant heterogeneity among the studies (P = 0.79, I2 = 0%), the fixed effect model was used. The meta-analysis results showed that z = 1.11, P = 0.27 > 0.05, and the difference was not statistically significant (Fig. 12). The combined effect was OR = 1.36, 95% CI: 0.79, 2.34, and the invalid value was 1.00 within 95% CI. The study suggested that there was no significant difference in the incidence of poor prognosis between the two groups of IMN patients.

Fig. 12
figure 12

Meta-analysis of adverse prognosis: serum anti-PLA2R antibody-positive group versus -negative group

Full size image

Comparison of adverse prognosis in the high-titer and low-titer anti-PLA2R antibody -positive subgroups

Three studies reported the occurrence of adverse prognosis in anti-PLA2R antibody-positive IMN patients disaggregated by high-titer (n = 96) and low-titer (n = 95) subgroups. Owing to significant heterogeneity among the studies (P = 0.23, I2 = 33%), the random effect was used. The results of meta-analysis were z = 1.46, P = 0.14 > 0.05, and the difference was not statistically significant (Fig. 13). The combined effects were OR 1.66, 95% CI: 0.84, 3.29, and the invalid value was within 95% CI. There was no significant difference in the incidence of adverse prognosis between the two sub-groups of anti-PLA2R antibody positive IMN patients.

Fig. 13
figure 13

Meta-analysis of adverse prognosis: high-titer versus low-titer subgroup of the serum anti-PLA2R antibody -positive group

Full size image

Assessment of publication bias

We also assessed publication bias using Egger’s test and Begg’s Test with Stata 13.0 software (Table 3). The results showed that for the comparison of serum anti-PLA2R antibody -positive and -negative groups, except for the age, all other factors were not statistically significant (P > 0.05); this suggested the absence of publication bias. For the comparison of serum anti-PLA2R antibody high- and low -titer subgroups, except for the remission rate, all other factors were not statistically significant (P > 0.05), which suggested that there was no publication bias. Comparison of serum albumin in serum anti-PLA2R antibody -positive and -negative groups and comparison of the remission rate in serum anti-PLA2R antibody high- and low -titer subgroups were associated with P value < 0.05, which was indicative of the presence of publication bias.

Table 3 Analysis of publication bias
Full size table

Discussion

IMN is the most common pathological type of nephrotic syndrome in the elderly people [28], and it is one of the major underlying causes of ESRD [2]. With the progress in understanding of its pathogenesis, IMN is now recognized as an autoimmune disease [29]. The clinical diagnosis of IMN mainly relies on renal biopsy. The patient’s condition and treatment effect are evaluated mainly by monitoring 24-h urine protein, serum albumin, and serum creatinine [30]. Although renal biopsy is the gold standard for diagnosis of IMN, the procedure is associated with a risk of bleeding and infection. Identification of relatively safe and convenient method for diagnosis and prognostic assessment of patients with IMN will confer a considerable leverage to nephrologists. As early as 2002, Debiec et al. [31] found that neutral endopeptidase is the target antigen of podocytes in membranous nephropathy; however, it is found in only a small proportion of IMN patients. A large number of studies have demonstrated the diagnostic relevance of serum anti-PLA2R antibodies in the context of IMN. In a meta-analysis [32], serum anti-PLA2R antibodies exhibited 68% sensitivity and 97% specificity for the diagnosis of IMN. A large body of evidence supports the relationship between PLA2R and the clinical course and prognosis of IMN. Wang J et al. [11] followed up 91 patients with pathologically confirmed IMN for 15 months. These included 78 serum anti-PLA2R antibody -positive patients and 13 serum anti-PLA2R antibody -negative patients; all patients were administered immunosuppressive therapy [glucocorticoid plus cyclophosphamide (n = 45); glucocorticoid plus calcineurin inhibitors (n = 46)]. They found that in the third and sixth month of treatment, the remission rate of serum anti-PLA2R antibody -positive patients was lower than that of -negative patients; in addition, serum anti-PLA2R antibody -negative patients showed a faster response to immunosuppressive therapy as compared to serum anti-PLA2R antibody -positive patients. Pang et al [33] found a positive correlation of serum anti-PLA2R antibody levels with serum albumin, serum creatinine, eGFR, and urinary protein. The glomerular PLA2R deposition intensity showed a weak correlation with proteinuria. They suggested that serum anti-PLA2R antibody more closely reflects the disease activity and renal function as compared to PLA2R. In a study by Wei et al. [34], serum anti-PLA2R antibody and renal tissue PLA2R positivity rates in IMN patients were 82.3 and 85.8%, respectively. Serum anti-PLA2R antibody titers were significantly associated with proteinuria in the first 20 months of follow-up. Moreover, changes in serum anti-PLA2R antibody levels preceded the changes in proteinuria. They concluded that serum PLA2R antibody titer, but not renal expression of PLA2R, reflects the prognosis of IMN. Studies [35] have also shown that the effect of immunosuppressive therapy on anti-PLA2R antibody titer in the first 3 months of treatment is a sensitive and specific predictor of therapeutic response at 6th and 9th month of treatment in patients with IMN; further, decrease in antibody at the 6th month was also shown to predict the response at the 12th month. These studies further suggest that serum anti-PLA2R antibodies and PLA2R are closely related to the disease activity and prognosis of IMN.

The present meta-analysis addresses a gap in contemporary literature in that this is the first meta-analysis of the clinical relevance and prognostic value of serum anti-PLA2R antibodies and renal expression of PLA2R in patients with IMN. The results showed that serum albumin and eGFR in serum anti-PLA2R antibody -positive group of IMN patients were lower than those in the serum anti-PLA2R antibody-negative group, while age and serum creatinine levels were higher in the former group. No significant between-group difference was observed with respect to 24-h urine protein. No significant difference was observed between renal tissue PLA2R -positive and -negative groups with respect to age, 24-h urine protein, eGFR, or serum albumin. In summary, serum anti-PLA2R antibody expression may correlate with the severity of IMN. The endpoints were sparsely including the serum albumin levels (Fig. 3), 24-h urine protein (Fig. 3) and the remission rate (Fig. 10) in our study, but they are 3 important index during the treatment of membranous nephropathy, which are used to reflect the severity of membranous nephropathy. Age (Fig. 5) and adverse prognosis (Fig. 13) are 2 established prognostic factors in membranous nephropathy. So, the above indicators are essential in our meta-analysis. Our findings are consistent with those of several previous clinical studies [33, 34], although some findings were different from other studies [33]. These may be attributable to differences with respect to the nature of research, objective, measurement technology used and clinical treatment methods. Due to inconsistent clinical data included in the study, we were unable to compare other factors such as blood lipids and blood pressure. For prognostic assessment of IMN patients, we found that serum anti-PLA2R antibody expression correlated with the remission rate of IMN patients, as the remission rate in the serum anti-PLA2R antibody-positive group was lower than that in the -negative group. Serum anti-PLA2R antibody expression levels were also associated with remission rates The high-titer group had a lower response rate; however, the expression of PLA2R in the renal tissue and the expression level were not significantly associated with remission rate. We did not conduct a meta-analysis about the relationship between the expression of PLA2R in the renal tissue and the poor prognosis of IMN, because only one study was included. However, for the reverse prognosis of IMN patients we did not conduct a meta-analysis because only one study of PLA2R in the renal tissue was included. In addition, the expression of serum anti-PLA2R antibody has no correlation to poor prognosis of IMN. In addition, serum anti-PLA2R antibody expression and the level of expression and IMN patients have no significant statistical significance. Although our meta-analysis results are different from the above results, serum anti-PLA2R antibody expression still has certain guiding significance for monitoring the severity of IMN patients and judging the prognosis. Meta-analysis aims to increase the credibility of conclusions and solve the inconsistency of research results by increasing the sample content. Although some endpoints were sparsely and inconsistently reported by some primary studies, meta-analysis can still increase the credibility of the original literatures and provide more powerful evidence for clinical work. Some limitations of our meta-analysis need to be considered while interpreting our results: (1) only 3 studies had reported data on PLA2R expression in renal tissues, and the sample size of patients was relatively small, which may have affected our results. (2) Lack of relevant data from individual studies may reflect the potential impact of publication bias. (3) The results of individual studies are liable to be influenced by the research subjects, measurement methods, and treatment modalities. Due to a large number of factors, no subgroup analysis was performed. Therefore, the source of heterogeneity among the included studies could not be assessed. (4) Due to the failure to obtain the original data of the included studies, what the specific PLA2R level and serum anti-PLA2R antibody titer was related to adverse prognosis of IMN were not indicated. Due to the failure to obtain the original data of the included studies, the specific PLA2R and serum anti-PLA2R antibody titer values were not indicated when introducing the relationship between PLA2R and its antibodies and IMN conditions. (5) There may be some potential factors in other studies that have not been included, resulting in biased selection in this meta-analysis. (6) We didn’t register our review in PROSPERO.

Future research may be improved in the following respects: (1) Expanding the sample size, designing a multi-center cohort study, and extending the follow-up time as much as possible. (2) For further clarification of the relationship of serum anti-PLA2R antibody and PLA2R titer with clinical course of IMN, it is best to provide a specific titer range.

Conclusion

As compared to PLAR2, serum anti-PLAR2 antibody is more closely related with iMN disease progression. Compared with negative group, serum anti-PLA2 antibody -positive group had lower serum albumin, higher age, lower eGFR, and lower remission rate. In serum anti-PLA2R antibody -positive group, the high-titer group had lower remission rate. The relationship of PLA2R expression in renal tissue with the clinical manifestations and prognosis of IMN patients cannot be ruled out.

Availability of data and materials

The datasets used and analysed in the current study are available from the corresponding authors on reasonable request.

Abbreviations

eGFR :

Estimated glomerular filtration rate

ELISA:

Enzyme-linked immunosorbent assay

ESRD:

End stage renal disease

GBM:

Glomerular basement membrane

IFA:

Indirect immunofluorescence assay

IMN:

Idiopathic membranous nephropathy

MD:

Mean difference

MN:

Membranous nephropathy

NOS:

Newcastle-Ottawa scale

OR:

Odds ratio

PLA2R:

M-type phospholipase A2 receptors

RCTs:

Randomized controlled trials

RR:

Relative risk

SMD:

Standardized mean difference

WB:

Western blotting

References

  1. Feng ZWS, Huang Y, Liang X, Shi W, Zhang B. A follow-up analysis of positron emission tomography/computed tomography in detecting hidden malignancies at the time of diagnosis of membranous nephropathy. Oncotarget. 2016;7(9):9645–51.

    Article  Google Scholar 

  2. Ronco P, Debiec H. Antigen identification in membranous nephropathy moves toward targeted monitoring and new therapy. J American Soc Nephrol: JASN. 2010;21(4):564–9.

    Article  CAS  Google Scholar 

  3. Boskovic J, Arnold JN, Stilion R, Gordon S, Sim RB, Rivera-Calzada A, Wienke D, Isacke CM, Martinez-Pomares L, Llorca O. Structural model for the mannose receptor family uncovered by electron microscopy of Endo180 and the mannose receptor. J Biol Chem. 2006;281(13):8780–7.

    Article  CAS  Google Scholar 

  4. Hoxha E, Harendza S, Zahner G, Panzer U, Steinmetz O, Fechner K, Helmchen U, Stahl RA. An immunofluorescence test for phospholipase-a (2)-receptor antibodies and its clinical usefulness in patients with membranous glomerulonephritis. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2011;26(8):2526–32.

    Article  CAS  Google Scholar 

  5. Ancian PLG, Mattéi MG, et al. the human 180-kDa receptor for secretory phospholipases A2. Molecular cloning, identification of a secreted soluble form, expression, and chromosomal localization. J Biol Chem. 1995;270(15):8963–70.

    Article  CAS  Google Scholar 

  6. Beck LH Jr, Salant DJ. Membranous nephropathy: from models to man. J Clin Invest. 2014;124(6):2307–14.

    Article  CAS  Google Scholar 

  7. Beck LH Jr, Bonegio RG, Lambeau G, Beck DM, Powell DW, Cummins TD, Klein JB, Salant DJ. M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy. N Engl J Med. 2009;361(1):11–21.

    Article  CAS  Google Scholar 

  8. Beck LH Jr, Fervenza FC, Beck DM, Bonegio RG, Malik FA, Erickson SB, Cosio FG, Cattran DC, Salant DJ. Rituximab-induced depletion of anti-PLA2R autoantibodies predicts response in membranous nephropathy. JAmerican Soc Nephrol: JASN. 2011;22(8):1543–50.

    Article  CAS  Google Scholar 

  9. Hoxha E, Thiele I, Zahner G, Panzer U, Harendza S, Stahl RA. Phospholipase A2 receptor autoantibodies and clinical outcome in patients with primary membranous nephropathy. J American Soc Nephrol: JASN. 2014;25(6):1357–66.

    Article  CAS  Google Scholar 

  10. Wang LJ , Shang MH , Zhuge YF , Huang YX , Rong S , Tang ZH , Bao JF , Yu Q , Yuan WJ. Expression of renal PLA2R in patients with idiopathic membranous nephropathy and its relationship with the curative effect of immunotherapy. National Med J China. 2016;96(1):4–8.

  11. Wang J, Xie Q, Sun Z, Xu N, Li Y, Wang L, Liu S, Xue J, Hao CM. Response to immunosuppressive therapy in PLA2R- associated and non-PLA2R- associated idiopathic membranous nephropathy: a retrospective, multicenter cohort study. BMC Nephrol. 2017;18(1):227.

    Article  Google Scholar 

  12. LJ W, MH S, YF Z, YX H, M R, ZH T, JF B, Q Y, WJ Y: expression of renal PLA2R in patients with idiopathic membranous nephropathy and its relationship with the curative effect of immunotherapy. National Med J China 2016(1):4–8.

  13. Liu H, Luo W, Gong S, Ding X. Detection and clinical significance of glomerular M-type phospholipase A2 receptor in patients with idiopathic membranous nephropathy. Intern Med J. 2016;46(11):1318–22.

    Article  CAS  Google Scholar 

  14. Pourcine F, Dahan K, Mihout F, Cachanado M, Brocheriou I, Debiec H, Ronco P. Prognostic value of PLA2R autoimmunity detected by measurement of anti-PLA2R antibodies combined with detection of PLA2R antigen in membranous nephropathy: a single-Centre study over 14 years. PLoS One. 2017;12(3):e0173201.

    Article  Google Scholar 

  15. Ramachandran R, Kumar V, Kumar A, Yadav AK, Nada R, Kumar H, Kumar V, Rathi M, Kohli HS, Gupta KL, et al. PLA2R antibodies, glomerular PLA2R deposits and variations in PLA2R1 and HLA-DQA1 genes in primary membranous nephropathy in south Asians. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2016;31(9):1486–93.

    Article  CAS  Google Scholar 

  16. Bech AP, Hofstra JM, Brenchley PE, Wetzels JF. Association of anti-PLA (2) R antibodies with outcomes after immunosuppressive therapy in idiopathic membranous nephropathy. Clin J American Soc Nephrol: CJASN. 2014;9(8):1386–92.

    Article  CAS  Google Scholar 

  17. Zhou GY, Wl Z, Wu C, Zhuang ZQ, Wang XT, Zhao YY. the relationship between serum anti-M-type phospholipase A2 receptor antibody and manifestation or therapeutic response of membranous nephropathy. Chin J Gerontol. 2017;14:3574–7.

    Google Scholar 

  18. Qin W, Beck LH Jr, Zeng C, Chen Z, Li S, Zuo K, Salant DJ, Liu Z. Anti-phospholipase A2 receptor antibody in membranous nephropathy. J American Soc Nephrol: JASN. 2011;22(6):1137–43.

    Article  CAS  Google Scholar 

  19. Oh YJ, Yang SH, Kim DK, Kang SW, Kim YS. Autoantibodies against phospholipase A2 receptor in Korean patients with membranous nephropathy. PLoS One. 2013;8(4):e62151.

    Article  CAS  Google Scholar 

  20. Kim YG, Choi YW, Kim SY, Moon JY, Ihm CG, Lee TW, Jeong KH, Yang SH, Kim YS, Oh YJ, et al. Anti-phospholipase A2 receptor antibody as prognostic Indicator in idiopathic membranous nephropathy. Am J Nephrol. 2015;42(3):250–7.

    Article  CAS  Google Scholar 

  21. Ruggenenti P, Debiec H, Ruggiero B, Chianca A, Pelle T, Gaspari F, Suardi F, Gagliardini E, Orisio S, Benigni A, et al. Anti-phospholipase A2 receptor antibody titer predicts post-rituximab outcome of membranous nephropathy. J American Soc Nephrol : JASN. 2015;26(10):2545–58.

    Article  CAS  Google Scholar 

  22. Timmermans SA, Abdul Hamid MA, Cohen Tervaert JW, Damoiseaux JG, van Paassen P, Limburg Renal R. Anti-PLA2R antibodies as a prognostic factor in PLA2R-related membranous nephropathy. Am J Nephrol. 2015;42(1):70–7.

    Article  CAS  Google Scholar 

  23. Hofstra JM, Debiec H, Short CD, Pelle T, Kleta R, Mathieson PW, Ronco P, Brenchley PE, Wetzels JF. Antiphospholipase A2 receptor antibody titer and subclass in idiopathic membranous nephropathy. J American Soc Nephrol : JASN. 2012;23(10):1735–43.

    Article  CAS  Google Scholar 

  24. Liang Y, Zhang XL, Zhu Q, Shao FM. Effect of adrenocorticosteroids combined with immunosuppressive agents on membranous nephropathy and its correlation with serum PLA2R antibody concentration. Guangdong Med J. 2017;38(12):1897–900.

    Google Scholar 

  25. Huang J, Li JW, Liang M, Qin SG, Zhou SS, Fu JZ. Titer of serum antiphospholipase A2 receptor antibody predicts clinical outcome of idiopathic membranous nephropathy. Guangdong Med J. 2017;38(9):1348–53.

    Google Scholar 

  26. Zhang D, Zou J, Zhang C, Zhang W, Lin F, Jiang G. Clinical and histological features of phospholipase A2 receptor-associated and Thrombospondin type-I domain-containing 7A-associated idiopathic membranous nephropathy: a single center retrospective study from China. Med Sci Monit : Int Med J Exp Clin Res. 2018;24:5076–83.

    Article  CAS  Google Scholar 

  27. Li Q, Zhang BR, He P, Qin XS, Zhao ZX, Zhang YZ, Wang YQ, Sun GP. Clinical application of serum PLA2R antibody detection inidiopathic membranous nephropathy. Chin J Pract Intern Med. 2018;38(12):63–66.

  28. Chen A, Frank R, Vento S, Crosby V, Chandra M, Gauthier B, Valderrama E, Trachtman H. Idiopathic membranous nephropathy in pediatric patients: presentation, response to therapy, and long-term outcome. BMC Nephrol. 2007;8:11.

    Article  Google Scholar 

  29. Pozdzik A, Brocheriou I, David C, Touzani F, Goujon JM, Wissing KM. Membranous nephropathy and anti-Podocytes antibodies: implications for the diagnostic workup and disease management. Biomed Res Int. 2018;2018:6281054.

    Article  Google Scholar 

  30. Sengupta U, Kumar V, Yadav AK, Marwaha N, Kohli HS, Sakhuja V, Jha V. Infusion of autologous bone marrow mononuclear cells leads to transient reduction in proteinuria in treatment refractory patients with idiopathic membranous nephropathy. BMC Nephrol. 2013;14:262.

    Article  Google Scholar 

  31. Debiec HGV, Mougenot B, Decobert F, Haymann JP, Bensman A, Deschênes G, Ronco PM. Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies. N Engl J Med. 2002;346(26):2053–60.

    Article  Google Scholar 

  32. Dai H, Zhang H, He Y. Diagnostic accuracy of PLA2R autoantibodies and glomerular staining for the differentiation of idiopathic and secondary membranous nephropathy: an updated meta-analysis. Sci Rep. 2015;5:8803.

    Article  CAS  Google Scholar 

  33. Pang L, Zhang AM, Li HX, Du JL, Jiao LL, Duan N, Liu Y, Yu D. Serum anti-PLA2R antibody and glomerular PLA2R deposition in Chinese patients with membranous nephropathy: a cross-sectional study. Medicine. 2017;96(24):e7218.

    Article  CAS  Google Scholar 

  34. Wei SY, Wang YX, Li JS, Zhao SL, Diao TT, Wang Y, Wang C, Qin Y, Cao Y, Wei Q, et al. Serum anti-PLA2R antibody predicts treatment outcome in idiopathic membranous nephropathy. Am J Nephrol. 2016;43(2):129–40.

    Article  CAS  Google Scholar 

  35. Segarra-Medrano A, Jatem-Escalante E, Carnicer-Caceres C, Agraz-Pamplona I, Salcedo MT, Valtierra N, Ostos-Roldan E, Arredondo KV, Jaramillo J. Evolution of antibody titre against the M-type phospholipase A2 receptor and clinical response in idiopathic membranous nephropathy patients treated with tacrolimus. Nefrologia : Publicacion oficial de la Sociedad Espanola Nefrologia. 2014;34(4):491–7.

    Google Scholar 

Download references

Acknowledgements

Not applicable

Funding

This study was supported by the Jilin Technology Department Natural Foundation of China (20160101122JC).

Author information

Author notes

  1. Dan Dong and Ting-ting Fan contributed equally to this work.

Authors and Affiliations

  1. Department of Nephrology, First Hospital of Jilin University, 71 Xinmin Street, Changchun, Jilin, 130021, People’s Republic of China

    Dan Dong, Ting-ting Fan, Lu Zhang, Li Song & Li Zhang

  2. Department of Nephrology, Binzhou People’s Hospital, Binzhou, Shandong, People’s Republic of China

    Ting-ting Fan

  3. Department of Nephrology, Jining No.1 People’s Hospital, Jining, Shandong, People’s Republic of China

    Ying-ying Wang

Authors
  1. Dan Dong
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Ting-ting Fan
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Ying-ying Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Lu Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Li Song
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Li Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Conception and design of the network meta-analysis: LZ, DD. Performance of the network meta-analysis: DD, TTF and LZ. Quality assessment of the network meta-analysis: TTF, LZ, LS and YYW. Analysis of study data: DD, TTF and LS. Writing of the paper: TTF, DD. All authors have read and approved the final version of the manuscript.

Corresponding author

Correspondence to Li Zhang.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dong, D., Fan, Tt., Wang, Yy. et al. Relationship between renal tissues phospholipase A2 receptor and its serum antibody and clinical condition and prognosis of idiopathic membranous nephropathy: a meta-analysis. BMC Nephrol 20, 444 (2019). https://doi.org/10.1186/s12882-019-1638-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12882-019-1638-x

Keywords

BMC Nephrology

ISSN: 1471-2369

Contact us