Association of interleukin-18 promoter polymorphisms with WHO pathological classes and serum IL-18 levels in Chinese patients with lupus nephritis

Lupus ◽  
2009 ◽  
Vol 18 (1) ◽  
pp. 29-37 ◽  
Author(s):  
DY Chen ◽  
CW Hsieh ◽  
KS Chen ◽  
YM Chen ◽  
FJ Lin ◽  
...  
2009 ◽  
Vol 36 (10) ◽  
pp. 2284-2289 ◽  
Author(s):  
DER-YUAN CHEN ◽  
YI-MING CHEN ◽  
HSIN-HUA CHEN ◽  
CHIA-WEI HSIEH ◽  
CHI-CHEN LIN ◽  
...  

Objective.Interleukin 18 (IL-18) has a central role in the pathogenesis of adult-onset Still’s disease (AOSD). We investigated the functional association of −607 (C/A) IL-18 promoter polymorphisms with disease course in Chinese patients with AOSD.Methods.Sequence-specific primer polymerase chain reaction and the restriction fragment-length polymorphism method were used to analyze the genotypes of IL-18 promoter polymorphism at position −607 in 96 unrelated patients with AOSD and 164 ethnically-matched healthy controls. Serum IL-18 levels were determined using ELISA in patients with active untreated AOSD.Results.Significantly lower frequencies of single-nucleotide polymorphism −607/AA were observed in patients with AOSD compared to healthy controls (18.8% vs 31.1%, respectively; p < 0.05). Median levels of serum IL-18 were significantly lower in AOSD patients with AA genotype compared to those with CA genotype or CC genotype (147.5 pg/ml vs 410.5 pg/ml or 262.4 pg/ml, respectively; both p < 0.05). Significantly lower IL-18 levels were demonstrated in AOSD patients with a monocyclic systemic course than in those with a polycyclic systemic course or a chronic articular course. The AA genotype was more frequently observed in patients with monocyclic systemic course, which had the best prognosis, than in those with the other 2 disease courses. In contrast, a lower frequency of the AA genotype than the CA or the CC genotype was observed in patients with chronic disabling arthritis (5.5% vs 25.0% or 19.2%, respectively).Conclusion.The SNP −607/AA genotype with lower IL-18 levels might be a genetically protective factor for the occurrence of AOSD in the Chinese population, against progression of chronic disabling arthritis.


2001 ◽  
Vol 59 (4) ◽  
pp. 1520-1528 ◽  
Author(s):  
Angela Yee Moon Wang ◽  
Peter Poon ◽  
Fernand Macmound Lai ◽  
Lymee Yu ◽  
Paul Cheung Lung Choi ◽  
...  

2016 ◽  
Vol 90 (6) ◽  
pp. 1357-1367 ◽  
Author(s):  
Yun Pang ◽  
Ying Tan ◽  
Yongzhe Li ◽  
Jianchun Zhang ◽  
Yongbing Guo ◽  
...  

2002 ◽  
Vol 46 (11) ◽  
pp. 3083-3095 ◽  
Author(s):  
Justus Faust ◽  
Julia Menke ◽  
J�rg Kriegsmann ◽  
Vicki Rubin Kelley ◽  
Werner J. Mayet ◽  
...  

2018 ◽  
Vol 33 (suppl_1) ◽  
pp. i384-i384
Author(s):  
Shaofan Wang ◽  
Yinghua Chen ◽  
Ke Zuo ◽  
Duqun Chen ◽  
Zhengzhao Liu ◽  
...  

2019 ◽  
Vol 46 (8) ◽  
pp. 912-919 ◽  
Author(s):  
Si-Jia Shao ◽  
Jin-Hua Hou ◽  
Guo-Tong Xie ◽  
Wen Sun ◽  
Dan-Dan Liang ◽  
...  

Objective.To assess how the longterm outcomes have changed over the past decades in Chinese patients with lupus nephritis (LN). The trends in patient manifestation at presentation, treatment pattern, and therapeutic effects were evaluated.Methods.A cohort of biopsy-proven patients with LN (n = 1945) from January 1994 to December 2010 was analyzed. Treatment regimens, treatment response, renal relapse, and renal outcome were compared at different time periods (1994–1998, 1999–2004, and 2005–2010).Results.Patients in the later periods had shorter duration of disease, lower serum creatinine value and chronicity at biopsy, and more frequent followup. They were more likely to receive standard-of-care therapies, which included cyclophosphamide, mycophenolate mofetil, and combination therapy. Patients in the later periods had higher probabilities of achieving remission (p < 0.001) and lower probabilities of experiencing renal flare (p = 0.007). The 5-year renal survival rates were 92.6%, 90.6%, and 94.3% in 1994–1998, 1999–2004, and 2005–2010, respectively. The 5-year risk of endstage renal disease (ESRD) did not differ between 1994–1998 and 1999–2004, but was significantly lower in 2005–2010 (HR 0.40, 95% CI 0.19–0.85 vs 1999–2004). In multivariable Cox analysis, standard therapy was independently associated with lower risk of ESRD (adjusted HR 0.72, 95% CI 0.52–0.98, p = 0.04). Variables of renal damage at biopsy (renal function, activity index, and chronicity index) were independently associated with poor outcome.Conclusion.The outcomes of Chinese patients with LN have improved from 1994 to 2010. With the increased use of standard therapies, the remission rates have increased and renal relapse has decreased.


2005 ◽  
Vol 6 (3) ◽  
pp. 211-216 ◽  
Author(s):  
J A Gracie ◽  
N Koyama ◽  
J Murdoch ◽  
M Field ◽  
F McGarry ◽  
...  

Lupus ◽  
2019 ◽  
Vol 28 (8) ◽  
pp. 995-1002 ◽  
Author(s):  
M A Elkoumi ◽  
A A Emam ◽  
M A N Allah ◽  
A H Sherif ◽  
N M Abdelaal ◽  
...  

Background Pediatric-onset SLE (pSLE) is a multisystem autoimmune disease. Recently, the ficolin-2 (FCN2) gene has emerged as a potential candidate gene for susceptibility to SLE. Objectives The objective of this study was to evaluate the association of the FCN2 gene polymorphisms at positions −986 (G/A), −602 (G/A), −4 (A/G) and SNP C/T (rs3124954) located in intron 1, with susceptibility to pSLE in Egyptian children and adolescents. Methods This was a multicenter study of 280 patients diagnosed with pSLE, and 280 well-matched healthy controls. The FCN2 promoter polymorphisms at –986 G/A (rs3124952), −602 G/A (rs3124953), −4 A/G (rs17514136) and SNP C/T (rs3124954) located in intron 1 were genotyped by polymerase chain reaction, while serum ficolin-2 levels were assessed using enzyme-linked immunosorbent assay. Results The frequencies of the FCN2 GG genotype and G allele at −986 and −602 positions were significantly more represented in patients with pSLE than in controls ( p < 0.001). Conversely, the FCN2 AA genotype and A allele at position −4 were more common in patients than in controls ( p < 0.001). Moreover, patients carrying the FCN2 GG genotype in −986 position were more likely to develop lupus nephritis (odds ratio: 2.6 (95% confidence interval: 1.4–4.78); p = 0.006). The FCN2 AA genotype at position −4 was also identified as a possible risk factor for lupus nephritis (odds ratio: 3.12 (95% confidence interval: 1.25–7.84); p = 0.024). Conclusion The FCN2 promoter polymorphisms may contribute to susceptibility to pSLE in Egyptian children and adolescents. Moreover, the FCN2 GG genotype at position −986 and AA genotype at position −4 were associated with low serum ficolin-2 levels and may constitute risk factors for lupus nephritis in pSLE.


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