scholarly journals IgA nephropathy associated with ankylosing spondylitis: occurrence in women as well as in men.

1989 ◽  
Vol 48 (5) ◽  
pp. 435-437 ◽  
Author(s):  
K N Lai ◽  
P K Li ◽  
B Hawkins ◽  
F M Lai
1986 ◽  
Vol 6 (4) ◽  
pp. 145-149 ◽  
Author(s):  
A. J. G. Swaak ◽  
I. Frankfort ◽  
R. S. Menon ◽  
J. M. Pekelharing ◽  
O. Planten

Rheumatology ◽  
1987 ◽  
Vol 26 (5) ◽  
pp. 396-397 ◽  
Author(s):  
E. KANTEREWICZ ◽  
R. SANMARTI ◽  
A. COLLADO ◽  
M. A. BRANCOS ◽  
A. TORRAS ◽  
...  

1988 ◽  
Vol 77 (12) ◽  
pp. 1888-1889
Author(s):  
Yuji NAKAMURA ◽  
Hiroko UTSUNOMIYA ◽  
Keiko YOSHIMOTO ◽  
Masahiko OKADA ◽  
Shigeki SAIMA

2021 ◽  
Vol 14 (1) ◽  
pp. e237713
Author(s):  
Charlotte Anne Baert ◽  
Selda Aydin ◽  
Philippe Leroy ◽  
Patrick Durez

We report the case of a 43-year-old man, suffering from ankylosing spondylitis and treated with Infliximab 5 mg/kg every 2 months, with an excellent disease control. During a follow-up consultation, an incipient renal insufficiency is detected. A urine analysis showed haematuria and proteinuria and a renal puncture-biopsy revealed an image of IgA nephropathy.Several cases of IgA nephropathy have been reported in the literature associated with ankylosing spondylitis. Some of them occur in patients treated with antitumour necrosis factor, but it is unclear whether this pathology is caused by the treatment or whether treatment failed to prevent its occurrence.Our clinical case highlights the importance of regular monitoring of renal function in patients with ankylosing spondylitis, as well as urinary spotting.The question of whether the disease itself, the treatment or other factors such as immune dysregulation could be held responsible for kidney disease will be addressed in the discussion.


2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Qin Xue ◽  
Guang Li Zhang ◽  
Zebo Tian

Abstract Background and Aims Renal involvement is one of the most common extra-articular complications caused by ankylosing spondylitis (AS). The main pathological manifestation is secondary IgA nephropathy(SIgAN) in Chinese AS patients. The difference between SIgAN and primary IgAN (PIgAN) remains unclear due to the lack of cases. Therefore, the aim of this retrospective study was to compare the clinical and pathological features of SIgAN of AS (SIgAN-AS) and PIgAN, to detect the pathogenesis of SIgAN Method Clinical characteristics and pathological data were collected in patients who were diagnosed with IgAN by renal biopsy in our hospital from Jan 2008 to Oct 2018. Patients with SIgAN-AS were recruited by the ratio 1:5 of patients with primary IgAN as the control group in the study. Fifteen patients with SIgAN-AS and Seventy-five patients with PIgAN were enrolled in this retrospective study. Results There were 15 cases in AS group, including 13 male and 2 female. The cohort of 75 patients with PIgAN included 34 male and 41 female. There were more males in AS group 13/15 (86.7%) vs 37/75(49.3%) ,P < 0.05. Compared with PIgAN patients, SIgAN-AS patients had higher incidences of hematuria( 13/15(86.7%)vs 44/75 (58.7%) , P < 0.05), lower levels of 24-hour urinary protein(0.85±0.68 vs 1.57±1.54g, P < 0.05), but higher levels of eGFR (CKD-MDRD formula) (117.60±37.33 vs 85.35±31.36, P < 0.05),eGFR (CKD-EPI formula) (128.01±41.58 vs 92.75±36.09, P < 0.05), Albumin (44.67±3.48 vs 41.09±7.07 g/L, P < 0.05) ESR (43.20 ±33.94 vs 18.79±16.26mm/h, P < 0.001) , and CRP (21.19±30.61 vs 2.11±4.58mg/L, P < 0.001) . From the perspective of renal pathology of PIgAN, SIgA-AS patients had fewer incidences of renal tubular atrophy / interstitial fibrosis of nephropathy (P <0.05). The immunohistostaining analysis showed higher incidences of dominant deposits of single IgA in mesangial cell area (P < 0.05). Conclusion Patients with SIgAN-AS is more common in male and display a milder progression than those with primary IgAN. Majority of the SIgAN-AS can be improved with early intervention.


2019 ◽  
Vol 30 (4) ◽  
pp. 648-656 ◽  
Author(s):  
Dafeng He ◽  
Rong Wang ◽  
Shaoshan Liang ◽  
Dandan Liang ◽  
Feng Xu ◽  
...  

2018 ◽  
Vol 33 (1) ◽  
pp. 85
Author(s):  
Do-Hyeong Lee ◽  
Geun-Tae Kim ◽  
Na-Kyoung Hwang ◽  
Eun-Heui Kim

2019 ◽  
Vol 8 (1) ◽  
pp. 39-43
Author(s):  
Mahmud Javed Hasan ◽  
ASM Ruhul Quddus ◽  
Nitai Chandra Ray

We are reporting a rare case with ankylosing spondylitis (AS), renal impairment with IgA nephropathy. Here, we discuss the course of diagnosis. A 32 year-old man with bilateral pain of the sacroiliac joints for 5 years and leg swelling for 10 days.  A Diagnosis of AS by HLA-B27 and pelvic X-ray tests, pathological diagnosis and IgA nephropathy based on renal biopsy. We administered methylprednisolone 500 mg/d for 3 consecutive days, followed by methylprednisolone 40 mg oral QD for a month. The patient was followed up once a month. In the sixth month, the patient's serum creatinine had decreased to 0.96 mg/dL, urine microalbumin creatinine ratio decreased to 173.3 mg/g, and albumin had risen to 33.1 g/L. Pain and morning stiffness were relieved. Although the causal relationship between AS and IgA nephropathy in this patient still needs to be established. In clinical practice, patients with AS need to be screened for renal complications. CBMJ 2019 January: vol. 08 no. 01 P: 39-43


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