Anti phospholipid Syndrome Nephropathy in Patients with Lupus Nephritis

Message:
Abstract:
Background
Increasing the Antiphospholipid-nephropathy (APS-N) alterations on lupus renal lesions cause renal disease progression and detoriation of prognosis. The aim of this study was to find some indicators in lupus patients that can predict the occurring of APS-N in them and can be construct the preventive treatments for prevention of more complications.
Methods
In this descriptive study, the renal biopsy specimens of 66 patients with lupus nephritis, were reviewed according to new classification of lupus nephritis ISN/RPS 2003 by a nephropathologist and synchronous alterations due to APS, were studied. Results were analyzed by SPSS-12 and statistical methods, independent sample test, chi-square.
Findings
The APS-N alterations were seen in 31.8% of patients. The most common class of lupus nephritis was IV. There was no significant difference between any one of the lupus nephritis class and the existence of synchronous APS-N alterations (P > 0.05), between lupus nephritis and APS-N with serum Cr level at the time of renal biopsy (P = 0.434) and also between the presence of anti phospholipid antibodies and the existence of synchronous APS-N alterations (P= 0.904). The difference between clinical signs (thrombosis, ischemia) and existence of the synchronous APS-N alterations, was strongly significant (P = 0.001).
Conclusion
This study recommend that pathologists should be careful to diagnose and report the existence of synchronous APS-N alterations in renal biopsy specimens related to lupus nephritis patients, because these alterations help the physician to carry out proper treatment and prevent of future vascular thrombotic events in lupus nephritis patients.
Language:
Persian
Published:
Journal Of Isfahan Medical School, Volume:26 Issue: 89, 2008
Page:
171
magiran.com/p553275  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!