Епидемиология на IgA нефропатията

  • Елена Митова
  • Юлиан Ананиев
  • Георги Стефанов
Keywords: Имуноглобулин A нефропатия, IgA нефропатия, епидемиология, болестност, заболеваемост

Abstract

IgA нефропатията (ORPHA код: 34145) е рядко, хронично прогресиращо имуно-медиирано бъбречно заболяване и представлява една от основните причини за бъбречна недостатъчност в световен мащаб. Диагнозата на IgAN може да бъде потвърдена само чрез извършването на пункционна бъбречна биопсия, която се явява „златен стандарт“ в диагностиката на този вид бъбречни заболявания. Клиничните прояви на IgAN могат да варират от асимптоматична микроскопска или интермитентна макроскопска хематурия, до бързо прогресиращ гломерулонефрит. Очакваната продължителност на живота при пациентите с IgAN е намалена средно с 10 години и смъртността при тях е два пъти по-висока в сравнение с общата популация.

В рамките на 10–20 години от поставяне на диагнозата близо 50% от пациентите с IgAN развиват терминална бъбречна недостатъчност, налагаща хемодиализа и бъбречна трансплантация. Съществуват доказателства, че епидемиологията, клиничната картина, прогресията на заболяването и дългосрочните резултати при IgAN се различават в различните етнически популации по света. Цел на настоящата публикация е да анализира епидемиологични данни за IgA нефропатията и да направи прогноза за разпространението на това заболяване в България.

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Published
2024-03-14
How to Cite
1.
Митова Е, Ананиев Ю, Стефанов Г. Епидемиология на IgA нефропатията. Редки болести и лекарства сираци [Internet]. 2024Mar.14 [cited 2024Nov.24];15(1):3-11. Available from: https://journal.raredis.org/index.php/RBLS/article/view/192
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