Артериол гипертония даволаш жараёнида беморларнинг давога риоя уилиши (комплаентлиги) терапия самарадорлигида уал уилувчи ауамиятга эга. Мазкур мацолада СОМТ гени A/G (Vall58Met) rs4680 полиморфизми генотиплари ва гипертония касаллиги мавжуд беморларнинг антигипертензив терапияга бўлган тарафдорлик даражаси ўртасидаги боглиҳлик таулил қилинди. Тадқиқот натижаларига кўра, ушбу геннинг GG генотипига эга шахсларда давога юкори даражада риоя уилиш эутимоли бошка генотипларга нисбатан сезиларли даражада юуори эканлиги аниуланди. Натижалар фармакогенетик ёндашувни амалиётга жорий этиш зарурлигини курсатади.
| Mualliflar | Мавлянов, И, Мавлянов, С, Мавлянов, З |
|---|---|
| Jurnal | Тиббиёт ва спорт |
| Nashr sanasi | 2026-06-14 |
| Son | 3 |
| Betlar | 63-64 |
| Til | O‘zbek |
гипертония, ген COMT, rs4680, полиморфизм, приверженность лечению, фармакотерапия, генетические факторы, hypertension, COMT gene, rs4680, polymorphism, compliance, pharmacotherapy, genetic factors, гипертония, COMT гени, rs4680, полиморфизм, комплаентлик, фармакотерапия, генетик омиллар
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