Homiladorlikning jigar ichi xolestazida paritetga bog‘liq bo‘lgan oshqozon osti bezining morfologik va morfometrik o‘zgarishlari: autopsiya tadqiqoti
Qabul qilingan: 2026-02-27
Nashr etilgan: 2026-04-30
Annotatsiya
Maqsad. Homiladorlikning intrahepatik xolestazi (HIX) tufayli vafot etgan ayollarda oshqozon osti bezi morfologik va morfometrik o‘zgarishlarini, shuningdek, ularning jigar shikastlanishi va homiladorliklar soni bilan bog‘liqligini tavsiflash.
Materiallar va usullar. O‘tkir miokard infarktidan vafot etgan 12 nafar tug‘ruq yoshidagi nazorat guruhi ayollari bilan taqqoslaganda, og‘ir HIX tufayli vafot etgan 51 nafar ayolning jigar va oshqozon osti bezi to‘qimalarida autopsiyaga asoslangan morfologik va miqdoriy morfometrik tadqiqot o‘tkazildi (Respublika patologik anatomiya ilmiy-amaliy markazi, 2013–2023-yillar). 28 ta asosiy holat va nazorat guruhidan olingan kesmalar gematoksilin-eozin bilan bo‘yalib, morfometriya (12 ta parametr) uchun raqamlashtirildi; o‘rtacha qiymatlar Styudentning t-mezoni yordamida taqqoslandi.
Natijalar. HIX kuzatilgan jigarlarda sentrilobulyar va midzonal gepatotsellyulyar xolestaz, o‘t pigmentining to‘planishi, gidropik distrofiya va nekrobioz (54,2%), 75% holatda esa kanalikulyar o‘t dimlanishi aniqlandi. Oshqozon osti bezida o‘tning yirik va bo‘lakchali yo‘llarga reflyuksi, segmentar atsinar nekroz, vakuolyar distrofiya, interstitsial shish, periduktal infiltratsiya va avj oluvchi fibroz kuzatildi. Barcha 12 morfometrik ko‘rsatkich nazorat guruhidan sezilarli darajada farq qildi (P<0,01–P<0,001) va o‘zgarishlar jiddiyligi homiladorliklar soniga qarab ortib, ayniqsa uchinchi va to‘rtinchi homiladorlikda yaqqol namoyon bo‘ldi.
Xulosa. HIX – bu o‘t kislotalari ta’sirida yuzaga keladigan tizimli toksik holat bo‘lib, u jigar xolestazi bilan birga oshqozon osti bezining miqdoriy jihatdan baholanadigan va homiladorliklar soniga bog‘liq bo‘lgan shikastlanishini keltirib chiqaradi. Bu esa og‘ir yoki qaytalanuvchi HIX holatlarida oshqozon osti bezini sinchkovlik bilan kuzatib borish zarurligini tasdiqlaydi.
Kalit so‘zlar
Adabiyotlar ro'yxati
-
Gandhi S, Barsanti-Innes B, Jolicoeur G, Nwokoro IN. Intrahepatic cholestasis of pregnancy. Clin Liver Dis. 2026;30(3):677–699. https://doi.org/10.1016/j.cld.2026.04.009.
-
Jurk S, Kremer A, Schleussner E. The latest on intrahepatic cholestasis of pregnancy – update 2026. Geburtshilfe Frauenheilkd. 2026;86(6):528–537. https://doi.org/10.1055/a-2845-6610.
-
Capatina N, Ovadia C. Meta-analyses in cholestatic pregnancy: the outstanding clinical questions. Obstet Med. 2024;17(3):147–151. https://doi.org/10.1177/1753495X241251425.
-
Niculae LE, Petca A. Intrahepatic cholestasis of pregnancy: neonatal impact through the lens of current evidence. Biomedicines. 2025;13(9):2066. https://doi.org/10.3390/biomedicines13092066.
-
Kothari S, Afshar Y, Friedman LS, Ahn J. AGA clinical practice update on pregnancy-related gastroin-testinal and liver disease: expert review. Gastroenterology. 2024;167(5):1033–1045. https://doi.org/10.1053/j.gastro.2024.06.014.
-
Zollner G, Trauner M. Mechanisms of cholestasis. Clin Liver Dis. 2008;12(1):1–26.
-
Yuan S, Zhou S. Mechanistic basis and translational potential of traditional Chinese medicine in the treatment of cholestasis: a narrative review. Hepat Med. 2026;18:609530. https://doi.org/10.2147/HMER.S609530.
-
Tang D, Yang J, Shi X, Gu X, Zhao L. Activation of the TGR5/cAMP/PKA/CREB axis in cholangiocytes mediates epithelial-mesenchymal transition and fibrosis in hepatolithiasis. Biol Direct. 2026;21(1). https://doi.org/10.1186/s13062-026-00783-7.
-
Huang X, Liao E, Chen A, Shao Y. Mechanism of mitochondrial dysfunction on placental trophoblastic cells in intrahepatic cholestasis of pregnancy. J Mol Histol. 2025;56(3):140. https://doi.org/10.1007/s107 35-025-10427-1.
-
Xu ZT, Ge LX, Luo L, Ma HY, Xiao H, Ding YB. PIP2 accumulation in the spongiotrophoblast drives trophoblast apoptosis in intrahepatic cholestasis of pregnancy. Mol Reprod Dev. 2026;93(4):e70105. https://doi.org/10.1002/mrd.70105.
-
Tyrmi JS, Karjalainen J, Venkatesh SS, Benoit-Pilven C, Lemmelä SM, Brunak S, et al. Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy. Nat Commun. 2026;17(1). https://doi.org/10.1038/s41467-026-73122-z.
-
English N, Rao J. Acute fatty liver of pregnancy with hypoglycaemia, diabetes insipidus and pancreatitis, preceded by intrahepatic cholestasis of pregnancy. BMJ Case Rep. 2015;2015:bcr2015209649. https://doi.org/10.1136/bcr-2015-209649.
-
Yosief S, Chen W, Wescoe K, Branch MS, Bashir M, Wegermann K. Perplexing severe cholestasis in the postpartum period. ACG Case Rep J. 2026;13(5):e02115. https://doi.org/10.14309/crj.00000000000021 15.
-
Beuers U. Drug insight: mechanisms and sites of action of ursodeoxycholic acid in cholestasis. Nat Clin Pract Gastroenterol Hepatol. 2006;3(6):318–328.
-
Chen Y, Zhang H, Ning W, Chen Y, Wen C. The impact of intrahepatic cholestasis on pregnancy outcomes: a retrospective cohort study. BMC Gastroenterol. 2023;23(1):16. https://doi.org/10.1186/s12876-023-02652-3.
-
Keles E, Kaya L, Ogunc YT, Kaya Z, Baydili KN, Kumru P. Impact of maternal nutrition and gesta¬tional weight gain on perinatal outcomes in intrahepatic cholestasis of pregnancy. Rev Assoc Med Bras. 2026;72(3):e20251795. https://doi.org/10.1590/1806-9282.20251795.
-
Öztürk Ö, Çirkin Tekeş G, Şimşek M, Küçükkayıkçı AS, Yakut Yücel K. The evaluation of Xenin-25 levels in intrahepatic cholestasis of pregnancy and comparison with healthy pregnant women. BMC Pregnancy Childbirth. 2026;26(1). https://doi.org/10.1186/s12884-026-09234-7.
-
Tsuru T, Watanabe T, Kouzu K, Yamagishi Y, Einama T, Yamasaki T, et al. A simple morphometric algorithm based on nuclear atypia features of invasive breast carcinoma: relationship with nuclear grade, Ki-67 level, and hormone receptor status. Breast Cancer. 2026;33(4):905–918. https://doi.org/10.1007/s1 2282-026-01870-3.
-
Ono D, Kawai H, Kuwahara H, Yokota T. Refining muscle morphometry through machine learning and spatial analysis. Neuropathol Appl Neurobiol. 2025;51(2):e70012. https://doi.org/10.1111/nan.70012.
-
Sales DC, Fontes CC, Zanella AP, Martinez C, Souza-Sporkens JC, Vanzela EC, et al. Maternal high-fat diet impairs pancreatic β-cell development and reduces VAMP-2 levels in islets of mouse offspring. J Dev Orig Health Dis. 2026;17:e32. https://doi.org/10.1017/S2040174426100646.
-
Kumar PU, Ramalaxmi BA, Venkiah K, Sesikeran B. Effect of maternal undernutrition on human foetal pancreas morphology in second trimester of pregnancy. Indian J Med Res. 2013;137(2):302–307.
-
Kodger J, Nadim H, Choucair I, Sutphin A, Eid T, El-Khoury JM. Rapid diagnosis of intrahepatic cholestasis of pregnancy (ICP): validation of an automated enzymatic total bile acid assay and assessment of ursodeoxycholic acid impact on bile acid profiles in an ICP cohort. J Appl Lab Med. 2026. https://doi.org/10.1093/jalm/jfag099.
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