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Hepatic steatosis in patients with acromegaly

机译:肢端肥大症患者的肝脂肪变性

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Objective Comorbid NAFLD is increasingly being diagnosed in patients with diabetes and nondiabetic endocrinopathies. The aim of this study was to assess hepatic steatosis noninvasively by transient elastography in patients with acromegaly. Design A cross‐sectional study including 22 patients with acromegaly. Methods Hepatic steatosis was quantified using controlled attenuation parameter (CAP) during elastography. Anthropometric measurements were obtained, serum liver function tests and lipid and hormone profiles were measured, and prosteatogenic gene variants were genotyped using standard assays. Results In total, 41% of patients were women (mean age 60?±?14.7?years, mean BMI 31.2?±?4.6?kg/msup2/sup). Hepatic steatosis, as defined by CAP??248?dB/m, was present in 66% of patients. Five (45%) of the patients with hepatic steatosis also had fibrosis, and one presented with cirrhosis. Nine patients were carriers of the PNPLA3 p.I148M prosteatogenic [M] risk allele, eight of whom were heterozygotes. CAP values were significantly ( P =?.045) higher in these patients and corresponded to advanced steatosis, as compared to patients with the wild‐type genotype, who demonstrated CAP values consistent with mild steatosis (311?±?33?dB/m. vs 254?±?62?dB/m). CAP values did not differ significantly in carriers of distinct TM6SF2 and MBOAT7 genotypes; however, carriers of the risk alleles displayed higher CAP as compared to wild‐type patients. Conclusions This study shows that in patients with acromegaly, carriers of the PNPLA3 susceptibility allele are at risk of developing hepatic steatosis, as assessed by CAP. Comorbid NAFLD might compound prognosis in such patients; thus, further research into the pathomechanisms and treatment of NAFLD in acromegaly is warranted.
机译:目的越来越多的糖尿病和非糖尿病性内分泌病变患者被诊断出患有共病NAFLD。这项研究的目的是通过瞬时弹性成像技术对肢端肥大症患者进行无创性肝脂肪变性评估。设计一项横断面研究,包括22例肢端肥大症患者。方法采用弹性衰减控制参数(CAP)定量肝脂肪变性。获得人体测量学数据,测量血清肝功能测试以及脂质和激素谱,并使用标准分析对促前列腺炎基因变异进行基因分型。结果总共有41%的患者为女性(平均年龄60?±?14.7?岁,平均BMI为31.2?±?4.6?kg / m 2 )。 CAP≥> 248?dB / m所定义的肝脂肪变性存在于66%的患者中。肝脂肪变性患者中有五名(45%)也有纤维化,其中一名患有肝硬化。 9名患者是PNPLA3 p.I148M促前列腺炎[M]风险等位基因的携带者,其中8名是杂合子。与野生型基因型患者相比,这些患者的CAP值显着高(P = ?. 045)​​,并对应于晚期脂肪变性,后者的CAP值与轻度脂肪变性一致(311?±?33?dB / m)比254?±?62?dB / m)。在不同的TM6SF2和MBOAT7基因型的携带者中,CAP值没有显着差异。但是,与野生型患者相比,风险等位基因携带者的CAP更高。结论该研究表明,根据CAP评估,在肢端肥大症患者中,PNPLA3易感性等位基因携带者有发生肝脂肪变性的风险。 NAFLD合并症可能会加重此类患者的预后。因此,有必要进一步研究肢端肥大症中NAFLD的发病机理和治疗方法。

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