National Institute for Health and Care Research (NIHR) Birmingham Biomedical Research Centre, Centre for Liver and Gastrointestinal Research and Gastrointestinal Research, National Institute of Health Research (NIHR) Birmingham Biomedical Research Centre (BRC), University of Birmingham, Birmingham, UK.
Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Aliment Pharmacol Ther. 2024 Jun;59(11):1366-1375. doi: 10.1111/apt.17944. Epub 2024 Apr 3.
Imaging markers of biliary disease in primary sclerosing cholangitis (PSC) have potential for use in clinical and trial disease monitoring. Herein, we evaluate how quantitative magnetic resonance cholangiopancreatography (MRCP) metrics change over time, as per the natural history of disease.
Individuals with PSC were prospectively scanned using non-contrast MRCP. Quantitative metrics were calculated using MRCP+ post-processing software to assess duct diameters and dilated and strictured regions. Additionally, a hepatopancreatobiliary radiologist (blinded to clinical details, biochemistry and quantitative biliary metrics) reported each scan, including ductal disease assessment according to the modified Amsterdam Cholangiographic Score (MAS).
At baseline, 14 quantitative MRCP+ metrics were found to be significantly different in patients with PSC (N = 55) compared to those with primary biliary cholangitis (N = 55), autoimmune hepatitis (N = 57) and healthy controls (N = 18). In PSC specifically, baseline metrics quantifying the number of strictures and the number and length of bile ducts correlated with the MAS, transient elastography and serum ALP values (p < 0.01 for all correlations). Over a median 371-day follow-up (range: 364-462), 29 patients with PSC underwent repeat MRCP, of whom 15 exhibited quantitative changes in MRCP+ metrics. Compared to baseline, quantitative MRCP+ identified an increasing number of strictures over time (p < 0.05). Comparatively, no significant differences in biochemistry, elastography or the MAS were observed between timepoints. Quantitative MRCP+ metrics remained stable in non-PSC liver disease.
Quantitative MRCP+ identifies changes in ductal disease over time in PSC, despite stability in biochemistry, liver stiffness and radiologist-derived cholangiographic assessment (trial registration: ISRCTN39463479).
原发性硬化性胆管炎(PSC)的胆道疾病影像学标志物具有用于临床和试验疾病监测的潜力。在此,我们根据疾病的自然史评估定量磁共振胰胆管成像(MRCP)指标随时间的变化情况。
前瞻性地对 PSC 患者进行非对比性 MRCP 扫描。使用 MRCP+后处理软件计算定量指标,以评估胆管直径和扩张及狭窄区域。此外,肝胆胰放射科医师(对临床细节、生物化学和定量胆道指标均不知情)根据改良阿姆斯特丹胆管造影评分(MAS)报告每次扫描的胆管疾病评估情况。
在基线时,PSC 患者(N=55)的 14 项定量 MRCP+指标与原发性胆汁性胆管炎(N=55)、自身免疫性肝炎(N=57)和健康对照(N=18)患者相比存在显著差异。具体到 PSC,定量评估狭窄数量、胆管数量和长度的基线指标与 MAS、瞬态弹性成像和血清 ALP 值相关(所有相关性的 p 值均<0.01)。在中位 371 天的随访期间(范围:364-462),29 例 PSC 患者接受了重复 MRCP,其中 15 例患者的 MRCP+指标定量发生变化。与基线相比,定量 MRCP+随时间推移识别出更多的狭窄(p<0.05)。相比之下,在各个时间点之间,生化、弹性成像或 MAS 没有显著差异。非 PSC 肝病患者的定量 MRCP+指标保持稳定。
尽管生化、肝硬度和放射科医师评估的胆管造影结果稳定,但定量 MRCP+可识别 PSC 患者胆管疾病随时间的变化(试验注册:ISRCTN39463479)。