Raychaudhuri Siba P, Abdelhafez Yasser G, Mazza Dario F, Raychaudhuri Smriti K, Cherry Simon R, Nardo Lorenzo, Badawi Ramsey D, Chaudhari Abhijit J
Department of Internal Medicine-Rheumatology, University of California Davis, Sacramento, CA, USA.
Northern California Veterans Affairs Medical Center, Mather, CA, USA.
Rheumatology (Oxford). 2025 Jun 1;64(6):3483-3491. doi: 10.1093/rheumatology/keae702.
To test the hypothesis that recently-developed total body-positron emission tomography (TB-PET) imaging with integrated computed tomography (CT) will enable low-dose, quantitative, domain-specific evaluation of the total inflammatory burden of psoriatic arthritis (PsA) and associate with established outcome measures of the clinical domains of PsA.
Seventy-one adult participants (40 with PsA, 16 with rheumatoid arthritis (RA), and 15 with osteoarthritis (OA)) underwent 20-min TB-PET/CT scans using [18F]FDG, a glucose analogue radiotracer. [18F]FDG uptake was assessed qualitatively and quantitatively. Rheumatological examinations were performed prior to the scan. For both evaluations, domain-specific assessments included 68 joints, 6 entheses, 20 nails, axial disease and dactylitis.
[18F]FDG PET uptake consistent with joint involvement and enthesitis was noted in 100% of participants with PsA. Other features included nail matrix pathology (53%), spinal involvement (60%), active sacroiliitis (13%) and dactylitis (10%). Patterns of [18F]FDG uptake in PsA differed from those in participants with RA or OA. There was a high concordance between TB-PET measures and the domain-specific assessments of the joint (75%), entheseal (79%) and nail (65%) pathology. TB-PET was positive for an additional 15% of joints, 20% of entheses and 13% of nails that were negative on clinical assessments.
TB-PET/CT identified inflammatory pathologies characteristic to all clinical domains of PsA and thus provided an in vivo evaluation of systemic PsA inflammatory burden. This promising tool may further contribute to identifying pathologies that may be occult, provide biomarkers to diagnose and differentiate PsA at an early stage, and to monitor early treatment response.
检验如下假设,即最近开发的结合计算机断层扫描(CT)的全身正电子发射断层扫描(TB-PET)成像技术能够实现对银屑病关节炎(PsA)的总炎症负担进行低剂量、定量、特定领域的评估,并与PsA临床领域既定的疗效指标相关联。
71名成年参与者(40名患有PsA,16名患有类风湿关节炎(RA),15名患有骨关节炎(OA))使用葡萄糖类似物放射性示踪剂[18F]FDG进行了20分钟的TB-PET/CT扫描。对[18F]FDG摄取情况进行了定性和定量评估。在扫描前进行了风湿病学检查。对于这两项评估,特定领域的评估包括68个关节、6个附着点、20个指甲、轴向疾病和指(趾)炎。
100%的PsA参与者中观察到与关节受累和附着点炎一致的[18F]FDG摄取。其他特征包括甲床病变(53%)、脊柱受累(60%)、活动性骶髂关节炎(13%)和指(趾)炎(10%)。PsA中[18F]FDG摄取模式与RA或OA参与者不同。TB-PET测量结果与关节(75%)、附着点(79%)和指甲(65%)病变的特定领域评估之间具有高度一致性。TB-PET在临床评估为阴性的关节中额外发现15%呈阳性,附着点中20%呈阳性,指甲中13%呈阳性。
TB-PET/CT识别出了PsA所有临床领域的特征性炎症病变,从而对系统性PsA炎症负担进行了体内评估。这一有前景的工具可能进一步有助于识别可能隐匿的病变,提供早期诊断和鉴别PsA的生物标志物,并监测早期治疗反应。