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Interventional AI-Human Collaboration for Steatotic Liver Disease Screening

2026년 5월 23일 업데이트: Yu Shi, Shengjing Hospital

AI-Driven Opportunistic Screening and Risk-Adapted Management of Steatotic Liver Disease

Steatotic liver disease (SLD) is one of the most prevalent chronic liver diseases worldwide, affecting nearly 30% of the global population and projected to exceed 55% by 2040. Timely identification and management of intermediate- and high-risk SLD patients are essential, yet early detection remains challenging because current diagnostic modalities, such as biopsy, ultrasonography, and serum indices, are invasive, insensitive, operator-dependent, or difficult to scale. In contrast, non-contrast CT is widely available in routine care and offers substantial potential for opportunistic SLD screening, although this value has not been fully utilized. Our previously developed MAOSS model accurately identifies intermediate- and high-risk individuals, with MAOSS score≥1.6 combined with Fibro Score ≥1.7, demonstrating high sensitivity and specificity in our large-scale retrospective study. However, despite these promising retrospective findings, the model has not undergone prospective interventional validation, and it remains unclear whether an AI-guided workflow can truly enhance clinical risk stratification, diagnostic yield, and downstream management in real-world SLD populations. Therefore, a prospective intervention study is needed to determine whether MAOSS-guided identification and recall of at-risk individuals can meaningfully improve fibrosis detection and optimize clinical care pathways for SLD.

연구 개요

상세 설명

The AIG-SLD Screening Project is a single-arm, open-label, prospective interventional study designed to evaluate the effectiveness of a MAOSS-guided identification and AI-human collaboration recall strategy for detecting individuals at intermediate or high risk of steatotic liver disease (SLD) and for assessing intervention outcomes. The trail will prospectively and consecutively enroll around 8000 eligible adults aged ≥18 years who undergo routine chest or abdominal non-contrast CT (NCCT) with adequate hepatic coverage .

The AI system i.e. MAOSS will be embedded within the standard clinical workflow to evaluate the real-world performance and the impact of AIG-SLD screening. All eligible NCCT scans will be evaluated through two parallel streams:

  1. Standard of Care (SoC) workflow: Radiologists perform independent assessments, first-line radiologists review followed by a senior radiologist finalizing the report.
  2. AIG workflow: The MAOSS system simultaneously analyzes the identical imaging data in real-time.

The system screens patients with clinically suspected SLD by flagging those with a MAOSS score ≥1.6 and a FIBRO Score ≥1.7 for recall. These algorithmic flags will be compared against radiologists' determinations of clinically significant SLD. Management pathways are defined as follows: (1) Concordant cases: If the Standard of Care (SoC) and the AIG pathway agree (both recommending recall or both recommending no recall), the agreed-upon decision will be executed. (2) Discordant cases: If the SoC and AIG pathways disagree, patients will be recalled for primary hepatology care to ensure safety.

Primary hepatology care begins with the collection of questionnaires regarding medical history, lifestyle, alcohol consumption, and metabolic risks (Type 2 Diabetes Mellitus, obesity, metabolic syndrome, significant alcohol consumption, or viral hepatitis) followed by further serum laboratory tests and Transient Elastography (e.g., FibroScan). Recalled patients will be managed according to the MAOSS pathway starting with FIB-4 stratification (<1.3, 1.3-2.67, >2.67), followed by FAST stratification (<0.35, ≥0.35) as needed. Intermediate-to-high-risk patients will proceed to escalated care involving MRE, MRI-PDFF, or liver biopsy. Management is then determined by MRE-derived Liver Stiffness Measurement (LSM): patients with LSM < 3.5 kPa will receive lifestyle interventions and annual reassessment; those with LSM 3.5-5.0 kPa (F2-F3) will receive pharmacological or therapeutic interventions; and those with LSM ≥ 5.0 kPa (F4) will undergo cirrhosis-based management. Patients in the latter two groups will be reassessed every six months to monitor changes in steatosis and fibrosis.

연구 유형

중재적

등록 (추정된)

7969

단계

  • 해당 없음

연락처 및 위치

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연구 장소

    • Liaoning
      • Shenyang, Liaoning, 중국, 110004
        • Shengjing Hospital of China Medical University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

설명

Inclusion Criteria:

  • Adults aged ≥18 years undergoing routine non-contrast or contrast-enhanced chest or abdominal CT examination.
  • CT images with adequate hepatic coverage and sufficient image quality for MAOSS analysis.
  • Willing to undergo the recall evaluation and either: having a FIB-4 result within the past 1 month, or willing to complete blood testing (ALT, AST, platelet count) required for FIB-4 calculation and undergo FibroScan or MRE assessment.
  • Willing to participate in the study and able to provide written informed consent at the time of recall.

Exclusion Criteria:

  • Known malignant liver tumors (e.g., HCC, cholangiocarcinoma) or a history of liver transplantation or major hepatic resection.
  • Known cirrhosis based on noninvasive fibrosis assessment tests, liver biopsy or complications of decompensated disease, or with a documented history of cirrhosis identified by clinical notes will be excluded.
  • Biliary obstruction, acute cholangitis, or other conditions that may interfere with interpretation of liver biochemistry or fibrosis risk assessment.
  • CT images with severe artifacts or incomplete liver coverage preventing reliable MAOSS analysis.
  • Severe acute systemic illness (e.g., sepsis, shock, acute heart failure), or pregnancy or breastfeeding.
  • Unwilling or unable to complete recall procedures, including required blood tests, FibroScan, or MRE when indicated, or unable to comply with study follow-up.
  • Severe comorbidity with an expected survival of less than 1 year (e.g., terminal malignancy).

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 상영
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: AI-human collaboration for SLD screening
In the prospective analysis phase, all eligible NCCT scans will be evaluated through two parallel streams: 1. Standard of Care (SoC) workflow: Radiologists perform independent assessments as per standard clinical procedures (e.g., first-line radiologists' reviews followed by senior radiologist finalizing the report). 2. AIG workflow: The MAOSS system simultaneously analyzes the identical imaging data in real-time.
The system screens patients with clinically suspected SLD by flagging those with a MAOSS score ≥1.6 and a FIBRO Score ≥1.7 for recall. These algorithmic flags will be compared against radiologists' determinations of clinically significant SLD. Management pathways are defined as follows: (1) Concordant cases: If the Standard of Care (SoC) and the AIG pathway agree (both recommending recall or both recommending no recall), the agreed-upon decision will be executed. (2) Discordant cases: If the SoC and AIG pathways disagree, patients will be recalled for primary hepatology care to ensure safety and avoid potential missed diagnosis.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Effective referral yield for escalated hepatology care
기간: 6 months
Effective referral yield: the proportion of patients referred for escalated hepatology care confirmed with clinically significant (or above) fibrosis by MRE/liver biposy. A non-inferiority test (and estimates of the associated absolute and relative differences) will be performed for effective referral yield between SoC and AIG workflow.
6 months

2차 결과 측정

결과 측정
측정값 설명
기간
Real-World Screening Specificity
기간: Duration of the study (12 months)
A critical safety endpoint is to determine if AIG-SLD care pathway maintains a high specificity to prevent false referral, thereby avoiding unnecessary interventions.
Duration of the study (12 months)
Real-World Screening Sensitivity
기간: Duration of the study (12 months)
A critical efficacy endpoint is to determine if AIG-SLD care pathway is sufficiently sensitive to identify patients who actually need interventions.
Duration of the study (12 months)
Real-World Screening Negative predictive value
기간: Duration of the study (12 months)
This evaluates the AIG-SLD care pathway's ability to correctly exclude low-risk patients who actually do not need interventions.
Duration of the study (12 months)
Intervention Success (Fibrosis Reversion)
기간: Duration of the study (12 months)
The proportion of patients referred for escalated care achieves fibrosis stage reversion.
Duration of the study (12 months)
Intervention Success (Steatosis Reversion)
기간: Duration of the study (12 months)
The proportion of patients referred for escalated care achieves steatosis stage Reversion.
Duration of the study (12 months)
Quantitative Liver Stiffness Trends
기간: Duration of the study (12 months)
The overall longitudinal changes in Liver Stiffness Measurement (LSM) values for all patients referred to escalated care.
Duration of the study (12 months)
Quantitative Liver Steatosis Trends
기간: Duration of the study (12 months)
The overall longitudinal changes in Liver Fat Content (CAP/PDFF) values for all patients referred to escalated care.
Duration of the study (12 months)
Intervention Patient Adherence
기간: Duration of the study (12 months)
The overall intervention adherence rate for all patients referred to escalated care.
Duration of the study (12 months)

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연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 2월 24일

기본 완료 (추정된)

2026년 8월 30일

연구 완료 (추정된)

2027년 2월 24일

연구 등록 날짜

최초 제출

2026년 5월 23일

QC 기준을 충족하는 최초 제출

2026년 5월 23일

처음 게시됨 (실제)

2026년 5월 29일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 23일

마지막으로 확인됨

2026년 5월 1일

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