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Imalife (IMAL)

Imalife is an additional assessment, performed in ~12,000 adult Lifelines participants in collaboration with the UMCG Department of Radiology.
The aim of Imalife was to use a new computed tomography (CT) scan technique to evaluate quantitative imaging biomarkers of early stages of lung cancer, chronic obstructive pulmonary disease (COPD) and cardiovascular disease (CVD) (the “Big-3”) at ultra-low radiation dose. Imaging biomarkers, combined with clinical and laboratory biomarkers and medical decision support systems, can in the future open up new avenues for effective prevention and/or early diagnostic and treatment protocols. This study provides an invaluable resource for the development and validation of biomarker profiles in the context of personalized medicine.

Protocol

Participants underwent ultra-low-dose CT scanning of lungs and heart with third-generation dual-source CT (SOMATOM Force, Siemens). Scanning was performed during suspended inspiration, according to the standard vendor recommended protocol, with tube current adjusted automatically by the system for body size based on the scout images. The scout images were followed by a CT scan of the lungs in inspiration, and, in a subset of 100 participants per 5-year age/gender category, also in expiration. The latter was performed to determine normal values for expiratory lung density.
To obtain a CT scan of the heart at the moment that the movement of the coronary arteries is the lowest, participants were fitted with ECG electrodes by CT personnel. The software of the CT scanner decided what the best moment is during a regular heartbeat to acquire the CT data of the heart, and subsequently the CT scan of heart was obtained.
The primary end-point was the establishment of reference values of:

  • lung density
  • bronchial wall thickness
  • vascular calcification
  • lung nodules

Participants with a lung nodule between 100-300 mm3 (~5,4% of all scanned participants) were invited for a repeat CT scan after 3-4 months for scientific purposes, to evaluate natural evolution of lung nodules in the general population.

Subcohort

Imalife ran from 2017 to 2022. The assessments were performed in ~12.000 Lifelines participants of 45+ years who completed a pulmonary function test.
To ensure sufficient participants in the older age groups, selection criteria were later adjusted to 60+ and, in the final phase, 75+.

Publications using Imalife data

Variables

A precise list of variables derived from CT-scans will be described later.

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imal.txt · Last modified: 2024/07/22 10:55 by trynke