Longitudinal Assessment of Transient Elastography in Cystic Fibrosis



Status:Enrolling by invitation
Conditions:Gastrointestinal, Pulmonary
Therapuetic Areas:Gastroenterology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:6 - 26
Updated:4/17/2018
Start Date:April 1, 2017
End Date:December 2020

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To determine if transient elastography (TE), when combined with ultrasound (US) pattern
characterization can improve the prediction of progression to a nodular pattern on US.

To confirm the feasibility of obtaining TE measurements in children with Cystic Fibrosis (CF)
To prospectively assess whether TE data are associated with conventional laboratory markers
of hepatic fibrosis To determine the variability of TE measurements taken at different sites
in the same patient

A noninvasive assessment of hepatic fibrosis is desperately needed to advance the care of
children with CF significant liver disease and to provide for measurements during clinical
trials. That global assessment might serve as both a predictor/descriptor of disease course
but also as a critical biomarker for clinical research. FibroScan® measurement of liver
stiffness has great potential to fill this void. The underlying hypothesis of this proposal
is that elastography in addition to US can improved the prediction of the development of a
nodular liver on US and development of portal hypertension over time in children and young
adults with CF.

Inclusion Criteria:

- Participants enrolled in CFLD NET PUSH study in longitudinal follow up at centers with
Fibroscan available (currently 8/11 centers)

- Entry criteria for that study were:

- CF as determined by sweat chloride >60 meq/l

- Pancreatic insufficiency

- Age 3-12 years old at entry

- For entry into the longitudinal follow up subjects were in one of two groups

- A screening US pattern of nodular liver (CIR), heterogeneous increased
echogenicity (HTG) or homogeneous increased echogenicity (HMG)

- A screening US pattern of normal (NL) matched to a HTG subject (2 NL:1HTG) by
age, center and pseudomonas status

Exclusion Criteria:

- Exited from the PUSH Study

- Unable / unwilling to sign consent
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