Not provided
Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| U01DK103149 | U.S. NIH Grant/Contract | View source | |
| U01DK103140 | U.S. NIH Grant/Contract | View source | |
| U01DK103135 | U.S. NIH Grant/Contract | View source | |
| U01DK084575 | U.S. NIH Grant/Contract | View source | |
| U01DK084538 | U.S. NIH Grant/Contract | View source | |
| U01DK084536 | U.S. NIH Grant/Contract | View source | |
| U01DK062503 | U.S. NIH Grant/Contract | View source | |
| U01DK062500 | U.S. NIH Grant/Contract | View source | |
| U01DK062497 | U.S. NIH Grant/Contract | View source | |
| U01DK062481 | U.S. NIH Grant/Contract | View source | |
| U01DK062470 | U.S. NIH Grant/Contract | View source | |
| U01DK062466 | U.S. NIH Grant/Contract | View source | |
| U01DK062456 | U.S. NIH Grant/Contract | View source | |
| U01DK062453 | U.S. NIH Grant/Contract | View source | |
| U01DK062452 | U.S. NIH Grant/Contract | View source | |
| U01DK062445 | U.S. NIH Grant/Contract | View source | |
| U01DK062436 | U.S. NIH Grant/Contract | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) | NIH |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Noninvasive monitoring of liver fibrosis is an unmet need within the clinical management of pediatric chronic liver disease. While liver biopsy is often used in the initial diagnostic evaluation, subsequent biopsies are rarely performed because of inherent invasiveness and risks. This study will evaluate the role of non-invasive FibroScan™ technology to detect and quantify liver fibrosis.
Noninvasive monitoring of liver fibrosis is an unmet and critical need within the clinical management of children with chronic liver disease. While liver biopsy is often used in the initial diagnostic evaluation of children with liver disease, subsequent surveillance liver biopsy is rarely performed in children because of its inherent invasiveness and risks. Therefore, our understanding of the natural history of fibrosis progression in children is limited. The patchy nature of fibrosis in many important pediatric liver diseases [e.g. biliary atresia (BA) and cystic fibrosis liver disease (CFLD)] limits the utility of sequential liver biopsy even if it were to be employed in clinical practice in pediatrics. Thus, non-invasive means of assessing liver fibrosis throughout the liver would be highly desirable and clinically useful in pediatric hepatology. ChiLDReN is poised and uniquely qualified to conduct a comprehensive longitudinal assessment of the utility of FibroScan™-specific elastography, liver stiffness measurement (LSM) as a measure of hepatic fibrosis in children with serious chronic cholestatic liver disease.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| All Subjects | All subjects will be recruited from the Children parent studies: LOGIC (NCT00571272), BASIC (NCT00345553) and PROBE (NCT00061828) and will undergo Liver Stiffness Measurement (LSM). Subjects in these studies have one or more of the following conditions: biliary atresia (BA), Alpha1 Anti-trypsin Deficiency (A1AT) or Alagille Syndrome (ALGS). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Liver Stiffness Measurement (LSM) | Other | LSM will be measured via transient elastography utilizing the non-invasive FibroScan™ ultrasound device. LSM will be measured at Baseline, Year 1 and Year 2 visits. |
| Measure | Description | Time Frame |
|---|---|---|
| Compare the distribution of LSM at enrollment between participants with and without portal hypertension | A linear model will be fit to FibroScan™ values at enrollment to assess the impact of portal hypertension on LSM, controlling for important covariates such as age, gender, and race | Enrollment |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Liver Stiffness Measurement (LSM) obtained via transient elastography from baseline to LSM at the Year 1 and Year 2 visits in participants with biliary atresia (BA). | The key secondary aim (Aim 2) compares the one- and two-year FibroScan™ values to those at enrollment in participants with BA. | Baseline, Year 1 Visit, Year 2 Visit |
| Measure | Description | Time Frame |
|---|---|---|
| Change from LSM Measurement obtained via transient elastography from baseline, to LSM at the Year 1 and Year 2 visits in participants with A1AT and ALGS | To prospectively explore changes in LSM over time by FibroScan™ in children with A1AT and ALGS. | Baseline, Year 1, and Year 2 Visits in children with A2AT, ALGS, and BA. |
Inclusion Criteria:
Age less than 21 years at the time of enrollment
Participants enrolled in a ChiLDReN based prospective observational cohort study (PROBE, BASIC, or LOGIC)
Willingness and ability to participate in the study for up to 24 months
One of the following three diagnoses
Exclusion Criteria:
Not provided
Not provided
Not provided
All children with an established diagnosis of BA (excluding those with known situs inversus or polysplenia/asplenia), who are actively followed at participating ChiLDReN sites and enrolled in PROBE or BASIC will be eligible for the trial. In addition, all children with A1AT or ALGS actively followed at one of these sites and enrolled in LOGIC will also be eligible.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Benjamin Shneider, MD | Baylor College of Medicine | Principal Investigator |
| Ed Doo, MD | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) | Study Director |
| Averell Sherker, MD | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) | Study Director |
| John Magee, MD | University of Michigan Medical Center, Ann Arbor | Principal Investigator |
| Lisa Henn, PhD | Arbor Research Collaborative of Health | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Children's Hospital Los Angeles | Los Angeles | California | 90027 | United States | ||
| University of California at San Francisco (UCSF) |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 20678019 | Background | Pinzani M, Macias-Barragan J. Update on the pathophysiology of liver fibrosis. Expert Rev Gastroenterol Hepatol. 2010 Aug;4(4):459-72. doi: 10.1586/egh.10.47. | |
| 25920084 | Background | Trautwein C, Friedman SL, Schuppan D, Pinzani M. Hepatic fibrosis: Concept to treatment. J Hepatol. 2015 Apr;62(1 Suppl):S15-24. doi: 10.1016/j.jhep.2015.02.039. |
| Label | URL |
|---|---|
| Childhood Liver Disease Research Network (ChiLDReN) website | View source |
Not provided
De-identified data will be shared via the NIDDK's Data Repository.
Not provided
Not provided
Not provided
Not provided
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Dec 12, 2019 |
Not provided
Not provided
Not provided
Not provided
Plasma and serum
|
| Number of participants in whom a valid FibroScan™ LSM can be obtained |
The investigators will define two measures of the feasibility of FibroScans™ in the participant populations with a "technically possible" FibroScan™, defined as the number of subjects with at least 10 FibroScan™ measurements obtained divided by the number assessed. The proportion of subjects with FibroScans™ of "acceptable quality" is defined as the number of subjects with FibroScan™ LSM with the ratio of the interquartile range and median of the 10 measurements <30%, of which at least 6 are completed, divided by the number assessed. The proportions and their 95% confidence intervals will be provided using the Wald method; however, the Wilson-Score methods will be used if the sample sizes are small or the proportion is small for a disease group. We will perform separate analyses for subjects <2 years of age and for those >2 years of age. |
| Baseline, Year 1 Visit, Year 2 Visit |
| FibroScan™ LSM values at enrollment and conventional laboratory determinants of liver disease ((Pediatric End Stage Liver Disease (PELD) and APRI (Aspartate Aminotransferase (AST) to Platelet Ratio Index)). | The analysis will be limited to subjects for whom a PELD can be calculated (i.e., those for whom the individual components of the PELD score are available). Note that PELD will be calculated for all pediatric participants including those greater than 12 years of age. PELD is calculated as PELD = 4.80 x [ln serum bilirubin (mg/dL)] + 18.57 x [ln INR] - 6.87 x [ln albumin (g/dL)] + 4.36(<1 year old) + 6.67(growth failure) [www.unos.org\ [blocked]] APRI is calculated as APRI = AST/upper limit of normal AST x 100 [U/L] Platelet Count (109/L) [U/L]) | Baseline |
| San Francisco |
| California |
| 94143 |
| United States |
| Children's Hospital Colorado | Aurora | Colorado | 80045 | United States |
| Children's Healthcare of Atlanta (Emory University) | Atlanta | Georgia | 30322 | United States |
| Ann & Robert H. Lurie Children's Hospital of Chicago | Chicago | Illinois | 60611 | United States |
| Riley Hospital for Children | Indianapolis | Indiana | 46202 | United States |
| Cincinnati Children's Memorial Hospital | Cincinnati | Ohio | 60190 | United States |
| Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 | United States |
| Children's Hospital of Pittsburgh | Pittsburgh | Pennsylvania | 15224 | United States |
| Texas Children's Hospital (Baylor College of Medicine) | Houston | Texas | 77030 | United States |
| University of Utah | Salt Lake City | Utah | 84113 | United States |
| Seattle Children's Hospital | Seattle | Washington | 98105 | United States |
| Hospital for Sick Children | Toronto | Ontario | M5G 1X8 | Canada |
| 22903006 | Background | Shneider BL, Abel B, Haber B, Karpen SJ, Magee JC, Romero R, Schwarz K, Bass LM, Kerkar N, Miethke AG, Rosenthal P, Turmelle Y, Robuck PR, Sokol RJ; Childhood Liver Disease Research and Education Network. Portal hypertension in children and young adults with biliary atresia. J Pediatr Gastroenterol Nutr. 2012 Nov;55(5):567-73. doi: 10.1097/MPG.0b013e31826eb0cf. |
| 25651489 | Background | Teckman JH, Rosenthal P, Abel R, Bass LM, Michail S, Murray KF, Rudnick DA, Thomas DW, Spino C, Arnon R, Hertel PM, Heubi J, Kamath BM, Karnsakul W, Loomes KM, Magee JC, Molleston JP, Romero R, Shneider BL, Sherker AH, Sokol RJ; Childhood Liver Disease Research Network (ChiLDReN). Baseline Analysis of a Young alpha-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension. J Pediatr Gastroenterol Nutr. 2015 Jul;61(1):94-101. doi: 10.1097/MPG.0000000000000753. |
| 11172184 | Background | Bonis PA, Friedman SL, Kaplan MM. Is liver fibrosis reversible? N Engl J Med. 2001 Feb 8;344(6):452-4. doi: 10.1056/NEJM200102083440610. No abstract available. |
| 20848612 | Background | Ozaslan E. Drug-induced autoimmune hepatitis: an easily reversible type of liver fibrosis? Hepatology. 2011 Jan;53(1):370. doi: 10.1002/hep.23858. Epub 2010 Jul 29. No abstract available. |
| 18193125 | Background | Saleh HA, Abu-Rashed AH. Liver biopsy remains the gold standard for evaluation of chronic hepatitis and fibrosis. J Gastrointestin Liver Dis. 2007 Dec;16(4):425-6. No abstract available. |
| 17440193 | Background | Huang JF, Hsieh MY, Dai CY, Hou NJ, Lee LP, Lin ZY, Chen SC, Wang LY, Hsieh MY, Chang WY, Yu ML, Chuang WL. The incidence and risks of liver biopsy in non-cirrhotic patients: An evaluation of 3806 biopsies. Gut. 2007 May;56(5):736-7. doi: 10.1136/gut.2006.115410. No abstract available. |
| 11230761 | Background | Falck-Ytter Y, McCullough AJ. The risks of percutaneous liver biopsy. Hepatology. 2001 Mar;33(3):764. doi: 10.1053/jhep.2001.0103303le01. No abstract available. |
| 22249806 | Background | Westheim BH, Ostensen AB, Aagenaes I, Sanengen T, Almaas R. Evaluation of risk factors for bleeding after liver biopsy in children. J Pediatr Gastroenterol Nutr. 2012 Jul;55(1):82-7. doi: 10.1097/MPG.0b013e318249c12a. |
| 22249089 | Background | El-Shabrawi MH, El-Karaksy HM, Okahsa SH, Kamal NM, El-Batran G, Badr KA. Outpatient blind percutaneous liver biopsy in infants and children: is it safe? Saudi J Gastroenterol. 2012 Jan-Feb;18(1):26-33. doi: 10.4103/1319-3767.91735. |
| 7588960 | Background | Lachaux A, Le Gall C, Chambon M, Regnier F, Loras-Duclaux I, Bouvier R, Pinzaru M, Stamm D, Hermier M. Complications of percutaneous liver biopsy in infants and children. Eur J Pediatr. 1995 Aug;154(8):621-3. doi: 10.1007/BF02079063. |
| 21235598 | Background | Castera L, Bernard PH, Le Bail B, Foucher J, Trimoulet P, Merrouche W, Couzigou P, de Ledinghen V. Transient elastography and biomarkers for liver fibrosis assessment and follow-up of inactive hepatitis B carriers. Aliment Pharmacol Ther. 2011 Feb;33(4):455-65. doi: 10.1111/j.1365-2036.2010.04547.x. |
| 25003372 | Background | Kim S, Kang Y, Lee MJ, Kim MJ, Han SJ, Koh H. Points to be considered when applying FibroScan S probe in children with biliary atresia. J Pediatr Gastroenterol Nutr. 2014 Nov;59(5):624-8. doi: 10.1097/MPG.0000000000000489. |
| Aug 27, 2024 |
| Prot_SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form | Dec 12, 2019 | Jan 24, 2020 | ICF_000.pdf |
| ID | Term |
|---|---|
| D001656 | Biliary Atresia |
| D016738 | Alagille Syndrome |
| D019896 | alpha 1-Antitrypsin Deficiency |
| D006975 | Hypertension, Portal |
| D008103 | Liver Cirrhosis |
| D002779 | Cholestasis |
| ID | Term |
|---|---|
| D001649 | Bile Duct Diseases |
| D001660 | Biliary Tract Diseases |
| D004066 | Digestive System Diseases |
| D004065 | Digestive System Abnormalities |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D002780 | Cholestasis, Intrahepatic |
| D008107 | Liver Diseases |
| D006330 | Heart Defects, Congenital |
| D018376 | Cardiovascular Abnormalities |
| D002318 | Cardiovascular Diseases |
| D000015 | Abnormalities, Multiple |
| D030342 | Genetic Diseases, Inborn |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D013352 | Subcutaneous Emphysema |
| D004646 | Emphysema |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D005355 | Fibrosis |
Not provided
Not provided