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Liver biopsy in modern clinical practice: a pediatric point-of-view

Ovchinsky, Nadia; Moreira, Roger K; Lefkowitch, Jay H; Lavine, Joel E
Liver biopsy remains the foundation of evaluation and management of liver disease in children, although the role of the liver biopsy is changing with development of alternative methods of diagnosis and advancement of hepatic imaging techniques. The indications for liver biopsy are evolving as current knowledge of etiologies, noninvasive biomarker alternatives, and treatment options in pediatric liver disease are expanding. The procedure can often be complicated in children by technical difficulties, cost, and smaller specimen size. Communication and partnership of clinicians with pathologists experienced in pediatric liver diseases are essential. DNA sequencing, novel imaging modalities, noninvasive biomarkers of fibrosis and apoptosis, proteomics, and genome-wide association studies offer potential alternative methods for evaluation of liver disease in children. This review presents specific indications, considerations, methods, complications, contraindications, and alternatives for pediatric liver biopsy.
PMCID:3404724
PMID: 22692288
ISSN: 1533-4031
CID: 5416452

Lower serum hepcidin and greater parenchymal iron in nonalcoholic fatty liver disease patients with C282Y HFE mutations

Nelson, James E; Brunt, Elizabeth M; Kowdley, Kris V; Abrams, Stephanie H; Angeli, Leanel; McCullough, Arthur J; Brandt, Patricia; Bringman, Diane; Dasarathy, Srinivasan; Dasarathy, Jaividhya; Hawkins, Carol; Liu, Yao-Chang; Rogers, Nicholette; Stager, Margaret; Whitwell, Judy; McCullough, Arthur J; Dasarathy, Srinivasan; Pagadala, Mangesh; Sargent, Ruth; Yerian, Lisa; Zein, Claudia; Merriman, Raphael; Nguyen, Anthony; Mohan, Parvathi; Nair, Kavita; DeVore, Stephanie; Kohli, Rohit; Lake, Kathleen; Xanthakos, Stavra; Cosme, Yohaime; Lavine, Joel E; Mencin, Ali; Ovchinsky, Nadia; Abdelmalek, Manal F; Buie, Stephanie; Diehl, Anna Mae; Gottfried, Marcia; Guy, Cynthia; Hanna, Meryt; Kigongo, Christopher; Killenberg, Paul; Kwan, Samantha; Pan, Yi-Ping; Piercy, Dawn; Smith, Melissa; Srivastava, Savita; Byam, Elizabeth; Chalasani, Naga; Cummings, Oscar W; Ghabril, Marwan; Klipsch, Ann; Molleston, Jean P; Ragozzino, Linda; Subbarao, Girish; Tandra, Sweta; Vuppalanchi, Raj; Devadason, Caroline; Pfeifer, Kimberly; Scheimann, Ann; Torbenson, Michael; Kerkar, Nanda; Narayanappa, Sreevidya; Suchy, Frederick; Dunne, Katherine; Fishbein, Mark H; Jacques, Katie; Quinn, Ann; Riazi, Cindy; Whitington, Peter F; Barlow, Sarah; Derdoy, Jose; King, Debra; Morris, Andrea; Siegner, Joan; Stewart, Susan; Neuschwander-Tetri, Brent A; Thompson, Judy; Behling, Cynthia; Collins, Jennifer; Durelle, Janis; Hassanein, Tarek; Lavine, Joel E; Loomba, Rohit; Morgan, Anya; Rose, Steven; Patton, Heather; Schwimmer, Jeffrey B; Sirlin, Claude; Stein, Tanya; Aouizerat, Bradley; Bambha, Kiran; Bass, Marissa; Bass, Nathan M; Ferrell, Linda D; Filipowski, Danuta; Fleck, Shannon; Gu, Bo; Hameed, Bilal; Langlois, Camille; Pabst, Mark; Rosenthal, Monique; Rosenthal, Philip; Steel, Tessa; Coffey, Melissa; Galdzicka, Sarah; Murray, Karen; Yeh, Matthew; Boyett, Sherry; Contos, Melissa J; Fuchs, Michael; Jones, Amy; Luketic, Velimir A C; Puri, Puneet; Sandhu, Bimalijit; Sanyal, Arun J; Sargeant, Carol; Noble, Kimberly; White, Melanie; Ackermann, Sarah; Kowdley, Kris V; Park, Jane; Pierce, Tracey; Mooney, Jody; Nelson, James; Shaw, Cheryl; Stead, Alice; Wang, Chia; Brunt, Elizabeth M; Kleiner, David E; Grave, Gilman D; Doo, Edward C; Hoofnagle, Jay H; Robuck, Patricia R; Sherker, Averell; Belt, Patricia; Brancati, Frederick L; Clark, Jeanne M; Colvin, Ryan; Donithan, Michele; Green, Mika; Hollick, Rosemary; Isaacson, Milana; Jin, Wana K; Lydecker, Alison; Mann, Pamela; May, Kevin P; Miriel, Laura; Sternberg, Alice; Tonascia, James; Unalp-Arida, Aynur; Van Natta, Mark; Vaughn, Ivana; Wilson, Laura; Yates, Katherine
UNLABELLED:Hepcidin regulation is linked to both iron and inflammatory signals and may influence iron loading in nonalcoholic steatohepatitis (NASH). The aim of this study was to examine the relationships among HFE genotype, serum hepcidin level, hepatic iron deposition, and histology in nonalcoholic fatty liver disease (NAFLD). Single-nucleotide polymorphism genotyping for C282Y (rs1800562) and H63D (rs1799945) HFE mutations was performed in 786 adult subjects in the NASH Clinical Research Network (CRN). Clinical, histologic, and laboratory data were compared using nonparametric statistics and multivariate logistic regression. NAFLD patients with C282Y, but not H63D mutations, had lower median serum hepcidin levels (57 versus 65 ng/mL; P = 0.01) and higher mean hepatocellular (HC) iron grades (0.59 versus 0.28; P < 0.001), compared to wild-type (WT) subjects. Subjects with hepatic iron deposition had higher serum hepcidin levels than subjects without iron for all HFE genotypes (P < 0.0001). Hepcidin levels were highest among patients with mixed HC/reticuloendothelial system cell (RES) iron deposition. H63D mutations were associated with higher steatosis grades and NAFLD activity scores (odds ratio [OR], ≥1.4; 95% confidence interval [CI]: >1.0, ≤2.5; P ≤ 0.041), compared to WT, but not with either HC or RES iron. NAFLD patients with C282Y mutations had less ballooning or NASH (OR, ≤0.62; 95% CI: >0.39, <0.94; P ≤ 0.024), compared to WT subjects. CONCLUSIONS/CONCLUSIONS:The presence of C282Y mutations in patients with NAFLD is associated with greater HC iron deposition and decreased serum hepcidin levels, and there is a positive relationship between hepatic iron stores and serum hepcidin level across all HFE genotypes. These data suggest that body iron stores are the major determinant of hepcidin regulation in NAFLD, regardless of HFE genotype. A potential role for H63D mutations in NAFLD pathogenesis is possible through iron-independent mechanisms.
PMCID:3462887
PMID: 22611049
ISSN: 0270-9139
CID: 2807682

Conjugated bile acids as potential early markers of parenteral nutrition-associated liver disease [Comment]

Ovchinsky, Nadia
PMID: 20852172
ISSN: 1941-2444
CID: 5416442

A new measure of placebo response and patient satisfaction in office encounters

Ovchinsky, Alexander; Ovchinsky, Nadia; Rosenfeld, Richard M
OBJECTIVES/OBJECTIVE:Placebo response is defined as a change in health status resulting from the symbolic significance attributed by the patient or proxy to the physician encounter. Our goals were to validate the PR12 survey as a measure of placebo response and to analyze the placebo response as a discrete and measurable component of everyday office encounters with the otolaryngologist. STUDY DESIGN/METHODS:This was a prospective, before-and-after clinical outcomes study of 95 children aged 6 months to 12 years conducted in an academic metropolitan pediatric otolaryngology practice. Caregivers completed the PR-12 survey at entry and at least 4 weeks later. The survey included 3 domains (4 questions each) reflecting the main components of the placebo response: meaningful explanation, care and concern, and mastery and control. PR-12 was correlated with longitudinal change in health status at least 1 to 2 months after the baseline visit. Outcome measures included direct and indirect measures of change in disease-specific quality of life and satisfaction with change. RESULTS:Test-retest reliability was fair for most PR-12 survey items (R = 0.41 to 0.76) but was higher for domains (0.60 to 0.66) and the overall survey score (0.66). PR-12 had excellent internal consistency (Cronbach's alpha 0.91) and appropriate construct validity. Caregiver satisfaction change at follow-up correlated with the PR-12 (r = -.25, P = 0.036). Conversely, no correlation was seen between the PR-12 and direct and indirect measures of change in disease specific quality of life. CONCLUSION/CONCLUSIONS:Placebo response is an important and potentially measurable aspect of clinical encounters. PR-12 is a promising first step at creating a brief, reliable, and valid instrument to assess the placebo response. SIGNIFICANCE/CONCLUSIONS:Reemphasizing the therapeutic potential of the doctor-patient relationship may improve quality of care and disease outcomes.
PMID: 15365548
ISSN: 0194-5998
CID: 5054382

Cytokeratins 7 & 20 in the diagnosis of Barrett's esophgus (BE) with and without dysplasia [Meeting Abstract]

Shen, E; Ovchinsky, N; Wong, RH; Hirota, WK; Baroni, DS; Das, KM; Griffel, LH
ISI:000168514702068
ISSN: 0016-5085
CID: 5416942