Metabolomic Analysis for Newborn Screening and Diagnosis of Metabolic Disorders

Similar documents
Newborn Screening & Methods for Diagnosing Inborn Errors of Metabolism

How MS/MS Revolutionized Newborn Screening

Positive Newborn Screens: What do you do next?

HA Convention 2016 Master course How to Handle Abnormal Newborn Metabolic Screening Results Causes, Management and Follow up

MS/MS APPROACHES TO CLINICAL TESTING FOR INBORN ERRORS OF METABOLISM

Newborn Screening: Focus on Treatment

e-learning Fatty Acid Oxidation Defects Camilla Reed and Dr Simon Olpin Sheffield Children s Hospital

Newborn Screen & Development Facts about the genetic diseases new since March 2006 (Excluding Cystic Fibrosis)

Overview of Newborn Screening, Potential Uses of Residual Dried Blood Spots, and Protection of Privacy

Newborn Screening: What s New?

Newborn Screening in Manitoba. Information for Health Care Providers

Routine Newborn Screening, Testing the Newborn Inherited Metabolic Disorders Update August 2015

For Your Baby s Health Department of Health

Metabolic Changes in ASD. Norma J. Arciniegas, MD Simón E. Carlo, MD Instituto Filius

Fatty Acid Oxidation Disorders- an update. Fiona Carragher Biochemical Sciences, GSTS Pathology St Thomas Hospital, London

INBORN ERRORS OF METABOLISM (IEM) IAP UG Teaching slides

[R23-13-MET/HRG] STATE OF RHODE ISLAND AND PROVIDENCE PLANTATIONS DEPARTMENT OF HEALTH. February October October 1992 (E) September 1995

Acylcarnitine measurement in blood spots: methodological aspects, problems and pitfalls with reference to the ERNDIM QA scheme

Inborn Errors of Metabolism (IEM)

Title: Assessing Recommendations Related To Timeliness of Newborn Screening

SCAD and GA-II: Truths and Confusions

Attachment 1. Newborn Screening Program Description

TIMELINESS OF NEWBORN SCREENING: RECOMMENDATIONS FROM ADVISORY COMMITTEE ON HERITABLE DISORDERS IN NEWBORNS AND CHILDREN

NEWBORN METABOLIC SCREEN, MINNESOTA

Lynne A. Wolfe, MS, ACNP, PNP, BC Department of Genetics Yale School of Medicine

Understanding metabolic disease

Use of Derivatization for LC- MS/MS Analysis in the Clinical Lab

INTEGRATIVE MEDICINE URINE, SPOT Result Range Units

Neonatal Screening using Shimadzu LCMS- 8040

Newborn Screening in Washington State Saving lives with a simple blood spot

Inborn Errors of Metabolism. Metabolic Pathway. Digestion and Fasting. How is Expanded Newborn Screening Different? MS/MS. The body is a factory.

The Compelling Benefits of Routine 2 nd NBS: A Fifteen-Year Review in Washington State. Saving lives with a simple blood spot

Neonatal Screening using Shimadzu LCMS-8040

DIAGNOSIS OF FATTY ACID OXIDATION DISORDERS BY MASS SPECTROMETRY

The spectrum and outcome of the. neonates with inborn errors of. metabolism at a tertiary care hospital

Alvaro Serrano Russi MD University of Iowa Hospitals and Clinics

Manipulation of the Nutrient Sensors (AMPK/TOR) with Anaplerotic Diet Therapy (Triheptanoin) An Alternative to Diet Restriction

Newborn screening for congenital metabolic diseases Optional out-of-pocket tests Information Sheet

Fatty Acid Beta-Oxidation Disorders: A Brief Review

Newborn Screening in Japan: Restructuring for the New Era

Xiaolei Xie, Marta Kozak. Thermo Fisher Scientific, 355 River Oaks Parkway, San Jose, CA Introduction

A Guide for Prenatal Educators

NEWBORN SCREENING. in Massachusetts: Answers for You and Your Baby. University of Massachusetts Medical School

Inborn Errors of Metabolism From Neonatal Screening to Metabolic Pathways

So Much More Than The PKU Test

Very-long-chain acyl-coa dehydrogenase deficiency

Urea Cycle Defects. Dr Mick Henderson. Biochemical Genetics Leeds Teaching Hospitals Trust. MetBioNet IEM Introductory Training

Most common is the congenital adrenogenital syndrome (AGS) or congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency.

Inborn Errors of Metabolism Clinical Approach to Diagnosis and Treatment

BIOB111 - Tutorial activity for Session 25

Selective newborn screening of amino acid, fatty acid and organic acid disorders in the Kingdom of Bahrain.

MISSOURI DEPARTMENT OF HEALTH AND SENIOR SERVICES

NEWBORN SCREENING. in Massachusetts: Information for You and Your Baby. University of Massachusetts Medical School

My Experiences and Understanding of VLCAD Deficiency and its Treatment Charles R. Roe, MD June 26, 2011 (Now retired)

Fatty acid oxidation. Naomi Rankin

Mitochondrial Fatty Acid Oxidation Deficiencies Prof. Niels Gregersen

Further expansion of the neonatal screening panel in the Netherlands

(f) "Birthing center" means any facility that is licensed by the Georgia Department of Community Health as a birthing center;

Considerations in Choosing Screening Conditions: One (US) Approach

MEDICAL COVERAGE GUIDELINES ORIGINAL EFFECTIVE DATE: 12/19/17 SECTION: MEDICINE LAST REVIEW DATE: LAST CRITERIA REVISION DATE: ARCHIVE DATE:

Genética e Hígado: Cómo contribuye la genética en el algoritmo diagnóstico de la enfermedad hepática pediátrica? Nicholas Ah Mew, MD

Metabolite identification in metabolomics: Database and interpretation of MSMS spectra

Metabolite identification in metabolomics: Metlin Database and interpretation of MSMS spectra

Nutritional Management of Inborn Errors of Metabolism. Kay Davis, RD, CSP Esther Berenhaut, RD, CSP, CSR Aug 28, 2017

Comprehensive cost-utility analysis of newborn screening strategies Carroll A E, Downs S M

AMINO ACID METABOLISM. Sri Widia A Jusman Dept. of Biochemistry & Molecular Biology FMUI

ANATOMY OF A METABOLIC CRISIS: FAOD-style. Mark S. Korson, MD Tufts Medical Center Boston, MA

Jana Novotná, Bruno Sopko. Department of the Medical Chemistry and Clinical Biochemistry The 2nd Faculty of Medicine, Charles Univ.

NEWBORN SCREENING. health.mo.gov/newbornscreening MISSOURI DEPARTMENT OF HEALTH AND SENIOR SERVICES

Beyond the case for NBS in South Africa. Chris Vorster 28/05/2016

History of Metabolic Tests. Dr Mick Henderson Biochemical Genetics Leeds and Manchester

OVERVIEW M ET AB OL IS M OF FR EE FA TT Y AC ID S

UK NATIONAL METABOLIC BIOCHEMISTRY NETWORK GUIDELINES FOR THE INVESTIGATION OF HYPERAMMONAEMIA

LIPID METABOLISM. Sri Widia A Jusman Department of Biochemistry & Molecular Biology FMUI

National Metabolic Biochemistry Network Guidelines for the investigation of hypoglycaemia in infants and children

Classification of amino acids: -

Providing the Right Fuels for FOD s. Elaina Jurecki, MS, RD Regional Metabolic Nutritionist Kaiser Permanente Medical Center Oakland, CA

Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry: Experience of the Pilot Study in Andhra Pradesh, India

THE GLUCOSE-FATTY ACID-KETONE BODY CYCLE Role of ketone bodies as respiratory substrates and metabolic signals

Intestinal Microbial Overgrowth

0091 Organix Comprehensive Profile Summary of abnormal results:

Integrative Metabolism: Significance

Screening for Phenylketonuria: A Literature Update for the U.S. Preventive Services Task Force

Introduction to Organic Acidemias. Hilary Vernon, MD PhD Assistant Professor of Genetic Medicine Johns Hopkins University 7.25.

Medium-chain acyl-coa dehydrogenase deficiency

Using the Organic Acids Test Part 3 Dr. Jeff Moss

Objectives By the end of lecture the student should:

Metabolic Disorders. Chapter Thomson - Wadsworth

Mary Seeterlin, PhD Michigan Department of Community Health. Prevent Disease Promote Wellness Improve Quality of Life

Secondary Energy Deficiencies in Organic Acidemias. Kimberly A Chapman MD PhD Children s National July 26, 2014

Lauren E. Cipriano, BSc, BA, 1 C. Anthony Rupar, PhD, 2 Gregory S. Zaric, PhD 1. Introduction

Short Term Follow Up Tandem Mass Spectrometry Workshop Agenda

Diagnose a broad range of metabolic disorders with a single test, Global MAPS

Mitochondrial Energy Metabolism:

Newborn Metabolic Screening Programme Annual Report

Simultaneous Analysis of Amino Acids and Acylcarnitines in Dried Blood Spots

Application of LC-MS-based metabolomics method in differentiating septic survivors from non-survivors

ICD-10 Physician Education. Medical Genetics

UREA CYCLE DISORDERS - The What, Why, How and When

2017 Newborn Screening and Genetic Testing Symposium September 10, 2017

Transcription:

Metabolomic Analysis for Newborn Screening and Diagnosis of Metabolic Disorders Mass Spectrometry and Separation Sciences for Laboratory Medicine Chicago October 1-2, 2015 Michael J. Bennett PhD, FRCPath, FACB, DABCC University of Pennsylvania Perelman School of Medicine & Children s Hospital of Philadelphia bennettmi@email.chop.edu

Learning goals The audience will be made aware of the public health significance of screening newborns for metabolic diseases The role that medium-chain acyl-coa dehydrogenase deficiency played in defining the expansion of newborn screening will be outlined The role of tandem mass spectrometry as a screening tool for metabolic disorders will be described Future trends in newborn screening using mass spectrometry will be discussed The use of untargeted metabolomics for the diagnosis of metabolic diseases will be described.

Conflicts of Interest no conflicts to declare

Phenylketonuria and blood spot collection

Robert Guthrie and the bacterial inhibition assay

Improved outcomes for patients with PKU In the unscreened population: patients are inevitably institutionalized with severe developmental delay $188K US per year in 2009* Screened population: essentially normal development on a restricted dietary regimen, no institutionalization Concerns about maintaining good metabolic control, particularly in girls of conceptional age * National Council for Disability

Other diseases added congenital adrenal hyperplasia congenital hypothyroidism sickle cell disease (other hemoglobinopathies) All demonstrate much improved clinical outcomes following early diagnosis

MCAD deficiency fulfills most screening requirements

Science. 1983 Jul 1;221(4605):73-5. Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-coa dehydrogenase in fibroblasts. Rhead WJ, Amendt BA, Fritchman KS, Felts SJ. Pediatr Res. 1983 Nov;17(11):877-84. Medium-chain acyl-coa dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. Stanley CA, Hale DE, Coates PM, Hall CL, Corkey BE, Yang W, Kelley RI, Gonzales EL, Williamson JR, Baker L. Br Med J (Clin Res Ed). 1984 Mar 31; 288(6422): 976. PMCID: PMC1442514 Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome. A J Howat, M J Bennett, S Variend, and L Shaw

The word about MCAD deficiency gets out 1980 s-90 s many more cases of MCAD described often associated with sudden death, from neonates to adults(46y). Estimated that 25% of cases die at first presentation. High morbidity in survivors Very high incidence of previous sibling deaths Population frequency estimated to be same as Phenylketonuria in Northern European populations (1 in 8,000-16,000) Regarded as treatable if diagnosed early (sibling studies)

The advent of tandem mass spectrometry as a tool for NBS David Millington s group at Duke University pioneered tandem mass spectrometry methodologies for measurement of amino acids for amino acid disorders and acylcarnitines for MCAD deficiency and other fatty acid oxidation defects and some organic acidemias The use of flow injection and Multiple Reaction Monitoring allows for simultaneous measurement of many acylcarnitine and amino acid species without chromatographic separation in a 2 minute analytic time Stable isotope-labeled internal standards allows for accurate quantitation

100% * 90% C 0 Normal acylcarnitine profile 80% Intensity 70% 60% 50% 40% 30% C 2 * * * * * 20% 10% 200 220 240 260 280 300 320 340 360 380 400 420 440 460 480 500m/z

Acylcarnitine profile from patient with isovaleric acidemia 100% C 5 90% 80% 70% Intensity 60% 50% 40% 30% 20% 10% C 0 C 2 * * * * * * 200 220 240 260 280 300 320 340 360 380 400 420 440 460 480 500

Distinctive acylcarnitine profiles in fatty acid oxidation defects Normal MCAD VLCAD CPT2 LCHAD Glutaric Acidemia2

carn C16 phe C2 Leu Ileu gly arg

Current status of newborn screening USA: Most states follow ACMG guidelines Australia: Includes most of ACMG recommended disorders UK: MCAD plus 4 more Germany: 14 conditions mandated Netherlands: 14 conditions Programs starting in many countries

10 Great public health achievements: Centers for Disease Control Vaccine preventable diseases Prevention and control of infectious diseases Tobacco control *Maternal and child health* folate supplementation, Newborn screening Motor vehicle safety Cardiovascular disease prevention Occupational safety Cancer prevention Childhood lead poisoning prevention Public health preparedness and response

Metabolomic analysis for metabolic diseases Screening designed for maximum sensitivity (least false negatives) Generates some false positives Requirement for confirmatory testing usually requires mass spectrometric analysis GC-MS for organic acids, untargeted metabolomics assay TMS or LC-MS/MS for plasma acylcarnitines, amino acids, lysosomal enzymes

Follow-up guidelines National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines: Follow-Up Testing for Metabolic Disease Identified by Expanded Newborn Screening Using Tandem Mass Spectrometry; Executive Summary Clin Chem 55: 1615-1626, 2009 www.aacc.org/nacb/guidelines

Urine organic acid analysis Untargeted approach to identification of metabolic intermediates indicating a specific defect of metabolism. amino acids, fatty acids, neurotransmitters, vitamin metabolism, cholesterol biosynthesis, other mitochondrial pathways, oxalate/peroxisomal metabolism, glutathione pathway, ketone body metabolism.

Normal organic acid chromatogram hip IS cit kg acon ox urea succ adip lac

3-methylcrotoyl-CoA carboxylase deficiency 3-MCG Hippurate IS

How low can we go? GC-MS with full scan 10µmol/mmol creatinine GC-MS with heavy isotope-labelled internal standard, selected ion monitoring 100nmol 10 µmol/mmol creatinine

Pre-analytical sources of urine metabolomic artifacts Endogenous, Metabolic Symbiotic Clinical Exogenous, Pharmacologic, prescribed Pharmacologic, not prescribed Nutritional/Xenobiotic

Metabolic artifacts Artifacts related to fasting: ketones up to 20mmol/mmol creatinine (DKA) dicarboxylic and 3-hydroxydicarboxlic acids (? mitochondrial leakage) Intermediates of ketogenic amino acid catabolic pathways Artifacts related to stress phenolic acid metabolites of catecholamines (HVA, VMA,)

Clinical artifacts Other disease states Liver disease of any etiology tyrosine metabolites, N-acetylated amino acids Catecholamine-secreting tumors catechol metabolites VMA, HVA, VLA Maternal disease (artifacts in newborns) maternal metabolic disease

Products of the microbiome Products of GI flora metabolism Volatile fatty acids propionate, butyrate (often further metabolized endogenously). Direct oxidation in gut epithelium TCA cycle intermediates succinate, citrate, isocitrate Products of bacterial metabolism of plant membranes p, m and o cresol, 4-hydroxyphenylacetate, 3 and 4- hydroxyhippurate, but not 2-hydroxyhippurate

Pharmacologic artifacts Prescribed and non-prescribed Anticonvulsants and their metabolites Phenytoin. Phenobarbital, valproate, carbamazepine NSAIDS Salicylates, acetominophen, ibuprofen Treatment for hyperammonemia benzoate hippurate, phenylacetate phenylacetylglutamate Any drug that is metabolized and excreted as a glucuronide

Nutritional/xenobiotic artifacts Nutritional support for failure to thrive Medium-chain triglycerides Medium chain dicarboxylic acids Additives to formula octenylsuccinic acid added to Nutramigen Products that make foods more palatable adipic acid added to yoghurt to make smooth, benzoic acid in soda to protect taste, metabolized to hippuric acid

Metabolomic Profile 1

Metabolomic Profile 2

Measurement of individual metabolites: targeted disease-related products of discovery investigations Requires a stable isotope labeled internal standard, [13C], [15N], [3H]

Ornithine trans carbamylase (OTC) deficiency X-linked urea cycle defect Males relatively easy to diagnose Females have variable X- chromosomal inactivation

Orotic Acid Molar mass =156.10 Internal standard, [1,3-15N] orotic acid, Molar mass = 158.10

Native and labeled spectra A bundance 1100000 1000000 Scan 956 (12.551 min): Orotic acid 254 900000 800000 700000 600000 native 357 500000 400000 73 300000 Abundance m /z--> 200000 100000 0 1100000 147 269 100 131 174 207 239 329 372 59 117 193 221 283 299 313 343 40 60 80 100 120 140 160 180 200 220 240 260 256 280 300 320 340 360 380 Scan 956 (12.551 min): 1,3-15 N Orotic acid 1000000 900000 800000 700000 600000 500000 73 Internal standard 359 400000 300000 m/z--> 200000 100000 0 147 59 271 101 131 175 207 241 331 87 117 161 193 221 285 301 315 345 374 60 80 100 120 140 160 180 200 220 240 260 280 300 320 340 360 380

Isotope dilution selected ion monitoring for gold standard quantification Abundance 1800000 12.514 Ion 254.00 (253.70 to 254.70): Orotic acid Abundance 180000 Ion 254.00 (253.70 to 254.70): 1209MT32.D\data.ms 160000 1400000 140000 1000000 120000 100000 600000 80000 60000 200000 0 Time--> Abundance 12.42 12.44 12.46 12.48 12.50 12.52 12.54 12.56 12.58 12.60 12.62 12.64 12.66 12.68 40000 20000 0 Time--> Abundance 12.514 12.599 12.4212.4412.4612.4812.5012.5212.5412.5612.5812.6012.6212.6412.6612.68 1800000 Ion 256.00 (255.70 to 256.70): Orotic acid 180000 160000 Ion 256.00 (255.70 to 256.70): 1209MT32.D\data.ms 12.514 1400000 140000 120000 1000000 100000 600000 12.514 80000 60000 Time--> 200000 0 12.42 12.44 12.46 12.48 12.50 12.52 12.54 12.56 12.58 12.60 12.62 12.64 12.66 12.68 40000 20000 0 Time--> 12.606 12.4212.4412.4612.4812.5012.5212.5412.5612.5812.6012.6212.6412.6612.68

Mass spectrometry for additional metabolic conditions Lysosomal enzymes- Gaucher, Pompe, Fabry disease- TMS Glycosylated proteins- carbohydrate deficient glycoprotein diseases- Time of Flight MS Acyl-CoA s, mitochondrial diseases-tms

Product Scan of Acetyl-CoA m/z = 810 507 m/z = 303 ACETYL_COA_DOU_3 1 (0.526) Cm (1) 303.2 100 54247424 Daughters of 810ES+ x10 5.42e7 % 201.0 135.9 7179008 4896256 159.0 2289920 428.1 6893312 0 100 150 200 250 300 350 400 450 500 550 600 650 700 750 800 850 m/z 809.9 201136

Neutral loss scan from wild-type mouse liver Free CoA C18:1-CoA IS 13C8-CoA IS C17-CoA C18-CoA C16-CoA Intens ity C2-CoA IS 13 C2CoA C4-CoA C6-CoA C12-CoA C10-CoA C16:1-CoA 3OH C20-CoA C22:1-CoA m/z

SCAD deficiency SCAD From Rinaldo, Matern, and Bennett. Annu. Rev. Physiol. 2002.

Andrew Palladino Ratio of acyl-coas in SCAD deficient/wt Mice

Thank You