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Obstetrics Genetics Update for the Busy OB/GYN: From Aneuploidy Screening to
Fragile X Carrier Testing
Jennifer Salcedo, MD, MPH, MPP, FACOGAssociate Professor & Residency Program DirectorSASGOG Liaison to ACOG Committee on Genetics
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Common Aneuploidies in Liveborn InfantsDisorder IncidenceTrisomy 21 (Down Syndrome) 1:700Trisomy 18 (Edward Syndrome) 1:3000Trisomy 13 (Patau Syndrome) 1:500045 X (Turner Syndrome) 1:2500 females47 XXY (Klinefelter Syndrome) 1:600 males47 XYY & 47 XXX 1:1500
ACOG Education in Women’s Genomic Counseling
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Case 1You’re seeing a 30 yo G1 at 10 weeks gestation. You counsel her that the aneuploidy screening option with the highest sensitivity and positive predictive value for T21 is:A. Nuchal translucency measurementB. Cell-free DNA screening (cfDNA)C. Quad screeningD. First trimester serum analyte screening
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Case 1You’re seeing a 30 yo G1 at 10 weeks gestation. You counsel her that the aneuploidy screening option with the highest sensitivity and positive predictive value for T21 is:A. Nuchal translucency measurementB. Cell-free DNA screening (cfDNA)C. Quad screeningD. First trimester serum analyte screening
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Age-Related Aneuploidy RiskAGE AT TERM RISK OF TRISOMY 21 RISK OF ANY CHROMOSOMAL
ABNORMALITY15 1:1578 1:45420 1:1480 1:52525 1:1340 1:47530 1:940 1:38435 1:353 1:17840 1:85 1:6245 1:35 1:18
Adapted from ACOG Practice Bulletin 163; Morris et al., Hook et al., Cuckle et al.
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Aneuploidy Screening Options - SerumTest GA
(weeks)Sensitivity for T21 (%)
Screen Positive Rate (%)*
Advantages Disadvantages Methods
Triple screen 15-22 69 5 Open defects & other adverse outcomes
Lower sensitivity; 2nd
tri
hcg, AFP, uE3
Quad screen 15-22 81 5 Open defects & other adverse outcomes
Lower sensitivity; 2nd
tri
hcg, AFP, uE3, DIA
Serum Integrated
Multiple 88 5 Increased sensitivity
2 samples; no 1st tri results
PAPP-A & Quad screen
Adapted from ACOG Practice Bulletin 163, Table 2
* Includes true & false positives
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Aneuploidy Screening Options - NTTest GA
(weeks)Sensitivity for T21 (%)
Screen Positive Rate (%)*
Advantages Disadvantages Methods
NT only 10-13 6/7
64-70 5 Additional fetal abnl; multiple gestations
Low sensitivity; certification
NT
1st trimester screening
10-13 6/7
82-87 5 Other adverse outcomes
Multiple tests NT, PAPP-A, hcg
Integrated Multiple 96 5 Highest sensitivity; open defects
Delayed results; multiple tests
NT, PAPP-A, quad screen
Sequential stepwise
Multiple 95 5 High sensitivity; 1st tri results provided
Multiple tests NT, PAPP-A, hcg, quad screen
Contingent Multiple possible
88-94 5 High sensitivity; 1st tri results provided
Complex process; multiple tests
2nd tri testing for intermediate risk
Adapted from ACOG Practice Bulletin 163, Table 2
* Includes true & false positives
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Aneuploidy Screening Options – Cell-free DNATest GA
(weeks)Sensitivity for T21 (%)
Screen Positive Rate (%)*
Advantages Disadvantages Methods
Cell free fetal DNA (cfDNA)
10+ 99 (if result obtained)
0.5 Highest sensitivity; highest PPV
Cost; limited info about other fetal risks
Molecular methods
Adapted from ACOG Practice Bulletin 163, Table 2
* Includes true & false positives
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Norten, ME et al. NEJM 2015; 372:1589-97
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Norten, ME et al. NEJM 2015; 372:1589-97
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Case 2 Your “low risk” patient chooses to pursue cfDNA screening and has a normal result. What do you recommend for subsequent NTD screening?A. 2nd trimester sonoB. 2nd trimester AFPC. 2nd trimester sono & AFPD. None of the aboveE. Any of the above
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Case 2 Your “low risk” patient chooses to pursue cfDNA screening and has a normal result. What do you recommend for subsequent NTD screening?A. 2nd trimester sonoB. 2nd trimester AFPC. 2nd trimester sono & AFPD. None of the aboveE. Any of the above
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Case 3A 24 yo G2P0 at 6 weeks sees you for her 1st prenatal visit. You counsel her that her pregnancy is at highest risk for what type of chromosomal disorder:A. A sex chromosome aneuploidyB. Trisomy 21C. Unbalanced translocationD. Microdeletion or microduplication
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Case 3 A 24 yo G2P0 at 6 weeks sees you for her 1st prenatal visit. You counsel her that her pregnancy is at highest risk for what type of chromosomal disorder:A. A sex chromosome aneuploidyB. Trisomy 21C. Unbalanced translocationD. Microdeletion or microduplication
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Common Microdeletion & Duplication Syndromes
Region Name Common Features22q11.21 DiGeorge VCFS CHD, clefting, ID, immune disorders5p13 Cri-du-chat ID, dysmorphia, characteristic cry17p11.2 Smith-Magenis ID, dysmorphia, self-mutilation17p13.3 Miller-Dieker Lissencephaly, seizures, CHD15q11q13 Prader-Willi ID, hypotonia, hyperphagia7q11.23 Williams-Beuren CHD, ID, growth deficiency1p36 ID, CHD, hearing loss17q21.31 ID, speech disorders, seizures15q11q13 Angelman ID, ataxia, seizures
ACOG Education in Women’s Genomic Counseling
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Case 4A 37 yo G3P0 at 7 weeks initiates care with you after achieving pregnancy via IVF (her eggs). She had aneuploidy screening (PGT-A) & transferred euploid embryos. What do you recommend in pregnancy for aneuploidy screening/testing?A. Nothing – she already had normal aneuploidy screeningB. Invasive testing only C. Her preferred screening or testing option (like non-ART pts)D. Referral to a genetic counselor
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Case 4A 37 yo G3P0 at 7 weeks initiates care with you after achieving pregnancy via IVF (her eggs). She had aneuploidy screening (PGT-A) & transferred euploid embryos. What do you recommend in pregnancy for aneuploidy screening/testing?A. Nothing – she already had normal aneuploidy screeningB. Invasive testing only C. Her preferred screening or testing option (like non-ART pts)D. Referral to a genetic counselor
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Aneuploidy Testing Confusion• Erroneous gestational age• ”Vanishing” twin• Selective reduction• Confined placental mosaicism (CPM)• Maternal malignancy• Maternal aneuploidy• Donor eggs
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Case 5You’re seeing a 28 yo G2P1 with a di-di twin gestation at 8 weeks. You counsel her that that the aneuploidy screening option best suited to twin pregnancies is:A. Nuchal translucency measurement (NT)B. Cell-free DNA screening (cfDNA)C. Quad screeningD. First trimester serum analyte screening
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Case 5You’re seeing a 28 yo G2P1 with a di-di twin gestation at 8 weeks. You counsel her that that the aneuploidy screening option best suited to twin pregnancies is:A. Nuchal translucency measurement (NT)B. Cell-free DNA screening (cfDNA)C. Quad screeningD. First trimester serum analyte screening
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Case 6Your patient, a 25 yo G3P2 at 14 weeks gestation had an abnormal NT followed by a normal CVS. You counsel her that her fetus is elevated risk of:A. Cardiac abnormalitiesB. Abdominal wall defectsC. Congenital diaphragmatic herniaD. All of the aboveE. None of the above
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Case 6Your patient, a 25 yo G3P2 at 14 weeks gestation had an abnormal NT followed by a normal CVS. You counsel her that her fetus is elevated risk of:A. Cardiac abnormalitiesB. Abdominal wall defectsC. Congenital diaphragmatic herniaD. All of the aboveE. None of the above
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Nuchal Translucency
www.fetalmedicine.org
• Performed by certified sonographer/clinician
• 10-13 6/7 weeks
• Abnormal measurements • Diagnostic testing• Targeted ultrasound• Fetal echo
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Cystic Hygroma
www.sonoworld.com
• 50% aneuploid• T21, 45X, T18
• 50% euploid• 50% major structural
malformation• <20% healthy liveborn
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Case 7 Your patient, a 37 yo G2P0 at 14 weeks gestation had a cfDNA screen that returned as “no result.” You counsel her that “no result” is associated with:A. ObesityB. AneuploidyC. Pregnancy dating inaccuracyD. LMWH useE. All of the above
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Case 7 Your patient, a 37 yo G2P0 at 14 weeks gestation had a cfDNA screen that returned as “no result.” You counsel her that “no result” is associated with:A. ObesityB. AneuploidyC. Pregnancy dating inaccuracyD. LMWH useE. All of the above
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Case 8 Your patient, a 36 yo G1 at 18 weeks had an abnormal cfDNA screen followed by a normal amniocentesis. You counsel her that her pregnancy is at elevated risk for:A. Hypertensive disorders of pregnancyB. Genetic metabolic disordersC. Preterm deliveryD. IUGR
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Case 8 Your patient, a 36 yo G1 at 18 weeks had an abnormal cfDNA screen followed by a normal amniocentesis. You counsel her that her pregnancy is at elevated risk for:A. Hypertensive disorders of pregnancyB. Genetic metabolic disordersC. Preterm deliveryD. IUGR
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Case 9According to ACOG, women who have not been previously screened & have a negative family history should be offered carrier testing for what condition(s) during preconception or prenatal care?A. Cystic fibrosisB. Fragile XC. Spinal Muscular Atrophy (SMA)D. A & CE. A, B, & C
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Case 9According to ACOG, women who have not been previously screened & have a negative family history should be offered carrier testing for what condition(s) during preconception or prenatal care?A. Cystic fibrosisB. Fragile XC. Spinal Muscular Atrophy (SMA)D. A & CE. A, B, & C
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Carrier Frequencies
Mayo Clinic
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Cystic Fibrosis Carrier Screening
ACOG Committee Opinion 691 (Reaffirmed 2019)
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Spinal Muscular Atrophy Carrier Screening• Progressive neuromuscular disorder• Complex genetics
– AR (SMN1 modified by SMN2*; ASAH1; IGHMBP2)– AD– X-linked
NIH Genetics Home Reference
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Spinal Muscular Atrophy Types
www.avexis.com
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Case 10 ACOG recommends Fragile X carrier screening for women with:A. Family history of unexplained intellectual disabilityB. Family history of autismC. Family history of Fragile XD. Premature ovarian insufficiencyE. All of the above
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Case 10 ACOG recommends Fragile X carrier screening for women with:A. Family history of unexplained intellectual disabilityB. Family history of autismC. Family history of Fragile XD. Premature ovarian insufficiencyE. All of the above
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Fragile X Expansion
ACOG Committee Opinion 691 (Reaffirmed 2019)
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Fragile X-Associated Tremor Ataxia Syndrome (FXTAS)
• Late onset, progressive disorder• Males more often & severely affected• Disorder of movement, cognition, & mood• Women may develop hypothyroidism or pain symptoms
before neuro symptoms present
NIH Genetics Home Reference
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Case 11 You are seeing a G1 couple for a 1st prenatal visit. The male partner is of Ashkenazi Jewish descent. The female partner is of Japanese descent. There’s no family history of genetic disease. What are your recommendations regarding carrier testing for genetic diseases of elevated prevalence in the Jewish population?A. No testing is indicated since the woman is JapaneseB. Both partners should be offered panel testingC. The male partner should be offered panel testingD. No testing is indicated given the negative family history
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Case 11You are seeing a G1 couple for a 1st prenatal visit. The male partner is of Ashkenazi Jewish descent. The female partner is of Japanese descent. There’s no family history of genetic disease. What are your recommendations regarding carrier testing for genetic diseases of elevated prevalence in the Jewish population?A. No testing is indicated since the woman is JapaneseB. Both partners should be offered panel testingC. The male partner should be offered panel testingD. No testing is indicated given the negative family history
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Recommended Carrier Screening –Ashkenazi Jewish Patients
ACOG• Tay Sachs• Familial dysautonomia• Canavan disease
ACMG• Tay Sachs• Familial dysautonomia• Canavan disease• Fanconi anemia C• Niemann-Pick A• Bloom syndrome• Mucolipidosis IV• Gaucher type 1
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Case 12 You are seeing a couple for preconception counseling. Both partners are of Ashkenazi Jewish descent and have family histories that include breast cancer. You counsel them that:A. Offspring have potential cancer risks similar to parentsB. BRCA1 mutation homozygosity is associated with fetal abnormalitiesC. BRCA 2 mutation homozygosity is associated with fetal abnormalitiesD. A&BE. A&C
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Case 12You are seeing a couple for preconception counseling. Both partners are of Ashkenazi Jewish descent and have family histories that include breast cancer. You counsel them that:A. Offspring have potential cancer risks similar to parentsB. BRCA1 mutation homozygosity is associated with fetal abnormalitiesC. BRCA 2 mutation homozygosity is associated with fetal abnormalitiesD. A&BE. A&C
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Aneuploidy Screening/Diagnosis Principles• All women should be offered screening & diagnostic
testing– Potential advantages of information gained– Differentiating between screening & diagnosis– What is/isn’t being screened/tested for
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Aneuploidy Screening/Diagnosis Principles• Pre- & Post-test counseling
– Pre-test risk– Residual risk– Unexpected information about parents
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Aneuploidy Screening/Diagnosis Principles• Standard approach to counseling
– Consider• Decision aids• Graphic representations• Questionnaires• Reminder systems/documentation prompts• Patient consent forms
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ACOG Education in Women’s Genomic Counseling
• Certificate • 18 CME credits• MOC Part 4 credit
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Questions?
https://www.acog.org/About-ACOG/ACOG-Departments/Genetics