Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes.

PURPOSE: Previous studies have reported that prenatal exome sequencing (pES) can detect monogenic diseases in fetuses with congenital anomalies with diagnostic yields ranging from 6% to 81%, but there are few reports of its clinical utility.
METHODS: We conducted a retrospective chart review of patients who had pES to determine whether results led to clinical management changes.
RESULTS: Of 20 patients, 8 (40%) received a definitive diagnosis. Seven patients (35%) had medical management changes based on the pES results, including alterations to their delivery plan and neonatal management (such as use of targeted medications, subspecialty referrals, additional imaging and/or procedures). All patients who received a definitive diagnosis and one who received a likely pathogenic variant (n = 9; 45%) received specific counseling about recurrence risk and the medical/developmental prognosis for the baby. In five (25%) cases, the result facilitated a diagnosis in parents and/or siblings.
CONCLUSION: pES results can have significant impacts on clinical management, some of which would not be possible if testing is deferred until after birth. To maximize the clinical utility, pES should be prioritized in cases where multiple care options are available and the imaging findings alone are not sufficient to guide parental decision-making, or where postnatal testing will not be feasible.

INTRODUCTION

Congenital anomalies and genetic conditions are noted in approximately 2–5% of pregnancies and are major causes of fetal demise and infant death.[1,2] Chromosomal microarray is recommended to evaluate for chromosomal abnormalities in fetuses with congenital anomalies, but 60–70% of fetuses remain without a genetic diagnosis after microarray, which can complicate counseling, prenatal management, and parental decision-making.[3,4]

With the decreasing cost and turnaround time (TAT) of genomic testing methodologies, broad testing approaches such as exome sequencing (ES) are being used more frequently for prenatal diagnosis of monogenic disorders not detectable by microarray. Current professional society opinions support the use of prenatal ES (pES) in select cases of anomalies suggestive of a genetic disorder with the input of a clinical geneticist.[3,5,6] Prior case series have reported highly variable diagnostic yields of pES from 6.2% to 89%, with most reporting yields of 20–40%.[7-20]

However, it remains to be determined whether this improved diagnostic yield is meaningful to the patient and family. The American College of Medical Genetics and Genomics defines the clinical utility of genetic testing as its “effects on diagnostic or therapeutic management, implications for prognosis, health and psychological benefits to patients and their relatives, and economic impact on health-care systems.”[21] Most genetics providers believe that pES will have clinical utility.[22-25] Previous studies of pES indicate that results can impact decision-making about continuation or termination, pre- or postnatal medical management, delivery planning, recurrence risk counseling, reproductive planning, and parental medical management.[8-10,13,18,20,26]

However, there are also risks and limitations of pES that must be considered. Since parents may choose to terminate their pregnancy based on the results, there is a potential for harm if results are ambiguous, unexpected, and/or misunderstood.[25,27] As in postnatal ES, there is a risk of discovering incidental or secondary findings. The interpretation of variants detected on pES can be also challenging because the prenatal-onset phenotypes of many disorders are poorly characterized and the phenotype information about a fetus is often limited.[19] Additionally, pES requires a rapid TAT if results are to be used for clinical management, which can be labor-intensive for both the clinical and laboratory teams. The cost of pES may pose a significant burden to patients because most US health-care insurance providers do not cover the cost of this test, citing a lack of evidence to support its clinical utility.[28]

Given the potential limitations, additional studies are needed to establish the clinical utility of pES to justify its use. Here, we examine the clinical utility of pES in a cohort of 20 patients seen at our institution for pregnancies affected by congenital anomalies.

MATERIALS AND METHODS

A retrospective chart review was conducted for patients evaluated in our fetal care center who had ES ordered during pregnancy or after a fetal demise or termination of pregnancy (TOP), which were all considered as pES for this study since the indications for testing were prenatally identified congenital anomalies. Our fetal care center is a tertiary referral center that evaluated approximately 1,100 patients from 2018 to 2019 (the timeframe where most of the patients included in this chart review were evaluated) for congenital anomalies and complications of multiple gestations. All patients underwent detailed prenatal phenotyping via ultrasound, fetal magnetic resonance imaging (MRI), and fetal echocardiogram, as well as evaluation by a multidisciplinary team including a clinical geneticist, genetic counselor, maternal fetal medicine specialist, neonatologist, and additional subspecialists as needed based on the fetal anomalies (e.g., fetal/pediatric surgeon, neurologist). Patients were considered eligible for pES if their fetus had congenital anomalies thought to be caused by an underlying genetic disorder but for which multigene panels were not felt to be suitable as determined by the clinical geneticist and genetic counselor. All patients underwent chromosomal microarray testing prior to or concurrently with pES. Some patients had additional testing, such as amniotic fluid viral studies, based on their indications. There were no gestational age restrictions for eligibility. Patients considering TOP, a comfort care approach, or full medical interventions were all eligible. Patients were eligible for this chart review if pES produced a result (i.e., no sample failure) and they were no longer pregnant at the time of chart review.

Fetal DNA was obtained via chorionic villus sampling, amniocentesis, or fetal tissue. Blood or saliva was collected from parents for duo or trio analysis. All patients received counseling about pES from a certified genetic counselor and provided written informed consent for the testing. ES was performed by CLIA-approved commercial or academic laboratories selected on a case-by-case basis based on patient-specific factors, such as gestational age, insurance considerations, and eligibility for a pES clinical trial. Variant interpretation and reporting were performed by individual laboratories per standard clinical practice.

Maternal and neonatal charts were reviewed to describe the prenatal phenotype, pregnancy and neonatal outcomes (when applicable), pES results, and clinical utility of the results. Clinical utility was defined as changes to prenatal management (e.g., decisions about prenatal surgical interventions, decision about pregnancy termination or perinatal palliative care), delivery management (e.g., change in location, mode, and/or timing of delivery), neonatal management (e.g., initiation of gene- or pathway-specific medication, subspecialist referrals), family planning (e.g., specific recurrence risk counseling, pursuit of preimplantation or prenatal genetic testing for future pregnancies), family medical care (e.g., diagnosis of a genetic disorder in parents and/or siblings), and other aspects of care (e.g., psychosocial interventions).

RESULTS

Cohort demographics

Twenty patients from March 2015 to October 2019 were identified who met the inclusion criteria (Table 1). One additional patient was excluded since exome was ordered based on the autopsy findings and was therefore not considered a prenatal exome. Most had pES in 2018 (n = 9) or 2019 (n = 9). Nineteen were completed as trios and one was a maternal/fetal duo as the father was unavailable.

Table 1

Results of clinical exome sequencing.

Case ID	GA at pES order	GA at pES result	TAT (days)	Prenatal findings	Gene(s)	Variant(s)	Interpretation	Inheritance	Diagnosis	Clinical utility	Outcome
Diagnostic results
1	Postdemise	Postdemise	99	Severe bilateral ventriculomegaly, abnormal brainstem, cerebellar hypoplasia, hydrops, small chest, hepatomegaly, decreased muscle mass, small kidneys, oligohydramnios	NMNAT2	NM_015039.4:c.403dup p.(Gln135Profs*44),mat NM_015039.4:c.695G>A p.(Arg232Gln),pat	Likely pathogenic Likely pathogenic	Autosomal recessive	Novel NMNAT2-related disorder	FP, FD	Fetal demise at 27 weeks gestation
2	28 2/7	32 4/7	30	Megalencephaly, polymicrogyria, gray matter heterotopia, enlarged globes with proptosis, thickened chin soft tissue, ambiguous genitalia	AKT1	NM_001014432.1:c.49G>A p.(Glu17Lys), de novo	Pathogenic	Somatic	Proteus syndrome	P, D, N, FP, O	Delivery at 35 0/7; 10 days in NICU; death at 6 months of age
3	30 2/7	Postmortem	40	Arthrogryposis and hydrops; previous sibling with similar presentation	SCN4A	NM_000334.4:c.608T>A p.(Met203Lys),mat NM_000334.4:c.175G>T p.(Glu59*),pat	Pathogenic Pathogenic	Autosomal recessive	SCN4A-related congenital myopathy	FP, FD	Delivery at 30 4/7; death on DOL 17
4	25 3/7	31 0/7	39	Severely hypoplastic nose, choanal stenosis, hypertelorism, micrognathia, cleft palate, hypogenesis of the corpus callosum, pelvocaliectasis	KANSL1	NM_001193466.1:c.808_809del p.(Leu270Valfs*11),de novo	Pathogenic	Autosomal dominant	Koolen–de Vries syndrome	N, FP	Delivery at 37 0/7; 111 days in NICU; currently 20 months old
5	26 1/7	DOL 18	133a	Microphthalmia, cleft palate, micrognathia, pectus excavatum, horseshoe kidney, hypoplastic left heart, polyhydramnios	KMT2D	NM_003482.4:c.9787_9791dup p.(Gln3265Serfs*67), non-matb	Pathogenic	Autosomal dominant	Kabuki syndrome	N, FP	Delivery at 37 0/7; 57 days in NICU/CICU; currently 19 months old
6	28 6/7	30 6/7	14	Arthrogryposis, deficient muscle mass, scoliosis, micrognathia, cleft palate, frontal bossing, soft tissue edema, small VSD, polyhydramnios	NEB	NM_001271208.1:c.13147C>T p.(Gln4383*),mat NM_001271208.1:c.25093C>T p.(Arg8365*),pat	Pathogenic Pathogenic	Autosomal recessive	Nemaline myopathy 2	P, D, N, FP, O	Delivery at 36 4/7; neonatal death
7	28 5/7	31 2/7	16	Short limbs, micrognathia, bell-shaped chest, generalized edema, hypoplastic left heart	COL2A1 PIEZO1	NM_001844.4:c.1358G>T p.(Gly453Val), de novo NM_001142864.2:c.1970G>A p.(Arg657His),mat NM_001142864.2:c.6905G>A p.(Arg2302His),pat	Pathogenic VUS VUS	Autosomal dominant Autosomal dominant/ recessive	COL2A1-related skeletal dysplasia PIEZO1-related disorder	FP, FD	Delivery at 32 weeks 0 days; neonatal death
8	Postdemise	Postdemise	8	Hydrops, short nasal bone, hypertelorism, mild ventriculomegaly, renal pelvocaliectasis	PTPN11	NM_002834.3:c.923A>G p.(Asn308Ser),mat	Pathogenic	Autosomal dominant	Noonan syndrome	FP, FD	Fetal demise at 25 weeks gestation
Inconclusive results
9	36 0/7	DOL 17	34	Severe micrognathia, cleft palate, midface hypoplasia, short ribs, pulmonary hypoplasia, polyhydramnios	ALPL	NM_000478.5:c.130C>T p.(Gln44*),pat	Likely pathogenic	Autosomal dominant/recessive	Hypophosphatasia (incidental finding) Primary diagnosis unknowne	N, FP, FD	Delivery at 37 6/7; 301 days in NICU; currently 2 years old
10	Postdemise	Postdemise	58	Hydrops, fetal akinesia, micrognathia, bilateral clubfoot	IGHMBP2 NEB	NM_002180.2:c.1488C>A p.(Cys496*),pat NM_001271208.1:c.24632_ 24633del p.(Pro8211Argfs*4),pat	Pathogenic Pathogenic	Autosomal recessive Autosomal recessive	Unknownc	–	Fetal demise at 22 weeks gestation
11	Post-TOP	Post-TOP	80	Severe bilateral ventriculomegaly, aqueductal stenosis, gray matter heterotopia, polyhydramnios	LAMC3 NF1	NM_006059.3:c.2572C>T p.(Arg858*),pat NM_001042492.2:c.4219A>G p.(Ser1407Gly),pat	Likely pathogenic VUS	Autosomal recessive Autosomal dominant	Unknownd	–	TOP
12	28 6/7	Postdemise	63	Hydrops, arthrogryposis, markedly small brain measurements (including brainstem), micrognathia, polyhydramnios	LAMA2	NM_000426.3:c.2462C>T p.(Thr821Met),mat NM_000426.3:c.5158G>C p.(Glu1720Gln),pat	VUS VUS	Autosomal recessive	Unknownf	–	Fetal demise at 30 2/7
13	23 2/7	25 2/7	14	Lower urinary tract obstruction, severe bilateral ventriculomegaly with suspected aqueductal stenosis, bilateral superior vena cavae	GLI3	NM_000168.5:c.1945C>T p.(Arg649Trp),mat	VUS	Autosomal dominant	Unknown	–	Delivery at 34 1/7; neonatal death
14	Post-TOP	Post-TOP	76	Severe bilateral ventriculomegaly, myelomeningocele, bilateral severe microphthalmia, small kidneys	FREM2	NM_207361.6:c.1921A>G p.(Thr541Ala),mat	VUS	Autosomal recessive	Unknown	–	TOP
15	27 2/7	Postmortem	17	Bilateral diaphragmatic hernia or eventration, severe pulmonary hypoplasia, small or absent stomach, growth restriction, cystic hygroma, small brain biometry, bilateral clenched hands, VSD	PKD1 WDR5	NM_001009944.2:c.651del p.(Gly218Alafs*72), mosaic (14%) NM_052821.3:c.512C>T p.(Ser171Leu), de novo	Pathogenic VUS	Autosomal dominant Unknown	Unknown	–	Delivery at 29 0/7; neonatal death
Negative results
16	30 4/7	DOL 12	42	Abnormal angulation and bowing of tibia/fibula, clenched hands	–	–	–	–	Amniotic bands (detected at delivery)	–	Delivery at 34 6/7; currently 2 years old
17	Post-TOP	Post-TOP	31	Gastroschisis, arthrogryposis	–	–	–	–	Unknown	–	TOP
18	32 2/7	35 2/7	21	Bilateral ventriculomegaly with aqueductal stenosis, partial thalamic fusion, sacral hypoplasia, preaxial polydactyly of the right foot, small for gestation age, and truncus arteriosus with large VSD; demise of the co-twin (zygosity not specified) was noted at 12 weeks gestation	–	–	–	–	Suspect diabetic embryopathy	–	Delivery at 37 0/7; death on DOL 19
19	27 4/7	28 6/7	9	Posterior fossa cyst, vermian hypoplasia, unusual calvarium shape, severe micrognathia, hypertelorism, cataracts, low-set ears, midline cleft lip and palate, decreased muscle mass, bowed femurs, hyperflexed wrists, tetralogy of Fallot	–	–	–	–	Unknown	–	Delivery at 32 0/7; neonatal death
20	29 2/7	30 6/7	11	Arthrogryposis, scoliosis, mild micrognathia, enlarged cisterna magna, supraventricular tachycardia	–	–	–	–	Unknown	–	Delivery at 38 1/7; death on DOL 13

CICU cardiac intensive care unit, D delivery management, DOL day(s) of life, FD familial diagnosis, FP family planning counseling and/or management, GA gestational age, N neonatal management, NICU neonatal intensive care unit, O other clinical management, P prenatal management, pES prenatal exome sequencing, TAT turnaround time, TOP termination of pregnancy, VSD ventricular septal defect, VUS variant of unknown significance.

aTAT extended due to delay in maternal sample collection.

bPaternal inheritance not ruled out as only fetal and maternal DNA were included in the analysis.

cDeletion/duplication analysis of IGHMBP2 and NEB were negative.

dFather with negative clinical evaluation for neurofibromatosis type 1.

ePostnatal genome sequencing performed with no causative variant identified.

fPostmortem LAMA2 histology not consistent with LAMA2-related disorder.

Fourteen (70%) were ordered during an ongoing pregnancy, 3 (15%) after fetal demise, and 3 (15%) after TOP. The average gestational age for the pES order during an ongoing pregnancy was 28 4/7 weeks gestation. For the eight patients who received results during their pregnancy, the average TAT was 19.3 days and the average gestational age at the time of the result was 30 5/7 weeks. For the remaining 12 patients, the average TAT was 56.8 days.

pES results

Eight patients (40%) received a diagnostic result from pES (Table 1). Of these diagnoses, three (cases 1, 3, and 6) were autosomal recessive disorders and one (case 8) was an autosomal dominant disorder inherited from a previously undiagnosed mother. The remaining four were de novo autosomal dominant (cases 4, 5, and 7) and somatic mosaic (case 2) disorders. Seven additional patients (35%) received an inconclusive result due to variants of uncertain clinical significance. In two cases (cases 1 and 16), variants in novel genes were reported. Of the five patients who received negative pES results, two received postnatal diagnoses of nongenetic disorders (cases 16 and 18).

Clinical utility of pES results

Nine patients (45%) had clinical management changes made based on the pES result, including all eight who received a diagnosis and one who received an inconclusive result (Table 2).

Table 2

Clinical management changes based on prenatal exome sequencing (pES) results.

Case ID	Diagnosis	Clinical management changes
		Prenatal	Delivery	Neonatal	Family planning	Familial diagnosis	Other
1	NMNAT2-related disorder	–	–	–	X	X	–
2	Proteus syndrome	X	X	X	X	–	X
3	SCN4A-related congenital myopathy	–	–	–	X	X	–
4	Koolen–de Vries syndrome	–	–	X	X	–	–
5	Kabuki syndrome	–	–	X	X	–	–
6	Nemaline myopathy 2	X	X	X	X	–	X
7	COL2A1-related skeletal dysplasia	–	–	–	X	X	–
8	Noonan syndrome	–	–	–	X	X	–
9	Hypophosphatasia (primary diagnosis unknown)	–	–	X	X	X	–

Case 1

Multiple brain malformations, hydrops, small chest, hepatomegaly, decreased muscle mass, small kidneys, and oligohydramnios detected by ultrasound at 20 5/7 weeks gestation

pES detected compound heterozygous likely pathogenic variants in NMNAT2, a novel gene with no established human phenotype. The parents had previously decided on palliative care based on the poor prognosis associated with the imaging findings (Fig. 1a). Phenotypes reported in animal studies of NMNAT2 were consistent with the fetal anomalies. The clinical team believed this was likely the diagnosis for the fetus, which facilitated counseling about a recurrence risk of 25% and prompted the parents to pursue preimplantation genetic testing (PGT) resulting in a healthy child. They later had another pregnancy affected by similar anomalies and underwent targeted prenatal diagnostic testing that confirmed the same NMNAT2 variants in this fetus. Functional studies established that these variants impair NMNAT2 function and supported this gene’s association with fetal akinesia deformation sequence.[29]

Fig. 1

Fetal magnetic resonance images (MRIs) demonstrating phenotypes of select prenatal exome sequencing (pES) cases.

(a) Case 1 at 26 3/7: severe hydrops fetalis, severe ventriculomegaly, abnormal brainstem morphology, cerebellar hypoplasia, and hepatomegaly. (b) Case 2 at 27 2/7: megalencephaly, frontal bossing, and thickened soft tissues of the chin. (c) Case 4 at 24 3/7: severely hypoplastic nose and micrognathia. (d) Case 6 at 24 4/7: significant scoliosis and slender limbs with deficient muscle mass. (e) Case 7 at 25 0/7: micrognathia, flattened facial profile, small and bell-shaped chest, pulmonary hypoplasia, shortened limbs, and generalized edema. (f) Case 9 at 30 4/7: severe micrognathia, small chest, and polyhydramnios.

Case 2

Megalencephaly, neuronal migration anomalies, enlarged globes, thickened chin soft tissue, and ambiguous genitalia detected by ultrasound at 23 2/7 weeks gestation

pES detected a pathogenic variant in AKT1 consistent with a diagnosis of Proteus syndrome (OMIM 176920). Based on the grave prognosis of Proteus syndrome in the context of the fetal anomalies (Fig. 1b), the parents enrolled in perinatal palliative care. At 35 weeks gestation, the fetal head circumference was greater than 2 standard deviations above the mean. Due to concerns that continued overgrowth of the head was likely and could result in maternal morbidity during delivery, her delivery timing was changed from 37 to 35 weeks gestation to reduce the risk of maternal morbidity and she delivered by an uncomplicated cesarean section with a low-transverse incision. After birth, the baby received a full-body MRI to screen for additional Proteus syndrome–related overgrowth. Her known diagnosis and enrollment in palliative care allowed her medical team to minimize the duration of her hospital stay and she was discharged at 10 days of life. She later developed seizures requiring polypharmacy, including the mTOR inhibitor sirolimus to target the AKT1 biochemical pathway. Unfortunately, she died of respiratory failure at 6 months. The parents were counseled about the negligible recurrence risk for future pregnancies due to the sporadic nature of Proteus syndrome. The parents reported psychosocial utility of the result as it facilitated their connection to Proteus syndrome support groups.

Case 3

Arthrogryposis and hydrops detected by ultrasound at 25 2/7 weeks gestation

Since the parents had a previous female child with arthrogryposis who died as a neonate and remained undiagnosed after a multigene panel for fetal akinesia, pES was felt to be the best test to identify a diagnosis in this fetus. The patient delivered shortly after pES was ordered and the baby died prior to the availability of results. pES detected compound heterozygous pathogenic variants in SCN4A associated with congenital myopathy, which confirmed the 25% recurrence risk and a diagnosis for their previous child. To our knowledge, the parents are investigating options for PGT to prevent further recurrence.

Case 4

Hypoplastic nose, micrognathia, hypogenesis of the corpus callosum, and pelvocaliectasis detected by ultrasound at 18 0/7 weeks gestation, with cystic hygroma detected at 11 3/7 weeks gestation

pES was recommended to guide the parental decision-making about neonatal management options due to the wide range outcomes associated with the fetal anomalies (Fig. 1c) and detected a de novo pathogenic variant in KANSL1 consistent with a diagnosis of Koolen–de Vries syndrome (KdVS; OMIM 610443). The parents opted for full intervention after receiving the genetic diagnosis. After birth, the baby received a screening electroencephalogram (EEG) and early placement of a gastrostomy tube due to the known risks for seizures and feeding problems associated with KdVS. He developed worsening respiratory distress and received a tracheostomy at 6 weeks of life. His postnatal X-rays demonstrated epiphyseal stippling in addition to his severely hypoplastic nose, consistent with chondrodysplasia punctata (CDP). His ES data were reanalyzed and a multigene deletion/duplication panel was ordered, but neither identified a genetic etiology for CDP. It remains unknown whether CDP represents an unrecognized phenotype of KdVS or if there is another etiology for this phenotype.

Case 5

Microphthalmia, micrognathia, pectus excavatum, horseshoe kidney, hypoplastic left heart syndrome, and polyhydramnios detected by ultrasound at 21 1/7 weeks gestation

pES was recommended to guide parental decision-making about whether to pursue neonatal surgical intervention for hypoplastic left heart syndrome in the context of multiple congenital anomalies, but the results were not available until 18 days after birth due to difficulties obtaining a maternal DNA sample. The mother had opted for full neonatal intervention prior to receiving the pES results of a presumed de novo pathogenic variant in KMT2D consistent with a diagnosis of Kabuki syndrome (OMIM 147920). Due to the risk for immunodeficiency associated with Kabuki syndrome, an immunology evaluation was performed at 3 weeks of life which demonstrated lymphopenia. At 18 months, he developed hypogammaglobulinemia requiring intravenous immunoglobulin. The diagnosis improved counseling about the long-term medical and developmental prognosis for this baby to inform future medical management decisions, as well as counseling about the likely low recurrence risk due to the presumed de novo nature of the variant.

Case 6

Arthrogryposis, deficient muscle mass, scoliosis, micrognathia, frontal bossing, soft tissue edema, ventricular septal defect, and polyhydramnios detected by ultrasound at 20 0/7 weeks gestation

Due to the anomalies visualized with prenatal imaging (Fig. 1d), the parents were counseled that their baby would likely need an ex utero intrapartum therapy (EXIT) delivery and a prolonged hospital. Therefore, pES was recommended to guide parental decision-making. pES detected compound heterozygous pathogenic variants in NEB consistent with nemaline myopathy 2 (OMIM 256030). After receiving the pES results, the prenatal care team recommended against performing an EXIT delivery due to the poor long-term prognosis of this condition and the increased risk of maternal complications associated with EXIT delivery. Instead, the care team and mother elected for a C-section delivery with attempt to intubate the infant while still on placental support. They also referred the parents to a perinatal palliative care team. Given the likely respiratory distress and lifelong need for mechanical ventilation, the parents requested intubation and a trial of mechanical ventilation after delivery but declined chest compressions and tracheostomy placement. The delivery and intubation were successful, and the baby ultimately remained ventilator dependent. His parents took time for valuable psychosocial interventions including memory-making activities and baptism prior to removal of his breathing tube. The diagnosis also allowed for counseling about the 25% recurrence risk.

Case 7

Short limbs, micrognathia, bell-shaped chest, edema, and hypoplastic left heart syndrome detected by ultrasound at 16 2/7 weeks gestation

The imaging findings of a complex heart defect and suspected pulmonary hypoplasia due to a bell-shaped chest (Fig. 1e) suggested a poor prognosis, so the parents sought a genetic diagnosis to inform their prenatal and neonatal decision-making. pES detected a de novo pathogenic variant in COL2A1 associated with skeletal dysplasia. While COL2A1 is known to be associated with multiple types of skeletal dysplasia, it had not been previously associated with heart defects. Therefore, it is uncertain whether this case expands the phenotype of COL2A1-related skeletal dysplasia or if the heart defect had a separate etiology. The prenatal genetic diagnosis supported the decision to pursue palliative care and facilitated counseling about the low recurrence risk for the skeletal dysplasia due to the de novo nature of the variant. pES also identified two variants in PIEZO1, a gene associated with autosomal dominant iron overload, splenomegaly, and gallstones (OMIM 194380), and autosomal recessive lymphedema (OMIM 616843). The father reported a personal history of splenomegaly and a family history of gallstones, so he was counseled that he likely has the autosomal dominant PIEZO1-related disorder, which has a 50% recurrence risk.

Case 8

Hydrops, short nasal bone, mild ventriculomegaly, and pelvocaliectasis detected by ultrasound at 18 4/7 weeks gestation, with cystic hygroma detected at 13 4/7 weeks gestation

pES performed after fetal demise identified a maternally inherited pathogenic variant in PTPN11 consistent with Noonan syndrome (OMIM 163950). The mother was referred to a RASopathy-specific genetics clinic where she was noted to have short stature, mitral valve regurgitation, and a bleeding tendency including easy bruising, heavy periods, gum bleeding, and significant bleeding after a previous surgery. It was recommended that her care include continued follow-up with this clinic, regular echocardiograms due to the increased risk of hypertrophic cardiomyopathy, and hematology screening for platelet anomalies. The diagnosis also facilitated accurate counseling of a 50% recurrence risk and the parents have expressed an interest in PGT.

Case 9

Severe micrognathia, midface hypoplasia, short ribs, pulmonary hypoplasia, and polyhydramnios detected by ultrasound at 24 5/7 weeks gestation, with cystic hygroma detected at 13 weeks gestation

pES was recommended to guide delivery planning as the severe fetal micrognathia (Fig. 1f) would likely necessitate an EXIT delivery to establish an airway, increasing the risk of maternal morbidity. The patient declined amniocentesis solely for genetic testing, so pES was sent at 36 weeks gestation when she required an amnioreduction due to polyhydramnios. The results were not available for delivery planning and she delivered by EXIT-to-tracheostomy due to severe fetal micrognathia (jaw index measured less than 5th percentile at 34 weeks gestation) and glossoptosis. She continues to be dependent on mechanical ventilation by tracheostomy at 2 years of life. pES results were reported 17 days after delivery and did not identify a conclusive primary diagnosis. However, it identified a paternally inherited likely pathogenic variant in ALPL thought to be consistent with a later-onset autosomal dominant form of hypophosphatasia (HPP; OMIM 146300). The baby had very poor bone mineralization, low alkaline phosphatase activity, and elevated vitamin B6, so she was treated with asfotase alfa, an HPP-targeted medication. This result also led to a paternal diagnosis of HPP and informed counseling about a 50% recurrence risk for HPP.

DISCUSSION

In our cohort, 40% of patients with severe and/or multiple fetal anomalies received a diagnosis from pES, which is comparable to the diagnostic yields previously reported for fetuses with similar presentations. In fetuses with multiple anomalies and/or suspected Mendelian disorders, the incremental diagnostic yield of pES over microarray is at least comparable to, if not better than, the 5–10% incremental diagnostic yield of microarray over karyotype. Thus, the value of pES in diagnosing genetic conditions should no longer be questioned. However, the clinical utility of pES still needs to be established.

In our cohort, pES led to clinical management changes in 45% of patients, most often related to family planning (45%) and neonatal medical management (25%), as well as diagnoses in family members (25%). Previously, two studies from the Netherlands reported that clinical management was directly impacted by pES results in 70% of their patients, where results were used to make decisions about pregnancy termination and pre- and postnatal medical management.[10,26] Notably, half of the patients in these studies with negative results had clinical management changes, primarily related to supporting their decision to continue their pregnancy and/or pursue intervention for the fetal anomalies, which further underscores the difference between diagnostic yield and clinical utility.

Surveys of clinicians and parents have reported that most believe that pES will have clinical utility related to diagnosing genetic conditions, impacting pregnancy management, facilitating decisions about pregnancy termination, preparing for childhood-onset conditions, and informing reproductive planning.[22,24,30-33] In stark contrast, a study of 14 US health-care insurance payers reported that none believed that decisions about TOP, withdrawal of intensive care, provision of palliative care, family planning, or directing families to disease-specific resources (e.g., support groups, research) were aspects of clinical utility of pES, and only a minority agreed that referral to a tertiary center for specialized care was an aspect of clinical utility.[28] Therefore, it will be challenging to reconcile the different perspectives of the various pES stakeholders to establish its clinical utility.

One argument against pES is that, given the availability of rapid postnatal ES, pES adds no value until in utero interventions for fetal genetic disorders are clinically available. However, the fetus is not the sole patient of concern in the prenatal period; the mother should also be considered since results can directly impact her health, as demonstrated by cases 2 and 6 where the genetic diagnosis led to modifications of the delivery plans to reduce maternal morbidity. These decisions would not have been possible if testing had been deferred to the postnatal period. Thus, it is imperative to consider maternal health outcomes as part of the clinical utility of pES.

The claim that rapid neonatal ES obviates the need for pES also overlooks the importance of perinatal medical management decisions for the baby, such as planning for optimal delivery room resuscitation and timely initiation of diagnosis-specific treatment. Kingsmore et al. recently reviewed studies of rapid ES and reported median TAT ranging from 9 to 23 days.[34] Given that some genetic conditions have targeted therapies available, such as cases 2 and 9 as well as 27% of Kingsmore’s cohort, treatment could be delayed for days to weeks while awaiting rapid neonatal results. As intensive neonatal care and targeted therapies are not available at all hospitals, prenatal genetic diagnosis can facilitate referrals to institutions that are able to provide the appropriate therapies without delay. A prenatal genetic diagnosis may also limit expensive or invasive diagnostic testing that may be performed while postnatal testing is pending.

Furthermore, the notion that in utero or neonatal treatments are the only clinically useful interventions ignores the value of perinatal palliative care, which empowers parents to consider their values and hopes for their child’s quality of life while ensuring that their physical and psychosocial needs are met. With earlier referrals to palliative care services, families form stronger bonds with their health-care team and have a healthier grieving process.[35,36] While families may choose to redirect to a palliative care approach after learning of a life-limiting diagnosis in their newborn, deciding to withdraw care that has already begun is often more difficult for families than avoiding invasive and painful care in the first place.[37] Indeed, the diagnoses in cases 2 and 6 facilitated prenatal enrollment in a perinatal palliative care program, allowing these families to request avoidance of futile, painful procedures such as chest compressions; decrease the baby’s inpatient hospital stay to maximize family bonding at home; and plan meaningful rituals, such as baptism and memory-making, prior to the baby’s death. Therefore, while it is not always possible to improve a baby’s long-term outcome, prenatal diagnosis can improve the baby’s quality of life and the overall experience of the family.

Another significant difference between pre- and postnatal genetic testing is that TOP may be considered during an ongoing pregnancy, but prenatal imaging findings may not be sufficient to guide this decision without knowledge of the underlying etiology. For example, parents of a baby with an isolated heart defect detected on ultrasound are more likely to terminate their pregnancy if an underlying genetic condition is identified.[38] As this decision is restricted to the prenatal period, access to prenatal genetic testing including pES is imperative for parents to make informed decisions about their pregnancy.

Certainly, there are important limitations of pES that must be considered. Due to the broad nature of the testing, there is the possibility of receiving variants of uncertain clinical significance, as seen in 35% of our cohort. Since parents may make irreversible decisions, such as pursuing pregnancy termination or declining intensive interventions, it is imperative that uncertain results are fully explained in both pre- and post-test counseling to limit the risk of harm. Additionally, since there is an inherent timeframe in which prenatal and delivery management decisions can be made, the TAT for pES results needs to be optimized.

In our cohort, the decision to perform pES was at the discretion of the multidisciplinary clinical team that included a clinical geneticist and was based on a high suspicion of a Mendelian genetic disorder. As a result, the diagnostic yield and rate at which clinical management changes occurred in our study are likely higher than cohorts of all prenatally diagnosed congenital anomalies. However, the data presented here may be representative of yields expected in actual clinical practice. Additionally, our cohort represents the patients with health insurance carriers who approved pES, personal financial resources to pay for the testing, or who qualified for free testing by other means, and thus excludes patients who lacked the financial ability to access this testing.

The retrospective nature of our study limited identification of clinical management changes to those explicitly documented in the patients’ medical records. While we made every effort possible to only report clinical management changes that specifically resulted from the pES results, including speaking with the clinical staff when the patients’ charts were unclear, it is possible that some decisions may have been influenced by other factors (e.g., progression of imaging findings). We did not identify any cases where clinical management changes were made based on the lack of a genetic diagnosis from an inconclusive or negative result, which may be in part because pregnancy termination is not common in our clinic’s population. Additionally, for our patients who had pES during an ongoing pregnancy, it was ordered in the late second to late third trimesters; we therefore cannot comment on the clinical utility of pES results in the first or early second trimesters. Future prospective studies should be performed to better evaluate and maximize the impact of positive, inconclusive, and negative pES results on clinical decision-making throughout pregnancy.

In conclusion, results from pES can have significant impacts on the clinical management of the mother, neonate, and other family members, such as reducing risks of maternal morbidity during delivery, planning for optimal neonatal resuscitation, early initiation of diagnosis-targeted treatments, avoiding futile neonatal interventions, diagnosing other family members, and facilitating informed reproductive decision-making. As some of these decisions are only possible in the prenatal period, deferring genetic testing to the postnatal period is not always ideal. In cases where a genetic etiology is suspected and parents are pursuing TOP or where intrauterine fetal demise is likely, pES may be the only feasible opportunity to establish a genetic diagnosis to guide future reproductive planning. Additionally, pES may have clinical utility in cases where multiple care options are available, such as intensive in utero or neonatal intervention, TOP, and palliative care, but where the imaging findings alone are not sufficient to guide parental decision-making.