Testing During Pregnancy. David G. Grenache, PhD University of Utah & ARUP Laboratories Salt Lake City, UT

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Testing During Pregnancy David G. Grenache, PhD University of Utah & ARUP Laboratories Salt Lake City, UT

Disclosures Abbott Point of Care, Inc. Honorarium/Expenses

Objectives Explain the clinical utility of hcg testing in the diagnosis and management of intrauterine and ectopic pregnancy Compare and contrast recommendations for screening and diagnosing gestational diabetes mellitus Describe how thyroid function tests are affected by pregnancy

Human Pregnancy Approximately 40 weeks from 1 st day of last normal menstrual period to expected day of confinement (delivery) Divided into 3 trimesters of ~13 weeks Term is considered 37-42 weeks Childbirth bowl with confinement-chamber scene, ca. 1530s

Expected Physiological Changes System Changes Circulatory Increased blood volume (~45%) Cardiac Increased output (30-40%) Renal Increased GFR Hepatic Increased synthesis of plasma proteins Endocrine Insulin resistance/glucose intolerance Respiratory Hyperventilation and mild respiratory alkalosis

Laboratory Management of the Pregnant Patient Test Amniotic fluid bilirubin Fetal fibronectin Fetal lung maturity tests hcg Kleihauer-Betke Liver function tests Maternal serum screening tests Oral glucose tolerance Thyroid function tests TORCH tests Urine total protein Condition Hemolytic disease of the newborn Preterm delivery Fetal lung maturity Pregnancy diagnosis; ectopic pregnancy Fetal-maternal hemorrhage HELLP syndrome; cholestasis of pregnancy Fetal defects Gestational diabetes mellitus Thyroid function; thyroid disorders Infectious disease Preeclampsia

Laboratory Management of the Pregnant Patient Test Amniotic fluid bilirubin Fetal fibronectin Fetal lung maturity tests hcg Kleihauer-Betke Liver function tests Maternal serum screening tests Oral glucose tolerance Thyroid function tests TORCH tests Urine total protein Condition Hemolytic disease of the newborn Preterm delivery Fetal lung maturity Pregnancy diagnosis; ectopic pregnancy Fetal-maternal hemorrhage HELLP syndrome; cholestasis of pregnancy Fetal defects Gestational diabetes mellitus Thyroid function; thyroid disorders Infectious disease Preeclampsia

Human Chorionic Gonadotropin PREGNANCY DIAGNOSIS ECTOPIC PREGNANCY ASSESSMENT

Human Chorionic Gonadotropin (hcg) Glycoprotein hormone family hcg LH FSH TSH

Human Chorionic Gonadotropin (hcg) Glycoprotein hormone family hcg LH hcgβ LHβ 80% 43% FSH 41% FSHβ TSH 40% Adapted from Trends Biochem Sci 2004; 29:119-126 TSHβ

hcg Synthesis Synthesized by syncytiotrophoblasts Extends functional life of corpus luteum Maintains increasing progesterone Serum concentrations increase progressively in early pregnancy Peak at 7 9 weeks of gestation Decrease until ~24 weeks then plateau Adapted from Expert Rev Mol Diag 2009;9:721-747

hcg Heterogeneity Numerous molecular forms of hcg present in pregnancy serum Dissociated or degraded molecules with no biological activity Serum & Urine Key β-containing variants Intact hcg Nicked hcg Free β subunit Nicked free β subunit β-core fragment (urine) Urine only Adapted from Clin Chem 1997;43:2233-2243

hcg in Normal Pregnancy Pregnancy diagnosis involves history & physical exam in conjunction with hcg testing Serum hcg detectable 9-11 days after LH surge ~3-5 days before expected menses Urine hcg detectable around same time or soon after More variable than serum Adapted from Fertil Steril 2005;83:1000-1111

How early can hcg detect pregnancy? Depends on several variables Length of menstrual cycle Time from ovulation to fertilization Time from fertilization to implantation How expected day of menses is determined Average cycle length Days relative to LH surge or LH peak

How early can urine hcg detect pregnancy? Method used to determine day of menses influences timing of pregnancy detection As reference point, LH surge shows less variability for pregnancy detection Adapted from Curr Med Res Opin 2009;25:741-748

Ectopic Pregnancy Extrauterine implantation of blastocyst ~95% occur in fallopian tube Incidence is estimated at 2% of all pregnancies Responsible for 5% of maternal deaths Classic symptoms include abdominal/pelvic pain (95%) and vaginal bleeding (70%) but some have no symptoms until rupture

Diagnosis of Ectopic Pregnancy Serial hcg Prolonged doubling time in ectopic pregnancy <53% increase in hcg over 48 h is 99% specific Transvaginal ultrasonography Gestational sac should be evident at 42 days after conception hcg discriminatory zone Surrogate marker for gestational age Concentration above which, if no IUP visualized by US, a healthy singleton gestation is not present 1,000 3,000 IU/L

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Adapted from Gala RB: Ectopic pregnancy. In Williams Gynecology. New York, McGraw-Hill, 2008

Reliability of the Discriminatory Zone 202 women who met the following Transvaginal sonogram with no evidence of an IUP Serum hcg measured on same day as sonogram Subsequent documentation of a viable IUP hcg concentrations (IU/L) 80% <1,000 9% 1000-1,499 6% 1,5000-1,999 5% 2,000+ Discriminatory zone should not be used to determine the management of a hemodynamically stable patient with suspected ectopic pregnancy Follow-up sonography and serial hcg recommended J Ultrasound Med 2011;30:1637-1642

Oral Glucose Tolerance Tests GESTATIONAL DIABETES MELLITUS

Gestational Diabetes Mellitus (GDM) Most frequent metabolic complication of pregnancy Any degree of glucose intolerance with onset or first recognition during pregnancy that is not overt diabetes Accounts for 90% of diabetes in pregnancy Affects ~7% of all pregnancies (range 1-14%) Highest in ethnic groups with high frequencies of type 2 diabetes (Hispanic, African, Native America, Asian, and Pacific Island ancestry)

Pathophysiology of GDM Mother Placenta Fetus Insulin availability (resistance) Glucose Anti-insulin hormones: Human placental lactogen Estrogens Progesterone Pancreas Insulin Excess nutrient storage Macrosomia Hypoglycemia

Consequences of GDM Maternal Morbidity Hypertension Preeclampsia Increased likelihood of C- section Development of diabetes after pregnancy Fetal Morbidity Macrosomia (excessive birth weight) Neonatal hypoglycemia Polycythemia Increased perinatal mortality Congenital malformation Hyperbilirubinemia Respiratory distress syndrome Hypocalcemia

Testing for GDM Oral glucose tolerance test Imprecise with fair reproducibility (~75%) Several testing protocols used world wide Impossible to compare different studies of GDM What is true prevalence of GDM? ACOG vs. ADA

ACOG vs. ADA ACOG Screening Test 50 g glucose (non-fasting) 1 h glucose result exceeds: - 130 mg/dl (85% sensitive) - 140 mg/dl (90% sensitive) Diagnostic Test 100 g glucose (fasting) 2 or more glucose results exceed cutoffs: - Fasting: 95 mg/dl - 1 h: 180 mg/dl - 2 h: 155 mg/dl - 3 h: 140 mg/dl Pregnancies diagnosed with GDM mg/dl x 0.0555 = mmol/l None 4 7% ~18% ADA 75 g glucose (fasting) 1 or more glucose results exceed cutoff: - Fasting: 92 mg/dl - 1 h: 180 mg/dl - 2 h: 153 mg/dl

ACOG vs. ADA ACOG Originally established in 1964 (O Sullivan & Mahan) Cutoffs calculated as 2 SD of the mean whole blood glucose for each time point Predicted increased risk of diabetes after pregnancy Required 2 abnormal results to avoid misclassification due to laboratory error Current cutoffs are adaptations of originals ADA Adopted recommendations of International Association of Diabetes in Pregnancy Study Groups (IADPSG) in 2011 IADPSG established new diagnostic criteria for GDM based on data from HAPO study HAPO showed strong, continuous associations between maternal glucose and adverse outcomes

Objective: to clarify the risks of adverse outcomes associated with various degrees of maternal glucose intolerance less severe than that in overt diabetes mellitus 23,316 pregnant women in 9 countries 75 gram 2 hour OGTT

NEJM 2008;358:1991-2002

IADPSG Cutoffs Glucose cutoffs were those at which the odds for three specific HAPO outcomes were increased 1.75 times greater than mean HAPO concentrations (reference) Birth weight >90th percentile Cord C-peptide >90th percentile Percent body fat >90th percentile Time relative to 75 g OGTT Glucose (mg/dl) Above cutoff (%) Above cutoff (cumulative %) Fasting 92 8.3 8.3 1 hour 180 5.7 14.0 2 hour 153 2.1 16.1 mg/dl x 0.0555 = mmol/l Diabetes Care 2010;33:676-682

IADPSG GDM Detection Strategy Fasting glucose, random glucose, or Hb A1c at 1 st prenatal visit Fasting 126 mg/dl or Random 200 mg/dl or HbA1c 6.5% Fasting 92-126 mg/dl Fasting <92 mg/dl Overt diabetes GDM 75 g 2 hour OGTT at 24-28 weeks mg/dl x 0.0555 = mmol/l Diabetes Care 2010;33:676-682

1. IADPSG criteria more than doubles the incidence of GDM 2. No evidence its use would produce clinically significant improvements in maternal and neonatal outcomes 3. Would significantly increase in health care costs

Which Protocol to Offer? No consensus on which protocol is best Get input of physicians May find it necessary to offer both

Thyroid Function Tests THYROID FUNCTION DURING PREGNANCY

The Thyroid & Pregnancy Pregnancy places large demands on thyroid gland 10% increase in size (higher with iodine-deficiency) 50% increase in hormone synthesis 50% increase in iodine requirement High prevalence of thyroid disorders in women of child-bearing age Revealed by stressors of pregnancy

Increased Thyroid-binding Globulin (TBG) Estrogen increases glycosylation of TBG Prolonged TBG half-life (from 15 min to 3 days) mg/l x 0.0185 = μmol/l Increased hepatic TBG synthesis Affinity for T4 and T3 unaltered Acta Endocrinol 1982;100:504-511

Increased Total T4 & T3 Increased TBD leads to increased total T4 and T3 Peak concentration at ~20 weeks Acta Endocrinol 1982;100:504-511 nmol/l / 12.87 = μg/dl

hcg Stimulation of the Thyroid hcg has weak thyrotropic activity TSH lowest at peak hcg concentration (~10 weeks) TSH may be below the nonpregnant reference interval (0.35-5.5 miu/l) J Endocrinol Metab 1990;71:276-287

Decreased Serum Free T4 Slight increase in 1 st trimester due to hcg stimulation of thyroid Remainder of pregnancy marked by decreased ft4 Due to increased TBG, increased iodine clearance, and overall increased demand for T4

Increased Serum Thyroglobulin Often increased during pregnancy, especially in later weeks A: 1 st trimester B: Late gestation C: Post-partum Associated with increase in thyroid gland volume (mean 10%) but goiter is rare in U.S. 5-15% of women at term Normal <30 ng/ml ng/ml x 1 = μg/l J Endocrinol Metab 1990;71:276

Increased Renal Iodine Clearance Increased GFR leads to increased iodine clearance Decreased circulating iodine produces compensatory loss of thyroidal iodine Clinically significant in iodine deficient states Increased dietary requirements of iodine American Thyroid Association & Endocrine Society: 250 μg/day

hcg stimulates thyroid TSH decreases as hcg increases Increased hepatic synthesis of TBG Increased TBG increases TT4 Increased iodine clearance and increased demand for T4 decreases ft4

Thyroid Function Tests During Pregnancy Test Comment TSH Use trimester-specific reference intervals if available otherwise use: - 0.1-2.5 miu/l (1 st trimester) - 0.2-3.0 miu/l (2 nd trimester) - 0.3-3.0 miu/l (3 rd trimester) TT4 & TT3 1.5x non-pregnant reference intervals ft4 & ft3 Best to use equilibrium dialysis/lc/ms/ms method Use method- and trimester-specific reference intervals Interpret low results with caution Thyroid 2011;21:1081-1125 Thyroid 2007;17:1159-1167

Summary hcg is an early marker of pregnancy but should not be solely relied in the evaluation of ectopic pregnancy Clear associations between maternal hyperglycemia and adverse outcomes but no consensus regarding optimal protocol for identifying gestational diabetes mellitus Several expected changes to thyroid status during pregnancy

Self-Assessment Questions 1. Use of a low hcg discriminatory zone will A. Increase the sensitivity for diagnosing an intrauterine gestation B. Increase the sensitivity for diagnosing an ectopic gestation C. Decrease the number of women diagnosed with an ectopic pregnancy D. Decrease the number of hcg tests performed per patient 2. According to criteria recommended by the IADPSG, a fasting plasma glucose concentration 92 125 mg/dl during pregnancy is consistent with: A. Gestational diabetes mellitus B. Normal glycemia C. Overt diabetes mellitus D. Type 1 diabetes mellitus E. Type 2 diabetes mellitus 3. TSH decreases and free T4 increases during the first trimester of pregnancy because: A. Estrogen stimulates hepatic synthesis of thyroxine-binding globulin B. hcg stimulates TSH-receptors in the thyroid gland C. Increased release of thyroxine from thyroglobulin D. Thyroid-stimulating antibodies are transiently present during the first trimester