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CLINICAL INVESTIGATION UNIT TESTS Presented by: ALAA MONJED Endocrinology fellow OUTLINE • Background- Provocative endocrine tests • CIU tests Indications Side effects / Contraindications Background What can we measure? basal hormone levels stimulated or suppressed hormone levels Why do we do dynamic endocrine testing? test of secretory reserve INSUFFICIENCY/DEFICIENCY Stimulate! OVERPRODUCTION Suppress! Clinical Investigation Unit - CIU Liz Froats, RN Room B5-502 http://dom.lhsc.on.ca/dom/divisions/endo/ciu.htm http://lhdomws.lhsc.on.ca/dom/divisions/endo/ciu.htm Available CIU Tests Pituitary Hormonal Disorders Tests Acromegaly Oral Glucose Tolerance test GH deficiency Insulin Tolerance test Arginine/GHRH Stimulation test Glucagon Stimulation test Adrenal insufficiency ACTH Stimulation test Insulin Tolerance test CRH Stimulation test Central hypothyroidism TRH Stimulation test Hypogonadotropic Hypogonadism GnRH Stimulation test Anterior Pituitary insufficiency (Double or Triple Bolus test) Insulin Tolerance test TRH Stimulation test GnRH Stimulation test Diabetes Insipidus Water Deprivation test Non-Pituitary Diseases Tests Medullary Thyroid Cancer/Calcitonin Calcium Stimulation test Pentagastrin test Hyperaldosteronism Saline Infusion test Pheochromocytoma Plasma Catecholamines test Hypoglycemia 8+ hour Fast test Mixed Meal test Examples EVALUATION OF GROWTH HORMONE DEFICIENCY • Screening test: low IGF-1 level • but normal IGF-1 does not exclude it • Dynamic tests: • because basal levels of GH are usually low, which do not distinguish between normal and GHdeficient patients. 1. Insulin induced hypoglycemia • Most reliable stimulus to GH secretion • A subnormal increase in serumGH (<5.1 ng/mL) confirms the diagnosis of growth hormone deficiency ITT 14 units of insulin given Time Glucose (mmol/l) GH (ug/L) 0 3.96 1.77 15 1.2 0.98 30 0.8 3.24 60 2.3 3.26 90 1.3 2.83 120 2.1 0.95 • Interpretation: • abnormal • Why? • Glucose fell to <2.2 mm • Normally GH should rise over 10 2. GHRH-Arginine test • 1mg GHRH combined with a 30-min infusion of Arginine IV to stimulate GH secretion • Possible side effects: mild flushing, metallic taste, N/V • Contraindications: severe liver or renal disease 3. Glucagon stimulation test • 1 mg Glucagon IM, followed by measurement of GH every 30 min for 3 hours • Useful when ITT is contraindicated or GHRH is not available • Side effects: nausea, vomiting and possible late hypoglycemia • Contraindications: malnourished patients • Failure of GH to rise > 3ng/ml is a positive test Evaluation Of GH Hypersecretion/Acromegaly • Screening test: high IGF-1 level • Dynamic tests: • Oral glucose tolerance test • Failure of GH suppression or paradoxical rise in GH level confirms Acromegaly • Also, seen in starvation, anorexia nervosa, and proteincalorie malnutrition • Side effects: nausea • If a radioimmunoassay method= GH level > 1mcg/L • If one of the newer, highly sensitive immunoradiometric GH assays is used= GH level > 0.3 mcg/L Time GLUCOSE (MM) GH (ug/L) 0 min 4.7 19.7 30 min 11.0 15 60 min 7.5 12 90 min 5.3 10.8 120 min 3.1 14.9 Interpretation? Evaluation Of LH/FSH Deficiency 1. Measurement of gonadal steroids (estradiol, testosterone). 2. Measurement of LH/FSH. • Primary gonadal failure • Low gonadal steroids, High LH/FSH • Hypogonadotrophic hypogonadism • Low gonadal steroids, LH,FSH 3. GnRH test • Assess LH/FSH secretory reserve by stimulating their secretion • Uncommonly performed Evaluation Of TSH(Secondary Hypothyroidism) 1. Measurement of TSH 2. Measurement of free T4/free T3 • If high TSH, low T4 ……. • If low/normal TSH, low T4 ……. 3. TRH stimulation test • is rarely done now because of the accurate methods of determining TSH and freeT4 EVALUATION OF HYPOPITUITARISM • Components: • Insulin Tolerance Test • GH deficiency, adrenal insufficiency • GnRH stimulation test • hypogonadotropic hypogonadism • TRH stimulation test • central hypothyroidism, hypoprolactinemia 1984. J Neurosurg 61(3):586-590 ACTH and Cortisol Secretion Kronenberg HM et al. Williams Textbook of Endocrinology. 11th edition. 2008 Saunders Elsevier. ACTH and Cortisol Secretion 24:00 08:00 12:00 20:00 pulsatile secretion circadian rhythm highest in a.m. Kronenberg HM et al. Williams Textbook of Endocrinology. 11th edition. 2008 Saunders Elsevier. Pituitary-Adrenal Reserve Dynamic Tests • Used to evaluate the ability of the HPA axis to respond to stress 1. ACTH stimulation test: directly stimulates adrenal secretion 2. Metyrapone test: inhibits cortisol synthesis and stimulates pituitary ACTH secretion 3. Insulin-induced hypoglycemia: stimulates ACTH secretion by increasing CRH 4. CRH test: stimulates directly the pituitary corticotrophs to release ACTH Adrenal Insufficiency Diagnosis Steps: 1. To rule out adrenal insufficiency - fasting 08:00 am cortisol if 08:00 am cortisol >524 nmol/L, adrenal insufficiency excluded if 08:00 am cortisol <83 nmol/L, adrenal insufficiency confirmed if 08:00 am cortisol between these values, is borderline – need further testing reviewed in Oelkers W. N Engl J Med 1996; 335(16):1206-1212 Adrenal Insufficiency Diagnosis Steps: 2. If suspect primary adrenal insufficiency, do both 08:00 am cortisol and ACTH low cortisol and high ACTH - primary • if cortisol normal – rules out primary, but does not exclude mild secondary adrenal insufficiency • in primary adrenal insufficiency – ACTH usually >22pmol/L low cortisol and low/normal ACTH – secondary/tertiary Adrenal Insufficiency Diagnosis • Dynamic Tests: To confirm adrenal insufficiency: High dose ACTH stimulation test Fasting is not required 250 mg cosyntropin (Cortrosyn) IV/IM Cortisol/ACTH at -15, 0, 30, 60 min If peak cortisol >500 nmol/L (preferably >550 nmol/L), rules out primary adrenal insufficiency Oelkers W. N Engl J Med 1996; 335(16):1206-1212 • A normal response to ACTH stimulation test: • Excludes primary AI • Excludes overt secondary AI with adrenal atrophy • Dose not rule out partial ACTH deficiency • pts with sufficient basal ACTH secretion to prevent adrenocortical atrophy • Or pts with recently developed secondary AI who have not yet undergone adrenal atrophy • In such patients, other pituitary-adrenal reserve dynamic testing may be indicated Adrenal Insufficiency Diagnosis • Low dose short ACTH stimulation test • must be undertaken in the morning • 1 mg cosyntropin (Cortrosyn) IV • Cortisol/ACTH at -15, 0, 30, 60 min • Normal peak cortisol >500 nmol/L • 2 meta-analyses comparing low vs. high dose tests had conflicting results: • Dorin et al. 2003 – no difference in sensitivity or specificity • Kazlauskaite et al. 2008 – low dose test had higher sensitivity Oelkers W. N Engl J Med 1996; 335(16):1206-1212 Adrenal Insufficiency Diagnosis • Insulin-induced hypoglycemia test: • It measures the integrity of the HPA axis and its ability to respond to stress • Normal plasma cortisol response: an increment >220nmol/l and a peak level >550 nmol/l • Normal ACTH response > 22pmol/l • A normal response exclude AI and decreased pituitary reserve i.e. no need to cortisol therapy during illness or stress • Contraindicated in: Elderly, CVD, CVA and seizure disorders Adrenal Insufficiency Diagnosis To distinguish secondary vs. tertiary adrenal insufficiency: CRH stimulation test (if you can get CRH!) 100 mg CRH IV ACTH, cortisol at -15, 0, 30, 60, 90 min low/absent ACTH = pituitary adrenal insufficiency (secondary) high ACTH = hypothalamic adrenal insufficiency (tertiary) (values not as well standardized as for ITT) Oelkers W. N Engl J Med 1996; 335(16):1206-1212 Posterior Pituitary Diabetes Insipidus • Central • Antidiuretic hormone deficiency • Responds to Desmopressin • Diagnosis: • Water Restriction Test Water Restriction Test Water Deprivation Test TIme Weight (kg) Urine osmol Serum osmol Serum Na 0800 82.6 150 290 144 0900 82.4 160 1000 82.1 200 295 148 1100 81.9 210 1200 81.6 225 300 149 1300 81.5 211 312 150 1400 81.1 231 298 145 1500 ** 487 • Interpretation: abnormal, consistent with central DI • Why? • Serum osmolality rose but urine osmolality remained relatively dilute still; similarly serum Na rose • [At ** time DDAVP was given and serum/urine/Na responded appropriately] REFRENCES Kronenberg HM et al. Williams Textbook of Endocrinology. 11th edition. 2008 Saunders Elsevier. Gardner DG & Shoback D (eds) Greenspan’s Basic & Clinical Endocrinology, 9th Edition. 2011 McGraw-Hill. www.uptodate.com http://dom.lhsc.on.ca/dom/divisions/endo/ciu.ht m THANK YOU