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Andrew Maclennan, MD April 23, 2010 Morning Report & Insulin Autoimmune Syndrome (Hirata disease)
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“Neuroglycopenic symptoms” Cognitive impairment, behavioral changes, psychomotor abnormalities, coma, death “Neurogenic symptoms” Tremors, palpitations, anxiety/arousal, sweating, hunger, paresthesias
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Whipple’s Triad: Symptoms consistent with hypoglycemia A low plasma glucose - measured with a precise method (not a glucometer) Relief of symptoms after glucose level normal Allen Oldfather Whipple
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Fast (overnight or post-prandial) 72 hr fast if initial fast is negative End fast when glucose ≤45 mg/dL Pt has signs/sx of hypoglycemia 72 hours have elapsed glucose <55 mg/dL if Whipple's triad documented previously Check Q6 hrs, more frequently when glucose < 60 mg/dL plasma glucose, insulin, C-peptide, proinsulin, BHOB, and oral hypoglycemic agents At end of fast IV glucagon and measure glucose 10, 20, and 30 minutes later Feed patient
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In symptomatic patients with hypoglycemia Insulin > 3 microU/mL is excess insulin; consistent w/ insulinoma Caution! Glucose 50 mg/dL in some patients with insulinoma. Proinsulin > 5 pmol/L consistent w/ insulinoma Beta-hydroxybutyrate - Insulin is antiketogenic BHOB levels lower in insulinoma patients than in normal subjects. C-peptide - distinguishes endogenous from exogenous hyperinsulinemia Sulfonylurea and meglitinide screen Glucose response to glucagon Insulin is antiglycogenolytic and hyperinsulinemia permits retention of glycogen within the liver. In insulin-mediated hypoglycemia, response to glucagon is release of glucose Normal patients have virtually exhausted hepatic glycogen stores after 72hrs and can’t respond as vigorously. (Insulin & insulin receptor antibodies)
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Radiologic studies — CT, MRI, transabdominal US can detect most insulinomas Arterial calcium stimulation — to distinguish between insulinoma and a diffuse process (islet cell hypertrophy/nesidioblastosis). Inject calcium gluconate into gastroduodenal, splenic and superior mesenteric artery Sample hepatic vein for insulin Increased insulin secretion localizes area of hyperfunctioning islets.
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Insulinoma – surgical resection of tumor Nesidioblastosis – partial or subtotal pancreatectomy Antibodies to insulin receptors – immunosuppressants (poor response) Antibodies to insulin – glucocorticoids (good response)
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Episodes of hyperinsulinemic hypoglycemia Often post-prandial, after exercise Paradoxic hyperglycemia May occur after meal or oral glucose challenge
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Extremely uncommon in West (58 case reports in non- Asian populations) 3 rd leading cause of hypoglycemia in Japan No sex preference Age > 40yrs Associated with rheumatologic disease SLE, RA, May see positive ANA, anti DSDNA, RF Association with medications Captopril, penicillamine, hydralazine, procainamide, INH, penicillin G Meds with sulfhydryl group (especially methimazole)
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1. Insulin secreted after meal bound by antibodies (IgG) 2. Hyperglycemia persists causing more insulin secretion (results in high A1C over time) 3. As hyperglycemia abates, insulin-bound to antibodies is released, with inappropriately high insulin levels 4. Hypoglycemia results.
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Autoimmune Forms of Hypoglycemia. Lupsa, Beatrice; Chong, Angeline; Cochran, Elaine; MSN, CRNP; Soos, Maria; Semple, Robert; MB, PhD; Gorden, Phillip Medicine. 88(3):141-153, May 2009. DOI: 10.1097/MD.0b013e3181a5b42e
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Lupsa BC et al, Autoimmune Forms of Hypoglycemia. Medicine, vol 88(3):141-153; May 2009. UpToDate
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