Mechanisms of Hypoglycemia in Patients Without Diabetes

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The goal of this study is to identify physiologic and molecular mechanisms that underlie hypoglycemia in the absence of diabetes (or medications that can cause hypoglycemia) and to investigate potential genetic and microbiome differences which contribute to hypoglycemia. We will test the hypothesis that hypoglycemia in the absence of diabetes is linked to genetic variation or the microbiome, and identify whether additional medical history or diagnoses are enriched in the population of patients with hypoglycemia.

2020-08-11

2024-06-01

2025-05-01

Active (not recruiting)

33

Inclusion Criteria: 1. For hypoglycemia group without a history of bariatric surgery: Males or females diagnosed with hypoglycemia with prior episodes of neuroglycopenia. 2. For hypoglycemia group with history of upper gastrointestinal surgery: Males or females diagnosed with ongoing hypoglycemia with prior episodes of neuroglycopenia. 3. For non-surgical controls only: Males or females with no history of upper gastrointestinal surgery and no history of hypoglycemia or diabetes. 4. Age 18-70 years of age, inclusive, at screening. 5. Willingness to provide informed consent and attend one study visit, with option to attend a second visit with mixed meal test, and follow all study procedures Exclusion Criteria: 1. Active treatment with any diabetes medications except for acarbose; 2. Known insulinoma, gastrinoma, or other neuroendocrine tumor; Additional exclusion criteria for those participating in optional Visit 2 (meal testing): 1. Chronic kidney disease stage 4 or 5 (including end-stage renal disease); 2. Hepatic disease, including serum alanine transaminase (ALT) or aspartate aminotransferase (AST) greater than or equal to 3 times the upper limit of normal; hepatic synthetic insufficiency as defined as serum albumin \< 3.0 g/dL; or serum bilirubin \> 2.0; 3. Congestive heart failure, New York Hear Association (NYHA) class II, III or IV; 4. History of myocardial infarction, unstable angina or revascularization within the past 6 months or 2 or more risk factors for coronary artery disease including diabetes, uncontrolled hypertension, uncontrolled hyperlipidemia, and active tobacco use; 5. History of syncope (unrelated to hypoglycemia) or diagnosed cardiac arrhythmia; 6. Concurrent administration of β-blocker therapy; 7. History of a cerebrovascular accident; 8. Seizure disorder (other than with suspect or documented hypoglycemia); 9. Active malignancy, except basal cell or squamous cell skin cancers; 10. Personal or family history of pheochromocytoma or disorder with increased risk of pheochromocytoma (MEN 2, neurofibromatosis, or Von Hippel-Lindau disease); 11. Major surgical operation within 30 days prior to screening; 12. Hematocrit \< 33% (women) or \<36% (men); 13. Bleeding disorder, treatment with warfarin, or platelet count \<50,000; 14. Blood donation (1 pint of whole blood) within the past 2 months; 15. Active alcohol abuse or substance abuse; 16. Current administration of oral or parenteral corticosteroids; 17. Pregnancy and/ or Lactation: For women of childbearing potential: there is a requirement for a negative urine pregnancy test and for agreement to use contraception during the study and for at least 1 month after participating in the study. Acceptable contraception includes birth control pill / patch / vaginal ring, Depo-Provera, Norplant, an intrauterine device (IUD), the double barrier method (the woman uses a diaphragm and spermicide and the man uses a condom), or abstinence. 18. Use of an investigational drug within 30 days prior to screening. There will be no involvement of special vulnerable populations such as fetuses, neonates, pregnant women, children, prisoners, institutionalized or incarcerated individuals, or others who may be considered vulnerable populations.

{'studyType': 'OBSERVATIONAL', 'patientRegistry': True, 'targetDuration': '3 Weeks', 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'CROSS_SECTIONAL'}, 'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': 'Blood and fecal samples will be stored for up to 5 years for future analyses of additional blood proteins and metabolites and microbiome species which may contribute to hypoglycemia. DNA will be stored for additional expanded genotyping, depending on results of targeted resequencing. Fecal samples and /or cultures from them may be used for mouse transfer experiments in the future. All samples will be labeled only with the study identifier (ID) and acrostic unique to each participant.'}, 'enrollmentInfo': {'count': 33, 'type': 'ACTUAL'}}

2024-01-05