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This prospective observational study evaluates a simplified biochemical screening strategy to differentiate Glucocorticoid-Remediable Aldosteronism (GRA) from Aldosterone-Producing Adenoma (APA). The approach combines a 1-mg overnight dexamethasone suppression test (ODST) with LC-MS/MS steroid profiling. We aim to establish diagnostic cut-off points for aldosterone and hybrid steroid (18-oxoF, 18-OHF) suppression rates as an efficient screening tool prior to genetic testing.
Background:
GRA is a rare form of primary aldosteronism where aldosterone secretion is regulated by ACTH. This study evaluates if a 1-mg ODST can effectively suppress aldosterone and hybrid steroids in GRA patients compared to the autonomous secretion observed in APA.Methods:
This initial phase establishes the diagnostic parameters, which will be further validated in a larger cohort to optimize the screening workflow for primary aldosteronism.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Aldosterone-producing adenoma | APA group (control group): Patients diagnosed with PA and whose adrenal imaging indicated the presence of a typical adrenal adenoma on one side, with AVS or Ga68-Pentixafor PET/CT suggesting that the adenoma side had a dominant secretion of aldosterone, and meeting any of the following criteria: (1) Post-surgical pathology clearly confirmed an adrenal cortical adenoma, with immunohistochemistry showing aldosterone synthase CYP11B2 (+); (2) Patients who underwent unilateral adrenal resection achieved complete biochemical remission and met the surgical outcome criteria for PA. Exclusion criteria: Patients with secondary hypertension caused by other reasons (such as Cushing's syndrome, pheochromocytoma), severe renal and cardiac dysfunction (eGFR < 30 mL/min/1.73m²), or those who could not cooperate to complete the trial process for any reason were excluded. |
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| Familial hyperaldosteronism type 1 | GRA group (case group): Patients who met the biochemical diagnostic criteria for primary aldosteronism, had a clear history of early-onset hypertension or hypertension in their families, and whose CYP11B1/CYP11B2 chimeric gene was confirmed by genetic testing. Exclusion criteria: Patients with secondary hypertension caused by other reasons (such as Cushing's syndrome, pheochromocytoma), severe renal or cardiac dysfunction (eGFR < 30 mL/min/1.73m²), or those who cannot cooperate to complete the trial process for various reasons are excluded. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 1 mg overnight dexamethasone inhibition test | Diagnostic Test | After the patient fasted overnight, venous blood was collected at 08:00 in the morning for baseline steroid profile analysis (including aldosterone, 18-oxycortisol, 18-hydroxy cortisol, etc., a total of 11 types of steroid hormones). At 24:00 that night, the patient took a single oral dose of 1mg dexamethasone tablets. At 08:00 the next morning, venous blood was collected again under the same collection conditions as the baseline to conduct the baseline steroid profile analysis. |
| Measure | Description | Time Frame |
|---|---|---|
| Percent suppression of Plasma Aldosterone Concentration (PAC) after 1-mg ODST | Post-1mg ODST (approximately 2 weeks after dexamethasone administration) |
| Measure | Description | Time Frame |
|---|---|---|
| Absolute concentration of Plasma Aldosterone (PAC) post-1mg ODST | Post-1mg ODST (approximately 2 weeks after dexamethasone administration) | |
| Absolute concentration and percent suppression of 11 steroids (including 18-oxoF and 18-OHF). | Post-1mg ODST (approximately2 weeks after dexamethasone administration) |
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Inclusion Criteria:
GRA Group: Genetically confirmed presence of the $CYP11B1/CYP11B2$ chimeric gene.
APA group:The patient was diagnosed with PA and the adrenal imaging showed a typical adrenal adenoma on one side. The AVS or Ga68-Pentixafor PET/CT indicated that the adrenal gland on the adenoma side had a dominant secretion of aldosterone. And any of the following conditions was met: (1) The postoperative pathology clearly confirmed an adrenal cortical adenoma, with immunohistochemistry showing aldosterone synthase CYP11B2 (+). (2) After unilateral adrenal resection, the biochemical results of the patient were completely relieved, meeting the surgical outcome criteria for PA.
Exclusion Criteria:
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The study population consists of 31 patients diagnosed with Primary Aldosteronism (PA), including 8 cases of genetically confirmed Glucocorticoid-Remediable Aldosteronism (GRA) and 23 cases of Aldosterone-Producing Adenoma (APA).
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peking Union Medical Colledge Hospital | Beijing | 李泽文 | 456350 | China |
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|
| ID | Term |
|---|---|
| D006929 | Hyperaldosteronism |
| ID | Term |
|---|---|
| D000308 | Adrenocortical Hyperfunction |
| D000307 | Adrenal Gland Diseases |
| D004700 | Endocrine System Diseases |
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