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Primary aldosteronism (PA) is the most common cause of secondary hypertension. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) is more accurate than the traditional radioimmunoassay method in measuring aldosterone. This study aims to establish a more precise diagnostic cutoff value for the captopril stimulation test (CCT) by measuring aldosterone levels using LC-MS/MS. The investigators will combine the detection results of CCT from healthy volunteers and suspected PA patients, etc., to determine the new CCT cutoff value. The investigators expect to improve the diagnostic accuracy of PA, helping clinicians identify this curable cause of hypertension earlier and more accurately, and achieving precise treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| normal sujects | Healthy volunteers with normal blood pressure, normal blood potassium levels, and no adrenal nodules. These individuals were used to establish the normal physiological range (lower limit) of aldosterone suppression after the test. |
| |
| Patients suspected of having primary aldosteronism | Patients suspected of having primary aldosteronism |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Captopril inhibition test(CCT) | Diagnostic Test | The subjects are required to stop using any drugs that affect the RAAS system in advance. At 08:00 on the test day, they are to remain seated and collect baseline blood samples. Then, they are to take 25mg of captopril orally. After taking the medicine, they are to remain seated and fast for 2 hours, and then collect blood samples again at 10:00. The blood samples collected at these two time points will undergo mass spectrometry analysis to detect plasma aldosterone and renin activity, and 24-hour urine samples will be collected to measure 24-hour urine sodium and 24-hour urine potassium. |
| Measure | Description | Time Frame |
|---|---|---|
| Plasma Aldosterone Concentration (PAC) by LC-MS/MS before and after captopril inhibition test | Two weeks after completing the captopril inhibition test | |
| Plasma Renin activity(PRA) by LC-MS/MS before and after captopril inhibition test | Two weeks after completing the captopril inhibition test | |
| Aldosterone-renin ratio(ARR)by LC-MS/MS before and after captopril inhibition test | Two weeks after completing the captopril inhibition test |
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Normal Control Group
Inclusion Criteria
Exclusion Criteria
Patients with suspected primary aldosteronism
Inclusion Criteria:
Exclusion Criteria:
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1)Healthy Controls to establish physiological suppression limits.2) Patients with suspected PA undergo captopril inhibition test to determine the cut-off point.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Tong Anli | Contact | +8613460884085 | tonganli@hotmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peking Union Medical Colledge Hospital | Recruiting | Beijing | Beijing Municipality | 456350 | China |
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|
| ID | Term |
|---|---|
| D006929 | Hyperaldosteronism |
| D004194 | Disease |
| ID | Term |
|---|---|
| D000308 | Adrenocortical Hyperfunction |
| D000307 | Adrenal Gland Diseases |
| D004700 | Endocrine System Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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