Describes the specimen type validated for testing
Defines the optimal specimen required to perform the test and the preferred volume to complete testing
Patient preparation: Patient should be on a normal sodium diet, 110 mEq of sodium. Patient should be in a recumbent posture for at least 30 minutes prior to drawing specimen. Diuretics, mineralocorticoids, glucocorticoids, estrogens, oral contraceptives, ACT medications and sodium, potassium, and posture all affect Angiotensin levels.
Specimen Type: Plasma
Specimen Volume: 3 mL
Collection Instructions: Draw blood in a lavender-top (EDTA) tube(s). Separate plasma from cells immediately after draw, and send 3 mL of EDTA plasma frozen in plastic vial.
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
| Hemolysis || Mild reject; Gross reject |
| Lipemia || Mild reject; Gross reject |
| Icterus || NA |
| Other || Specimens other than Plasma ETDA. Test is strict frozen |
Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test
Angiotensin I is a ten amino acid peptide formed by Renin cleavage of
Angiotensinogen (Renin Substrate). Angiotensin I has little biological
activity except that high levels can stimulate Catecholamine production.
It is metabolized to its biologically active byproduct Angiotensin II by
Angiotensin Converting Enzyme (ACE). The formation of Angiotensin I is
controlled by negative feedback of Angiotensin II and II on Renin
release and by Aldosterone concentration. Levels of Angiotensin I are
increased in many types of hypertension. Angiotensin I levels are used
to determine Renin activity. Angiotensin I is excreted directly into the
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
- Authorized users can sign in to Test Prices for detailed fee information.
- Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.
This test was performed using a kit that has not been cleared or
approved by the FDA and is designated as research use only.
The analytic performance characteristics of this test have been
determined by Inter Science Institute. This test is not intended for
diagnosis or patient management decisions without confirmation
by other medically established means.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CPT codes are provided by the performing laboratory.
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.
||Test Order Name
Order LOINC Value
||Angiotensin I, P
||Test Result Name
Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
||Angiotensin I, P
Test Setup Resources
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.
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SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.
SI Normal Reports |
SI Abnormal Reports