2001575
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Renin, Direct

RENIND
Example Reports
Standard

Ordering Recommendation

The combined aldosterone/renin tests are preferred when screening for hyperaldosteronism. Refer to Aldosterone/Renin Activity Ratio (0070073) or Aldosterone and Renin Direct, With Ratio (3005949).

Methodology

Quantitative Chemiluminescent Immunoassay

Performed

Mon, Wed, Fri

Reported

1-5 days

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation

Collect midmorning (i.e., 7am - 10am) after patient has been sitting, standing, or walking for at least 30 minutes and seated for 5-15 minutes. If the patient is supine, ensure that the patient is in this position for at least 30 minutes prior to collection. Fasting specimens are recommended but not required.

Collect

Lavender (EDTA) from a supine or upright patient.. Do not collect in refrigerated tubes nor store tubes on ice. Process blood at room temperature and centrifuge tubes in a non-refrigerated centrifuge.

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL plasma to an ARUP Standard Transport Tube and freeze immediately. (Min: 1 mL)

Storage/Transport Temperature

Frozen

Unacceptable Conditions

Serum. Specimens collected in citrate, heparin, or oxalate. Grossly hemolyzed or refrigerated specimens.

Remarks
Stability

Ambient: 8 hours; Refrigerated: Unacceptable; Frozen: 4 weeks

Reference Interval

Upright ≤40 yr: 4.2-52.2 pg/mL
Upright >40 yr: 3.6-81.6 pg/mL
Supine ≤40 yr: 3.2-33.2 pg/mL
Supine >40 yr: 2.5-45.1 pg/mL

Interpretive Data



Compliance Category

FDA

Note

Do not use this test for patients treated with Cathepsin B. Menstruating females and those taking estrogen-containing medications may have lower renin direct concentrations, resulting in falsely high aldosterone-renin ratio (ARR). In these cases, order Aldosterone/Renin Activity Ratio (ARUP Test code 0070073). Refer to the Additional Technical Information for Endocrine Society recommendations for patient preparation, specimen collection, medications for hypertension control during confirmatory testing for primary aldosteronism, and factors that may lead to false-positive or false-negative ARR results.

Hotline History

View Hotline History

 

Hotline History

Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
07/05/2022
X
X
X
X
N/A

CPT Codes

84244

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Components

Component Test Code* Component Chart Name LOINC
2001576 Direct Renin 35570-1
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Direct Renin
Renin, Direct