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Plasma renin activity

Plasma renin activity (PRA), also known as the renin (active) assay or random plasma renin, is a measure of the activity of the plasma enzyme renin, which plays a major role in the body's regulation of blood pressure, thirst, and urine output. Measure of direct renin concentration (DRC) is technically more demanding, and hence PRA is used instead. DRC assays are still in evolution, and generally a conversion factor of PRA (ng/mL/h) to DRC (mU/L) is 8.2. A recently developed and already commonly used automated DRC assay uses the conversion factor of 12.[1] PRA is sometimes measured, specially in case of certain diseases which present with hypertension or hypotension. PRA is also raised in certain tumors.[2] A PRA measurement may be compared to a plasma aldosterone concentration as an aldosterone-to-renin ratio (ARR).

Measurement and Values

Measurement is done from a sample of venous blood using immunological measuring mechanisms like ELISA, RIA, etc. Often these are done by automated machines to minimize human error.

Considerations for variation

Factors to take into account when interpreting results[1]

Normal values

Reference ranges for blood tests of plasma renin activity can be given both in mass and in international units (μIU/mL or equivalently mIU/L, improperly shown as μU/mL or U/L, confusing mcU/mL used where Greek μ not available), with the former being roughly convertible to the latter by multiplying with 11.2.[3] The following table gives the lower limit (2.5th percentile) and upper limit (97.5th percentile) for plasma renin activity by mass and MCU, with different values owing to various factors of variability of reference ranges:

Results and explanations

Please go through the physiology of renin and of the renin–angiotensin system to understand why the following occur.

Higher-than-normal levels may indicate:[7][8][9][10][11]

Lower-than-normal levels may indicate:

References

  1. ^ a b "Primary Aldosteronism Guideline Resources".
  2. ^ Hamilton Regional Laboratory Medicine Program - Laboratory Reference Centre Manual. Renin Direct.
  3. ^ a b c New Assays for Aldosterone, Renin and Parathyroid Hormone Archived 2011-10-27 at the Wayback Machine University of Washington, Department of Laboratory Medicine. Retrieved Mars 2011
  4. ^ a b Converted from values in μIU/mL by dividing with a factor of 11.2 μIU/mL per ng/(mL*hour), as given in:
    • New Assays for Aldosterone, Renin and Parathyroid Hormone Archived 2011-10-27 at the Wayback Machine University of
    Washington, Department of Laboratory Medicine. Retrieved Mars 2011
  5. ^ a b Pratt, R.; Flynn, J.; Hobart, P.; Paul, M.; Dzau, V. (1988). "Different secretory pathways of renin from mouse cells transfected with the human renin gene". The Journal of Biological Chemistry. 263 (7): 3137–3141. doi:10.1016/S0021-9258(18)69046-5. PMID 2893797.
  6. ^ a b Converted from values in ng/(mL*hour) by multiplying with a factor of 11.2 μIU/mL per ng/(mL*hour), as given in:
    • New Assays for Aldosterone, Renin and Parathyroid Hormone Archived 2011-10-27 at the Wayback Machine University of
    Washington, Department of Laboratory Medicine. Retrieved Mars 2011
  7. ^ Fujino T, Nakagawa N, Yuhki K, Hara A, Yamada T, Takayama K, Kuriyama S, Hosoki Y, Takahata O, Taniguchi T, Fukuzawa J, Hasebe N, Kikuchi K, Narumiya S and Ushikubi F. (2004) Decreased susceptibility to renovascular hypertension in mice lacking the prostaglandin I2 receptor IP. J. Clin. Invest. 114:805-812.
  8. ^ Human renin gene: structure and sequence analysis. 1984 Aug; PubMed Free text.
  9. ^ Cloning and sequence analysis of cDNA for human renin precursor. PubMed.
  10. ^ Pivotal role of the renin/prorenin receptor in angiotensin II production and cellular responses to renin. 2002 Jun; PubMed.
  11. ^ Different secretory pathways of renin from mouse cells transfected with the human renin gene. 1988 Mar 5; PubMed Free text.

Further reading