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Sorted By Test Name - Mayo Medical Laboratories

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FSTAC<br />

91655<br />

80327<br />

STEM<br />

hospitalization due to cardiovascular disease using a cutpoint of 35 ng/mL. In addition, mortality risk was<br />

significantly higher in patients with ST2 >35 ng/mL.(4) The risk appears early and persists throughout the<br />

follow-up period. Clinical risk categories are substantiated by results from several large chronic heart<br />

failure studies: -Low risk: < or =35.0 ng/mL -High risk: >35.0 ng/mL (high risk) Results should be<br />

interpreted in the context of the individual patient presentation. Elevated ST2 results indicate an increased<br />

risk for adverse outcomes and signal the adverse remodeling and progression of disease. The reference<br />

interval was derived from normal donors without a history of cardiovascular disease, stroke, diabetes,<br />

renal disease, liver disease, or autoimmune diseases. The reference range is gender dependent; however, it<br />

is the clinical cutpoint that is recognized as providing the most utility. Knowledge of ST2 results in a<br />

heart failure patient may assist in cardiovascular risk stratification and lead to more aggressive<br />

management. There are no specific ST2 inhibitors available at this time and heart failure patients with<br />

elevated ST2 concentrations should be treated and monitored according to established guidelines.<br />

Angiotensin receptor blockers (ARBs) and aldosterone antagonists are thought to be particularly effective.<br />

Reference Values:<br />

Males:<br />

or =18 years: < or =52.0 ng/mL<br />

Females:<br />

or =18 years: < or =38.7 ng/mL<br />

Clinical References: 1. Weintraub NL, Collins SP, Pang PS, et al: Acute heart failure syndromes:<br />

emergency department presentation, treatment, and disposition: Current approaches and future aims: a<br />

scientific statement from the American Heart Association. Circulation 2010;122:1975-1996 2. Kakkar R,<br />

Lee R: The IL-33/ST2 Pathway: therapeutic target and novel biomarker. Nat Rev Drug Discov<br />

2008;7:827-8403 3. Seki K, Sanada S, Kudinova AY, et al: Interleukin-33 prevents apoptosis and<br />

improves survival after experimental myocardial infarction through ST2 signaling. Circ Heart Fail<br />

2009;2(6):684-691 4. Whellan DJ, Oâ€Connor CM, Lee, KL, et al: HF-ACTION Trial Investigators.<br />

Heart failure and a controlled trial investigating outcomes of exercise training (HF-ACTION): design and<br />

rationale. Am Heart J 2007;153(2):201-221 5. Dieplinger B, Januzzi J, Steinmair M, et al: Analytical and<br />

clinical evaluation of a novel high-sensitivity assay for measurement of soluble ST2 in human plasma -<br />

The Presage ST2 Assay. Clin Chim Acta 2009;409:33-40<br />

Stachybotrys Panel II<br />

Reference Values:<br />

Stachybotrys chartarum/atra IgE:

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