Loewe additivity

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In toxicodynamics and pharmacodynamics, Loewe additivity (or dose additivity) is one of several common reference models used for measuring the effects of drug combinations.[1][2][3]

Definition

Let d1 and d2 be doses of compounds 1 and 2 producing in combination an effect e. We denote by De1 and De2 the doses of compounds 1 and 2 required to produce effect e alone (assuming this conditions uniquely define them, i.e. that the individual dose-response functions are bijective). De1/De2 quantifies the potency of compound 1 relatively to that of compound 2.

d2De1/De2 can be interpreted as the dose d2 of compound 2 converted into the corresponding dose of compound 1 after accounting for difference in potency.

Loewe additivity is defined as the situation where d1+d2De1/De2=De1 or d1/De1+d2/De2=1.

Geometrically, Loewe additivity is the situation where isoboles are segments joining the points (De1,0) and (0,De2) in the domain (d1,d2).

If we denote by f1(d1), f2(d2) and f12(d1,d2) the dose-response functions of compound 1, compound 2 and of the mixture respectively, then dose additivity holds when

d1f11(f12(d1,d2))+d2f21(f12(d1,d2))=1

Testing

The Loewe additivity equation provides a prediction of the dose combination eliciting a given effect. Departure from Loewe additivity can be assessed informally by comparing this prediction to observations. This approach is known in toxicology as the model deviation ratio (MDR).[4]

This approach can be rooted in a more formal statistical method with the derivation of approximate p-values with Monte Carlo simulation, as implemented in the R package MDR.[5]Template:Clarify

References

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