Vertaile menetelmiä

	Annosvasteen meta-analyysi	Metaregressio
Tieteenala	Näytön synteesi	Meta-analyysi
Menetelmäperhe	Process / pipeline	Regression model
Syntyvuosi	1992	2002
Kehittäjä	Greenland & Longnecker (1992), Advanced by Orsini et al. (2012)	Simon Thompson & Julian Higgins
Tyyppi	Method	Weighted regression for effect-size heterogeneity
Alkuperäislähde	Greenland, S., & Longnecker, M. P. (1992). Methods for trend estimation of environmental health risks, with application to exposure to contaminated groundwater. Statistics in Medicine, 11(14‐15), 1837–1847.	Thompson, S. G., & Higgins, J. P. T. (2002). How should meta-regression analyses be undertaken and interpreted? Statistics in Medicine, 21(11), 1559–1573.
Rinnakkaisnimet	Dose-Response Relationship, Non-Linear Meta-Analysis, Dose-Effect Synthesis	Meta-Analytic Regression, Weighted Regression in Meta-Analysis, Moderator Analysis, Meta-regresyon
Liittyvät	1	2
Tiivistelmä	Dose-response meta-analysis is a specialized evidence synthesis method that models the relationship between exposure dose (or intensity, duration, quantity) and health outcome across multiple studies, assessing whether effects follow a linear trend, nonlinear curve, or threshold pattern. Pioneered by Greenland and Longnecker (1992) and refined by Orsini et al. (2012), dose-response meta-analysis answers critical questions like 'Does cardiovascular disease risk increase consistently with salt intake, or is there a threshold above which risk plateaus?' and 'Does the benefit of physical activity increase linearly with exercise duration, or do diminishing returns occur at high doses?' This method is essential for risk assessment, policy-setting on safe exposure limits, and optimizing treatment dosing.	Meta-regression is a statistical technique that extends conventional meta-analysis by regressing study-level effect sizes on one or more study characteristics (moderators) to explain between-study heterogeneity. Formalized by Thompson and Higgins in 2002, it uses weighted least squares — weighting each study by the inverse of its variance — within a mixed-effects framework, allowing researchers to identify which study features systematically account for variation in observed effects across the literature.