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In an ab initio context, it may be calculated within many-body perturbation theory or time-dependent density-functional theory, but the quantitative accuracy is currently limited by the available functionals for exchange and correlation in dynamically evolving systems. To circumvent this limitation, the spin susceptibility is here alternatively formulated as the solution of an initial-value problem. In this way, the challenge of accurately describing exchange and correlation in many-electron systems is shifted to the stationary initial state, which is much better understood. 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