27 research outputs found

    A Faster Algorithm for Two-Variable Integer Programming

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    We show that a 2-variable integer program, defined by mm constraints involving coefficients with at most φ\varphi bits can be solved with O(m+φ)O(m + \varphi) arithmetic operations on rational numbers of size~O(φ)O(\varphi). This result closes the gap between the running time of two-variable integer programming with the sum of the running times of the Euclidean algorithm on φ\varphi-bit integers and the problem of checking feasibility of an integer point for mm~constraints

    Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

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    Background: Regular, detailed reporting on population health by underlying cause of death is fundamental for public health decision making. Cause-specific estimates of mortality and the subsequent effects on life expectancy worldwide are valuable metrics to gauge progress in reducing mortality rates. These estimates are particularly important following large-scale mortality spikes, such as the COVID-19 pandemic. When systematically analysed, mortality rates and life expectancy allow comparisons of the consequences of causes of death globally and over time, providing a nuanced understanding of the effect of these causes on global populations. Methods: The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 cause-of-death analysis estimated mortality and years of life lost (YLLs) from 288 causes of death by age-sex-location-year in 204 countries and territories and 811 subnational locations for each year from 1990 until 2021. The analysis used 56 604 data sources, including data from vital registration and verbal autopsy as well as surveys, censuses, surveillance systems, and cancer registries, among others. As with previous GBD rounds, cause-specific death rates for most causes were estimated using the Cause of Death Ensemble model—a modelling tool developed for GBD to assess the out-of-sample predictive validity of different statistical models and covariate permutations and combine those results to produce cause-specific mortality estimates—with alternative strategies adapted to model causes with insufficient data, substantial changes in reporting over the study period, or unusual epidemiology. YLLs were computed as the product of the number of deaths for each cause-age-sex-location-year and the standard life expectancy at each age. As part of the modelling process, uncertainty intervals (UIs) were generated using the 2·5th and 97·5th percentiles from a 1000-draw distribution for each metric. We decomposed life expectancy by cause of death, location, and year to show cause-specific effects on life expectancy from 1990 to 2021. We also used the coefficient of variation and the fraction of population affected by 90% of deaths to highlight concentrations of mortality. Findings are reported in counts and age-standardised rates. Methodological improvements for cause-of-death estimates in GBD 2021 include the expansion of under-5-years age group to include four new age groups, enhanced methods to account for stochastic variation of sparse data, and the inclusion of COVID-19 and other pandemic-related mortality—which includes excess mortality associated with the pandemic, excluding COVID-19, lower respiratory infections, measles, malaria, and pertussis. For this analysis, 199 new country-years of vital registration cause-of-death data, 5 country-years of surveillance data, 21 country-years of verbal autopsy data, and 94 country-years of other data types were added to those used in previous GBD rounds. Findings: The leading causes of age-standardised deaths globally were the same in 2019 as they were in 1990; in descending order, these were, ischaemic heart disease, stroke, chronic obstructive pulmonary disease, and lower respiratory infections. In 2021, however, COVID-19 replaced stroke as the second-leading age-standardised cause of death, with 94·0 deaths (95% UI 89·2–100·0) per 100 000 population. The COVID-19 pandemic shifted the rankings of the leading five causes, lowering stroke to the third-leading and chronic obstructive pulmonary disease to the fourth-leading position. In 2021, the highest age-standardised death rates from COVID-19 occurred in sub-Saharan Africa (271·0 deaths [250·1–290·7] per 100 000 population) and Latin America and the Caribbean (195·4 deaths [182·1–211·4] per 100 000 population). The lowest age-standardised death rates from COVID-19 were in the high-income super-region (48·1 deaths [47·4–48·8] per 100 000 population) and southeast Asia, east Asia, and Oceania (23·2 deaths [16·3–37·2] per 100 000 population). Globally, life expectancy steadily improved between 1990 and 2019 for 18 of the 22 investigated causes. Decomposition of global and regional life expectancy showed the positive effect that reductions in deaths from enteric infections, lower respiratory infections, stroke, and neonatal deaths, among others have contributed to improved survival over the study period. However, a net reduction of 1·6 years occurred in global life expectancy between 2019 and 2021, primarily due to increased death rates from COVID-19 and other pandemic-related mortality. Life expectancy was highly variable between super-regions over the study period, with southeast Asia, east Asia, and Oceania gaining 8·3 years (6·7–9·9) overall, while having the smallest reduction in life expectancy due to COVID-19 (0·4 years). The largest reduction in life expectancy due to COVID-19 occurred in Latin America and the Caribbean (3·6 years). Additionally, 53 of the 288 causes of death were highly concentrated in locations with less than 50% of the global population as of 2021, and these causes of death became progressively more concentrated since 1990, when only 44 causes showed this pattern. The concentration phenomenon is discussed heuristically with respect to enteric and lower respiratory infections, malaria, HIV/AIDS, neonatal disorders, tuberculosis, and measles. Interpretation: Long-standing gains in life expectancy and reductions in many of the leading causes of death have been disrupted by the COVID-19 pandemic, the adverse effects of which were spread unevenly among populations. Despite the pandemic, there has been continued progress in combatting several notable causes of death, leading to improved global life expectancy over the study period. Each of the seven GBD super-regions showed an overall improvement from 1990 and 2021, obscuring the negative effect in the years of the pandemic. Additionally, our findings regarding regional variation in causes of death driving increases in life expectancy hold clear policy utility. Analyses of shifting mortality trends reveal that several causes, once widespread globally, are now increasingly concentrated geographically. These changes in mortality concentration, alongside further investigation of changing risks, interventions, and relevant policy, present an important opportunity to deepen our understanding of mortality-reduction strategies. Examining patterns in mortality concentration might reveal areas where successful public health interventions have been implemented. Translating these successes to locations where certain causes of death remain entrenched can inform policies that work to improve life expectancy for people everywhere. Funding: Bill & Melinda Gates Foundation

    An Interpolating Sequent Calculus for Quantifier-Free Presburger Arithmetic.

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    Craig interpolation has become a versatile tool in formal verification, used for instance to generate program assertions that serve as candidates for loop invariants. In this paper, we consider Craig interpolation for quantifier-free Presburger arithmetic (QFPA). Until recently, quantifier elimination was the only available interpolation method for this theory, which is, however, known to be potentially costly and inflexible. We introduce an interpolation approach based on a sequent calculus for QFPA that determines interpolants by annotating the steps of an unsatisfiability proof with partial interpolants. We prove our calculus to be sound and complete. We have extended the Princess theorem prover to generate interpolating proofs, and applied it to a large number of publicly available Presburger arithmetic benchmarks. The results document the robustness and efficiency of our interpolation procedure. Finally, we compare the procedure against alternative interpolation methods, both for QFPA and linear rational arithmetic. © 2011 Springer Science+Business Media B.V

    Integer Programs with Prescribed Number of Solutions and a Weighted Version of Doignon-Bell-Scarf’s Theorem

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    peer reviewedIn this paper we study a generalization of the classical fesibility problem in integer linear programming, where an ILP needs to have a prescribed number of solutions to be considered solved. We first provide a generalization of the famous Doignon-Bell-Scarf theorem: Given an integer k, we prove that there exists a constant c(k, n), depending only on the dimension n and k, such that if a polyhedron {x : Ax ≤ b} contains exactly k integer solutions, then there exists a subset of the rows of cardinality no more than c(k,n), defining a polyhedron that contains exactly the same k integer solutions. The second contribution of the article presents a structure theory that characterizes precisely the set Sg≥k (A) of all vectors b such that the problem Ax = b, x ≥ 0, x ∈ Zn , has at least k-solutions. We demonstrate that this set is finitely generated, a union of translated copies of a semigroup which can be computed explicitly via Hilbert bases computation. Similar results can be derived for those right-hand-side vectors that have exactly k solutions or fewer than k solutions. Finally we show that, when n, k are fixed natural numbers, one can compute in polynomial time an encoding of Sg≥k(A) as a generating function, using a short sum of rational functions. As a consequence, one can identify all right-hand-side vectors that have exactly k solutions (similarly for at least k or less than k solutions). Under the same assumptions we prove that the k-Frobenius number can be computed in polynomial time
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