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"Lancet"[JOURNAL]

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Plasma biomarkers for Alzheimer's disease among middle-aged individuals.

Rosenberg A, Ngandu T

Lancet · 2026 May · PMID 42208551 · Publisher ↗

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Integrating peripheral immune control and brain health in the multiple sclerosis continuum.

Cocco E

Lancet · 2026 May · PMID 42208550 · Publisher ↗

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A new era in neurology.

The Lancet

Lancet · 2026 May · PMID 42208549 · Publisher ↗

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Advances in ophthalmic artificial intelligence.

Liu Z, Wu X, Lin H

Lancet · 2026 May · PMID 42202838 · Publisher ↗

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The PHEIC for Ebola disease caused by Bundibugyo virus: an inflection point for solidarity and health equity.

Phelan AL, Nuzzo JB, Gostin LO

Lancet · 2026 Jun · PMID 42184811 · Publisher ↗

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The Lancet Commission on precision health: equitable, data-driven health outcomes for all.

Franks PW, Lim LL, Ramsay M … +21 more , Chotirmall SH, Abedalthagafi MS, Ali R, K SB, Ford J, Giordano GN, Hamdi Y, Kieling C, Leal J, Li F, Lopes-Cendes I, Lyons L, Misra S, Owolabi MO, Rosenquist R, Tandon N, Tsosie KS, Udler MS, Smeden MV, Verguet S, Wason J

Lancet · 2026 May · PMID 42184810 · Publisher ↗

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Cruise ship hantavirus outbreak in remote island communities.

Dryden M, Blumberg L, Weyer J … +5 more , Hardy W, Verhoeven V, Asplin J, Plessis JD, Wright N

Lancet · 2026 Jun · PMID 42184809 · Publisher ↗

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The death of the assisted dying bill is an opportunity.

Sallnow L, Smith R

Lancet · 2026 Jun · PMID 42173106 · Publisher ↗

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The recursive care law: artificial intelligence reinforcing feedback loops and health inequity.

Car J, Wong TY, Atun R

Lancet · 2026 Jun · PMID 42173105 · Publisher ↗

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Failure to introduce alcohol health-warning labels in Ireland.

Rutledge SM, Murray F

Lancet · 2026 Jun · PMID 42173104 · Publisher ↗

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Microvascular dysfunction in atherosclerotic coronary disease.

Escaned J, Mejía-Rentería H

Lancet · 2026 Jun · PMID 42167299 · Publisher ↗

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Coronary microvascular dysfunction and cardiovascular outcomes (Multicenter FLOW-CMD Registry): a prospective, multicentre cohort study in South Korea.

Lee JM, Lee SH, Gim DH … +19 more , Lee SY, Choi KH, Ahn JH, Hong YJ, Kim HK, Lee KY, Choo EH, Jeon KH, Kim H, Kang MG, Koh JS, Joh HS, Park TK, Yang JH, Song YB, Choi SH, Gwon HC, Hahn JY, Multicenter FLOW-CMD investigators

Lancet · 2026 Jun · PMID 42167298 · Publisher ↗

BACKGROUND: Coronary microvascular dysfunction often coexists with epicardial coronary artery disease. Data regarding its prevalence and prognosis in patients undergoing invasive coronary angiography are scarce. This stu... BACKGROUND: Coronary microvascular dysfunction often coexists with epicardial coronary artery disease. Data regarding its prevalence and prognosis in patients undergoing invasive coronary angiography are scarce. This study aimed to evaluate the prevalence and prognosis of coronary microvascular dysfunction in patients undergoing clinically indicated invasive coronary angiography in routine practice. METHODS: In this prospective, multicentre cohort study done in seven tertiary medical hospitals in South Korea, consecutive patients aged 18 years and older who were referred for clinically indicated invasive coronary angiography were systematically screened and evaluated by coronary physiological assessment. Obstructive epicardial coronary artery disease was defined as an intermediate stenosis (40-90% diameter stenosis), with fractional flow reserve of 0·80 or less or severe stenosis (>90% of diameter stenosis) treated with revascularisation without fractional flow reserve measurement. Coronary microvascular dysfunction was identified as coronary flow reserve below 2·0 and index of microcirculatory resistance of ≥25. The primary endpoint was a composite of all-cause death, myocardial infarction, clinically driven repeat revascularisation, or hospitalisation for heart failure. The Multicenter FLOW-CMD Registry study is registered with ClinicalTrials.gov (NCT05369182). FINDINGS: Between April 22, 2022, and Nov 19, 2024, 5764 patients were screened and 1003 patients were enrolled (756 men and 247 women). Among these patients, coronary microvascular dysfunction was observed in 123 (21·5%) of 573 patients with obstructive epicardial coronary artery disease and in 40 (9·3%) of 430 patients without obstructive epicardial coronary artery disease. At a median follow-up of 1·9 years, the primary endpoint occurred in 26 patients (2-year Kaplan-Meier estimate 18·8%) with coronary microvascular dysfunction and 70 patients (2-year Kaplan-Meier estimate 10·5%) with preserved microvascular function (hazard ratio 1·91 [95% CI 1·22-2·99]; p=0·0047). INTERPRETATION: In patients with suspected ischaemic heart disease undergoing invasive coronary angiography, coronary microvascular dysfunction coexisted with epicardial coronary artery disease and was associated with a higher risk of the composite of all-cause death, myocardial infarction, clinically driven repeat revascularisation, or hospitalisation for heart failure. FUNDING: Abbott Vascular and Boston Scientific.

Announcing the Lancet Commission on schizophrenia and psychotic disorders.

Leboyer M, Pedraz-Petrozzi B, Spangemacher M … +2 more , Berk M, Lancet Commission on schizophrenia and psychotic disorders

Lancet · 2026 Jun · PMID 42167297 · Publisher ↗

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Updated trends in the global prevalence and burden of mental disorders, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

GBD 2023 Mental Disorder Collaborators

Lancet · 2026 May · PMID 42167272 · Publisher ↗

BACKGROUND: The 2023 iteration of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) estimated prevalence, incidence, and health burden for 375 diseases and injuries, including 12 mental disorders. We... BACKGROUND: The 2023 iteration of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) estimated prevalence, incidence, and health burden for 375 diseases and injuries, including 12 mental disorders. We assess past, current, and emerging trends in the prevalence and burden of mental disorders across sexes and age groups, for 21 regions, 204 countries and territories, and by Socio-demographic Index (SDI) quintile, from 1990 to 2023. METHODS: Mental disorders included in GBD 2023 were anxiety disorders, major depressive disorder, dysthymia, bipolar disorder, schizophrenia, autism spectrum disorders, conduct disorder, attention-deficit hyperactivity disorder, anorexia nervosa, bulimia nervosa, idiopathic developmental intellectual disability, and a residual category of other mental disorders. A literature review identified epidemiological data for each disorder. These were analysed via a Bayesian meta-regression to estimate prevalence by disorder, sex, age, location, and year. Disorder-specific prevalence was multiplied by disability weights representing the severity of health loss associated with each disorder to estimate years lived with disability (YLDs). Deaths due to anorexia nervosa were assessed with a Cause of Death Ensemble modelling strategy to estimate deaths by sex, age, location, and year, and then multiplied by the standard life expectancy at age of death to estimate years of life lost (YLLs). YLDs equalled disability-adjusted life-years (DALYs) for all mental disorders except anorexia nervosa (the only mental disorder considered as an underlying cause of death in GBD), for which DALYs represented the sum of YLDs and YLLs. We presented prevalence, deaths, YLDs, YLLs, and DALYs as counts, age-specific rates per 100 000 population, and age-standardised rates per 100 000 population. FINDINGS: We estimated 1·17 billion (95% uncertainty interval 1·06-1·31) prevalent cases of mental disorders globally in 2023, equivalent to an age-standardised prevalence rate of 14 210·7 cases (12 849·5-15 940·1) per 100 000 population. These estimates represented a 95·5% (75·0-121·2) increase in prevalent cases and 24·2% (11·4-41·4) increase in age-standardised prevalence rate between 1990 and 2023. All mental disorders showed increases in prevalent cases between 1990 and 2023, while notable increases were seen in age-standardised prevalence rates for anxiety disorders, major depressive disorder, dysthymia, anorexia nervosa, bulimia nervosa, schizophrenia, and conduct disorder. There were an estimated 171 million (127-228) DALYs due to mental disorders globally across sex and age in 2023, equivalent to an age-standardised DALY rate of 2070·5 DALYs (1519·1-2750·5) per 100 000 population. Mental disorders contributed to 6·1% (4·8-7·6) of all-cause DALYs in 2023, making them the fifth leading cause of global DALYs (up from 12th in 1990). DALYs were almost entirely composed of YLDs. Mental disorders were the leading cause of YLDs in 2023 (up from second in 1990), explaining 17·3% (14·8-20·6) of all-cause global YLDs. Leading causes of mental disorder DALYs were anxiety disorders (ranked 11th among the 304 diseases and injuries at Level 4 of the GBD cause hierarchy), major depressive disorder (15th), and schizophrenia (41st). Globally in 2023, mental disorder age-standardised DALY rates were higher among females (2239·6 [1643·7-3014·1] per 100 000) than among males (1900·2 [1399·8-2510·8] per 100 000), and peaked in the 15-19 years age group (2617·3 [1850·6-3696·8] per 100 000). All locations showed increased mental disorder DALY rates in 2023 compared with 1990, ranging across countries and territories from 1302·4 (952·7-1683·7) per 100 000 in Viet Nam to 3555·8 (2661·9-4715·0) per 100 000 in the Netherlands. Across SDI quintiles, DALY rates ranged from 1853·0 (1352·1-2469·3) per 100 000 for middle SDI to 2184·1 (1606·1-2890·3) per 100 000 for high SDI. INTERPRETATION: A significant health burden was imposed by mental disorders in all countries and territories in 2023, irrespective of the health resources available. In some instances, this burden has increased over time and is unevenly distributed across populations. Stronger surveillance systems, particularly in low-income and middle-income countries, are required. Additionally, we need more coordinated and inclusive policies to reduce the burden through early treatment and prevention, tailored to sex and age differences across locations. Responding to the mental health needs of our global population, especially those most vulnerable, is an obligation, not a choice. FUNDING: Gates Foundation, Queensland Health, and University of Queensland.

Department of Error.

Lancet · 2026 May · PMID 42167271 · Publisher ↗

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Department of Error.

Lancet · 2026 May · PMID 42167270 · Publisher ↗

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Outcome measure limitations in the SCIENCE trial - Authors' reply.

Perry DC, Kounali D, Zimmermann A … +2 more , Achten J, Costa ML

Lancet · 2026 May · PMID 42167269 · Publisher ↗

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Outcome measure limitations in the SCIENCE trial.

Kalra A, Chhina H, Cooper A

Lancet · 2026 May · PMID 42167268 · Publisher ↗

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Challenging narratives on Syria's health system - Authors' reply.

Irfan B, Kaadan MI, Tarab B

Lancet · 2026 May · PMID 42167267 · Publisher ↗

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Challenging narratives on Syria's health system.

Shalabi S, Abbara A, Safadi S … +2 more , Aljerk W, Alkhalil M

Lancet · 2026 May · PMID 42167266 · Publisher ↗

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