Cell cycle (Georgetown, Tex.) · 2011
Tracking the intermediate stages of epithelial-mesenchymal transition in epithelial stem cells and cancer.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАОбзорНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
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Dziewierz Artur, Malinowski Krzysztof, Dardzińska Natalia, Jaskulska Paulina, Zabojszcz Michał, Tkaczyk Filip, Rakowski Tomasz, Siudak Zbigniew
Аннотация
INTRODUCTION: ST‑segment elevation myocardial infarction (STEMI) onset follows a circadian rhythm, yet data from large contemporary national registries remain limited, particularly regarding how the onset time influences treatment delays and coronary pathology.
OBJECTIVES: We aimed to examine circadian patterns of STEMI onset and their impact on treatment delays, culprit vessel involvement, and periprocedural mortality.
PATIENTS AND METHODS: We retrospectively analyzed 153 543 STEMI patients from the Polish National Percutaneous Intervention Registry hospitalized between 2014 and 2022. We examined the hourly distribution of symptom onset and its associations with patient characteristics, treatment delays, and infarct‑related artery location.
RESULTS: STEMI onset showed pronounced circadian variation, peaking at 8:00 AM. Although the overall pattern was similar between sexes (P for interaction = 0.15), median onset time occurred earlier in men than women (10:00 AM vs 11:00 AM; P = 0.007). Nocturnal onset (eg, 3:00 AM) was associated with substantially longer median pain‑to‑first‑medical‑contact times than daytime onset (180 vs 90 min at 1:00 PM; P <0.001). We identified a novel opposing circadian rhythm for the infarct‑related artery location-the left anterior descending (LAD) artery seemed to be the main culprit during nocturnal hours with a nadir at noon, while the right coronary artery (RCA) involvement demonstrated an inverse pattern (P <0.001). Despite delayed presentation, periprocedural mortality did not vary significantly by onset time.
CONCLUSIONS: This large nationwide cohort demonstrates that STEMI onset follows a robust circadian pattern significantly affecting system delays. The discovery of opposing circadian rhythms for LAD and RCA involvement suggests that time of day influences not only STEMI triggering but also its pathophysiological manifestation.
OBJECTIVES: We aimed to examine circadian patterns of STEMI onset and their impact on treatment delays, culprit vessel involvement, and periprocedural mortality.
PATIENTS AND METHODS: We retrospectively analyzed 153 543 STEMI patients from the Polish National Percutaneous Intervention Registry hospitalized between 2014 and 2022. We examined the hourly distribution of symptom onset and its associations with patient characteristics, treatment delays, and infarct‑related artery location.
RESULTS: STEMI onset showed pronounced circadian variation, peaking at 8:00 AM. Although the overall pattern was similar between sexes (P for interaction = 0.15), median onset time occurred earlier in men than women (10:00 AM vs 11:00 AM; P = 0.007). Nocturnal onset (eg, 3:00 AM) was associated with substantially longer median pain‑to‑first‑medical‑contact times than daytime onset (180 vs 90 min at 1:00 PM; P <0.001). We identified a novel opposing circadian rhythm for the infarct‑related artery location-the left anterior descending (LAD) artery seemed to be the main culprit during nocturnal hours with a nadir at noon, while the right coronary artery (RCA) involvement demonstrated an inverse pattern (P <0.001). Despite delayed presentation, periprocedural mortality did not vary significantly by onset time.
CONCLUSIONS: This large nationwide cohort demonstrates that STEMI onset follows a robust circadian pattern significantly affecting system delays. The discovery of opposing circadian rhythms for LAD and RCA involvement suggests that time of day influences not only STEMI triggering but also its pathophysiological manifestation.
Предметные рубрики MeSH
AcetylationAnimalsBreast NeoplasmsCadherinsCell DifferentiationCell LineCell PolarityEmbryo ImplantationEmbryo, MammalianEpigenesis, GeneticEpithelial CellsEpithelial-Mesenchymal TransitionFemaleFibroblast Growth Factor 4Gene Knockdown TechniquesHumansMAP Kinase Kinase Kinase 4MiceNeoplasm InvasivenessPlacentaPregnancySignal TransductionSnail Family Transcription FactorsStem CellsTranscription FactorsTrophoblasts