Developmental programming of cardiovascular function: a translational perspective

2020 ◽  
Vol 134 (22) ◽  
pp. 3023-3046
Author(s):  
Stephane L. Bourque ◽  
Sandra T. Davidge

Abstract The developmental origins of health and disease (DOHaD) is a concept linking pre- and early postnatal exposures to environmental influences with long-term health outcomes and susceptibility to disease. It has provided a new perspective on the etiology and evolution of chronic disease risk, and as such is a classic example of a paradigm shift. What first emerged as the ‘fetal origins of disease’, the evolution of the DOHaD conceptual framework is a storied one in which preclinical studies played an important role. With its potential clinical applications of DOHaD, there is increasing desire to leverage this growing body of preclinical work to improve health outcomes in populations all over the world. In this review, we provide a perspective on the values and limitations of preclinical research, and the challenges that impede its translation. The review focuses largely on the developmental programming of cardiovascular function and begins with a brief discussion on the emergence of the ‘Barker hypothesis’, and its subsequent evolution into the more-encompassing DOHaD framework. We then discuss some fundamental pathophysiological processes by which developmental programming may occur, and attempt to define these as ‘instigator’ and ‘effector’ mechanisms, according to their role in early adversity. We conclude with a brief discussion of some notable challenges that hinder the translation of this preclinical work.

2014 ◽  
Vol 4 (5) ◽  
pp. 20140009 ◽  
Author(s):  
Michael R. Irwin

Sleep quality is important to health, and increasingly viewed as critical in promoting successful, resilient aging. In this review, the interplay between sleep and mental and physical health is considered with a focus on the role of inflammation as a biological pathway that translates the effects of sleep on risk of depression, pain and chronic disease risk in aging. Given that sleep regulates inflammatory biologic mechanisms with effects on mental and physical health outcomes, the potential of interventions that target sleep to reduce inflammation and promote health in aging is also discussed.


2021 ◽  
Vol 3 (1) ◽  
pp. 132-178
Author(s):  
Meagan E Crowther ◽  
Sally A Ferguson ◽  
Grace E Vincent ◽  
Amy C Reynolds

Shift work is associated with adverse chronic health outcomes. Addressing chronic disease risk factors including biomedical risk factors, behavioural risk factors, as well as sleep and perceived health status, affords an opportunity to improve health outcomes in shift workers. The present study aimed to conduct a systematic review, qualitative synthesis, and meta-analysis of non-pharmacological interventions targeting chronic disease risk factors, including sleep, in shift workers. A total of 8465 records were retrieved; 65 publications were eligible for inclusion in qualitative analysis. Random-effects meta-analysis were conducted for eight eligible health outcomes, including a total of thirty-nine studies. Interventions resulted in increased objective sleep duration (Hedges’ g = 0.73; CI: 0.36, 1.10, k = 16), improved objective sleep efficiency (Hedges’ g = 0.48; CI: 0.20, 0.76, k = 10) and a small increase in both subjective sleep duration (Hedges’ g = 0.11; CI: −0.04, 0.27, k = 19) and sleep quality (Hedges’ g = 0.11; CI: −0.11, 0.33, k = 21). Interventions also improved perceived health status (Hedges’ g = 0.20; CI: −0.05, 0.46, k = 8), decreased systolic (Hedges’ g = 0.26; CI: −0.54, 0.02, k = 7) and diastolic (Hedges’ g = 0.06; CI: −0.23, 0.36, k = 7) blood pressure, and reduced body mass index (Hedges’ g = −0.04; CI: −0.37, 0.29, k = 9). The current study suggests interventions may improve chronic disease risk factors and sleep in shift workers; however, this could only be objectively assessed for a limited number of risk factor endpoints. Future interventions could explore the impact of non-pharmacological interventions on a broader range of chronic disease risk factors to better characterise targets for improved health outcomes in shift workers.


2009 ◽  
Vol 1 (1) ◽  
pp. 49-85 ◽  
Author(s):  
Heather Royer

The fetal origins hypothesis asserts that nutrient deprivation in utero can raise chronic disease risk. Within economics, this hypothesis has gained acceptance as a leading explanation for the correlations between birth weight, a proxy for fetal nutrient intake, and adult outcomes. Exploiting birth-weight differences between twins using (a) a newly-created dataset of twins from 1960–1982 California birth records and (b) the Early Childhood Longitudinal Study Birth Cohort, I find birth weight is related to educational attainment, later pregnancy complications, and the birth weight of the next generation. These effects are generally small. However, the protective effects of birth weight vary across the birth-weight distribution. (JEL: I12, I21, J13)


Author(s):  
Kate Marsh ◽  
Angela Saunders ◽  
Carol Zeuschner

While foods of animal origin, including red meat, poultry, seafood, eggs and dairy foods, are good sources of protein and other nutrients including iron, zinc, calcium, vitamin B12 and omega-3 fatty acids, there is increasing evidence to suggest that regular consumption of animal foods may negatively impact health and disease risk. This chapter reviews the evidence linking high intakes of animal foods with chronic disease risk, particularly type 2 diabetes, cardiovascular disease and cancer, and discusses some of the possible mechanisms to explain the association between animal food intake and disease risk. The benefits of plant-based and low-animal food options as solutions to reducing these risks are also discussed, along with implications and recommendations for adopting such diets.


2016 ◽  
Vol 71 ◽  
pp. 4
Author(s):  
Sonja Entringer ◽  
Elissa Epel ◽  
Jue Lin ◽  
Claudia Buss ◽  
Elizabeth Blackburn ◽  
...  

1994 ◽  
Vol 10 (6) ◽  
pp. 367-371 ◽  
Author(s):  
Carol Friedman ◽  
Ross C. Brownson ◽  
Dan E. Peterson ◽  
Joan C. Wilkerson

2021 ◽  
Vol 22 (13) ◽  
pp. 6933
Author(s):  
Yuqi Wu ◽  
Chong-Zhi Wang ◽  
Jin-Yi Wan ◽  
Haiqiang Yao ◽  
Chun-Su Yuan

The gut microbiota exists throughout the full life cycle of the human body, and it has been proven to have extensive impacts on health and disease. Accumulating evidence demonstrates that the interplay between gut microbiota and host epigenetics plays a multifaceted role in health maintenance and disease prevention. Intestinal microflora, along with their metabolites, could regulate multiple epigenetic pathways; e.g., DNA methylation, miRNA, or histone modification. Moreover, epigenetic factors can serve as mediators to coordinate gut microbiota within the host. Aiming to dissect this interplay mechanism, the present review summarizes the research profile of gut microbiota and epigenetics in detail, and further interprets the biofunctions of this interplay, especially the regulation of intestinal inflammation, the improvement of metabolic disturbances, and the inhibition of colitis events. This review provides new insights into the interplay of epigenetics and gut microbiota, and attempts to reveal the mysteries of health maintenance and disease prevention from this new perspective.


Author(s):  
Mariana Zogbi Jardim ◽  
Bruna Vieira de Lima Costa ◽  
Milene Cristine Pessoa ◽  
Camila Kümmel Duarte

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