اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدAllometric metabolic scaling and fetal and placental weight
267
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We tested the hypothesis that the fetal-placental relationship scales allometrically and identified modifying factors. Among women delivering after 34 weeks but prior to 43 weeks gestation, 24,601 participants in the Collaborative Perinatal Project (CPP) had complete data for placental gross proportion measures, specifically, disk shape, larger and smaller disk diameters and thickness, and umbilical cord length. The allometric metabolic equation was solved for alpha and beta by rewriting PW= alpha(BW)^beta as Log (PW) = Log(alpha) + beta*Log(BW). Mean beta was 0.78+ 0.02 (range 0.66, 0.89), 104% of that predicted by a supply-limited fractal system (0.75). Gestational age, maternal age, maternal BMI, parity, smoking, socioeconomic status, infant sex, and changes in placental proportions each had independent and significant effects on alpha. Conclusions: In the CPP cohort, the placental - birth weight relationship scales to approximately 3/4 power.
قيم البحث
اقرأ أيضاً
We present a version of Kleibers scaling law for fetus and placenta.
Our empirical modeling suggests that deformation of placental vascular growth is associated with abnormal placental chorionic surface shape. Altered chorionic surface shape is associated with lowered placental functional efficiency. We hypothesize th
at placentas with deformed chorionic surface vascular trees and reduced functional efficiency also have irregular vascular arborization that will be reflected in increased variability of placental thickness and a lower mean thickness. We find that non-centrality of the umbilical cord insertion is strongly and significantly correlated with disk thickness (Spearmans rho=0.128, p=0.002). Deformed shape is strongly and significantly associated with lower overall thickness and higher variability of thickness with beta between -0.173 and -0.254 (p<0.001) . Both lower mean thickness and high variability of thickness are strongly correlated with higher beta (reduced placental efficiency) (p<0.001 and p=0.038 respectively). Greater thickness variability is correlated with higher beta independent of the other placental shape variables p=0.004.
Metabolism plays a central role in cell physiology because it provides the molecular machinery for growth. At the genome-scale, metabolism is made up of thousands of reactions interacting with one another. Untangling this complexity is key to underst
and how cells respond to genetic, environmental, or therapeutic perturbations. Here we discuss the roles of two complementary strategies for the analysis of genome-scale metabolic models: Flux Balance Analysis (FBA) and network science. While FBA estimates metabolic flux on the basis of an optimisation principle, network approaches reveal emergent properties of the global metabolic connectivity. We highlight how the integration of both approaches promises to deliver insights on the structure and function of metabolic systems with wide-ranging implications in discovery science, precision medicine and industrial biotechnology.
The prediction and prevention of traumatic brain injury, spinal injury and general musculo-skeletal injury is a very important aspect of preventive medical science. Recently, in a series of papers, I have proposed a new coupled loading-rate hypothesi
s as a unique cause of all above injuries. This new hypothesis states that the main cause of all mechanical injuries is a Euclidean Jolt, which is an impulsive loading that strikes any part of the human body (head, spine or any bone/joint) - in several coupled degrees-of-freedom simultaneously. It never goes in a single direction only. Also, it is never a static force. It is always an impulsive translational and/or rotational force, coupled to some human mass eccentricity. Keywords: traumatic brain injury, spinal injury, musculo-skeletal injury, coupled loading-rate hypothesis, Euclidean jolt
Mathematical models of cardiac electrical excitation are increasingly complex, with multiscale models seeking to represent and bridge physiological behaviours across temporal and spatial scales. The increasing complexity of these models makes it comp
utationally expensive to both evaluate long term (>60 seconds) behaviour and determine sensitivity of model outputs to inputs. This is particularly relevant in models of atrial fibrillation (AF), where individual episodes last from seconds to days, and inter-episode waiting times can be minutes to months. Potential mechanisms of transition between sinus rhythm and AF have been identified but are not well understood, and it is difficult to simulate AF for long periods of time using state-of-the-art models. In this study, we implemented a Moe-type cellular automaton on a novel, topologically correct surface geometry of the left atrium. We used the model to simulate stochastic initiation and spontaneous termination of AF, arising from bursts of spontaneous activation near pulmonary veins. The simplified representation of atrial electrical activity reduced computational cost, and so permitted us to investigate AF mechanisms in a probabilistic setting. We computed large numbers (~10^5) of sample paths of the model, to infer stochastic initiation and termination rates of AF episodes using different model parameters. By generating statistical distributions of model outputs, we demonstrated how to propagate uncertainties of inputs within our microscopic level model up to a macroscopic level. Lastly, we investigated spontaneous termination in the model and found a complex dependence on its past AF trajectory, the mechanism of which merits future investigation.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
