語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
FindBook
Google Book
Amazon
博客來
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function./
作者:
Moody, Alexander J.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2022,
面頁冊數:
123 p.
附註:
Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
Contained By:
Dissertations Abstracts International84-01B.
標題:
Medical imaging. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29213366
ISBN:
9798834033141
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function.
Moody, Alexander J.
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function.
- Ann Arbor : ProQuest Dissertations & Theses, 2022 - 123 p.
Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
Thesis (Ph.D.)--The University of Texas Health Science Center at San Antonio, 2022.
This item must not be sold to any third party vendors.
Cardiac Magnetic Resonance imaging (CMR) is a technique shown to accurately characterize function, structure, and composition in a metabolically deficient heart. The present study aims to demonstrate the sensitivity of CMR for cardiometabolic imaging applications in three parts: (i) measure the longitudinal effects of aging on cardiac function and myocardial strain in a baboon Intrauterine Growth Restriction (IUGR) model, (ii) evaluate the longitudinal progression of interstitial fibrosis in an IUGR baboon model with aging, and (iii) establish the effects of pioglitazone on cardiometabolic function and cardiac adiposity in Type 2 Diabetes Mellitus (T2DM). Baboon models were born from dams experiencing a 30% calorie reduction compared to control dams during gestation and nursing. After weaning, subjects were fed a normal caloric diet. CMR scans of baboon subjects were acquired in youth and again in late adulthood. Feature tracking image analysis was used to measure cardiac function and myocardial strain. Interstitial fibrosis was evaluated with a late-gadolinium enhanced T1-mapping method. In human subjects with T2DM, pioglitazone was used to ameliorate insulin resistance. The effects of pioglitazone on the cardiometabolic function were assessed as modulations in diastolic function and cardiac adiposity. Baboon subjects presented with decreased cardiac function and global myocardial strain in all directions in YOUTH, but recovered to a level similar to controls in MIDDLE AGE. Control function and strain remained constant from YOUTH to MIDDLE AGE. Improvements in systolic wall thickening velocity were significantly greater in IUGR compared to normal control subjects (p = 0.04). Ventricular sphericity remained relatively stable in control subjects, but was significantly elevated in IUGR between YOUTH and MIDDLE AGE by comparison (p = 0.03). Extracellular volume (ECV) of the myocardium increased globally from normal aging in both control (p = 0.02) and IUGR (p = 0.03). In human subjects with T2DM, pioglitazone significantly decreased insulin resistance, leading to ameliorations in epicardial adiposity (p = 0.03). The secondary effects of insulin resistance reduction were assessed as modulations in cardiac adiposity. The present study demonstrates three primary novel findings: (i) detrimental impacts from IUGR developmental programming on cardiac function and myocardial strain renormalize from YOUTH to MIDDLE AGE, (ii) progression of myocardial fibrosis and pathological ventricular remodeling (PVR) due to normal aging is accelerated in IUGR subjects compared to controls, and (iii) pioglitazone reduces insulin resistance, leading to reductions in cardiac adiposity associated with gains in myocardial function in T2DM. We propose that increased progression of PVR in IUGR causes an adaptative response that renormalizes cardiac function to supply bodily organs with sufficient blood flow. Additionally, pioglitazone interventions aimed at improving insulin tolerance are associated with ameliorations in cardiac adiposity.
ISBN: 9798834033141Subjects--Topical Terms:
3172799
Medical imaging.
Subjects--Index Terms:
Cardiac magnetic resonance imaging
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function.
LDR
:04353nmm a2200385 4500
001
2350951
005
20221028161059.5
008
241004s2022 ||||||||||||||||| ||eng d
020
$a
9798834033141
035
$a
(MiAaPQ)AAI29213366
035
$a
AAI29213366
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Moody, Alexander J.
$0
(orcid)0000-0003-1834-2175
$3
3690489
245
1 0
$a
Biomarkers in Cardiac Magnetic Resonance Imaging: Indicators of Aging and Metabolic Function.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2022
300
$a
123 p.
500
$a
Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
500
$a
Advisor: Clarke, Geoffrey.
502
$a
Thesis (Ph.D.)--The University of Texas Health Science Center at San Antonio, 2022.
506
$a
This item must not be sold to any third party vendors.
520
$a
Cardiac Magnetic Resonance imaging (CMR) is a technique shown to accurately characterize function, structure, and composition in a metabolically deficient heart. The present study aims to demonstrate the sensitivity of CMR for cardiometabolic imaging applications in three parts: (i) measure the longitudinal effects of aging on cardiac function and myocardial strain in a baboon Intrauterine Growth Restriction (IUGR) model, (ii) evaluate the longitudinal progression of interstitial fibrosis in an IUGR baboon model with aging, and (iii) establish the effects of pioglitazone on cardiometabolic function and cardiac adiposity in Type 2 Diabetes Mellitus (T2DM). Baboon models were born from dams experiencing a 30% calorie reduction compared to control dams during gestation and nursing. After weaning, subjects were fed a normal caloric diet. CMR scans of baboon subjects were acquired in youth and again in late adulthood. Feature tracking image analysis was used to measure cardiac function and myocardial strain. Interstitial fibrosis was evaluated with a late-gadolinium enhanced T1-mapping method. In human subjects with T2DM, pioglitazone was used to ameliorate insulin resistance. The effects of pioglitazone on the cardiometabolic function were assessed as modulations in diastolic function and cardiac adiposity. Baboon subjects presented with decreased cardiac function and global myocardial strain in all directions in YOUTH, but recovered to a level similar to controls in MIDDLE AGE. Control function and strain remained constant from YOUTH to MIDDLE AGE. Improvements in systolic wall thickening velocity were significantly greater in IUGR compared to normal control subjects (p = 0.04). Ventricular sphericity remained relatively stable in control subjects, but was significantly elevated in IUGR between YOUTH and MIDDLE AGE by comparison (p = 0.03). Extracellular volume (ECV) of the myocardium increased globally from normal aging in both control (p = 0.02) and IUGR (p = 0.03). In human subjects with T2DM, pioglitazone significantly decreased insulin resistance, leading to ameliorations in epicardial adiposity (p = 0.03). The secondary effects of insulin resistance reduction were assessed as modulations in cardiac adiposity. The present study demonstrates three primary novel findings: (i) detrimental impacts from IUGR developmental programming on cardiac function and myocardial strain renormalize from YOUTH to MIDDLE AGE, (ii) progression of myocardial fibrosis and pathological ventricular remodeling (PVR) due to normal aging is accelerated in IUGR subjects compared to controls, and (iii) pioglitazone reduces insulin resistance, leading to reductions in cardiac adiposity associated with gains in myocardial function in T2DM. We propose that increased progression of PVR in IUGR causes an adaptative response that renormalizes cardiac function to supply bodily organs with sufficient blood flow. Additionally, pioglitazone interventions aimed at improving insulin tolerance are associated with ameliorations in cardiac adiposity.
590
$a
School code: 0853.
650
4
$a
Medical imaging.
$3
3172799
650
4
$a
Aging.
$3
543123
650
4
$a
Physiology.
$3
518431
653
$a
Cardiac magnetic resonance imaging
653
$a
Cardiometabolism
653
$a
Developmental programming
653
$a
Intrauterine growth restriction
653
$a
Pioglitazone
653
$a
Type 2 diabetes
690
$a
0574
690
$a
0493
690
$a
0719
710
2
$a
The University of Texas Health Science Center at San Antonio.
$b
Radiology.
$3
3346989
773
0
$t
Dissertations Abstracts International
$g
84-01B.
790
$a
0853
791
$a
Ph.D.
792
$a
2022
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29213366
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9473389
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入