نتایج جستجو برای: family history fh

تعداد نتایج: 739379  

2011
Matti I. Uusitupa Alena Stančáková Markku Peltonen Johan G. Eriksson Jaana Lindström Sirkka Aunola Pirjo Ilanne-Parikka Sirkka Keinänen-Kiukaanniemi Jaakko Tuomilehto Markku Laakso

OBJECTIVE We aimed to investigate the influence of positive family history (FH+) of diabetes and 19 known genetic risk loci on the effectiveness of lifestyle changes and their predictive value on the incidence of type 2 diabetes in the Finnish Diabetes Prevention Study (DPS). RESEARCH DESIGN AND METHODS A total of 522 subjects with impaired glucose tolerance (IGT) were randomized into the con...

Journal: :Hypertension 1998
K Masuo H Mikami T Ogihara M L Tuck

This study evaluated the effects of a positive family history of hypertension (FH+) on the contributions of sympathetic nervous system (SNS) activity and insulin to blood pressure elevation (BPE). The study design was longitudinal and evaluated BP, body mass index (BMI), and fasting plasma insulin and norepinephrine (NE) levels for 10 years in 557 young, nonobese Japanese men who were normotens...

2012
Hideki Ota Masato Furuhashi Shutaro Ishimura Masayuki Koyama Yusuke Okazaki Tomohiro Mita Takahiro Fuseya Tomohisa Yamashita Marenao Tanaka Hideaki Yoshida Kazuaki Shimamoto Tetsuji Miura

BACKGROUND Fatty acid-binding protein 4 (FABP4/A-FABP/aP2), a lipid chaperone, is expressed in both adipocytes and macrophages. Recent studies have shown secretion of FABP4 from adipocytes and association of elevated serum FABP4 level with obesity, insulin resistance, and atherosclerosis. However, little is known about the role of FABP4 in essential hypertension. METHODS We first examined ser...

Journal: :American journal of physiology. Endocrinology and metabolism 2007
Kenneth Cusi Sangeeta Kashyap Amalia Gastaldelli Mandeep Bajaj Eugenio Cersosimo

Elevated plasma FFA cause beta-cell lipotoxicity and impair insulin secretion in nondiabetic subjects predisposed to type 2 diabetes mellitus [T2DM; i.e., with a strong family history of T2DM (FH+)] but not in nondiabetic subjects without a family history of T2DM. To determine whether lowering plasma FFA with acipimox, an antilipolytic nicotinic acid derivative, may enhance insulin secretion, n...

2012
Ademola Lukman Adelekan Elizabeth Ronami Edoni

Women with Family History (FH) of Breast Cancer (BRCA) in first-degree relative have a relative risk >4 due to inherited genetic mutation genes. This study therefore assessed knowledge and practices of BRCA prevention among women with FH of BRCA in the study area. This is a cross-sectional study. Snowball sampling technique was used to select 189 women with FH of BRCA. A semi-structured questio...

2017
Natália Portela Josária Ferraz Amaral Pedro Augusto de Carvalho Mira Livia Victorino de Souza Daniel Godoy Martinez Mateus Camaroti Laterza

Background: A family history of hypertension is associated with vascular and autonomic abnormalities, as well as an impaired neurohemodynamic response to exercise. Objective: To test the hypothesis that normotensive individuals with a family history of hypertension present an impaired peripheral vascular resistance response to exercise. Methods: The study included 37 normotensive volunteers...

Journal: :Hypertension 2012
Paolo Mulatero Philipp Tauber Maria-Christina Zennaro Silvia Monticone Katharina Lang Felix Beuschlein Evelyn Fischer Davide Tizzani Anna Pallauf Andrea Viola Laurence Amar Tracy Ann Williams Tim M Strom Elisabeth Graf Sascha Bandulik David Penton Pierre-François Plouin Richard Warth Bruno Allolio Xavier Jeunemaitre Franco Veglio Martin Reincke

Primary aldosteronism is the most frequent cause of endocrine hypertension. Three forms of familial hyperaldosteronism (FH) have been described, named FH-I to -III. Recently, a mutation of KCNJ5 has been shown to be associated with FH-III, whereas the cause of FH-II is still unknown. In this study we searched for mutations in KCNJ5 in 46 patients from 21 families with FH, in which FH-I was excl...

Journal: :American journal of human genetics 2000
B K Suarez J Lin J K Burmester K W Broman J L Weber T K Banerjee K A Goddard J S Witte R C Elston W J Catalona

Analysis of a genome screen of 504 brothers with prostate cancer (CaP) who were from 230 multiplex sibships identified five regions with nominally positive linkage signals, on chromosomes 2q, 12p, 15q, 16p, and 16q. The strongest signal in these data is found on chromosome 16q, between markers D16S515 and D16S3040, a region suspected to contain a tumor-suppressor gene. On the basis of findings ...

Journal: :International journal of psychophysiology : official journal of the International Organization of Psychophysiology 2004
Rebecca J Houston Lance O Bauer Victor M Hesselbrock

Decrements in P300 amplitude have been associated with familial risk for alcoholism as well as several other psychiatric disorders characterized by disinhibited behavior. The present study examined the P300 in relation to Borderline Personality Disorder (BPD) features in adolescents with a paternal history of alcohol or drug dependence. One hundred and seventy-five males and females, aged 14-20...

Journal: :Journal of atherosclerosis and thrombosis 2018
Mariko Harada-Shiba Takao Ohta Akira Ohtake Masatsune Ogura Kazushige Dobashi Atsushi Nohara Shizuya Yamashita Koutaro Yokote

This paper describes consensus statement by Joint Working Group by Japan Pediatric Society and Japan Atherosclerosis Society for Making Guidance of Pediatric Familial Hypercholesterolemia (FH) in order to improve prognosis of FH.FH is a common genetic disease caused by mutations in genes related to low density lipoprotein (LDL) receptor pathway. Because patients with FH have high LDL cholestero...

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