Last Posted: Jan 05, 2017
- Association between family history of diabetes and cardiovascular disease and lifestyle risk factors in the United States population: The 2009-2012 National Health and Nutrition Examination Survey.
Akhuemonkhan Eboselume et al. Preventive medicine 2016 Dec - Role of telomeres and associated maintenance genes in Type 2 Diabetes Mellitus: A review.
Sethi Itty et al. Diabetes research and clinical practice 2016 Dec 12292-100 - Precision Medicine, Genomics, and Public Health
DK ARnett et al, Diabetes Care, December 2016 - The Microbiome and Risk for Obesity and Diabetes
AL Komaroff, JAMA, December 22, 2016 - Simultaneous Emergence of Multidrug-Resistant Candida auris on 3 Continents Confirmed by Whole-Genome Sequencing and Epidemiological Analyses.
Lockhart Shawn R et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2016 Oct - The Application of Genomics in Diabetes: Barriers to Discovery and Implementation.
Floyd James S et al. Diabetes care 2016 Nov 39(11) 1858-1869 - Precision Medicine, Diabetes, and the U.S. Food and Drug Administration.
Meyer Robert J et al. Diabetes care 2016 Nov 39(11) 1874-1878 - Precision Medicine, Genomics, and Public Health.
Arnett Donna K et al. Diabetes care 2016 Nov 39(11) 1870-1873 - The Impact of Precision Medicine in Diabetes: A Multidimensional Perspective.
Rich Stephen S et al. Diabetes care 2016 Nov 39(11) 1854-1857 - Does Gene Testing Spur Healthier Habits? Maybe Not
N Bakalar, New York Times, December 2, 2016 - The Need for a Privacy Standard for Medical Devices That Transmit Protected Health Information Used in the Precision Medicine Initiative for Diabetes and Other Diseases.
Klonoff David C et al. Journal of diabetes science and technology 2016 Dec - Variation in PCSK9 and HMGCR and Risk of Cardiovascular Disease and Diabetes
BA Ference et al, NEJM, November 30, 2016 - Announcement: National Family History Day - November 24, 2016.
et al. MMWR. Morbidity and mortality weekly report 2016 Nov 65(46) 1305 - Knowing genetic risk for diabetes may not prompt lifestyle changes: study
Globe and Mail, November 30, 2016 - Lifestyle Advice Combined with Personalized Estimates of Genetic or Phenotypic Risk of Type 2 Diabetes, and Objectively Measured Physical Activity: A Randomized Controlled Trial.
Godino Job G et al. PLoS medicine 2016 Nov 13(11) e1002185 - Lifestyle Advice Combined with Personalized Estimates of Genetic or Phenotypic Risk of Type 2 Diabetes, and Objectively Measured Physical Activity: A Randomized Controlled Trial
Godino JG et al, PLOS Medicine, November 2016
From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- It's Your Life. Treat Your Diabetes Well.
- Type 2 Diabetes: All in the Family?
- What's New in diabetes: Prediabetes Awareness Campaign
CDC Diabetes, January 2016 - What is Gestational Diabetes?
- The Diabetes Report Card 2014
- The Diabetes Report Card 2014
From CDC-Authored Genomics Publication Database
This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.
- Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
Tomer Yaron et al. J. Autoimmun. 2015 Jun 6032-9 - Use of genomic panels to determine risk of developing type 2 diabetes in the general population: a targeted evidence-based review.
Palomaki Glenn E et al. Genet. Med. 2013 Aug 15(8) 600-11 - Personal history of diabetes, genetic susceptibility to diabetes, and risk of brain glioma: a pooled analysis of observational studies.
Kitahara Cari M et al. Cancer Epidemiol. Biomarkers Prev. 2014 Jan 23(1) 47-54 - Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study.
Kanakatti Shankar Roopa et al. Pediatr Diabetes 2013 May 14(3) 174-80 - Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: results from the SEARCH for Diabetes in Youth.
Pihoker Catherine et al. J. Clin. Endocrinol. Metab. 2013 Oct 98(10) 4055-62
From Implementation Database
This database focuses on state and national activities that integrate genomics into public health programs and clinical practice
- WISEWOMAN
[Disease: Stroke|Familial Hypercholesterolemia|Heart Disease; Type: Program; State: Multiple States] - Statewide Screening of Fifth Graders Leads to Identification and Treatment of Those With Genetic Predisposition to Early-Onset Heart Disease
[Disease: Heart Disease|Familial Hypercholesterolemia|Stroke; Type: Data|Program; State: West Virginia] - The Ohio Plan to Prevent Heart Disease and Stroke 2008-2012
[Disease: Heart Disease|Stroke|Familial Hypercholesterolemia; Type: Data|Policy|Program; State: Ohio] - Ohio Department of Health Heart Disease and Stroke Prevention Program Take Heart: Know Your Heart Disease and Stroke Family Health History
[Disease: Stroke|Heart Disease|Familial Hypercholesterolemia; Type: Education|Tools; State: Ohio] - Your Family History and Heart Disease[PDF 207.58 KB]
[Disease: Heart Disease|Familial Hypercholesterolemia; Type: Education|Tools; State: Oregon]
From Guideline Database
This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.
- Key-interventions derived from three evidence based guidelines for management and follow-up of patients with HFE haemochromatosis.
Published 2016 (The haemochromatosis working group) (The haemochromatosis working group) - Identification and treatment of patients with homozygous familial hypercholesterolaemia: information and recommendations from a Middle East advisory panel.
Published 2015 (Expert panel) - ISPAD Clinical Practice Consensus Guidelines 2014. The diagnosis and management of monogenic diabetes in children and adolescents.
Published 2015 (International Society for Pediatric and Adolescent Diabetes (ISPAD)) - [Diagnosis and treatment of familial hypercholesterolemia in Spain: Consensus document.]
Published 2015 (Expert panel) - ACOG committee opinion no. 527: Personalized genomic testing for disease risk.
Published 2012 (American College of Obstetricians and Gynecologists (ACOG) - Committee on Genetics)
From Tier Table Database
CDC Office of Public Health Genomics (OPHG) conducts horizon scanning (a systematic research method to find and follow novel technologies appearing in the literature) to identify and track the progress of genomic tests as they move from research into clinical and public health practice. As an aid in organizing horizon scanning results, OPHG ranks genomic tests, and family health history applications, by levels of evidence. See detail.
| Disease/Disorder | Test to be Assessed | Intended Use | Tier Classified | Detail |
|---|---|---|---|---|
| Type 2 diabetes | TCF7L2 genotyping | Risk prediction | Tier 3  | |
| Type 2 diabetes | SNP panels | Risk prediction | Tier 3 | |
| Type 2 diabetes in adults, glycemic control | G6PD | Pharmacogenomic for glyburide | Tier 2 | |
| Type 2 diabetes in adults, glycemic control | G6PD | Pharmacogenomic for glimepiride | Tier 2 | |
| Type 2 diabetes in adults, glycemic control | G6PD | Pharmacogenomic for glimepiride | Tier 2 |
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Vitamin D receptor gene FokI variant in diabetic foot ulcer and its relation with oxidative stress.
Gene 2017 Jan 599 87-91.
Soroush Negin, Radfar Mania, Hamidi Armita Kakavand, Abdollahi Mohammad, Qorbani Mostafa, Razi Farideh, Esfahani Ensieh Nasli, Amoli Mahsa - [Correlation of Thrombosis and Prothrombotic State with Coagulation Factor V Gene Polymorphism and APCR. HHcy].
Zhongguo shi yan xue ye xue za zhi 2016 Dec 24 (6): 1850-1855.
Gao Li-Xia, Ding Qiu-Lan, Wu Ke-Xiong, Hu Jun, Wang Xue-Feng, Dong Chuan-Ling, Dai Qin, Zhang Bing, Dai Jin, He Ping, Zhang Xue-Ping, Wang Yun-X - An IFIH1 gene polymorphism associated with risk for autoimmunity regulates canonical antiviral defence pathways in Coxsackievirus infected human pancreatic islets.
Scientific reports 2016 Dec 6 39378.
Domsgen Erna, Lind Katharina, Kong Lingjia, Hühn Michael H, Rasool Omid, van Kuppeveld Frank, Korsgren Olle, Lahesmaa Riitta, Flodström-Tullberg Mal - Association of ZFHX3 gene variation with atrial fibrillation, cerebral infarction, and lung thromboembolism: An autopsy study.
Journal of cardiology 2016 Dec .
Zaw Khin Thet Thet, Sato Noriko, Ikeda Shinobu, Thu Kaung Si, Mieno Makiko Naka, Arai Tomio, Mori Seijiro, Furukawa Tetsushi, Sasano Tetsuo, Sawabe Motoji, Tanaka Masashi, Muramatsu Masaa - Estrogen-related receptor ? gene (ESRRG) rs1890552 A>G polymorphism in a Korean population: Association with urinary prostaglandin F2? concentration and impaired fasting glucose or newly diagnosed type 2 diabetes.
Diabetes & metabolism 2016 Dec .
Kim M, Kim M, Yoo H J, Yun R, Lee S-H, Lee J
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