LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 8 of total 8

Search options

  1. Article: Multisystem Inflammatory Syndrome in Children, the Real Disease of COVID-19 in Pediatrics - A Multicenter Case Series From Al-Ahsa, Saudi Arabia.

    Almoosa, Zainab A / Al Ameer, Heba H / AlKadhem, Sajjad M / Busaleh, Fadi / AlMuhanna, Fatimah A / Kattih, Osama

    Cureus

    2020  Volume 12, Issue 10, Page(s) e11064

    Abstract: ... MIS-C), especially after the peak of the wave in Al-Ahsa, Saudi Arabia, in early June to mid-July ...

    Abstract Fortunately, coronavirus disease 2019 (COVID-19) infection in pediatric populations exhibits a mild course of disease. However, a small number have recently been identified who develop a significant systemic inflammatory response, a new disease entity called multisystem inflammatory syndrome in children (MIS-C), especially after the peak of the wave in Al-Ahsa, Saudi Arabia, in early June to mid-July. In MIS-C children usually present a few days to a few weeks after recovery from COVID-19 with high grade fever, GI symptoms, Kawasaki-like picture or even toxic shock-like syndrome. Raising awareness about this disease entity is very fundamental to enable pediatricians and other health care providers to identify and manage these patients before it is too late. We describe 10 different cases of MIS-C with different risk factors and presentations.
    Language English
    Publishing date 2020-10-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.11064
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: Multisystem Inflammatory Syndrome in Children Temporally Related to COVID-19: A Case Report From Saudi Arabia.

    Al Ameer, Heba H / AlKadhem, Sajjad M / Busaleh, Fadi / AlKhwaitm, Sami / Llaguno, Maria Blesilda B

    Cureus

    2020  Volume 12, Issue 9, Page(s) e10589

    Abstract: The World Health Organization is still revising the epidemiology of multi-system inflammatory syndrome in children (MIS-C) and the preliminary case definition, although there is a dearth of robust evidence regarding the clinical presentations, severity, ... ...

    Abstract The World Health Organization is still revising the epidemiology of multi-system inflammatory syndrome in children (MIS-C) and the preliminary case definition, although there is a dearth of robust evidence regarding the clinical presentations, severity, and outcomes. Researchers, epidemiologists, and clinicians are struggling to characterize and describe the disease phenomenon while taking care of the diseased persons at the forefronts. This report tackles the first case of a 13-year-old Saudi female with the MIS-C mimicking Kawasaki disease. Her main manifestations were fever, gastrointestinal symptoms, evidence of organ failure with an increase in inflammatory markers, and a history of coronavirus disease (COVID-19) infection. She had glucose-6-phosphate dehydrogenase (G6PD) deficiency and no significant previous history of any disease. She presented with signs of acute illness: high-grade fever (39.6°C) for five days accompanied by sore throat, malaise, reduced oral intake, abdominal pain, diarrhea, skin rash, bilateral non-suppurative conjunctivitis, and erythematous, cracked lips. Eventually, she died despite aggressive management based on the Centers for Disease Control and Prevention and the Saudi Ministry of Health guidelines for COVID-19 management. Based on this case, we suggest that pediatricians need to be aware of such atypical presentations and early referral to tertiary care is imperative for further early diagnosis and management. MIS-C is a rare yet severe and highly critical complication of COVID-19 infection in pediatrics, leading to serious and life-threatening illnesses. Knowledge about the wide spectrum of presenting signs and symptoms and disease severity, including early detection and treatment, is pivotal to prevent a tragic outcome.
    Keywords covid19
    Language English
    Publishing date 2020-09-22
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.10589
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article: Multisystem Inflammatory Syndrome in Children, the Real Disease of COVID-19 in Pediatrics - A Multicenter Case Series From Al-Ahsa, Saudi Arabia

    Almoosa, Zainab A. / Al Ameer, Heba H. / AlKadhem, Sajjad M. / Busaleh, Fadi AlMuhanna Fatimah A. / Kattih, Osama

    Cureus

    Abstract: ... MISC), especially after the peak of the wave in Al-Ahsa, Saudi Arabia, in early June to mid-July In MIS ...

    Abstract Fortunately, coronavirus disease 2019 (COVID-19) infection in pediatric populations exhibits a mild course of disease However, a small number have recently been identified who develop a significant systemic inflammatory response, a new disease entity called multisystem inflammatory syndrome in children (MISC), especially after the peak of the wave in Al-Ahsa, Saudi Arabia, in early June to mid-July In MIS-C children usually present a few days to a few weeks after recovery from COVID-19 with high grade fever, GI symptoms, Kawasaki-like picture or even toxic shock-like syndrome Raising awareness about this disease entity is very fundamental to enable pediatricians and other health care providers to identify and manage these patients before it is too late We describe 10 different cases of MIS-C with different risk factors and presentations
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #907537
    Database COVID19

    Kategorien

  4. Article: Multisystem Inflammatory Syndrome in Children Temporally Related to COVID-19: A Case Report From Saudi Arabia

    Al Ameer, Heba H. / AlKadhem, Sajjad M. / Busaleh, Fadi / AlKhwaitm, Sami / Llaguno, Maria Blesilda B.

    Cureus

    Abstract: The World Health Organization is still revising the epidemiology of multi-system inflammatory syndrome in children (MIS-C) and the preliminary case definition, although there is a dearth of robust evidence regarding the clinical presentations, severity, ... ...

    Abstract The World Health Organization is still revising the epidemiology of multi-system inflammatory syndrome in children (MIS-C) and the preliminary case definition, although there is a dearth of robust evidence regarding the clinical presentations, severity, and outcomes Researchers, epidemiologists, and clinicians are snuggling to characterize and describe the disease phenomenon while taking care of the diseased persons at the forefronts This report tackles the first case of a 13-year-old Saudi female with the MIS-C mimicking Kawasaki disease Her main manifestations were fever, gastrointestinal symptoms, evidence of organ failure with an increase in inflammatory markers, and a history of coronavirus disease (COVID-19) infection She had glucose-6-phosphate dehydrogenase (G6PD) deficiency and no significant previous history of any disease She presented with signs of acute illness: high-grade fever (39 6 degrees C) for five days accompanied by sore throat, malaise, reduced oral intake, abdominal pain, diarrhea, skin rash, bilateral non-suppurative conjunctivitis, and erythematous, cracked lips Eventually, she died despite aggressive management based on the Centers for Disease Control and Prevention and the Saudi Ministry of Health guidelines for COVID-19 management Based on this case, we suggest that pediatricians need to be aware of such atypical presentations and early referral to tertiary care is imperative for further early diagnosis and management MIS-C is a rare yet severe and highly critical complication of COVID-19 infection in pediatrics, leading to serious and life-threatening illnesses Knowledge about the wide spectrum of presenting signs and symptoms and disease severity, including early detection and treatment, is pivotal to prevent a tragic outcome
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #836397
    Database COVID19

    Kategorien

  5. Article ; Online: Analysis and prediction pathways of natural products and their cytotoxicity against HeLa cell line protein using docking, molecular dynamics and ADMET.

    Al-Jumaili, Mohammed Hadi Ali / Siddique, Farhan / Abul Qais, Faizan / Hashem, Heba E / Chtita, Samir / Rani, Abida / Uzair, Muhammad / Almzaien, Kahtan A

    Journal of biomolecular structure & dynamics

    2021  Volume 41, Issue 3, Page(s) 765–777

    Abstract: ... for designing compounds against the HeLa cell line.Communicated by Ramaswamy H. Sarma. ... are expected to be AMES-positive, suggesting that the other compounds are not mutagenic. The result ... total clearance property and no AMES mutagenicity or hERG inhibition properties. These compounds (3,4,15 ...

    Abstract Natural product such as flavonoids and their derivatives have a discernible capability to inhibit tumor formation and the growth of cancer cell, which have a vital link between diet and chronic disease prevention. Several plants and spices that contain flavonoid derivatives have been used in traditional medicine as disease preventative and therapeutic agents. Therefore, flavonoids could be used as chemotherapeutic drugs, indicating their potential clinical utility in cancer treatment. The purpose of this research was to discover and produce innovative pharmaceuticals from natural sources by introducing structural changes into flavonoids' backbones and changing their structures to improve biological activity and anticancer effects. In the current study, it was expected that the percent unbound values for the 15 compounds in human plasma would be low, ranging between 0.188 and 0.391. However, all compounds have a safe range and are not toxic to the brain. Compounds 2, 10, and 13 were shown to be permeable to the CNS (log PS > -3), but all other compounds had difficulty penetrating the CNS. Furthermore, all compounds had a low total clearance, ranging from 0.038 to 1.216 ml/min/kg, indicating that these compounds have a long half-life. None of the compounds caused skin sensitization (SS), and only compounds 1, 11, and 12 are expected to be AMES-positive, suggesting that the other compounds are not mutagenic. The result of the study showed based on the Drug-likeness and ADMET studies, only 3 compounds, including 3, 4, and 15, have a good pharmacokinetics propriety, the lowest toxicity, and good binding affinity towards Caspase 3 V266APDB (ID: 5I9B) as potential inhibitor candidates for the HeLa cell line, they have a low total clearance property and no AMES mutagenicity or hERG inhibition properties. These compounds (3,4,15) were examined to act as new cytotoxic drug candidates and would have an interest as starting point for designing compounds against the HeLa cell line.Communicated by Ramaswamy H. Sarma.
    MeSH term(s) Humans ; HeLa Cells ; Molecular Docking Simulation ; Biological Products/pharmacology ; Biological Products/chemistry ; Molecular Dynamics Simulation ; Flavonoids
    Chemical Substances Biological Products ; Flavonoids
    Language English
    Publishing date 2021-12-03
    Publishing country England
    Document type Journal Article
    ZDB-ID 49157-3
    ISSN 1538-0254 ; 0739-1102
    ISSN (online) 1538-0254
    ISSN 0739-1102
    DOI 10.1080/07391102.2021.2011785
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Effect of novel water soluble curcumin derivative on experimental type- 1 diabetes mellitus (short term study).

    Abdel Aziz, Mohamed T / El-Asmar, Mohamed F / El-Ibrashy, Ibrahim N / Rezq, Ameen M / Al-Malki, Abdulrahman L / Wassef, Mohamed A / Fouad, Hanan H / Ahmed, Hanan H / Taha, Fatma M / Hassouna, Amira A / Morsi, Heba M

    Diabetology & metabolic syndrome

    2012  Volume 4, Issue 1, Page(s) 30

    Language English
    Publishing date 2012-07-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2518786-7
    ISSN 1758-5996 ; 1758-5996
    ISSN (online) 1758-5996
    ISSN 1758-5996
    DOI 10.1186/1758-5996-4-30
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Effect of novel water soluble curcumin derivative on experimental type- 1 diabetes mellitus (short term study)

    Abdel Aziz Mohamed T / El-Asmar Mohamed F / El-Ibrashy Ibrahim N / Rezq Ameen M / Al-Malki Abdulrahman L / Wassef Mohamed A / Fouad Hanan H / Ahmed Hanan H / Taha Fatma M / Hassouna Amira A / Morsi Heba M

    Diabetology & Metabolic Syndrome , Vol 4, Iss 1, p

    2012  Volume 30

    Abstract: Abstract Background Diabetes mellitus type 1 is an autoimmune disorder caused by lymphocytic infiltration and beta cells destruction. Curcumin has been identified as a potent inducer of heme-oxygenase-1 (HO-1), a redoxsensitive inducible protein that ... ...

    Abstract Abstract Background Diabetes mellitus type 1 is an autoimmune disorder caused by lymphocytic infiltration and beta cells destruction. Curcumin has been identified as a potent inducer of heme-oxygenase-1 (HO-1), a redoxsensitive inducible protein that provides protection against various forms of stress. A novel water soluble curcumin derivative (NCD) has been developed to overcome low in vivo bioavailability of curcumin. The aim of the present work is to evaluate the anti diabetic effects of the “NCD” and its effects on diabetes-induced ROS generation and lipid peroxidation in experimental type- 1 diabetes mellitus. We also examine whether the up regulation of HO-1 accompanied by increased HO activity mediates these antidiabetic and anti oxidant actions. Materials and methods Rats were divided into control group, control group receiving curcumin derivative, diabetic group, diabetic group receiving curcumin derivative and diabetic group receiving curcumin derivative and HO inhibitor ZnPP. Type-1 diabetes was induced by intraperitoneal injection of streptozotocin. Curcumin derivative was given orally for 45 days. At the planned sacrification time (after 45 days), fasting blood samples were withdrawn for estimation of plasma glucose, plasma insulin and lipid profile . Animals were sacrificed; pancreas, aorta and liver were excised for the heme oxygenase - 1 expression, activity and malondialdehyde estimation. Results NCD supplementation to diabetic rats significantly lowered the plasma glucose by 27.5% and increased plasma insulin by 66.67%. On the other hand, the mean plasma glucose level in the control group showed no significant difference compared to the control group receiving the oral NCD whereas, NCD supplementation to the control rats significantly increased the plasma insulin by 47.13% compared to the control. NCD decreased total cholesterol, triglycerides, LDL cholesterol and increased HDL cholesterol levels. Also, it decreased lipid peroxides (malondialdehyde) in the pancreas, aorta and liver. Conclusion The (NCD) by its small dose possesses antidiabetic actions and that heme oxygenase induction seems to play an important role in its anti-diabetic effects. NCD also improves the lipid profile and oxidative status directly, proved by decreasing lipid peroxides (malondialdehyde) in pancreas, liver & aorta. The new water soluble curcumin derivative still retains the essential potencies of natural curcumin.
    Keywords Diabetes Type 1 ; Heme oxygenase −1 ; Curcumin ; Insulin secretion ; Oxidative stress ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Subject code 571
    Language English
    Publishing date 2012-07-01T00:00:00Z
    Publisher BioMed Central
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

    Forouzanfar, Mohammad H / Alexander, Lily / Anderson, H Ross / Bachman, Victoria F / Biryukov, Stan / Brauer, Michael / Burnett, Richard / Casey, Daniel / Coates, Matthew M / Cohen, Aaron / Delwiche, Kristen / Estep, Kara / Frostad, Joseph J / Astha, K C / Kyu, Hmwe H / Moradi-Lakeh, Maziar / Ng, Marie / Slepak, Erica Leigh / Thomas, Bernadette A /
    Wagner, Joseph / Aasvang, Gunn Marit / Abbafati, Cristiana / Abbasoglu Ozgoren, Ayse / Abd-Allah, Foad / Abera, Semaw F / Aboyans, Victor / Abraham, Biju / Abraham, Jerry Puthenpurakal / Abubakar, Ibrahim / Abu-Rmeileh, Niveen M E / Aburto, Tania C / Achoki, Tom / Adelekan, Ademola / Adofo, Koranteng / Adou, Arsène K / Adsuar, José C / Afshin, Ashkan / Agardh, Emilie E / Al Khabouri, Mazin J / Al Lami, Faris H / Alam, Sayed Saidul / Alasfoor, Deena / Albittar, Mohammed I / Alegretti, Miguel A / Aleman, Alicia V / Alemu, Zewdie A / Alfonso-Cristancho, Rafael / Alhabib, Samia / Ali, Raghib / Ali, Mohammed K / Alla, François / Allebeck, Peter / Allen, Peter J / Alsharif, Ubai / Alvarez, Elena / Alvis-Guzman, Nelson / Amankwaa, Adansi A / Amare, Azmeraw T / Ameh, Emmanuel A / Ameli, Omid / Amini, Heresh / Ammar, Walid / Anderson, Benjamin O / Antonio, Carl Abelardo T / Anwari, Palwasha / Argeseanu Cunningham, Solveig / Arnlöv, Johan / Arsenijevic, Valentina S Arsic / Artaman, Al / Asghar, Rana J / Assadi, Reza / Atkins, Lydia S / Atkinson, Charles / Avila, Marco A / Awuah, Baffour / Badawi, Alaa / Bahit, Maria C / Bakfalouni, Talal / Balakrishnan, Kalpana / Balalla, Shivanthi / Balu, Ravi Kumar / Banerjee, Amitava / Barber, Ryan M / Barker-Collo, Suzanne L / Barquera, Simon / Barregard, Lars / Barrero, Lope H / Barrientos-Gutierrez, Tonatiuh / Basto-Abreu, Ana C / Basu, Arindam / Basu, Sanjay / Basulaiman, Mohammed O / Batis Ruvalcaba, Carolina / Beardsley, Justin / Bedi, Neeraj / Bekele, Tolesa / Bell, Michelle L / Benjet, Corina / Bennett, Derrick A / Benzian, Habib / Bernabé, Eduardo / Beyene, Tariku J / Bhala, Neeraj / Bhalla, Ashish / Bhutta, Zulfiqar A / Bikbov, Boris / Bin Abdulhak, Aref A / Blore, Jed D / Blyth, Fiona M / Bohensky, Megan A / Bora Başara, Berrak / Borges, Guilherme / Bornstein, Natan M / Bose, Dipan / Boufous, Soufiane / Bourne, Rupert R / Brainin, Michael / Brazinova, Alexandra / Breitborde, Nicholas J / Brenner, Hermann / Briggs, Adam D M / Broday, David M / Brooks, Peter M / Bruce, Nigel G / Brugha, Traolach S / Brunekreef, Bert / Buchbinder, Rachelle / Bui, Linh N / Bukhman, Gene / Bulloch, Andrew G / Burch, Michael / Burney, Peter G J / Campos-Nonato, Ismael R / Campuzano, Julio C / Cantoral, Alejandra J / Caravanos, Jack / Cárdenas, Rosario / Cardis, Elisabeth / Carpenter, David O / Caso, Valeria / Castañeda-Orjuela, Carlos A / Castro, Ruben E / Catalá-López, Ferrán / Cavalleri, Fiorella / Çavlin, Alanur / Chadha, Vineet K / Chang, Jung-Chen / Charlson, Fiona J / Chen, Honglei / Chen, Wanqing / Chen, Zhengming / Chiang, Peggy P / Chimed-Ochir, Odgerel / Chowdhury, Rajiv / Christophi, Costas A / Chuang, Ting-Wu / Chugh, Sumeet S / Cirillo, Massimo / Claßen, Thomas K D / Colistro, Valentina / Colomar, Mercedes / Colquhoun, Samantha M / Contreras, Alejandra G / Cooper, Cyrus / Cooperrider, Kimberly / Cooper, Leslie T / Coresh, Josef / Courville, Karen J / Criqui, Michael H / Cuevas-Nasu, Lucia / Damsere-Derry, James / Danawi, Hadi / Dandona, Lalit / Dandona, Rakhi / Dargan, Paul I / Davis, Adrian / Davitoiu, Dragos V / Dayama, Anand / de Castro, E Filipa / De la Cruz-Góngora, Vanessa / De Leo, Diego / de Lima, Graça / Degenhardt, Louisa / del Pozo-Cruz, Borja / Dellavalle, Robert P / Deribe, Kebede / Derrett, Sarah / Des Jarlais, Don C / Dessalegn, Muluken / deVeber, Gabrielle A / Devries, Karen M / Dharmaratne, Samath D / Dherani, Mukesh K / Dicker, Daniel / Ding, Eric L / Dokova, Klara / Dorsey, E Ray / Driscoll, Tim R / Duan, Leilei / Durrani, Adnan M / Ebel, Beth E / Ellenbogen, Richard G / Elshrek, Yousef M / Endres, Matthias / Ermakov, Sergey P / Erskine, Holly E / Eshrati, Babak / Esteghamati, Alireza / Fahimi, Saman / Faraon, Emerito Jose A / Farzadfar, Farshad / Fay, Derek F J / Feigin, Valery L / Feigl, Andrea B / Fereshtehnejad, Seyed-Mohammad / Ferrari, Alize J / Ferri, Cleusa P / Flaxman, Abraham D / Fleming, Thomas D / Foigt, Nataliya / Foreman, Kyle J / Paleo, Urbano Fra / Franklin, Richard C / Gabbe, Belinda / Gaffikin, Lynne / Gakidou, Emmanuela / Gamkrelidze, Amiran / Gankpé, Fortuné G / Gansevoort, Ron T / García-Guerra, Francisco A / Gasana, Evariste / Geleijnse, Johanna M / Gessner, Bradford D / Gething, Pete / Gibney, Katherine B / Gillum, Richard F / Ginawi, Ibrahim A M / Giroud, Maurice / Giussani, Giorgia / Goenka, Shifalika / Goginashvili, Ketevan / Gomez Dantes, Hector / Gona, Philimon / Gonzalez de Cosio, Teresita / González-Castell, Dinorah / Gotay, Carolyn C / Goto, Atsushi / Gouda, Hebe N / Guerrant, Richard L / Gugnani, Harish C / Guillemin, Francis / Gunnell, David / Gupta, Rahul / Gupta, Rajeev / Gutiérrez, Reyna A / Hafezi-Nejad, Nima / Hagan, Holly / Hagstromer, Maria / Halasa, Yara A / Hamadeh, Randah R / Hammami, Mouhanad / Hankey, Graeme J / Hao, Yuantao / Harb, Hilda L / Haregu, Tilahun Nigatu / Haro, Josep Maria / Havmoeller, Rasmus / Hay, Simon I / Hedayati, Mohammad T / Heredia-Pi, Ileana B / Hernandez, Lucia / Heuton, Kyle R / Heydarpour, Pouria / Hijar, Martha / Hoek, Hans W / Hoffman, Howard J / Hornberger, John C / Hosgood, H Dean / Hoy, Damian G / Hsairi, Mohamed / Hu, Guoqing / Hu, Howard / Huang, Cheng / Huang, John J / Hubbell, Bryan J / Huiart, Laetitia / Husseini, Abdullatif / Iannarone, Marissa L / Iburg, Kim M / Idrisov, Bulat T / Ikeda, Nayu / Innos, Kaire / Inoue, Manami / Islami, Farhad / Ismayilova, Samaya / Jacobsen, Kathryn H / Jansen, Henrica A / Jarvis, Deborah L / Jassal, Simerjot K / Jauregui, Alejandra / Jayaraman, Sudha / Jeemon, Panniyammakal / Jensen, Paul N / Jha, Vivekanand / Jiang, Fan / Jiang, Guohong / Jiang, Ying / Jonas, Jost B / Juel, Knud / Kan, Haidong / Kany Roseline, Sidibe S / Karam, Nadim E / Karch, André / Karema, Corine K / Karthikeyan, Ganesan / Kaul, Anil / Kawakami, Norito / Kazi, Dhruv S / Kemp, Andrew H / Kengne, Andre P / Keren, Andre / Khader, Yousef S / Khalifa, Shams Eldin Ali Hassan / Khan, Ejaz A / Khang, Young-Ho / Khatibzadeh, Shahab / Khonelidze, Irma / Kieling, Christian / Kim, Daniel / Kim, Sungroul / Kim, Yunjin / Kimokoti, Ruth W / Kinfu, Yohannes / Kinge, Jonas M / Kissela, Brett M / Kivipelto, Miia / Knibbs, Luke D / Knudsen, Ann Kristin / Kokubo, Yoshihiro / Kose, M Rifat / Kosen, Soewarta / Kraemer, Alexander / Kravchenko, Michael / Krishnaswami, Sanjay / Kromhout, Hans / Ku, Tiffany / Kuate Defo, Barthelemy / Kucuk Bicer, Burcu / Kuipers, Ernst J / Kulkarni, Chanda / Kulkarni, Veena S / Kumar, G Anil / Kwan, Gene F / Lai, Taavi / Lakshmana Balaji, Arjun / Lalloo, Ratilal / Lallukka, Tea / Lam, Hilton / Lan, Qing / Lansingh, Van C / Larson, Heidi J / Larsson, Anders / Laryea, Dennis O / Lavados, Pablo M / Lawrynowicz, Alicia E / Leasher, Janet L / Lee, Jong-Tae / Leigh, James / Leung, Ricky / Levi, Miriam / Li, Yichong / Li, Yongmei / Liang, Juan / Liang, Xiaofeng / Lim, Stephen S / Lindsay, M Patrice / Lipshultz, Steven E / Liu, Shiwei / Liu, Yang / Lloyd, Belinda K / Logroscino, Giancarlo / London, Stephanie J / Lopez, Nancy / Lortet-Tieulent, Joannie / Lotufo, Paulo A / Lozano, Rafael / Lunevicius, Raimundas / Ma, Jixiang / Ma, Stefan / Machado, Vasco M P / MacIntyre, Michael F / Magis-Rodriguez, Carlos / Mahdi, Abbas A / Majdan, Marek / Malekzadeh, Reza / Mangalam, Srikanth / Mapoma, Christopher C / Marape, Marape / Marcenes, Wagner / Margolis, David J / Margono, Christopher / Marks, Guy B / Martin, Randall V / Marzan, Melvin B / Mashal, Mohammad T / Masiye, Felix / Mason-Jones, Amanda J / Matsushita, Kunihiro / Matzopoulos, Richard / Mayosi, Bongani M / Mazorodze, Tasara T / McKay, Abigail C / McKee, Martin / McLain, Abigail / Meaney, Peter A / Medina, Catalina / Mehndiratta, Man Mohan / Mejia-Rodriguez, Fabiola / Mekonnen, Wubegzier / Melaku, Yohannes A / Meltzer, Michele / Memish, Ziad A / Mendoza, Walter / Mensah, George A / Meretoja, Atte / Mhimbira, Francis Apolinary / Micha, Renata / Miller, Ted R / Mills, Edward J / Misganaw, Awoke / Mishra, Santosh / Mohamed Ibrahim, Norlinah / Mohammad, Karzan A / Mokdad, Ali H / Mola, Glen L / Monasta, Lorenzo / Montañez Hernandez, Julio C / Montico, Marcella / Moore, Ami R / Morawska, Lidia / Mori, Rintaro / Moschandreas, Joanna / Moturi, Wilkister N / Mozaffarian, Dariush / Mueller, Ulrich O / Mukaigawara, Mitsuru / Mullany, Erin C / Murthy, Kinnari S / Naghavi, Mohsen / Nahas, Ziad / Naheed, Aliya / Naidoo, Kovin S / Naldi, Luigi / Nand, Devina / Nangia, Vinay / Narayan, K M Venkat / Nash, Denis / Neal, Bruce / Nejjari, Chakib / Neupane, Sudan P / Newton, Charles R / Ngalesoni, Frida N / Ngirabega, Jean de Dieu / Nguyen, Grant / Nguyen, Nhung T / Nieuwenhuijsen, Mark J / Nisar, Muhammad I / Nogueira, José R / Nolla, Joan M / Nolte, Sandra / Norheim, Ole F / Norman, Rosana E / Norrving, Bo / Nyakarahuka, Luke / Oh, In-Hwan / Ohkubo, Takayoshi / Olusanya, Bolajoko O / Omer, Saad B / Opio, John Nelson / Orozco, Ricardo / Pagcatipunan, Rodolfo S / Pain, Amanda W / Pandian, Jeyaraj D / Panelo, Carlo Irwin A / Papachristou, Christina / Park, Eun-Kee / Parry, Charles D / Paternina Caicedo, Angel J / Patten, Scott B / Paul, Vinod K / Pavlin, Boris I / Pearce, Neil / Pedraza, Lilia S / Pedroza, Andrea / Pejin Stokic, Ljiljana / Pekericli, Ayfer / Pereira, David M / Perez-Padilla, Rogelio / Perez-Ruiz, Fernando / Perico, Norberto / Perry, Samuel A L / Pervaiz, Aslam / Pesudovs, Konrad / Peterson, Carrie B / Petzold, Max / Phillips, Michael R / Phua, Hwee Pin / Plass, Dietrich / Poenaru, Dan / Polanczyk, Guilherme V / Polinder, Suzanne / Pond, Constance D / Pope, C Arden / Pope, Daniel / Popova, Svetlana / Pourmalek, Farshad / Powles, John / Prabhakaran, Dorairaj / Prasad, Noela M / Qato, Dima M / Quezada, Amado D / Quistberg, D Alex A / Racapé, Lionel / Rafay, Anwar / Rahimi, Kazem / Rahimi-Movaghar, Vafa / Rahman, Sajjad Ur / Raju, Murugesan / Rakovac, Ivo / Rana, Saleem M / Rao, Mayuree / Razavi, Homie / Reddy, K Srinath / Refaat, Amany H / Rehm, Jürgen / Remuzzi, Giuseppe / Ribeiro, Antonio L / Riccio, Patricia M / Richardson, Lee / Riederer, Anne / Robinson, Margaret / Roca, Anna / Rodriguez, Alina / Rojas-Rueda, David / Romieu, Isabelle / Ronfani, Luca / Room, Robin / Roy, Nobhojit / Ruhago, George M / Rushton, Lesley / Sabin, Nsanzimana / Sacco, Ralph L / Saha, Sukanta / Sahathevan, Ramesh / Sahraian, Mohammad Ali / Salomon, Joshua A / Salvo, Deborah / Sampson, Uchechukwu K / Sanabria, Juan R / Sanchez, Luz Maria / Sánchez-Pimienta, Tania G / Sanchez-Riera, Lidia / Sandar, Logan / Santos, Itamar S / Sapkota, Amir / Satpathy, Maheswar / Saunders, James E / Sawhney, Monika / Saylan, Mete I / Scarborough, Peter / Schmidt, Jürgen C / Schneider, Ione J C / Schöttker, Ben / Schwebel, David C / Scott, James G / Seedat, Soraya / Sepanlou, Sadaf G / Serdar, Berrin / Servan-Mori, Edson E / Shaddick, Gavin / Shahraz, Saeid / Levy, Teresa Shamah / Shangguan, Siyi / She, Jun / Sheikhbahaei, Sara / Shibuya, Kenji / Shin, Hwashin H / Shinohara, Yukito / Shiri, Rahman / Shishani, Kawkab / Shiue, Ivy / Sigfusdottir, Inga D / Silberberg, Donald H / Simard, Edgar P / Sindi, Shireen / Singh, Abhishek / Singh, Gitanjali M / Singh, Jasvinder A / Skirbekk, Vegard / Sliwa, Karen / Soljak, Michael / Soneji, Samir / Søreide, Kjetil / Soshnikov, Sergey / Sposato, Luciano A / Sreeramareddy, Chandrashekhar T / Stapelberg, Nicolas J C / Stathopoulou, Vasiliki / Steckling, Nadine / Stein, Dan J / Stein, Murray B / Stephens, Natalie / Stöckl, Heidi / Straif, Kurt / Stroumpoulis, Konstantinos / Sturua, Lela / Sunguya, Bruno F / Swaminathan, Soumya / Swaroop, Mamta / Sykes, Bryan L / Tabb, Karen M / Takahashi, Ken / Talongwa, Roberto T / Tandon, Nikhil / Tanne, David / Tanner, Marcel / Tavakkoli, Mohammad / Te Ao, Braden J / Teixeira, Carolina M / Téllez Rojo, Martha M / Terkawi, Abdullah S / Texcalac-Sangrador, José Luis / Thackway, Sarah V / Thomson, Blake / Thorne-Lyman, Andrew L / Thrift, Amanda G / Thurston, George D / Tillmann, Taavi / Tobollik, Myriam / Tonelli, Marcello / Topouzis, Fotis / Towbin, Jeffrey A / Toyoshima, Hideaki / Traebert, Jefferson / Tran, Bach X / Trasande, Leonardo / Trillini, Matias / Trujillo, Ulises / Dimbuene, Zacharie Tsala / Tsilimbaris, Miltiadis / Tuzcu, Emin Murat / Uchendu, Uche S / Ukwaja, Kingsley N / Uzun, Selen B / van de Vijver, Steven / Van Dingenen, Rita / van Gool, Coen H / van Os, Jim / Varakin, Yuri Y / Vasankari, Tommi J / Vasconcelos, Ana Maria N / Vavilala, Monica S / Veerman, Lennert J / Velasquez-Melendez, Gustavo / Venketasubramanian, N / Vijayakumar, Lakshmi / Villalpando, Salvador / Violante, Francesco S / Vlassov, Vasiliy Victorovich / Vollset, Stein Emil / Wagner, Gregory R / Waller, Stephen G / Wallin, Mitchell T / Wan, Xia / Wang, Haidong / Wang, JianLi / Wang, Linhong / Wang, Wenzhi / Wang, Yanping / Warouw, Tati S / Watts, Charlotte H / Weichenthal, Scott / Weiderpass, Elisabete / Weintraub, Robert G / Werdecker, Andrea / Wessells, K Ryan / Westerman, Ronny / Whiteford, Harvey A / Wilkinson, James D / Williams, Hywel C / Williams, Thomas N / Woldeyohannes, Solomon M / Wolfe, Charles D A / Wong, John Q / Woolf, Anthony D / Wright, Jonathan L / Wurtz, Brittany / Xu, Gelin / Yan, Lijing L / Yang, Gonghuan / Yano, Yuichiro / Ye, Pengpeng / Yenesew, Muluken / Yentür, Gökalp K / Yip, Paul / Yonemoto, Naohiro / Yoon, Seok-Jun / Younis, Mustafa Z / Younoussi, Zourkaleini / Yu, Chuanhua / Zaki, Maysaa E / Zhao, Yong / Zheng, Yingfeng / Zhou, Maigeng / Zhu, Jun / Zhu, Shankuan / Zou, Xiaonong / Zunt, Joseph R / Lopez, Alan D / Vos, Theo / Murray, Christopher J

    Lancet (London, England)

    2015  Volume 386, Issue 10010, Page(s) 2287–2323

    Abstract: Background: The Global Burden of Disease, Injuries, and Risk Factor study 2013 (GBD 2013) is the first of a series of annual updates of the GBD. Risk factor quantification, particularly of modifiable risk factors, can help to identify emerging threats ... ...

    Abstract Background: The Global Burden of Disease, Injuries, and Risk Factor study 2013 (GBD 2013) is the first of a series of annual updates of the GBD. Risk factor quantification, particularly of modifiable risk factors, can help to identify emerging threats to population health and opportunities for prevention. The GBD 2013 provides a timely opportunity to update the comparative risk assessment with new data for exposure, relative risks, and evidence on the appropriate counterfactual risk distribution.
    Methods: Attributable deaths, years of life lost, years lived with disability, and disability-adjusted life-years (DALYs) have been estimated for 79 risks or clusters of risks using the GBD 2010 methods. Risk-outcome pairs meeting explicit evidence criteria were assessed for 188 countries for the period 1990-2013 by age and sex using three inputs: risk exposure, relative risks, and the theoretical minimum risk exposure level (TMREL). Risks are organised into a hierarchy with blocks of behavioural, environmental and occupational, and metabolic risks at the first level of the hierarchy. The next level in the hierarchy includes nine clusters of related risks and two individual risks, with more detail provided at levels 3 and 4 of the hierarchy. Compared with GBD 2010, six new risk factors have been added: handwashing practices, occupational exposure to trichloroethylene, childhood wasting, childhood stunting, unsafe sex, and low glomerular filtration rate. For most risks, data for exposure were synthesised with a Bayesian meta-regression method, DisMod-MR 2.0, or spatial-temporal Gaussian process regression. Relative risks were based on meta-regressions of published cohort and intervention studies. Attributable burden for clusters of risks and all risks combined took into account evidence on the mediation of some risks such as high body-mass index (BMI) through other risks such as high systolic blood pressure and high cholesterol.
    Findings: All risks combined account for 57·2% (95% uncertainty interval [UI] 55·8-58·5) of deaths and 41·6% (40·1-43·0) of DALYs. Risks quantified account for 87·9% (86·5-89·3) of cardiovascular disease DALYs, ranging to a low of 0% for neonatal disorders and neglected tropical diseases and malaria. In terms of global DALYs in 2013, six risks or clusters of risks each caused more than 5% of DALYs: dietary risks accounting for 11·3 million deaths and 241·4 million DALYs, high systolic blood pressure for 10·4 million deaths and 208·1 million DALYs, child and maternal malnutrition for 1·7 million deaths and 176·9 million DALYs, tobacco smoke for 6·1 million deaths and 143·5 million DALYs, air pollution for 5·5 million deaths and 141·5 million DALYs, and high BMI for 4·4 million deaths and 134·0 million DALYs. Risk factor patterns vary across regions and countries and with time. In sub-Saharan Africa, the leading risk factors are child and maternal malnutrition, unsafe sex, and unsafe water, sanitation, and handwashing. In women, in nearly all countries in the Americas, north Africa, and the Middle East, and in many other high-income countries, high BMI is the leading risk factor, with high systolic blood pressure as the leading risk in most of Central and Eastern Europe and south and east Asia. For men, high systolic blood pressure or tobacco use are the leading risks in nearly all high-income countries, in north Africa and the Middle East, Europe, and Asia. For men and women, unsafe sex is the leading risk in a corridor from Kenya to South Africa.
    Interpretation: Behavioural, environmental and occupational, and metabolic risks can explain half of global mortality and more than one-third of global DALYs providing many opportunities for prevention. Of the larger risks, the attributable burden of high BMI has increased in the past 23 years. In view of the prominence of behavioural risk factors, behavioural and social science research on interventions for these risks should be strengthened. Many prevention and primary care policy options are available now to act on key risks.
    Funding: Bill & Melinda Gates Foundation.
    MeSH term(s) Environmental Exposure/adverse effects ; Female ; Global Health/statistics & numerical data ; Global Health/trends ; Health Behavior ; Humans ; Male ; Metabolic Diseases/epidemiology ; Nutritional Status ; Occupational Diseases/epidemiology ; Occupational Exposure/adverse effects ; Risk Assessment/methods ; Risk Factors ; Sanitation/trends
    Language English
    Publishing date 2015-09-11
    Publishing country England
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(15)00128-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top