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Coexpression of type 2 immune targets in sputum-derived epithelial and dendritic cells from asthmatic patients

Bleck, Bertram; Kazeros, Angeliki; Bakal, Keren; Garcia-Medina, Lymaris; Adams, Alexandra; Liu, Mengling; Lee, Richard A; Tse, Doris B; Chiu, Amanda; Grunig, Gabriele; Egan, John P 3rd; Reibman, Joan
BACKGROUND: Noninvasive sputum sampling has enabled the identification of biomarkers in asthmatic patients. Studies of discrete cell populations in sputum can enhance measurements compared with whole sputum in which changes in rare cells and cell-cell interactions can be masked. OBJECTIVE: We sought to enrich for sputum-derived human bronchial epithelial cells (sHBECs) and sputum-derived myeloid type 1 dendritic cells (sDCs) to describe transcriptional coexpression of targets associated with a type 2 immune response. METHODS: A case-control study was conducted with patients with mild asthma (asthmatic cases) and healthy control subjects. Induced sputum was obtained for simultaneous enrichment of sHBECs and sDCs by using flow cytometry. Quantitative PCR was used to measure mRNA for sHBEC thymic stromal lymphopoietin (TSLP), IL33, POSTN, and IL25 and downstream targets in sDCs (OX40 ligand [OX40L], CCL17, PPP1R14A, CD1E, CD1b, CD80, and CD86). RESULTS: Final analyses for the study sample were based on 11 control subjects and 13 asthmatic cases. Expression of TSLP, IL33, and POSTN mRNA was increased in sHBECs in asthmatic cases (P = .001, P = .05, and P = .04, respectively). Expression of sDC OX40L and CCL17 mRNA was increased in asthmatic cases (P = .003 and P = .0001, respectively). sHBEC TSLP mRNA expression was strongly associated with sDC OX40L mRNA expression (R = 0.65, P = .001) and less strongly with sDC CCL17 mRNA expression. sHBEC IL33 mRNA expression was associated with sDC OX40L mRNA expression (R = 0.42, P = .04) but not sDC CCL17 mRNA expression. CONCLUSIONS: Noninvasive sampling and enrichment of select cell populations from sputum can further our understanding of cell-cell interactions in asthmatic patients with the potential to enhance endotyping of asthmatic patients.
PMID: 25813919
ISSN: 1097-6825
CID: 1518952

Association between Arsenic Exposure from Drinking Water and Longitudinal Change in Blood Pressure among HEALS Cohort Participants

Jiang, Jieying; Liu, Mengling; Parvez, Faruque; Wang, Binhuan; Wu, Fen; Eunus, Mahbub; Bangalore, Sripal; Newman, Jonathan D; Ahmed, Alauddin; Islam, Tariqul; Rakibuz-Zaman, Muhammad; Hasan, Rabiul; Sarwar, Golam; Levy, Diane; Slavkovich, Vesna; Argos, Maria; Scannell Bryan, Molly; Farzan, Shohreh F; Hayes, Richard B; Graziano, Joseph H; Ahsan, Habibul; Chen, Yu
BACKGROUND: Cross-sectional studies have shown associations between arsenic exposure and prevalence of high BP; however, studies examining the relationship of arsenic exposure with longitudinal changes in blood pressure are lacking. METHOD: We evaluated associations of arsenic exposure in relation to longitudinal change in blood pressure in 10,853 participants in the Health Effects of Arsenic Longitudinal Study (HEALS). Arsenic was measured in well water and in urine samples at baseline and in urine samples every two years after baseline. Mixed effect models were used to estimate the association of baseline well and urinary creatinine-adjusted arsenic with blood pressure annual change during follow-up (median, 6.7 years). RESULT: In the HEALS population, the median water arsenic concentration at baseline was 62 microg/L. Individuals in the highest quartile of baseline water arsenic or urinary creatinine-adjusted arsenic had a greater annual increase in SBP compared with those in the reference group (beta=0.48 mmHg/year; 95% CI: 0.35-0.61, and beta=0.43 mmHg/year; 95% CI: 0.29-0.56) for water arsenic and urinary creatinine-adjusted arsenic, respectively) in fully adjusted models. Likewise, individuals in the highest quartile of baseline arsenic exposure had a greater annual increase in DBP (beta=0.39 mmHg/year; 95% CI: 0.30, 0.49, and beta=0.45 mmHg/year; 95% CI: 0.36, 0.55) for water arsenic and urinary creatinine-adjusted arsenic, respectively) compared with those in the lowest quartile. CONCLUSION: Our findings suggest that long-term arsenic exposure may accelerate age-related increases in blood pressure. These findings may help explain associations between arsenic exposure and cardiovascular disease.
PMCID:4529016
PMID: 25816368
ISSN: 1552-9924
CID: 1519062

Detection and Treatment of Mental Health Issues by Pediatric PCPs in New York State: An Evaluation of Project TEACH

Kerker, Bonnie D; Chor, Ka Ho Brian; Hoagwood, Kimberly E; Radigan, Marleen; Perkins, Matthew B; Setias, Jade; Wang, Rui; Olin, S Serene; Horwitz, Sarah M
OBJECTIVE: The authors evaluated Project TEACH (PT), a statewide training and consultation program for pediatric primary care providers (PCPs) on identification and treatment of mental health conditions. METHODS: An intervention group of 176 PCPs who volunteered for PT training was compared with a stratified random sample of 200 PCPs who did not receive PT training. Data on prescription practices, diagnoses, and follow-up care were from New York State Medicaid files (2009-2013) for youths seen by the trained (N=21,784) and untrained (N=46,607) PCPs. RESULTS: The percentage of children prescribed psychotropic medication increased after PT training (9% to 12%, p<.001), a larger increase than in the untrained group (4% to 5%, p<.001) (comparison, p<.001). Fewer differences were noted in diagnoses and in medication use and follow-up care among children with depression. CONCLUSIONS: This intervention may have an impact on providers' behaviors, but further research is needed to clarify its effectiveness.
PMCID:4384126
PMID: 25828984
ISSN: 1557-9700
CID: 1519382

Extended-release naltrexone to prevent relapse among opioid dependent, criminal justice system involved adults: Rationale and design of a randomized controlled effectiveness trial

Lee, Joshua D; Friedmann, Peter D; Boney, Tamara Y; Hoskinson, Randall A Jr; McDonald, Ryan; Gordon, Michael; Fishman, Marc; Chen, Donna T; Bonnie, Richard J; Kinlock, Timothy W; Nunes, Edward V; Cornish, James W; O'Brien, Charles P
BACKGROUND: Extended-release naltrexone (XR-NTX, Vivitrol(R); Alkermes Inc.) is an injectable monthly sustained-release mu opioid receptor antagonist. XR-NTX is a potentially effective intervention for opioid use disorders and as relapse prevention among criminal justice system (CJS) populations. METHODS: This 5-site open-label randomized controlled effectiveness trial examines whether XR-NTX reduces opioid relapse compared with treatment as usual (TAU) among community dwelling, non-incarcerated volunteers with current or recent CJS involvement. The XR-NTX arm receives 6 monthly XR-NTX injections at Medical Management visits; the TAU group receives referrals to available community treatment options. Assessments occur every 2weeks during a 24-week treatment phase and at 12- and 18-month follow-ups. The primary outcome is a relapse event, defined as either self-report or urine toxicology evidence of >/=10days of opioid use in a 28-day (4week) period, with a positive or missing urine test counted as 5days of opioid use. RESULTS: We describe the rationale, specific aims, and design of the study. Alternative design considerations and extensive secondary aims and outcomes are discussed. CONCLUSIONS: XR-NTX is a potentially important treatment and relapse prevention option among persons with opioid dependence and CJS involvement. ClinicalTrials.gov: NCT00781898.
PMCID:4380547
PMID: 25602580
ISSN: 1559-2030
CID: 1520542

Comparison of parent and child versus child-only weight management interventions in the patient-centered medical home

Berner, Natalie; Jay, Melanie
ORIGINAL:0009635
ISSN: 1079-6533
CID: 1516482

Obesogenic behaviors among adolescents: the role of generation and time in the United States

Almeida, Joanna; Duncan, Dustin T; Sonneville, Kendrin R
OBJECTIVES: To examine how obesogenic behaviors (consumption of sugary drinks, physical activity, and/or sedentary behaviors) differ among adolescents within and across generation. DESIGN: Data come from the 2008 Boston Youth Survey, a population-based sample of 9th-12th-graders in 22 public high schools in Boston, MA. We used self-reported information to calculate generation and obesogenic behaviors (i.e. physical activity in past 7 days, consumption of sugar-sweetened beverages in past 7 days, and TV/computer/video game use on an average school day). Multivariable models were conducted to estimate the association between generation and obesogenic behaviors, adjusting for race/ethnicity, sex, age, family structure, and school. RESULTS: Relative to first generation youth, 1.5 generation (RR=1.74, 95% CI=1.10, 2.77) and second generation (RR=1.45, 95% CI=1.02, 2.07) youth were more likely to consume soda. Second (RR=1.60, 95% CI=1.20, 2.14) and third generation (RR=2.29, 95% CI=1.43, 3.65) youth were significantly more likely to consume other sugary drinks. Only third generation youth were more likely to watch >/=2 hours/day of TV when compared to first generation youth (RR=1.53, 95% CI=1.07, 2.18). No differences were seen by generation for levels of moderate-to-vigorous physical activity or computer/video games. CONCLUSIONS: Greater consumption of sugary drinks is seen across generation among adolescents. Sugary drinks, which are aggressively marketed to immigrant youth, may contribute to excess weight gain seen among foreign-born youth upon arrival in the United States.
PMID: 25812253
ISSN: 1049-510x
CID: 1515122

Validation of the substance use brief screen in primary care [Meeting Abstract]

McNeely, J; Strauss, S; Halkitis, P N; Saitz, R; Rotrosen, J; Shelley, D; Cleland, C; Gourevitch, M N
Aims: Implementation of substance use screening in general medical settings is hindered by the lack of a brief yet precise and comprehensive screening tool that is compatible with clinical workflows. To address this need, we developed the Substance Use Brief Screen (SUBS); a 4-item screener for tobacco, alcohol, and drug use (illicit and prescription) that is self-administered and may be easily integrated with electronic health records. Methods: Adult patients were recruited consecutively in the waiting area of an urban safety net primary care clinic. The SUBS was self-administered in English on touchscreen tablet computers. Reference standard measures of unhealthy substance use and substance use disorders were then administered, including self reported measures and saliva drug tests. The SUBS was compared against the reference standards to determine its sensitivity, specificity, and area under the curve (AUC) for each substance class. Results: Among the 390 participants, rates of past year use reported on the SUBS were 37% tobacco, 43% alcohol (4+ drinks/day), 20% illicit drugs, and 12% prescription drugs. Sensitivity and specificity of the SUBS for detecting past year unhealthy use were: tobacco 99% and 91% (AUC = .95); alcohol 94% and 68% (AUC = .81); drugs (illicit or prescription) 84% and 89% (AUC = .86). Sensitivity was lower for prescription drugs (57%) than for illicit drugs (78%). For detecting a substance use disorder, sensitivity and specificity were: tobacco 100% and 73% (AUC = .87); alcohol 93% and 64% (AUC = .79); drugs 85% and 82% (AUC = .84). Conclusions: The SUBS accurately identified unhealthy tobacco, alcohol, and drug use in this primary care sample, and had high sensitivity but lower specificity for identifying substance use disorders. Individuals screening positive on the SUBS should receive further assessment. Our findings support use of the SUBS for substance use screening in primary care, but additional tools may be needed for prescription drugs
EMBASE:71802006
ISSN: 0376-8716
CID: 1514442

Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013

Wang, H; Lozano, R; Davis, A; Liang, X; Zhou, M; Vollset, SE; Ozgoren, AA; Abdalla, S; Abd-Allah, F; Aziz, MIA; Abera, SF; Aboyans, V; Abraham, B; Abraham, JP; Abuabara, KE; Abubakar, I; Abu-Raddad, LJ; Abu-Rmeileh, NME; Achoki, T; Adelekan, A; Ademi, Z; Adofo, K; Adou, AK; Adsuar, JC; Arnlov, J; Agardh, EE; Akena, D; Al Khabouri, MJ; Alasfoor, D; Albittar, M; Alegretti, MA; Aleman, AV; Alemu, ZA; Alfonso-Cristancho, R; Alhabib, S; Ali, MK; Ali, R; Alla, F; Al Lami, F; Allebeck, P; AlMazroa, MA; Al-Shahi, Salman, R; Alsharif, U; Alvarez, E; Alviz-Guzman, N; Amankwaa, AA; Amare, AT; Ameli, O; Amini, H; Ammar, W; Anderson, HR; Anderson, BO; Antonio, CAT; Anwari, P; Apfel, H; Cunningham, SA; Arsenijevic, VSA; Artaman, A; Asad, MM; Asghar, RJ; Assadi, R; Atkins, LS; Atkinson, C; Badawi, A; Bahit, MC; Bakfalouni, T; Balakrishnan, K; Balalla, S; Banerjee, A; Barber, RM; Barker-Collo, SL; Barquera, S; Barregard, L; Barrero, LH; Barrientos-Gutierrez, T; Basu, A; Basu, S; Basulaiman, MO; Beardsley, J; Bedi, N; Beghi, E; Bekele, T; Bell, ML; Benjet, C; Bennett, DA; Bensenor, IM; Benzian, H; Bertozzi-Villa, A; Beyene, TJ; Bhala, N; Bhalla, A; Bhutta, ZA; Bikbov, B; Abdulhak, AB; Biryukov, S; Blore, JD; Blyth, FM; Bohensky, MA; Borges, G; Bose, D; Boufous, S; Bourne, RR; Boyers, LN; Brainin, M; Brauer, M; Brayne, CEG; Brazinova, A; Breitborde, N; Brenner, H; Briggs, ADM; Brown, JC; Brugha, TS; Buckle, GC; Bui, LN; Bukhman, G; Burch, M; Campos Nonato, IR; Carabin, H; Cardenas, R; Carapetis, J; Carpenter, DO; Caso, V; Castanda-Orjuela, CA; Castro, RE; Catala-Lopez, F; Cavalleri, F; Chang, J-C; Charlson, FC; Che, X; Chen, H; Chen, Y; Chen, JS; Chen, Z; Chiang, PP-C; Chimed-Ochir, O; Chowdhury, R; Christensen, H; Christophi, CA; Chuang, T-W; Chugh, SS; Cirillo, M; Coates, MM; Coffeng, LE; Coggeshall, MS; Cohen, A; Colistro, V; Colquhoun, SM; Colomar, M; Cooper, LT; Cooper, C; Coppola, LM; Cortinovis, M; Courville, K; Cowie, BC; Criqui, MH; Crump, JA; Cuevas-Nasu, L; Da, Costa, Leite, I; Dabhadkar, KC; Dandona, L; Dandona, R; Dansereau, E; Dargan, PI; Dayama, A; De la Cruz-Gongora, V; De La Vega, SF; De Leo, D; Degenhardt, L; Del Pozo-Cruz, B; Dellavalle, RP; Deribe, K; Des, Jarlais, DC; Dessalegn, M; DeVeber, GA; Dharmaratne, SD; Dherani, M; Diaz-Ortega, J-L; Diaz-Torne, C; Dicker, D; Ding, EL; Dokova, K; Dorsey, ER; Driscoll, TR; Duan, L; Duber, HC; Durrani, AM; Ebel, BE; Edmond, KM; Ellenbogen, RG; Elshrek, Y; Ermakov, SP; Erskine, HE; Eshrati, B; Esteghamati, A; Estep, K; Furst, T; Fahimi, S; Fahrion, AS; Faraon, EJA; Farzadfar, F; Fay, DFJ; Feigl, AB; Feigin, VL; Felicio, MM; Fereshtehnejad, S-M; Fernandes, JG; Ferrari, AJ; Fleming, TD; Foigt, N; Foreman, K; Forouzanfar, MH; Fowkes, FGR; Paleo, UF; Franklin, RC; Futran, ND; Gaffikin, L; Gambashidze, K; Gankpe, FG; Garc-Guerra, FA; Garcia, AC; Geleijnse, JM; Gessner, BD; Gibney, KB; Gillum, RF; Gilmour, S; Ginawi, IAM; Giroud, M; Glaser, EL; Goenka, S; Dantes, HG; Gona, P; Gonzalez-Medina, D; Guinovart, C; Gupta, R; Gosselin, RA; Gotay, CC; Goto, A; Gouda, HN; Graetz, N; Greenwell, KF; Gugnani, HC; Gunnell, D; Gutiierez, RA; Haagsma, J; Hafezi-Nejad, N; Hagan, H; Hagstromer, M; Halasa, YA; Hamadeh, RR; Hamavid, H; Hammami, M; Hancock, J; Hankey, GJ; Hansen, GM; Harb, HL; Harewood, H; Haro, JM; Havmoeller, R; Hay, RJ; Hay, SI; Hedayati, MT; Pi, IBH; Heuton, KR; Heydarpour, P; Higashi, H; Hijar, M; Hoek, HW; Hoffman, HJ; Hornberger, JC; Hosgood, HD; Hossain, M; Hotez, PJ; Hoy, DG; Hsairi, M; Hu, G; Huang, JJ; Huffman, MD; Hughes, AJ; Husseini, A; Huynh, C; Iannarone, M; Iburg, KM; Idrisov, BT; Ikeda, N; Innos, K; Inoue, M; Islami, F; Ismayilova, S; Jacobsen, KH; Jassal, S; Jayaraman, SP; Jensen, PN; Jha, V; Jiang, G; Jiang, Y; Jonas, JB; Joseph, J; Juel, K; Kabagambe, EK; Kan, H; Karch, A; Karimkhani, C; Karthikeyan, G; Kassebaum, N; Kaul, A; Kawakami, N; Kazanjan, K; Kazi, DS; Kemp, AH; Kengne, AP; Keren, A; Kereselidze, M; Khader, YS; Ali Hassan Khalifa, SE; Khan, EA; Khan, G; Khang, Y-H; Kieling, C; Kinfu, Y; Kinge, JM; Kim, D; Kim, S; Kivipelto, M; Knibbs, L; Knudsen, AK; Kokubo, Y; Kosen, S; Kotagal, M; Kravchenko, MA; Krishnaswami, S; Krueger, H; Defo, BK; Kuipers, EJ; Kucuk, Bicer, B; Kulkarni, C; Kulkarni, VS; Kumar, K; Kumar, RB; Kwan, GF; Kyu, H; Lai, T; Balaji, AL; Lalloo, R; Lallukka, T; Lam, H; Lan, Q; Lansingh, VC; Larson, HJ; Larsson, A; Lavados, PM; Lawrynowicz, AEB; Leasher, JL; Lee, J-T; Leigh, J; Leinsalu, M; Leung, R; Levitz, C; Li, B; Li, Y; Liddell, C; Lim, SS; De Lima, GMF; Lind, ML; Lipshultz, SE; Liu, S; Liu, Y; Lloyd, BK; Lofgren, KT; Logroscino, G; London, SJ; Lortet-Tieulent, J; Lotufo, PA; Lucas, RM; Lunevicius, R; Lyons, RA; Ma, S; Pedro, Machado, VM; MacIntyre, MF; Mackay, MT; MacLachlan, JH; Magis-Rodriguez, C; Mahdi, AA; Majdan, M; Malekzadeh, R; Mangalam, S; Mapoma, CC; Marape, M; Marcenes, W; Margono, C; Marks, GB; Marzan, MB; Masci, JR; Mashal, MT; Masiye, F; Mason-Jones, AJ; Matzopolous, R; Mayosi, BM; Mazorodze, TT; McGrath, JJ; McKay, AC; McKee, M; McLain, A; Meaney, PA; Mehndiratta, MM; Mejia-Rodriguez, F; Melaku, YA; Meltzer, M; Memish, ZA; Mendoza, W; Mensah, GA; Meretoja, A; Mhimbira, FA; Miller, TR; Mills, EJ; Misganaw, A; Mishra, SK; Mock, CN; Moffitt, TE; Ibrahim, NM; Mohammad, KA; Mokdad, AH; Mola, GL; Monasta, L; De La Cruz, Monis, J; Hernandez, JCM; Montico, M; Montine, TJ; Mooney, MD; Moore, AR; Moradi-Lakeh, M; Moran, AE; Mori, R; Moschandreas, J; Moturi, WN; Moyer, ML; Mozaffarian, D; Mueller, UO; Mukaigawara, M; Mullany, EC; Murray, J; Mustapha, A; Naghavi, P; Naheed, A; Naidoo, KS; Naldi, L; Nand, D; Nangia, V; Narayan, KMV; Nash, D; Nasher, J; Nejjari, C; Nelson, RG; Neuhouser, M; Neupane, SP; Newcomb, PA; Newman, L; Newton, CR; Ng, M; Ngalesoni, FN; Nguyen, G; Nguyen, NTT; Nisar, MI; Nolte, S; Norheim, OF; Norman, RE; Norrving, B; Nyakarahuka, L; Odell, S; O'Donnell, M; Ohkubo, T; Ohno, SL; Olusanya, BO; Omer, SB; Opio, JN; Orisakwe, OE; Ortblad, KF; Ortiz, A; Otayza, MLK; Pain, AW; Pandian, JD; Panelo, CI; Panniyammakal, J; Papachristou, C; Paternina, Caicedo, AJ; Patten, SB; Patton, GC; Paul, VK; Pavlin, B; Pearce, N; Pellegrini, CA; Pereira, DM; Peresson, SC; Perez-Padilla, R; Perez-Ruiz, FP; Perico, N; Pervaiz, A; Pesudovs, K; Peterson, CB; Petzold, M; Phillips, BK; Phillips, DE; Phillips, MR; Plass, D; Piel, FB; Poenaru, D; Polinder, S; Popova, S; Poulton, RG; Pourmalek, F; Prabhakaran, D; Qato, D; Quezada, AD; Quistberg, DA; Rabito, F; Rafay, A; Rahimi, K; Rahimi-Movaghar, V; Rahman, SUR; Raju, M; Rakovac, I; Rana, SM; Refaat, A; Remuzzi, G; Ribeiro, AL; Ricci, S; Riccio, PM; Richardson, L; Richardus, JH; Roberts, B; Roberts, DA; Robinson, M; Roca, A; Rodriguez, A; Rojas-Rueda, D; Ronfani, L; Room, R; Roth, GA; Rothenbacher, D; Rothstein, DH; Rowley, JTF; Roy, N; Ruhago, GM; Rushton, L; Sambandam, S; Soreide, K; Saeedi, MY; Saha, S; Sahathevan, R; Sahraian, MA; Sahle, BW; Salomon, JA; Salvo, D; Samonte, GMJ; Sampson, U; Sanabria, JR; Sandar, L; Santos, IS; Satpathy, M; Sawhney, M; Saylan, M; Scarborough, P; Schottker, B; Schmidt, JC; Schneider, IJC; Schumacher, AE; Schwebel, DC; Scott, JG; Sepanlou, SG; Servan-Mori, EE; Shackelford, K; Shaheen, A; Shahraz, S; Shakh-Nazarova, M; Shangguan, S; She, J; Sheikhbahaei, S; Shepard, DS; Shibuya, K; Shinohara, Y; Shishani, K; Shiue, I; Shivakoti, R; Shrime, MG; Sigfusdottir, ID; Silberberg, DH; Silva, AP; Simard, EP; Sindi, S; Singh, JA; Singh, L; Sioson, E; Skirbekk, V; Sliwa, K; So, S; Soljak, M; Soneji, S; Soshnikov, SS; Sposato, LA; Sreeramareddy, CT; Stanaway, JD; Stathopoulou, VK; Steenland, K; Stein, C; Steiner, C; Stevens, A; Stockl, H; Straif, K; Stroumpoulis, K; Sturua, L; Sunguya, BF; Swaminathan, S; Swaroop, M; Sykes, BL; Tabb, KM; Takahashi, K; Talongwa, RT; Tan, F; Tanne, D; Tanner, M; Tavakkoli, M; Ao, BT; Teixeira, CM; Templin, T; Tenkorang, EY; Terkawi, AS; Thomas, BA; Thorne-Lyman, AL; Thrift, AG; Thurston, GD; Tillmann, T; Tirschwell, DL; Tleyjeh, IM; Tonelli, M; Topouzis, F; Towbin, JA; Toyoshima, H; Traebert, J; Tran, BX; Truelsen, T; Trujillo, U; Trillini, M; Dimbuene, ZT; Tsilimbaris, M; Tuzcu, EM; Ubeda, C; Uchendu, US; Ukwaja, KN; Undurraga, EA; Vallely, AJ; Van, De, Vijver, S; Van, Gool, CH; Varakin, YY; Vasankari, TJ; Vasconcelos, AMN; Vavilala, MS; Venketasubramanian, N; Vijayakumar, L; Villalpando, S; Violante, FS; Vlassov, VV; Wagner, GR; Waller, SG; Wang, J; Wang, L; Wang, X; Wang, Y; Warouw, TS; Weichenthal, S; Weiderpass, E; Weintraub, RG; Wenzhi, W; Werdecker, A; Wessells, KRR; Westerman, R; Whiteford, HA; Wilkinson, JD; Williams, TN; Woldeyohannes, SM; Wolfe, CDA; Wolock, TM; Woolf, AD; Wong, JQ; Wright, JL; Wulf, S; Wurtz, B; Xu, G; Yang, YC; Yano, Y; Yatsuya, H; Yip, P; Yonemoto, N; Yoon, S-J; Younis, M; Yu, C; Jin, KY; El Sayed, Zaki M; Zamakhshary, MF; Zeeb, H; Zhang, Y; Zhao, Y; Zheng, Y; Zhu, J; Zhu, S; Zonies, D; Zou, XN; Zunt, JR; Vos, T; Lopez, AD; Murray, CJL; Alcala-Cerra, G; Balala, S; Chang, C-C; Gosslin, RA; Hu, H; Karam, N; Sabin, N; Temesgen, AM
BACKGROUND: Up-to-date evidence on levels and trends for age-sex-specific all-cause and cause-specific mortality is essential for the formation of global, regional, and national health policies. In the Global Burden of Disease Study 2013 (GBD 2013) we estimated yearly deaths for 188 countries between 1990, and 2013. We used the results to assess whether there is epidemiological convergence across countries. METHODS: We estimated age-sex-specific all-cause mortality using the GBD 2010 methods with some refinements to improve accuracy applied to an updated database of vital registration, survey, and census data. We generally estimated cause of death as in the GBD 2010. Key improvements included the addition of more recent vital registration data for 72 countries, an updated verbal autopsy literature review, two new and detailed data systems for China, and more detail for Mexico, UK, Turkey, and Russia. We improved statistical models for garbage code redistribution. We used six different modelling strategies across the 240 causes; cause of death ensemble modelling (CODEm) was the dominant strategy for causes with sufficient information. Trends for Alzheimer's disease and other dementias were informed by meta-regression of prevalence studies. For pathogen-specific causes of diarrhoea and lower respiratory infections we used a counterfactual approach. We computed two measures of convergence (inequality) across countries: the average relative difference across all pairs of countries (Gini coefficient) and the average absolute difference across countries. To summarise broad findings, we used multiple decrement life-tables to decompose probabilities of death from birth to exact age 15 years, from exact age 15 years to exact age 50 years, and from exact age 50 years to exact age 75 years, and life expectancy at birth into major causes. For all quantities reported, we computed 95% uncertainty intervals (UIs). We constrained cause-specific fractions within each age-sex-country-year group to sum to all-cause mortality based on draws from the uncertainty distributions. FINDINGS: Global life expectancy for both sexes increased from 65.3 years (UI 65.0-65.6) in 1990, to 71.5 years (UI 71.0-71.9) in 2013, while the number of deaths increased from 47.5 million (UI 46.8-48.2) to 54.9 million (UI 53.6-56.3) over the same interval. Global progress masked variation by age and sex: for children, average absolute differences between countries decreased but relative differences increased. For women aged 25-39 years and older than 75 years and for men aged 20-49 years and 65 years and older, both absolute and relative differences increased. Decomposition of global and regional life expectancy showed the prominent role of reductions in age-standardised death rates for cardiovascular diseases and cancers in high-income regions, and reductions in child deaths from diarrhoea, lower respiratory infections, and neonatal causes in low-income regions. HIV/AIDS reduced life expectancy in southern sub-Saharan Africa. For most communicable causes of death both numbers of deaths and age-standardised death rates fell whereas for most non-communicable causes, demographic shifts have increased numbers of deaths but decreased age-standardised death rates. Global deaths from injury increased by 10.7%, from 4.3 million deaths in 1990 to 4.8 million in 2013; but age-standardised rates declined over the same period by 21%. For some causes of more than 100,000 deaths per year in 2013, age-standardised death rates increased between 1990 and 2013, including HIV/AIDS, pancreatic cancer, atrial fibrillation and flutter, drug use disorders, diabetes, chronic kidney disease, and sickle-cell anaemias. Diarrhoeal diseases, lower respiratory infections, neonatal causes, and malaria are still in the top five causes of death in children younger than 5 years. The most important pathogens are rotavirus for diarrhoea and pneumococcus for lower respiratory infections. Country-specific probabilities of death over three phases of life were substantially varied between and within regions. INTERPRETATION: For most countries, the general pattern of reductions in age-sex specific mortality has been associated with a progressive shift towards a larger share of the remaining deaths caused by non-communicable disease and injuries. Assessing epidemiological convergence across countries depends on whether an absolute or relative measure of inequality is used. Nevertheless, age-standardised death rates for seven substantial causes are increasing, suggesting the potential for reversals in some countries. Important gaps exist in the empirical data for cause of death estimates for some countries; for example, no national data for India are available for the past decade. FUNDING: Bill & Melinda Gates Foundation.
PMCID:4340604
PMID: 25530442
ISSN: 1474-547x
CID: 1514472

Scientific evidence supports stronger limits on ozone

Rice, Mary B; Guidotti, Tee L; Cromar, Kevin R
PMID: 25536009
ISSN: 1535-4970
CID: 1514622

Hepatitis C virus incidence among HIV+ men who have sex with men: The role of non-injection drug use [Meeting Abstract]

Hagan, H; Neurer, J; Jordan, A E; Des, Jarlais D C; Wu, J; Dombrowski, K; Khan, B; Braithwaite, S; Kessler, J
Aims: There has been a rise in hepatitis C virus (HCV) infection in HIV- positive (HIV+) men who have sex with men (MSM). HIV/HCV co-infection complicates management of HIV and HCV, and increases the risk of serious liver disease. The aim of this study was to carry out a systematic review and meta-analysis to characterize the epidemiology of sexually transmitted HCV infection in this population. Methods: The search encompassed EMBASE, PubMed and BIOSIS, plus proceedings of scientific conferences and footnote chasing. To be eligible, reports must be published or presented 1990-2013, and include data on HCV incidence or risk factors for infection in HIV +MSM who were not injecting drugs. Studies were assigned quality ratings based on the Newcastle-Ottawa Scale. Results: The search retrieved 687 abstracts after duplicates were removed. After screening, there were 12 eligible studies from Europe, Australia, North America and Asia including 10 cohort and 2 case-control studies. HCV seroconversion rates ranged between 0 and 1.18/100 person-years (PYs), median 0.39/100PYs (n = 67,426 PYs). Two studies reported that sex while high on methamphetamine (AOR 28.6) and rectal trauma or bleeding (AOR = 6.2) were significantly associated with HCV seroconversion. Few studies examined the role of non-injection drug use in HCV infection. Conclusions: Evidence points to blood as the medium of sexual HCV transmission in HIV +MSM, and the role of drug use appears to be via the facilitation of mucosally traumatic sexual practices. The shared use of implements to administer drugs intranasally has received little attention as a possible risk factor for HCV infection in this population
EMBASE:71802264
ISSN: 0376-8716
CID: 1514842