7 research outputs found

    Plantes alimentaires spontanées de la région du Fromager (Centre- Ouest de la CÎte d\'Ivoire) : flore, habitats et organes consommés.

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    Une enquĂȘte ethnobotanique, visant Ă  inventorier les plantes spontanĂ©es alimentaires encore prĂ©sentes dans la rĂ©gion du Fromager (Centre-Ouest) de la CĂŽte d\'Ivoire, a Ă©tĂ© menĂ©e auprĂšs des populations rurales. Les espĂšces recensĂ©es sont au nombre de 72, rĂ©parties entre 61 genres et 42 familles. Les familles les plus reprĂ©sentĂ©es sont les Sterculiaceae, les Arecaceae et les Solanaceae. L\'habitat de ces plantes spontanĂ©es a Ă©tĂ© dĂ©terminĂ©; il s\'agit des forĂȘts, des jachĂšres et des vergers de cacaoyers et de cafĂ©iers. Les organes les plus consommĂ©s sont les fruits (38 %), les feuilles (33 %) et les graines (19 %). Ces enquĂȘtes ont montrĂ© qu\'il existe encore un nombre Ă©levĂ© d\'espĂšces spontanĂ©es alimentaires dans la RĂ©gion du Fromager.A ethnobotanic survey, aimed at the inventory of the food spontaneous plants present in the “fromager” region (Western Center) of CĂŽte d\'Ivoire, was carried out with the collaboration of the rural populations. The number of species inventoried is 72, belonging to 61 generas and 42 families. The most represented families are Sterculiaceae, Arecaceae and Solanaceae. The habitats of these spontaneous plants species were forests, fallows and the cocoa and coffee plantations. The most consumed organs were fruits (38 %), leaves (33 %) and seeds (19 %). These investigations showed a high number of food spontaneous species in the “fromager” region. Keywords: Spontaneous food plants, habitats, consumed organs, CĂŽte d\'IvoireSciences & Nature Vol. 5 (1) 2008: pp. 61-7

    Test d’efficacitĂ© d’un herbicide en culture d’ananas, Ă  la station d’expĂ©rimentation et de production d’AnguĂ©dĂ©dou en CĂŽte d’Ivoire

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    Objectif : Un produit Ă  base de glyphosate (Dominator 360) est testĂ© en vue d’évaluer son efficacitĂ© sur les adventices des cultures d’ananas. Ceci pour Ă©largir la gamme des produits dans cette culture et de minimiser les coĂ»ts de traitement en jouant sur les doses tout en veillant Ă  leur efficacitĂ©.MĂ©thodologie et rĂ©sultats : Le Dominator 360 est comparĂ© Ă  des herbicides de rĂ©fĂ©rence en usage sur la culture d’ananas dans la station expĂ©rimentale d’AnguĂ©dĂ©dou. Ces herbicides sont le Kalach, Ă©galement Ă  base de glyphosate et le Special 30 Ă  base de diuron + bromacile. L’essai a Ă©tĂ© conduit suivant un bloc de Fisher randomisĂ©, dont le dispositif est celui des tĂ©moins adjacents. Le Dominator 360 est expĂ©rimentĂ© Ă  trois doses : 2, 3 et 4 l/ha et les deux tĂ©moins Ă  une seule dose : 4 l/ha pour le Kalach et 4 kg/ha pour le Special 30.Les efficacitĂ©s observĂ©es sont diffĂ©rentes selon les doses utilisĂ©es. Le Dominator, les tĂ©moins Kalach et le SpĂ©cial 30 se sont montrĂ©s efficaces pratiquement au mĂȘme titre aux doses maximales utilisĂ©es (4 l/ha et 4 kg/ha). La dose de 3 l/ha du Dominator est apparue la plus faible dose expĂ©rimentĂ©e qui prĂ©sente une bonne efficacitĂ©.Conclusion et application : La dose de 3 l/ha du Dominator 360 constitue la faible dose du produit, comparĂ©e aux deux tĂ©moins utilisĂ©s dans cette Ă©tude, qui prĂ©sente une bonne efficacitĂ© dans la lutte contre les adventices en cultures d’ananas. Ceci en rapport avec la baisse des doses efficaces, recommandĂ©es, pour minimiser les coĂ»ts d’achat des herbicides. Cette dose de 3 l/ha du Dominator 360 est ainsi la dose par excellence Ă  vulgariser.Mots clefs : Herbicide, glyphosate, Dominator, efficacitĂ©, anana

    A Trial of Early Antiretrovirals and Isoniazid Preventive Therapy in Africa

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    BACKGROUND: In sub-Saharan Africa, the burden of human immunodeficiency virus (HIV)-associated tuberculosis is high. We conducted a trial with a 2-by-2 factorial design to assess the benefits of early antiretroviral therapy (ART), 6-month isoniazid preventive therapy (IPT), or both among HIV-infected adults with high CD4+ cell counts in Ivory Coast. METHODS: We included participants who had HIV type 1 infection and a CD4+ count of less than 800 cells per cubic millimeter and who met no criteria for starting ART according to World Health Organization (WHO) guidelines. Participants were randomly assigned to one of four treatment groups: deferred ART (ART initiation according to WHO criteria), deferred ART plus IPT, early ART (immediate ART initiation), or early ART plus IPT. The primary end point was a composite of diseases included in the case definition of the acquired immunodeficiency syndrome (AIDS), non-AIDS-defining cancer, non-AIDS-defining invasive bacterial disease, or death from any cause at 30 months. We used Cox proportional models to compare outcomes between the deferred-ART and early-ART strategies and between the IPT and no-IPT strategies. RESULTS: A total of 2056 patients (41% with a baseline CD4+ count of ≄500 cells per cubic millimeter) were followed for 4757 patient-years. A total of 204 primary end-point events were observed (3.8 events per 100 person-years; 95% confidence interval [CI], 3.3 to 4.4), including 68 in patients with a baseline CD4+ count of at least 500 cells per cubic millimeter (3.2 events per 100 person-years; 95% CI, 2.4 to 4.0). Tuberculosis and invasive bacterial diseases accounted for 42% and 27% of primary end-point events, respectively. The risk of death or severe HIV-related illness was lower with early ART than with deferred ART (adjusted hazard ratio, 0.56; 95% CI, 0.41 to 0.76; adjusted hazard ratio among patients with a baseline CD4+ count of ≄500 cells per cubic millimeter, 0.56; 95% CI, 0.33 to 0.94) and lower with IPT than with no IPT (adjusted hazard ratio, 0.65; 95% CI, 0.48 to 0.88; adjusted hazard ratio among patients with a baseline CD4+ count of ≄500 cells per cubic millimeter, 0.61; 95% CI, 0.36 to 1.01). The 30-month probability of grade 3 or 4 adverse events did not differ significantly among the strategies. CONCLUSIONS: In this African country, immediate ART and 6 months of IPT independently led to lower rates of severe illness than did deferred ART and no IPT, both overall and among patients with CD4+ counts of at least 500 cells per cubic millimeter. (Funded by the French National Agency for Research on AIDS and Viral Hepatitis; TEMPRANO ANRS 12136 ClinicalTrials.gov number, NCT00495651.)

    Effect of isoniazid preventive therapy on risk of death in west African, HIV-infected adults with high CD4 cell counts: long-term follow-up of the Temprano ANRS 12136 trial.

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    BACKGROUND: Temprano ANRS 12136 was a factorial 2 × 2 trial that assessed the benefits of early antiretroviral therapy (ART; ie, in patients who had not reached the CD4 cell count threshold used to recommend starting ART, as per the WHO guidelines that were the standard during the study period) and 6-month isoniazid preventive therapy (IPT) in HIV-infected adults in CĂŽte d'Ivoire. Early ART and IPT were shown to independently reduce the risk of severe morbidity at 30 months. Here, we present the efficacy of IPT in reducing mortality from the long-term follow-up of Temprano. METHODS: For Temprano, participants were randomly assigned to four groups (deferred ART, deferred ART plus IPT, early ART, or early ART plus IPT). Participants who completed the trial follow-up were invited to participate in a post-trial phase. The primary post-trial phase endpoint was death, as analysed by the intention-to-treat principle. We used Cox proportional models to compare all-cause mortality between the IPT and no IPT strategies from inclusion in Temprano to the end of the follow-up period. FINDINGS: Between March 18, 2008, and Jan 5, 2015, 2056 patients (mean baseline CD4 count 477 cells per ÎŒL) were followed up for 9404 patient-years (Temprano 4757; post-trial phase 4647). The median follow-up time was 4·9 years (IQR 3·3-5·8). 86 deaths were recorded (Temprano 47 deaths; post-trial phase 39 deaths), of which 34 were in patients randomly assigned IPT (6-year probability 4·1%, 95% CI 2·9-5·7) and 52 were in those randomly assigned no IPT (6·9%, 5·1-9·2). The hazard ratio of death in patients who had IPT compared with those who did not have IPT was 0·63 (95% CI, 0·41 to 0·97) after adjusting for the ART strategy (early vs deferred), and 0·61 (0·39-0·94) after adjustment for the ART strategy, baseline CD4 cell count, and other key characteristics. There was no evidence for statistical interaction between IPT and ART (pinteraction=0·77) or between IPT and time (pinteraction=0·94) on mortality. INTERPRETATION: In CĂŽte d'Ivoire, where the incidence of tuberculosis was last reported as 159 per 100 000 people, 6 months of IPT has a durable protective effect in reducing mortality in HIV-infected people, even in people with high CD4 cell counts and who have started ART. FUNDING: National Research Agency on AIDS and Viral Hepatitis (ANRS)

    Naturally occurring chalcones and their biological activities

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