is known about how changes in initial E-2 during the course of care might signal increasing patient acuity or risk of death. We hypothesized that changes from baseline serum E-2 during the course of critical illness are more strongly associated with mortality than a single E-2 level at admission.\n\nSTUDY DESIGN: A prospective cohort of 1,408 critically ill or injured nonpregnant adult patients requiring ICU care for >= 48 hours with admission and subsequent E-2 levels was studied. Demographics, illness severity, and E-2 levels were examined, and the probability of mortality was modeled with multivariate logistic regression. Changes in E-2 were examined by both analysis of variance and logistic regression.\n\nRESULTS: Overall mortality was find more 14.1% [95% 3-deazaneplanocin A solubility dmso confidence interval (CI) 12.3% to 16%]. Both admission and subsequent E-2 levels were independently associated with mortality [admission E-2 odds ratio 1.1
(CI 1.0 to 1.2); repeat estradiol odds ratio 1.3 (CI 1.2 to 1.4)], with subsequent values being stronger. Changes in E-2 were independently associated with mortality [odds ratio 1.1 (CI 1.0 to 1.16)] and improved regression model performance. The regression model produced an area under the receiver operating characteristic curve of 0.80 (CI 0.77 to 0.83).\n\nCONCLUSIONS: Although high admission levels of E-2 are associated with mortality, changes from baseline E-2 in critically ill or injured adults are independently associated with mortality. Future studies of E-2 dynamics may yield new indicators of patient acuity and illuminate underlying mechanisms for targeted therapy. (J Am Coll Surg 2011;212:703-713. (C) 2011 by the American College of Surgeons)”
“In 1999, Golub et al. proposed for the first time microarray-based transcriptional profiling to be used as a new technology for the differential
diagnosis of acute myeloid leukemias and acute lymphocytic leukemias. This very preliminary study sparked great enthusiasm beyond the leukemias. Over the last 10 years, numerous studies addressed the use of gene expression profiling of peripheral JNK-IN-8 ic50 blood from patients with malignancies, infectious diseases, autoimmunity and even cardiovascular diseases. Despite this great effort, no single test has yet been established using microarray-based transcriptional profiling of peripheral blood. Here we highlight the advances in the field of blood transcriptomics during the last 10 years and also critically discuss the issues that need to be resolved before blood transcriptomics will become part of daily diagnostics in the leukemias, as well as in other diseases showing involvement of peripheral blood.”
“Phylogenetic hypotheses of species of Leptodactylus have been proposed but relationships often consider few species and high-level groups are supported by few, homoplasious morphological characters.
The toxicity of these ketone toxins have not been fully characterized nor are the pathogenesis and sequelae of poisoning completely understood. The objective of the current study was to characterize and describe the clinical and pathologic changes of rayless
goldenrod toxicity in goats. Fifteen goats were gavaged with rayless goldenrod to obtain benzofuran ketone doses of 0, 10, 20, 40, and 60 mg/kg/day. After 7 treatment days, check details the goats were euthanized, necropsied, and tissues were processed for microscopic studies. After 5 or 6 days of treatment, the 40-mg/kg and 60-mg/kg goats were reluctant to move, stood with an erect stance, and became exercise intolerant. They had increased resting heart rate, prolonged recovery following exercise, and increased serum aspartate aminotransferase, alanine aminotransferase, lactate dehydrogenase, and creatinine kinase activities. All treated animals developed skeletal myopathy with dose-related distribution and severity. The goats dosed with 20 mg/kg and higher also developed myocardial degeneration and necrosis. Although skeletal myonecrosis was patchy and widely distributed, the quadriceps femoris was consistently damaged, even in low-dosed animals. Myocardial lesions were most severe in the papillary muscles of 60-mg/kg dosed animals. This indicates
that goats are highly susceptible to rayless goldenrod poisoning, and that the characteristic lesion of poisoning is buy Buparlisib skeletal and cardiac
“Purple acid phosphatase (PAP; EC 22.214.171.124) enzymes are metallophosphoesterases that hydrolysis phosphate ester bonds in a wide range of substrates. Twenty-nine PAP-encoding loci have been identified in the Arabidopsis genome, many of which have multiple transcript variants expressed in response to diverse environmental conditions. Having analyzed T-DNA insertion see more mutants, we have provided strong pieces of evidence that AtPAP9 locus encodes at least two types of transcripts, designated as AtPAP9-1 and AtPAP9-2. These transcript variants expressed distinctly during the course of growth in medium containing sufficient phosphate or none. Further histochemical analysis by the use of AtPAP9-1 promoter fused to B-glucuronidase reporter gene indicated the expression of this gene is regulated in a tissue-specific manner. AtPAP9-1 was highly expressed in stipule and vascular tissue, particularly in response to fungal infection. Subcellular localization of AtPAP9-1:green fluorescent fusion protein showed that it must be involved in plasma membrane and cell wall adhesion. (C) 2014 Published by Elsevier B.V.”
“Flixweed (Descurainia Sophia L) is a problematic weed in winter wheat fields in China, which causes great loss of wheat yield. A total of 46 flixweed accessions from winter wheat-planting areas were collected and used for the survey of resistance to tribenuron-methyl and Pro197 mutation diversity.
44 mu M) with leucine (88 mu M). The regenerated shoots were elongated on the same medium. Elongated shoots were transferred Vorinostat research buy to the MS medium fortified with BA (4.44 mu M), leucine (88 mu M), and putrescine (62 mu M) for root induction. Rooted plants were hardened and successfully established in soil with a 90% survival rate.”
“AIM: To screen the differential expressed genes in colorectal cancer and polyp tissue samples.\n\nMETHODS:
Tissue specimens containing 16 cases of colorectal adenocarcinoma and colorectal polyp vs normal mucosae were collected and subjected to cDNA microarray and bioinformatical analyses. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to confirm some of the cDNA microarray data.\n\nRESULTS: The experimental data showed that eight genes were differentially expressed, most of which were upregulated in adenomatous polyp lesions. Forty-six genes expressions were altered in colorectal cancers, of which 29 were upregulated and 17 downregulated, as compared to the normal mucosae. In addition, 18 genes were similarly altered in both adenomatous polyps and colorectal cancer. qRT-PCR analyses confirmed the cDNA microarray data for four of those 18 genes: MTA1, PDCD4, TSC1 and PDGFRA.\n\nCONCLUSION: These differentially expressed genes likely represent biomarkers for early detection of colorectal cancer
and may be potential therapeutic targets after confirmed by further studies. (C) 2012 Baishideng. All rights reserved.”
“In this study the effect of different particle sizes of inorganic suspended solids (ISS) on the ISS accumulation in an activated sludge system was investigated. The volume mean particle diameters SRT1720 (Dv) of ISS were 26, 73, 106, 165, and
210 gm. There are four fates of ISS in an activated sludge system: (1) suspending in the activated sludge, (2) depositing at the bottom of the reactors, (3) discharged from the reactors via excess sludge, and lastly (4) discharged from the reactors via effluent. The accumulated ISS in the bioreactor was unevenly distributed. Based on the accumulation proportion check details of ISS in bioreactor, an ISS accumulation model was established, from which the ISS accumulation concentration and the MLVSS/MLSS could be predicted. The proportion of ISS suspending in activated sludge was 0.22, 0.21, 0.042 and 0.031. The proportion of ISS depositing at the bottom of bioreactors was 0.31, 0.47, 0.75, 0.76 and 0.92. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.”
“Background: The racial/ethnic composition of the United States is shifting rapidly, with non-Hispanic Asian-Americans, Native Hawaiians/Pacific Islanders (NHs/PIs), and mixed-race individuals the fastest growing segments of the population. We determined new drug use estimates for these rising groups. Prevalences among Whites were included as a comparison.\n\nMethods: Data were from the 2005-2011 National Surveys on Drug Use and Health.
However, the role that epistasis plays in the genetic architecture of quantitative traits is controversial. Here, we compared the genetic architecture of three Drosophila
life history traits in the sequenced inbred lines of the Drosophila melanogaster Genetic Reference Panel (DGRP) and a large outbred, advanced intercross population derived from 40 DGRP lines (Flyland). We assessed allele frequency changes between pools of individuals at the extremes of the distribution for each trait in the Flyland population by deep DNA sequencing. The genetic architecture of all traits was highly polygenic GW4869 Apoptosis inhibitor in both analyses. Surprisingly, none of the SNPs associated with the traits in Flyland replicated in the DGRP and vice versa. However, the majority
of these SNPs participated in at least one epistatic interaction in the DGRP. Despite apparent additive effects at largely distinct loci in the two populations, the epistatic interactions perturbed common, biologically plausible, and highly connected genetic networks. Our analysis underscores the importance of epistasis as a principal factor that determines variation for quantitative traits and provides a means to uncover genetic networks affecting these traits. Knowledge of epistatic networks will contribute to our understanding of the genetic basis of evolutionarily and clinically important traits and enhance predictive ability at an individualized level in medicine and agriculture.”
“In the title compound, C(19)H(16)Cl(4)O(4), the two halves of the molecule are related by a crystallographic twofold rotation axis passing through the central spiro-C selleckchem atom. The two non-planar six-membered heterocycles both adopt chair conformations, and the dihedral angle between the two benzene rings is 76.6 (1)degrees. In the crystal structure, intermolecular C-H center dot center dot center dot O hydrogen bonds link the molecules into chains along the c axis.”
“A two-stage process, composed of growth under nutrient-rich
conditions followed by cultivation under nitrogen starvation and controlled conditions of phosphate, light intensity, aeration, and carbon sources was applied for lipid production selleck products by the green alga Chlorella vulgar’s. Using conditions without addition of nitrogen, 2 mg/L PO4-P, light intensity of 100 mu mol/m(2)/s and 0.25 vvm of air, about 43% of dry cell weight accumulated as lipids after 12 h, which equates to a lipid productivity of 77.8 mg/L/d. In a medium containing 5 mg/L NO3-N and 2 mg/L PO4-P, and at a light intensity of 100 mu mol/m(2)/s and 0.25 vvm of 2% CO2, about 53% of dry cell weight consisted of lipids after 24 h, representing a lipid productivity of 77.1 mg/L/d. The low amount of nutrients, moderate aeration and light intensity were helpful for increasing lipid productivity. (C) 2012 Elsevier Ltd. All rights reserved.
In this Account, we examine the characteristics of the enzymes responsible for constructing AviCys to evaluate possibilities for generating high yields of bioactive AviCys- or AviMeCys-containing peptides for research and clinical
use.\n\nThe gene cluster for the biosynthesis of epidermin has been studied in depth, leading to the proposal for Barasertib Cell Cycle inhibitor a mechanism of AviCys formation. First, a serine residue upstream of the C-terminus is enzymatically dehydrated to form a dehydroalanine residue. Then, the C-terminal cysteine residue is oxidatively decarboxylated to form an enethiolate, which subsequently cyclizes onto the dehydroalanine to give the AviCys ring. Extensive research on EpiD, the enzyme responsible for the oxidative decarboxylation reaction, has led to its purification and cocrystallization with a model substrate peptide, yielding an X-ray crystal structure. An in vitro assay of the enzyme with a library of synthetic heptapeptides has resulted in the discovery that EpiD has low absolute substrate specificity and can oxidatively decarboxylate a wide variety of C-terminal cysteine-containing peptides.\n\nRecently, the gene duster for the biosynthesis of cypemycin
was also identified. Despite certain structural similarities between cypemycin and the lantibiotic peptides, analysis of the biosynthetic genes suggests that cypemycin ABT-263 mouse production is quite different from that of the lantibiotics. In particular, the AviCys residue in cypemycin is formed from two cysteine Napabucasin research buy residues instead of one serine and one cysteine, and the CypD enzyme that catalyzes the oxidative decarboxylation of the C-terminal cysteine shows little homology to EpiD.\n\nThe knowledge accrued from studying EpiD and CypD could be used to develop a semisynthetic methodology to produce
AviCys-containing peptides. In particular, suitable precursor peptides could be synthesized on solid support before being fed to either of these enzymes in vitro to generate the C-terminal AviCys moiety. Exploring the potential of this methodology could lead to the efficient production of epidermin, cypemycin, and analogues thereof.”
“The aims of this study were to investigate mechanisms of action involved in H2AX phosphorylation by DNA interstrand crosslinking (ICL) agents and determine whether gamma H2AX could be a suitable pharmacological marker for identifying potential ICL cellular chemosensitivity. In normal human fibroblasts, after treatment with nitrogen mustard (HN2) or cisplatin, the peak gamma H2AX response was detected 2-3 h after the peak of DNA ICLs measured using the comet assay, a validated method for detecting ICLs in vitro or in clinical samples. Detection of gamma H2AX foci by immunofluorescence microscopy could be routinely detected with 6-10 times lower concentrations of both drugs compared to detection of ICLs using the comet assay.
4 +/- 1.6 s (foam), and 21.0 +/- 2.9 s (firm), 3.3 +/- 1.6s (foam), respectively. For TG, there was an order effect (P<.001) but no age, sex or BMI effects. FTN demonstrated a dominant arm preference (P<.001), sex (P=.006),
BM I (P=.043) and order effects (P<.001). SLS demonstrated an order effect on the firm surface (P=.009) and an order (P<.001) and BMI (P=.001) effect on foam. Intra-rater reliability, as measured by ICC (3,3), demonstrated that TG and FTN had excellent reliability compared to SLS. FIN and TG should continue to be used in test batteries to determine neurological function in sports-related concussion. (C) FRAX597 2009 Sports Medicine Australia. Published by Elsevier Ltd. All rights reserved.”
“Background: Some Nigerian studies have reported cases of the metabolic syndrome in the population. This study aims to assess the prevalence of the components of the metabolic syndrome in type 2 diabetes mellitus (T2DM) patients using the International Diabetes Federation (IDF) worldwide definition. Methods: Eighty-nine T2DM
patients were studied after an overnight fast. The patients’ blood pressure, anthropometric indices, and biochemical parameters were measured. The components of the metabolic syndrome-raised blood pressure, waist circumference, triglycerides (TGs), Bucladesine and reduced high-density lipoprotein cholesterol (HDL-C)-were calculated using the IDF definition for the European ethnic group. Results: About 25% of the patients had raised blood pressure ( bigger than 130/85 mmHg), with the male patients having higher prevalence of raised systolic blood pressure (SBP bigger than 130 mmHg) than the female patients (73.3 vs. 52.3%, P smaller than 0.05). Although the prevalence of raised TGs
did not differ in gender, more females than males had reduced HDL-C (77.3 vs. 46.7%, P smaller than 0.001). Although generalized obesity is similar in both gender (17.8% vs. 31.8%, P bigger than 0.05), abdominal obesity predominates significantly in female patients (97.7 vs. 68.9%, P smaller than 0.001). Overall, total obesity (P smaller than 0.05), raised blood pressure (P smaller than 0.05), raised TGs, and reduced HDL-C are significantly clustered selleck products in abdominally obese patients. Conclusion: It is concluded that the abdominally obese T2DM patients had a higher cluster of the components of the metabolic syndrome and are consequently at greater risk of cardiovascular disease (CVD). We recommend that diabetes education emphasizing the risk of CVD in patients with increased abdominal fat should be intensified in the developing countries.”
“Background/Aim: Lymphoma, the most common hematopoietic cancer in dogs is sensitive to chemotherapy which is the dominant treatment method.
The PCL nanoparticles containing about 12.5% (w/w) of the naproxen (sample A3) was chosen for complementary studies of stability and in vivo release in rats. Nanoparticles did not suffer alteration during stability studies. In vivo release was sustained by one month. Thus, nanoparticles showed potential to act as an implantable sustained P005091 release system for chronic inflammatory
“Faulty epigenetic reprogramming of somatic nuclei is likely to be a major cause of low success observed in all mammals produced through somatic cell nuclear transfer (SCNT). It has been demonstrated that the developmental competence of SCNT embryos in several species were significantly enhanced via treatment of histone deacetylase inhibitors (HDACi) such as trichostatin A (TSA) to increase histone acetylation. Here we report that 50 nM TSA for 10 h after activation increased the developmental competence of porcine SCNT embryos constructed from Landrace
fetal fibroblast cells (FFCs) in this website vitro and in vivo, but not at higher concentrations. Therefore, we optimized the application of another novel HDACi, Scriptaid, for development of porcine SCNT embryos. We found that treatment with 500 nM Scriptaid significantly enhanced the development SCNT embryos to the blastocyst stage when outbred Landrace FFCs and ear fibroblast cells (EFCs) were used as donors compared to the untreated group. Scriptaid increased the overall cloning efficiency from 0.4% (untreated group)
to 1.6% for Landrace FFCs and 0 to 3.7% for Landrace EFCs. Moreover, treatment of SCNT embryos with Scriptaid improved the histone acetylation on Histone H4 at lysine 8 (AcH4K8) SN-38 in a pattern similar to that of the in vitro fertilized (IVF) embryos.”
“Purpose: Individuals who experience stroke have a higher likelihood of subsequent stroke events, making it imperative to plan for future medical care. In the event of a further serious health event, engaging in the process of advanced care planning (ACP) can help family members and health care professionals (HCPs) make medical decisions for individuals who have lost the capacity to do so. Few studies have explored the views and experiences of patients with stroke about discussing their wishes and preferences for future medical events, and the extent to which stroke HCPs engage in conversations around planning for such events. In this study, we sought to understand how the process of ACP unfolded between HCPs and patients post-stroke. Patients and methods: Using grounded theory (GT) methodology, we engaged in direct observation of HCP and patient interactions on an acute stroke unit and two stroke rehabilitation units. Using semi-structured interviews, 14 patients and four HCPs were interviewed directly about the ACP process.
New therapies that prevent invasion and metastasis in combination with current treatments could therefore significantly reduce cancer recurrence and morbidity. Metastasis is driven by altered signaling pathways that induce changes in cell-cell adhesion, the cytoskeleton, integrin function, protease expression, epithelial-to-mesenchymal transition and
cell survival. The ribosomal S6 kinase (RSK) family of kinases is a group of extracellular signal-regulated kinase/mitogen-activated protein kinase (ERK/MAPK) effectors that can regulate these steps of metastasis by phosphorylating both nuclear and cytoplasmic targets. However, our understanding of RSK function in metastasis remains incomplete check details and is complicated by the fact that the four RSK isoforms perform nonredundant, sometimes BI 2536 opposing functions. Although some isoforms promote cell motility and invasion by altering transcription and integrin activity, others impair cell motility and invasion through effects on the actin cytoskeleton. The mechanism of RSK action depends both on the isoform and the cancer type. However, despite the variance in RSK-mediated outcomes, chemical inhibition of this group of kinases has proven effective in blocking invasion and metastasis of several solid tumors in preclinical models. RSKs are therefore a promising drug target for antimetastatic cancer treatments that could supplement and improve current therapeutic
approaches. This review highlights contradiction and agreement in the current data on the function of RSK isoforms in metastasis and suggests ways forward in developing RSK inhibitors
as new antimetastasis drugs. Cancer Res; 73(20); 6099-105. (C) 2013 AACR.”
“The prevention of infectious diseases is a global health priority area. The early detection of possible epidemics is the first and important defense line against infectious diseases. However, conventional surveillance systems, e. g., the Centers for Disease Control and Prevention (CDC), rely on clinical data. The CDC publishes the surveillance results weeks after epidemic outbreaks. To improve the early detection of epidemic outbreaks, we designed a syndromic surveillance system to predict the epidemic trends based on disease-related Google search volume. Specifically, we first represented the epidemic trend with multiple alert GSK923295 levels to reduce the noise level. Then, we predicted the epidemic alert levels using a continuous density HMM, which incorporated the intrinsic characteristic of the disease transmission for alert level estimation. Respective models are built to monitor both national and regional epidemic alert levels of the U. S. The proposed system can provide real-time surveillance results, which are weeks before the CDC’s reports. This paper focusses on monitoring the infectious disease in the U. S., however, we believe similar approach may be used to monitor epidemics for the developing countries as well.
Using the delocalization
and charge transfer descriptors, we obtain all couplings between these three states. Our results are important in the context of DNA photophysics, since the calculated couplings can be used to parametrize effective Hamiltonians to model extended DNA stacks. Our calculations Bioactive Compound Library screening also suggest that the 5′-purine-pyrimidine-3′ sequence favors the formation of charge transfer excited states. (C) 2014 AIP Publishing LLC.”
“Human detection is a significant and challenging task with applications in various domains. In real-time systems, the speed of detection is crucial to the performance of system, while the accuracy is also taken into consideration. In this work, a human detection approach based on Histograms of Oriented Gradients (HOG) feature and differential evolution (DE), termed as HOG-SVM-DE, is proposed to achieve both fast and accurate detection. The proposed method considers the problem of locating an objective detection window as a search problem, and speeds up the detection stage by solving the search problem with DE. DE is chosen as the optimizer as it is characterized by fast and global convergence. The proposed system trains only one linear-SVM, and allows tradeoffs between the detection rate and the detection
time to satisfy different applications by simply tuning one parameter. Experiments are conducted on a set of images from the INRIA Person Dataset, and the results validate that the proposed HOG-SVM-DE is promising in terms of both speed and accuracy. (C) 2014 Elsevier B.V. All rights reserved.”
“Background IgE binds to mast cells and basophils via
its high-affinity GSK1120212 supplier receptor, GM6001 concentration Fc epsilon RI, and cross-linking of Fc epsilon RI-bound IgE molecules by allergen leads to the release of allergic mediators characteristic of type I hypersensitivity reactions. Previous work has shown that cross-linking of Fc epsilon RI with Fc gamma RIIb, an ITIM-containing IgG receptor, leads to inhibition of basophil triggering. 2G10, a chimeric human IgG1 anti-idiotype, has broad reactivity with human IgE and as such has the potential to bind simultaneously to Fc epsilon RI-bound IgE, via its Fab regions, and the negative regulatory receptor, Fc gamma RIIb, via its Fc region.\n\nObjective To assess the ability of human 2G10 to inhibit anti-IgE and allergen-driven basophil degranulation through cross-linking of Fc epsilon RI-bound IgE with Fc gamma RIIb.\n\nMethods 2G10 was assessed for its ability to bind to Fc gamma RIIb on transfected cells and on purified basophils. In the basophil degranulation assay, basophils were purified from peripheral blood of atopic individuals and activated with either anti-IgE or the house dust mite allergen Der p 1, in the presence or absence of human 2G10. Basophil activation was quantified by analysis of CD63 and CD203c expression on the cell surface, and IL-4 expression intracellularly, using flow cytometery.
“Background\n\nAssisted reproduction techniques (ART) such as in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI) can help subfertile couples to create a family. It is necessary to induce multiple follicles; this is achieved by follicle stimulating hormone (FSH) injections. Current
treatment regimens prescribe daily injections of FSH (urinary FSH with or without luteinizing hormone (LH) injections or recombinant FSH (rFSH)).\n\nRecombinant DNA technologies have produced a new recombinant molecule which is a long-acting FSH, named corifollitropin alfa (Elonva) or FSH-CTP. Birinapant chemical structure A single dose of long-acting FSH is able to keep the circulating FSH level above the threshold necessary to support multi-follicular growth for an entire week. The optimal dose of long-acting FSH is still being determined. A single injection of long-acting FSH can replace seven daily FSH injections during the first week of controlled selleck compound ovarian stimulation (COS) and can make assisted reproduction
more patient friendly.\n\nObjectives\n\nTo compare the effectiveness of long-acting FSH versus daily FSH in terms of pregnancy and safety outcomes in women undergoing IVF or ICSI treatment cycles.\n\nSearch methods\n\nWe searched the following electronic databases, trial registers and websites: the Cochrane Central Register of Controlled Trials (CENTRAL), the Menstrual Disorders and Subfertility Group (MDSG) Specialised Register, MEDLINE, EMBASE, PsycINFO, CINAHL, electronic trial registers for ongoing and registered trials, citation indexes, conference abstracts in the ISI Web of Knowledge, LILACS, Clinical Study Results (for clinical trial results of marketed pharmaceuticals), PubMed and OpenSIGLE (10 October 2011). We also carried
out handsearches.\n\nSelection criteria\n\nAll randomised controlled trials (RCTs) comparing long-acting FSH versus daily FSH in women who were part of a couple with subfertility and undertaking IVF or ICSI treatment cycles with a GnRH antagonist or agonist protocol were included.\n\nData collection and analysis\n\nData extraction and assessment of risk of bias was independently done by two review authors. Original trial authors were contacted in the case of missing data. We calculated Peto odds ratios for each outcome; our primary outcomes were live Selleck JNK inhibitor birth rate and ovarian hyperstimulation syndrome (OHSS) rate.\n\nMain results\n\nWe included four RCTs with a total of 2335 participants. A comparison of long-acting FSH versus daily FSH did not show evidence of difference in effect on overall live birth rate (Peto OR 0.92; 95% CI 0.76 to 1.10, 4 RCTs, 2335 women) or OHSS (Peto OR 1.12; 95% CI 0.79 to 1.60, 4 RCTs, 2335 women). We compared subgroups by dose of long-acting FSH. There was evidence of reduced live birth rate in women who received lower doses (60 to 120 mu g) of long-acting FSH compared to daily FSH (Peto OR 0.60; 95% CI 0.40 to 0.91, 3 RCTs, 645 women).