Janet M. Roscoe
University of Toronto
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Featured researches published by Janet M. Roscoe.
The New England Journal of Medicine | 1989
Daniel C. Cattran; Terry Delmore; Janet M. Roscoe; Edward Cole; Carl Cardella; Richard Charron; Susan Ritchie
We conducted a prospective randomized study in which patients with biopsy-confirmed idiopathic membranous nephropathy were assigned to receive either a six-month course of prednisone given on alternate days (45 mg per square meter of body-surface area; n = 81) or no specific treatment (n = 77). The mean duration of follow-up was 48 months. Patients in the prednisone group (median age, 46 years) entered with a mean disease duration of 15 months, a median creatinine clearance of 1.2 ml per second per 1.73 m2 (range, 0.25 to 2.6), and a median rate of urinary protein excretion of 6.8 g per day (0.3 to 26). The annual change in the corrected creatinine clearance at six months did not differ between the prednisone group and the control group (0.10 vs. 0.06 ml per second; P = 0.8), or at the last follow-up evaluation (-0.07 vs. -0.02 ml per second; P = 0.2; 95 percent confidence interval on the difference, -0.03 to 0.13). The proportion of patients with complete remission of proteinuria was also similar in the groups at 6 and 12 months and after a mean of 48 months. Outcomes were similar in the two groups with respect to progression to renal failure (3 vs. 4 patients), death (3 vs. 1 patient), complete remission of proteinuria at 36 months (16 vs. 19 patients), and a decline of 25 percent or more in the creatinine clearance at 60 months (32 vs. 25 percent of patients). A multivariate analysis, which adjusted for differences at entry in sex distribution, urinary protein excretion, and creatinine concentration, as well as other prognostic variables, failed to provide an explanation for the lack of effect of prednisone. We conclude that a six-month course of therapy in which prednisone is given on alternate days is of no benefit to patients with idiopathic membranous nephropathy.
Journal of The American Society of Nephrology | 2003
Sarbjit V. Jassal; Murray Krahn; Gary Naglie; Jeffrey S. Zaltzman; Janet M. Roscoe; Edward Cole; Donald A. Redelmeier
Transplantation offers superior life expectancy and quality of life compared with dialysis in young patients with end-stage renal failure. However, the initial risks of mortality and morbidity are high. This study used a decision analysis model to evaluate the costs and benefits of kidney transplantation versus continued dialysis for older patients with renal failure. A decision analytic model comparing cadaveric renal transplantation to continued hemodialysis treatment was developed. The base case considered a theoretical cohort of patients aged 65 yr without known comorbidity or contraindications to transplantation who would have to wait 2 yr for a cadaveric transplant. Separate models were constructed for patients with diabetes or cardiovascular disease and for patients receiving an organ after a variety of wait-list times. Probability, utility, and survival data were obtained from published reports and renal registries. For 65-yr-old patients, quality-adjusted life expectancy increased by 1.1 quality-adjusted life years (QALY) at an incremental cost of
Forensic Science International-genetics | 2015
Andrew J. Pakstis; Eva Haigh; Lotfi Cherni; Amel Benammar Elgaaied; Alison Barton; Baigalmaa Evsanaa; Ariunaa Togtokh; Jane E. Brissenden; Janet M. Roscoe; Ozlem Bulbul; Gonul Filoglu; Cemal Gurkan; Kelly A. Meiklejohn; James M. Robertson; Cai-Xia Li; Yi-Liang Wei; Hui Li; Usha Soundararajan; Haseena Rajeevan; Judith R. Kidd; Kenneth K. Kidd
67,778 per QALY. Assuming a 2-yr wait-listed time, transplantation remained economically attractive for 70-yr-old patients (incremental cost effectiveness [ICE],
Human Biology | 2015
Jane E. Brissenden; Judith R. Kidd; Baigalmaa Evsanaa; Ariunaa Togtokh; Andrew J. Pakstis; Françoise R. Friedlaender; Kenneth K. Kidd; Janet M. Roscoe
79,359 per QALY) but was less economically attractive for those over 75 yr of age (ICE,
Peritoneal Dialysis International | 2015
Baigalmaa Evsanaa; Babak Aliazardeh; Sara Mahdavi; Gursarn Bajwa; Jerry Gula; Michelle Tam; Elena Sze; Janet M. Roscoe; Paul Y. Tam; Tabo Sikaneta
99,553) or for 70-yr-olds with either cardiovascular disease or diabetes (ICE,
International Journal of Legal Medicine | 2018
Ozlem Bulbul; Andrew J. Pakstis; Usha Soundararajan; Cemal Gurkan; Jane E. Brissenden; Janet M. Roscoe; Baigalmaa Evsanaa; Ariunaa Togtokh; Peristera Paschou; Elena L. Grigorenko; David Gurwitz; Sharon Wootton; Robert Lagace; Joseph Chang; William C. Speed; Kenneth K. Kidd
126,751 and
Journal of The American Society of Nephrology | 1998
Sarbjit V. Jassal; Janet M. Roscoe; Jeffrey S. Zaltzman; Tony Mazzulli; Mel Krajden; Maryann Gadawski; Daniel C. Cattran; Carl J. Cardella; Shelley Elizabeth Albert; Edward Cole
161,090 per QALY, respectively). The analytic results were sensitive only to the time spent waiting for the graft. The cost-effectiveness reduced such that the costs associated with one QALY were in excess of
Kidney International | 1985
Daniel C. Cattran; Carl Cardella; Janet M. Roscoe; Richard Charron; Phillip C. Rance; Susan Ritchie; Paul Corey
100,000/yr when the probability of a complication was > or = 50% per 3-mo cycle and when the utility of transplantation fell below 0.62. If available within a timely period, transplantation may offer substantial clinical benefits to older patients at a reasonable financial cost. Prolonged waiting times dramatically decrease the clinical benefits and economic attractiveness of transplantation, suggesting that living donor transplantation may be of particular benefit in this population.
Kidney International | 1993
Janet M. Roscoe; Jane E. Brissenden; E. Alexander Williams; Anne L. Chery; Mel Silverman
Ancestry inference for a person using a panel of SNPs depends on the variation of frequencies of those SNPs around the world and the amount of reference data available for calculation/comparison. The Kidd Lab panel of 55 AISNPs has been incorporated in commercial kits by both Life Technologies and Illumina for massively parallel sequencing. Therefore, a larger set of reference populations will be useful for researchers using those kits. We have added reference population allele frequencies for 52 population samples to the 73 previously entered so that there are now allele frequencies publicly available in ALFRED and FROG-kb for a total of 125 population samples.
Kidney International | 1976
Janet M. Roscoe; Marc B. Goldstein; Mitchell L. Halperin; Douglas R. Wilson; Bobby J. Stinebaugh
ABSTRACT Genetic data on North and Central Asian populations are underrepresented in the literature, especially for autosomal markers. In the present study we used 812 single nucleotide polymorphisms (SNPs) distributed across all the human autosomes and extensively studied at Yale to examine the affinities of two recently collected samples of populations: rural and cosmopolitan Mongolians from Ulaanbaatar and nomadic, Turkic-speaking Tsaatan from Mongolia near the Siberian border. We compare these two populations with each other and with a global set of populations and discuss their relationships to New World populations. Specifically, we analyze data on 521 autosomal loci (single SNPs and multi-SNP haplotypes) studied in 57 populations representing all the major geographical regions of the world. We conclude that these North and Central Asian populations are genetically distinct from all other populations in our study and may be close to the ancestral lineage leading to the New World populations.