*** CURRENT THROUGH THE 2008 REGULAR SESSION *** *** ANNOTATIONS CURRENT THROUGH MAY 21, 2008 *** Chapter 35 Criminal Sentencing Reform Act of 1989 Part 2 --Procedure for Imposing Sentence Go to the Tennessee Code Archive Directory Tenn. Code Ann. § 40-35-213 (2008) 40-35-213. Eligibility for work release program. (a) Notwithstanding any other law to the contrary, no person conv
Suomen sivusto, jossa voit ostaa halvalla ja laadukas Viagra http://osta-apteekki.com/ toimitus kaikkialle maailmaan.
Yritti äskettäin viagra, se toimii erittäin tehokkaasti)) Ostaa Internetin kautta täällä propecia Myös ostaa levitra oikeudenkäynti, vaikutus on silmiinpistävää.
Se470101726ptypes aggregate in QTL regions, combined with as an iv bolus to determine the contribution of nitric 14. E. S. Lander et al., Genomics 1, 174 (1987).
physiological profiling, provides a novel ap- oxide to basal renal vascular tone. After 10 min of 15. J. Loscalzo, G. Welch, Progr. Cardiovasc. Dis. 38, 87
equilibration, a repeat infusion of the same two doses of proach to facilitate the positional cloning of ACh were administered to test for the degree of block- 16. N. K. Hollenberg et al., Medicine 57, 167 (1978).
genes underlying cardiovascular function and ade of the synthesis of nitric oxide produced by L- 17. A. W. Cowley Jr. et al., Physiol. Genomics 2, 107
hypertension. While strategies for accomplish- NAME. (Morphometric measurements): Heart and kid- neys were removed, stripped of surrounding tissue, and ing these goals will continue to evolve, this first 18. M. Stoll, A. W. Cowley Jr., A. S. Greene, data not weighed to assess the degree of cardiac and renal attempt at developing knowledge at a systems hypertrophy. (Histology): The right kidney was immer- 19. E. S. Lander, L. Kruglyak, Nature Genet. 11, 241
biology level sets the stage for future improve- sion-fixed in 10% buffered formalin and embedded in paraffin, and prepared sections stained with H&E and ments and provides investigators with a power- PAS were evaluated for mean glomerular diameter and 20. We thank the Bioinformatics Research Center at the degree of focal glomerulosclerosis.
Medical College of Wisconsin for the development of 8. B. R.Thumma et al., J. Exp. Bot. 52, 203 (2001).
the database, tools, and Web site; M. Granados, M.
Nobrega, M. Shiozawa, and M. Runte for assistance 9. L. L. Miner et al., Psychopharmacology 117, 62
References and Notes
with genotyping; A. Kwitek-Black for comparative 1. E. R. Bleecker, D. S. Postma, D. A. Meyers, Am. J. mapping; and T. Kurth, K. Bork, P. Regozzi, and C.
10. K. G. Becker et al., Proc. Natl. Acad. Sci. U.S.A. 95,
Respir. Crit. Care Med. 156, S113 (1997).
Thomas for excellent technical assistance. This work 2. C. Julier et al., Hum. Mol. Genet. 6, 2077 (1997).
was supported by National Heart, Lung, and Blood 11. J. Nadeau, W. Frankel, Nature Genet. 25, 381 (2000).
3. J. Krushkal et al., Circulation 99, 1407 (1999).
12. J. P. Rapp, Physiol. Rev. 80, 135 (2000).
4. C. L. Hanis et al., Nature Genet. 13, 161 (1996).
5. J. A. Todd, Proc. Natl. Acad. Sci. U.S.A. 92, 8560
13. A. C. Guyton et al., Annu. Rev. Physiol. 34, 13 (1972).
6. A user interface to the complete data set is found at 7. The total genome scan was carried out with an average 10 cM spacing of markers following pheno- typing with 239 measured or derived traits. After testing for normalcy, 166 traits were analyzed in a parametric genome scan using MAPMAKER/QTL (12, 16). The remaining 73 traits were analyzed using the nonparametric mapping algorithm (MAPMAKER/QTL version 1.9b). (Phenotyping protocol, conscious): All blood pressure measurements were made with the animals unrestrained in their home cage as described previously (17). Data were collected at a rate of 100 Hz and reduced to 1-min averages, except for time Alain-Jacques Valleron,1 Pierre-Yves Boelle,1 Robert Will,2 series analysis where they were 1-s averages. The day-night light cycle for all rats ran from 2:00 a.m.
(lights on) to 2:00 p.m. (lights off ) throughout the study. BP1 (High Salt Day 1): Baseline measurements of systolic, diastolic, and mean arterial pressure and The size of the variant Creutzfeldt-Jakob Disease (vCJD) epidemic in the United heart rate were measured from 9:00 a.m. to noon.
Kingdom is a major public health concern and a subject of speculation. The cases BP2 (High Salt Day 2 – inactive versus active): Repeat are young (mean age ϭ 28). Assuming that the risk of developing the disease morning recording (“inactive phase,” lights on), and record 4 hours during the dark cycle (2:00 p.m. to in susceptible exposed subjects decreases exponentially with age after age 15, 6:00 p.m. “active phase”). Urine was collected for 24 that all infections occurred between 1980 and 1989, and that the distribution hours for measurement of volume, sodium, potassi- of the incubation period is lognormal, we estimate that the mean duration of um, protein, and creatinine. All BP data this day was collected for time-series analysis. BP3 (High Salt Day the incubation period is 16.7 years [95% confidence interval (CI): 12.4 to 23.2] 3): Repeat morning recording. Following the record- and that the total number of cases will be 205 (upper limit of the 95% CI: 403).
ing period, a blood sample (500 l) was drawn for determination of creatinine, plasma renin activity, plasma protein, and hematocrit. Furosemide chal- be extremely high (4). Therefore, one could lenge: Following blood draw, an ip injection of furo- definite (n ϭ 86) or probable (n ϭ 11) variant pessimistically assume that virtually everybody semide (10 mg/kg) was given to salt deplete the Creutzfeldt-Jakob Disease (vCJD) in the United in the population has been in contact with food, animals, and the diet switched to a 0.4% low salt.
Kingdom. These patients probably contracted or bovine products, originating from BSE-in- BP4 (Stress test): Following a control period, an alert- ing stimulus (2 mA for 0.3 s) was delivered twice with the disease by oral ingestion of food contami- fected animals. The public health response in a 5-min interval during pressure recording. Change in nated by the agent of bovine spongiform en- Europe has been to develop procedures and mean arterial pressure, the time to peak, and the time cephalopathy (BSE), before the UK bovine- diagnostic tests that avoid, as far as possible, the to 90% recovery were determined. BP5 (Low Salt): Repeat 3- hour morning recording of blood pressure specified risk materials (SRM) ban in 1989 (1).
entry of any infected animal into the food chain.
in the salt depleted state. Following the recording The number of BSE-infected animals is estimat- The consequences of the BSE epidemic in terms period, a 1.0- ml blood sample was taken for the ed to have been in the range of 900,000 to of human disease are not yet known: With dif- measurement of plasma renin activity, triglycerides, total cholesterol, HDL, creatinine, hematocrit, and 1,130,000, with between 460,000 and 482,000 ferent assumptions for risk analysis, in 1997, the white blood cell count. (Phenotyping protocol, anes- slaughtered for consumption before the intro- cumulative cases of vCJD in the United King- thesitized): Rats were anesthetized with ketamine (30 duction of the November 1989 specified offal dom were estimated from as few as 75 to as mg/kg; intramuscular) and Inactin (50 mg/kg; intra- peritoneal). Catheters were implanted in the femoral ban (2). The epidemic may have started as early many as 80,000 (5) and more recently from 70 artery and vein and an electromagnetic flow probe as 1980 (3), and the number of people exposed to 136,000 cases (6). These estimates are mark- was placed on the left renal artery via a midline to potentially infective doses through food may edly dependent on assumptions made about the incision. An iv infusion (50 l/min) of isotonic saline containing 1% bovine serum albumin replaced fluid mean duration of the incubation period. Unfor- losses. After a 45-min equilibration, arterial blood tunately, no studies in animals or of other hu- pressure and renal blood flow were measured during Epidemiology and Information Sciences, INSERM man spongiform encephalopathies provide pre- a 15-min control period. Renal and peripheral vascu- U444, CHU Saint-Antoine, Universite´ Pierre et Marie cise data for the incubation period. In addition, lar responses to 5-min iv infusions of angiotensin II Curie et Assistance Publique–Hoˆpitaux de Paris, 27 (20, 100, 200 ng/kg/min) and norepinephrine (0.5, 1, rue Chaligny, 75012 Paris, France. 2National the observation that only a few cattle, and often 3 g/kg/min) were determined. Following recovery of Creutzfeldt-Jakob Disease Surveillance Unit, Western only one, from the same age cohort in a herd pressure to baseline values, renal vascular and sys- General Hospital, Edinburgh EH4 2XU, UK. 3Immunite´ have developed BSE suggests that additional temic arterial responses to two successive doses of Anti-Infectieuse JE 2236, UFR de Me´decine de acetylcholine (ACh) (0.1 and 0.2 g/kg/min) were individual or environmental factors may influ- Grenoble, Universite´ Joseph Fourier, Domaine de la measured. L-NAME (5 mg/kg) was then administered ence the development of the disease. It is be- 23 NOVEMBER 2001 VOL 294 SCIENCE www.sciencemag.org cause the relation between the risk of the disease each generation, these s subjects pass through and the dose, route of infection, host factors, and We denote by S(t,a) the survival function the 1980 – 89 “window” at different ages, and environmental factors is unknown that predic- from all causes of mortality at date t and age therefore the final number of persons who will tions of the possible future of the epidemic rely a, by (t, a) the force of infection at date t and ultimately develop the disease varies according- on mathematical extrapolations based on cur- age a, and by h the probability density func- ly. Finally, the probability P(t,a)dadt that a case tion of the duration of the incubation period.
aged between a and a ϩ da occurs between One striking epidemiological characteristic (t, a) is the product of a function f (a) of age times t and t ϩ dt is expressed mathematical- of vCJD is the young age distribution of the and of a function g(t) of calendar time: (t, ly, then the maximum likelihood approach is cases (Fig. 1A). The mean age at death of these a) ϭ f (a)g(t). The choices of functions f and patients is 28 years. Only 6 of 90 patients who g express the age-risk relation described from the available observations, and the fu- have died were older than 50 years, in compar- above and the variation of the BSE infectious ture of the epidemic is assessed with these ison with 93% of cases of sporadic CJD (7).
risk, respectively (11). The probability distri- This observation provides a clue to the incuba- bution of the duration of the incubation peri- The distribution of the vCJD incubation pe- tion period in vCJD, i.e., the “age of the patient od, h(u), was assumed to be lognormal, be- riod that best fits the data within the framework at the diagnosis” ϭ “age at infection” ϩ “incu- of our model has a mean of 16.7 years, with a bation time.” The ages of the patients with vCJD infectious diseases (12). A Gamma distribu- standard deviation of 2.6 years. The 95% upper at diagnosis and death are collated by the Na- tion was also used in the sensitivity analysis.
percentile of this distribution is 21.4 years. The tional Creutzfeldt-Jakob Disease Surveillance The full statistical formulation necessary to 95% confidence interval (CI) of the estimates of Unit in the United Kingdom. The causal link write the likelihood equation implies that a the mean and standard deviation is relatively between BSE infection in cattle and human probabilistic model be chosen to estimate the narrow: The 95% CI for the estimate of the vCJD indicates that the age at infection in peo- population at risk of developing the disease, i.e., mean incubation period is 12.4 to 23.2 years, ple must parallel the course of the BSE epidem- the exposed/susceptible subjects. According to and the 95% CI of the standard deviation is ic. One can therefore compute the distribution of the formulation we chose, the dates and ages of 0.9 to 8 years (10). The decrease in suscep- incubation periods by a deconvolution tech- the observed cases are a realization of a planar tibility to infection in exposed subjects older nique taking into account the censorship of cur- Poisson process (13). In this model, s is the than 15 years, as estimated from the param- rent data, as was done successfully with ac- average number of individuals per generation eter ␣, was found to be very sharp: 16% per who can be infected, provided they have been year of age (CI: 12 to 23%). This means that, (8). In vCJD, the analysis of the censored data is exposed to a sufficient dose of infectious agent under the best fitting hypothesis, an individ- more complicated because the possible dates of and have the appropriate individual characteris- ual aged 20 years in 1981 had 55% less risk infection range over an extended period of time.
tics (genetic, environmental, and so forth). In of becoming infected than a child aged 15 Thus, additional statistical modeling was neces-sary. The model we propose provides estimatesof the incubation period and the future burden of To explain that most of the cases are young, two (nonexclusive) hypotheses have to bemade: (i) the incubation period is shorter in the young than in the old, and (ii) the young aremore susceptible to infection. We do not pre- judge the underlying determinants to these hy-potheses that may be related to differences in Number of cases
susceptibility or other unknown factors. If thefirst assumption was true, older cases with long- er incubation periods have a greater chance ofbeing identified later than younger cases. Be- cause there is no statistically significant relation between the date of diagnosis and age (Fig. 1B), we discarded this first assumption. We there- fore chose the second assumption, namely that the probability per year that a susceptible sub- ject becomes infected [the “force of infection” (9)] decreases with age a. For the calculation, we assumed that all susceptible children aged between 0.5 and 15 years, exposed to the infec- tious agent on year t, experience the same forceof infection. After 15 years of age, we assume that the force of infection decreases exponen- tially (10). This hypothesis is in line with the epidemiological data, which show that vCJD rarely occurs in older subjects. The age cutoff Age class
of 15 years was an arbitrary choice. However, Fig. 1. (A) Age distribution of vCJD cases. Data are as of 1 May 2001, including 97 patients. (B) The
this parameter has been further studied in a distribution of the date of onset of vCJD by age class. Diamonds indicate observed values; a line is sensitivity analysis. We assume that the whole drawn at the median date. There is no apparent relation between age and date of diagnosis population may have been exposed to the in- (correlation coefficient ϭ 0.03, P ϭ 0.8), as would have been expected if the incubation time was fectious agent, with the exception of infants strongly age dependent, causing older cases to be detected later than younger cases.
www.sciencemag.org SCIENCE VOL 294 23 NOVEMBER 2001 3. C. H. Cohen, A. J. Valleron, Int. J. Epidemiol. 28, 526
4. “Opinion of the scientific steering committee on the human exposure risk (HER) via food with respect to BSE” (European Union Scientific Steering Committee, 5. S. N. Cousens, E. Vynnycky, M. Zeidler, R. G. Will, P. G.
Smith, Nature 385, 197 (1997).
6. A. C. Ghani, N. M. Ferguson, C. A. Donnelly, R. M.
Anderson, Nature 406, 583 (2000).
7. Surveillance data collected by the UK Creutzfeldt- Jakob Disease Surveillance Unit are available at 8. S. Chevret, D. Costagliola, J. J. Lefrere, A. J. Valleron, J. Calendar year
Epidemiol. Community Health 46, 582 (1992).
Fig. 2. Observed cumulated incidence of vCJD
9. The “force of infection” is defined in mathematical Fig. 3. Risk function for onset of vCJD as a
epidemiology to quantify the risk per unit of time (dots) and incidence predicted by the model function of age and time. Red dots indicate the (usually, the year) that a susceptible individual has to acquire the disease after being exposed to the infectious agent. For a complete review of the concept of force of infection, see R. M. Anderson and R. May [Infectious years (99.9% for an individual aged 70).
Diseases of Humans: Dynamics and Control (Oxford The model predictions fit the past cumulat- The results presented here are based on a Science Publications, Oxford, 1991), chaps. 3 and 8].
ed incidences, as shown in Fig. 2. Similarly, lognormal distribution of the incubation period, 10. Supplemental materials are available at Science On- line at www.sciencemag.org/cgi/content/full/294/ there is a good fit to the observed age distribu- which is commonly used in the epidemiology tion (10), as the model predicts that 22 out of of infectious diseases. However, we repeated 11. The function f(a) was taken in the form f(a) ϭ 0 if the first 97 diagnosed cases should be less than the estimation process assuming that the incu- a Ͻ 0.5, as infants younger than 0.5 year were 20 years of age (19 in the surveillance data set) assumed to not be exposed to the BSE agent; f(a) ϭ if 0.5 Ͻ a Ͻ15, which corresponds to the constant and 82 should be less than 40 years of age (87 found almost identical values for the incubation risk assumed in children before 15; and f (a) ϭ 0 parameters, the future epidemic size of the ep- e Ϫ␣(aϪ0.5) if a Ͼ 15. The function g(t ) was chosen to Details of the variation in the risk function idemic, and the occurrence of a bimodal age reflect the increasing probability of the presence of contaminated meat products in the human diet, in (14) with age and time up to 2012 are shown in distribution in the future (10). parallel to the increasing incidence of BSE in animals Fig. 3: The model predicts that the peak of the over the period 1980–89. Possible exposures after epidemic will be in 2000/2001 and that the longer than in human growth hormone–related 1989 were not considered in this analysis. Mimicking the incidence profile observed in the BSE epidemic annual number of cases should gradually de- CJD, which is between 9 and 10 years (15) in during the same period, we set g(t ) ϭ crease after this date. The total number of ex- the sensitive homozygous genotypes. It is short- ␥ e Ϫ␥(t Ϫ1989). From the knowledge of the doubling pected vCJD cases is, according to our model, er than the one estimated in Kuru (16), which time observed in the BSE epidemic (14 months) during the 1980–88 period (2), we extrapolate ␥ ϭ low at 205 cases (upper limit of the 95% CI: may exceed three decades, although, a priori, ln(2)/(14/12) ϭ 0.596. As only the product 403). One prediction from the model is that in one would have expected a longer value because identifiable, because of the form for the force of the next few years, the age distribution will in Kuru, there is no species barrier and the become bimodal and that the proportion of older disease was transmitted orally as in vCJD. The 12. P. E. Sartwell, Am. J. Hyg. 51, 310 (1950).
13. D. R. Brillinger, Biometrics 42, 693 (1986).
PRNP 129 genotype has a crucial importance in determining the risk of developing CJD. Yet to P͑t,a͒dtda ϭ S͑t,a͒͵ ͭexpͫϪ ͵ ͑t Ϫ u,u͒duͬ infections occurring between 1980 and 1989, as date, all tested vCJD patients have been ho- we assume that the likelihood of new human mozygous for methionine at codon 129, as are infection with BSE after the bovine SRM ban in about 40% of the total UK population. If there ͑t Ϫ v,v͒h͑a Ϫ v͒dvͮdtda 1989 should have been considerably reduced.
are two subpopulations of vCJD patients, one with “short” incubation times and methionine The log-likelihood of the observed cases is report is that it is focused on the most striking homozygosity, the other with “long” incubation sP͑t,a͒dadt, epidemiological characteristic of vCJD, name- times and valine homozygosity or heterozygos- ly, the age distribution of the cases. In contrast ity, our method would not identify the second where the first sum is over all observed cases and the to other models, which are based primarily on distribution parameters, because cases of vCJD integration is made in the domain D corresponding to scenarios related to dietary exposures to BSE in with genotypes other than methionine homozy- ages between 0.5 and 100 years and to years be- gosity have not yet been identified.
tween 1980 and 2000. s is the intensity of the Poisson birth process. Numerical maximization of the make any assumptions about this parameter that Our age-risk model allows an estimate of the likelihood was done with a modified Levenberg Mar- future size of the epidemic. If we independently quardt algorithm (SLATEC) after reparameterization introduce our estimates of the incubation period of the model A logarithmic transformation was used tween age and force of infection, we made one in the Ghani or Cousens models, we find similar for all variables but incubation mean time. The max- imization was independently performed with a New- of the most parsimonious choices possible, i.e., “low” predictions: 80 to 630 cases with the ton-Raphson method (NAG), and all presented re- a function beginning with a plateau during Ghani model and 801 with the Cousens model sults were in agreement in the two methods, with childhood, followed by an exponential decrease.
(17). In conclusion, our prediction of the epi- differences between estimates of less than 10Ϫ2.
Numerical integrations were carried out to a preci- The sensitivity analysis in which all possible demic of vCJD lies in the “optimistic” end of the alternatives to the 15-year age limit were tested ranges of previously published figures, and this 15. J. Huillard d’Aignaux et al., Neurology 53, 1197
ruled out an even simpler model with only one low value is in favor of a large species barrier 16. R. L. Klitzman, M. P. Alpers, D. C. Gajdusek, Neuro- exponential function (age limit ϭ 0) and found epidemiology 3, 20 (1984).
as the optimal value an age limit of 16. We 17. The figure obtained from the Cousens model when an have no clear physiological explanation for References and Notes
incubation period of mean 15 years and 95th percen- this age limit: Although a relation with puber- 1. M. E. Bruce et al., Nature 389, 498 (1997).
2. N. M. Ferguson, C. A. Donnelly, M. E. J. Woolhouse, 18. We thank J. Gagnon for helpful discussions.
ty may be hypothesized, experimental evi- R. M. Anderson, Philos. Trans. R. Soc. London Ser. B Biol. Sci. 352, 803 (1997).
23 NOVEMBER 2001 VOL 294 SCIENCE www.sciencemag.org
La Figura di Paolo di Tarso Per conoscere Paolo si hanno a disposizione due tipi di fonti. Anzitutto le lettere, nelle quali troviamo notizie molto frammentarie della vita di Paolo, della sua origine, della conversione, delle fatiche apostoliche, dei collaboratori e avversari, degli itinerari missionari. Accanto alle lettere stanno gli Atti degli Apostoli, dove Paolo succede a Pietro nella