ライフサイエンスコーパス: IPT

1 IPT alone does not cure existing infections in the major

2 IPT and prolonged exposure improved quality of life and

3 IPT confers protection against incident TB among HIV-neg

4 IPT exposure during pregnancy was not negatively associa

5 IPT exposure during pregnancy was not negatively associa

6 IPT for acute-phase depression had moderate-to-large eff

7 IPT had (nonsignificantly) lower attrition and higher re

8 IPT had little effect on frequencies or cytokine coexpre

9 IPT had significant effects on eating disorders, but the

10 IPT in subthreshold depression significantly prevented t

11 IPT is effective in the acute treatment of depression an

12 IPT may also be effective in the treatment of eating dis

13 IPT of malaria improves the health and cognitive ability

14 IPT reduced the incidence of malaria parasitemia and cli

15 IPT reduced the risk of TB by approximately 30% (aHR, 0.

16 IPT was associated with loss of QGIT positivity, the pot

17 IPT was well tolerated; the most common side effects wer

18 IPT with dihydroartemisinin-piperaquine given every 4 we

19 IPT with MQAS administered to patients with SCD during r

20 IPTs and drug experimentation were modestly heritable (5

21 pregnancy outcome compared to 23 of 82 (23%) IPT-unexposed participants.

22 rse pregnancy outcome compared with 23 (28%) IPT-unexposed women.

23 Among 56 IPT-DP recipients (26 children, 30 pregnant women) with

24 Of the 69 IPT-exposed participants, 11 (16%) had an adverse pregna

25 Of the 69 IPT-exposed women, 11 (16%) had an adverse pregnancy out

26 cipants who were revaccinated with BCG after IPT (n = 33) or without prior IPT (n = 39).

27 ry, 34 (12%) reverted to QGIT-negative after IPT.

28 Although IPT prevented malaria, the hematological benefit it adde

29 lower in IST (5.7%) than in SST (12.6%) and IPT (10.6%) clusters.

30 g recovery rates were equivalent for CBT and IPT at posttreatment (64 [79%] of 81 vs 59 [73%] of 81)

31 Both behavioral therapies (CBT and IPT) were manual guided and were delivered in individual

32 ot lie within blade 5 of the SEMA domain and IPT domains 2-3, both of which are thought to bind to HG

33 ne (SP) in Malawi, the impacts of IST-DP and IPT-SP on the development and maintenance of malaria ant

34 ough ART has been widely rolled out, ICF and IPT have not.

35 and daily iron for 12 weeks, daily iron and IPT with SP placebo, IPT and daily iron placebo, or dail

36 aily iron placebo, or daily iron placebo and IPT with SP placebo (double placebo).

37 where malaria transmission is seasonal, and IPT an appropriate malaria intervention in children, com

38 Two months after treatment, both SPT and IPT resulted in significant reductions in serum CRP comp

39 on was induced by pollination in both WT and IPT corollas, but this increase was delayed in IPT flowe

40 se to examine associations between antenatal IPT exposure and adverse pregnancy outcomes, maternal TB

41 reassuring regarding the safety of antenatal IPT, with the greatest benefits against TB disease obser

42 oglobulin superfamily in a subclass known as IPT domains.

43 -specific efficacy of interventions, such as IPT and bacillus Calmette-Guerin (BCG) vaccination for p

44 Surgical resection of asymptomatic IPT is controversial.

45 noncurative resection of their asymptomatic IPT.

46 s (RR) for pulmonary TB associated with BCG, IPT, and latent TB infection.

47 gression to evaluate the association between IPT exposure and adverse pregnancy outcomes (fetal demis

48 gression to evaluate the association between IPT exposure and adverse pregnancy outcomes (fetal demis

49 At 2-year follow-up, both IPT and CBTgsh resulted in greater remission from binge

50 restraint decreased more quickly in CBT but IPT had equivalent levels by later follow-ups.

51 bitory potency, whereas contacts provided by IPT might strengthen the Fe-N bond.

52 d randomized controlled trials that compared IPT to placebo or alternative regimen in HIV-positive, t

53 nducted a randomized 14-week trial comparing IPT, prolonged exposure (an exposure-based exemplar), an

54 In high-incidence settings, continuous IPT should be integrated with HIV care.

55 nity volunteers could be employed to deliver IPT during the peak malaria-transmission season and also

56 proven efficacious treatment for depression (IPT).

57 In anxiety disorders, IPT had large effects compared with control groups, and

58 trates for dimethylallyl diphosphate (DMAPP) IPT activity.

59 amine fail in children by day 14, the 2-dose IPT with sulfadoxine-pyrimethamine regimen continues to

60 Four trials compared 2-dose IPT with sulfadoxine-pyrimethamine to case management or

61 Eleven IPTs were resected without a morbidity event: eight for

62 e conducted to identify all trials examining IPT for any mental health problem.

63 rovement of >30% in CAPS score, were 63% for IPT, 47% for prolonged exposure, and 38% for relaxation

64 re 2.8 for BWL, 2.9 for CBTgsh, and 0.73 for IPT; for self-esteem, they were 2.4 for BWL, 1.9 for CBT

65 ere 2.4 for BWL, 1.9 for CBTgsh, and 0.9 for IPT.

66 -life of piperaquine makes it attractive for IPT.

67 DP appears well tolerated and effective for IPT.

68 DP appears well tolerated and effective for IPT.

69 for SPT, P = 0.030 and 0.8 +/- 0.2 mg/L for IPT, P = 0.001).

70 CAPS outcomes for IPT and prolonged exposure differed by 5.5 points (not s

71 er, the optimal drug and dosing regimens for IPT remain to be determined.

72 The chemorepellent Sema3F is required for IPT axon pruning, dendritic spine remodeling, and repuls

73 iduals [70.5%]) was more than twice that for IPT (24 [32.0%]) (relative risk, 2.20 [95% CI, 1.51-3.22

74 per week for CGT vs 0.75 points per week for IPT [t633 = 3.85; P < .001]), and the rate of improvemen

75 s of identifying those who will benefit from IPT are needed to permit appropriate targeting of this i

76 at proportions of patients will benefit from IPT if implemented without targeting according to TST st

77 ould be classified as likely to benefit from IPT if similar frequency thresholds were applied.

78 Flowers from IPT plants were less sensitive to exogenous ethylene and

79 Group IPT is a viable alternative to group CBT for the treatme

80 compares the effects of group CBT and group IPT across BED-related symptoms among overweight individ

81 weekly sessions of either group CBT or group IPT.

82 NCLUSIONS/SIGNIFICANCE: In most settings, if IPT is administered to PLWH pre-ART without assessment o

83 or adherence interventions when implementing IPT on a wider scale.

84 In IPT clusters, participants received the fixed-dose combi

85 ars in CMX (95% CI, 105.4-112.2) and 90.1 in IPT-SP (95% CI, 86.8-93.4) (not significant).

86 clusters, compared with 11.6% (61 of 528) in IPT clusters (relative risk [RR] 0.59, 95% CI 0.42-0.83,

87 9 were enrolled (744 in SST clusters, 681 in IPT clusters, and 854 in IST clusters).

88 T corollas, but this increase was delayed in IPT flowers.

89 irming that floral senescence was delayed in IPT plants.

90 5 (95%CI: 1.0, 6.5; p=0.048) times higher in IPT-unexposed women compared to IPT-exposed women after

91 interval, 1.0-6.5; P = .048) times higher in IPT-unexposed women compared with IPT-exposed women afte

92 auxin-mediated bud inhibition, and increased IPT transcript levels are not needed for bud release fol

93 dy demonstrated noninferiority of individual IPT for PTSD compared with the gold-standard treatment.

94 e no differences between women who initiated IPT antepartum or postpartum.

95 refore be taken into account when initiating IPT.

96 Scale-up of TB screening at ART initiation, IPT, and ART adherence interventions could significantly

97 eived three treatments at 4-month intervals (IPT n=3535, placebo n=3223).

98 ') plants expressing ISOPENTENYLTRANSFERASE (IPT; encoding the enzyme that mediates the rate-limiting

99 sion of at least one ISOPENTENYLTRANSFERASE (IPT) CK biosynthetic gene in the stem.

100 spite these recommendations, household-level IPT programs are rarely implemented in high TB burden se

101 e onset of major depression, and maintenance IPT significantly reduced relapse.

102 eekly, twice-monthly, or monthly maintenance IPT monotherapy for 2 years or until a recurrence of the

103 These results suggest that maintenance IPT, even at a frequency of only one visit per month, is

104 and the null hypothesis of more than minimal IPT inferiority was rejected (p=0.035).

105 Monthly IPT with dihydroartemisinin-piperaquine is a promising a

106 Monthly IPT with DP offered remarkable protection against clinic

107 Monthly IPT-DP was associated with an 84% reduction in the incid

108 Monthly IPT-DP was associated with fewer serious adverse events

109 in their first or second pregnancy, monthly IPT resulted in less placental malaria (RR, 0.34; 95% CI

110 1 dose than were women randomized to monthly IPT (relative risk, 16.4 [95% confidence interval, 4.0-6

111 Three trials compared 2-dose with monthly IPT with sulfadoxine-pyrimethamine during pregnancy.

112 ersonal psychotherapy for depressed mothers (IPT-MOMS), a nine-session intervention based on standard

113 have an N-terminal signal peptide, multiple IPTs and PbH1 repeats, a single transmembrane span (TM),

114 5 years and one in pregnant women), and nine IPT trials (five in children younger than 5 years, one i

115 thirty-six months of isoniazid (36H) and no IPT for HIV-infected patients in India.

116 severe illness than did deferred ART and no IPT, both overall and among patients with CD4+ counts of

117 .22 for 36H at three years as compared to no IPT.

118 ively at three-year follow-up compared to no IPT.

119 .33 to 0.94) and lower with IPT than with no IPT (adjusted hazard ratio, 0.65; 95% CI, 0.48 to 0.88;

120 ly-ART strategies and between the IPT and no-IPT strategies.

121 At least 26%, and maybe up to 57%, of IPT patients of European-American descent carried possib

122 After cessation of IPT, children who had previously received dihydroartemis

123 extended for up to 1 year after cessation of IPT.

124 luate the risk of malaria after cessation of IPT.

125 The combination of IPT and iron supplementation was most effective in the t

126 as being at higher risk of non-completion of IPT.

127 Thirty patients with diagnoses of IPT underwent standard ophthalmologic evaluation that in

128 ebo iron, after adjustment for the effect of IPT-SP, was 9.1 g/L (95% CI: 6.4, 11.8) and 8.2 g/L (4.0

129 or limiting the rollout and effectiveness of IPT and ICF is the limitations of existing tools to both

130 Further, the cost-effectiveness of IPT has not been studied in India.

131 l randomized trials examining the effects of IPT for all mental health problems was conducted.

132 We estimate the age-specific efficacy of IPT and BCG for preventing TB disease using data from a

133 sulfadoxine-pyrimethamine on the efficacy of IPT during pregnancy in Africa.

134 Data on the safety and efficacy of IPT in pregnant women living with HIV (PWLHIV) are mixed

135 Data on the efficacy of IPT with sulfadoxine-pyrimethamine on placental and peri

136 Efficacy of IPT with sulfadoxine-pyrimethamine was lower among women

137 In addition, O-Man glycosylation of IPT/TIG domains of plexins and hepatocyte growth factor

138 e impact of community-wide implementation of IPT for TB-HIV coinfected individuals on the dynamics of

139 f TST is not a requirement for initiation of IPT.

140 rican country, immediate ART and 6 months of IPT independently led to lower rates of severe illness t

141 The aim was to evaluate predictors of IPT non-completion.

142 arch is needed to confirm both the safety of IPT and new short-course TB preventive therapies during

143 research is needed to evaluate the safety of IPT and new short-course tuberculosis preventive therapi

144 rteen patients had 1-hour weekly sessions of IPT from the same supervised therapist (E.M.).

145 Intervention Twenty sessions of IPT or BWL or 10 sessions of CBTgsh during 6 months.

146 We aimed to compare two dosing strategies of IPT with dihydroartemisinin-piperaquine in young Ugandan

147 d, double-blind, placebo-controlled trial of IPT was done in 30 primary schools in western Kenya.

148 Nine trials of IPT with sulfadoxine-pyrimethamine during pregnancy in A

149 These findings support the use of IPT in older children and young-adult household contacts

150 acebo-controlled study comparing 28 weeks of IPT antepartum versus postpartum, were tested by QuantiF

151 performed genome-wide association studies of IPTs to identify regions and genes that account for this

152 Sixteen sessions of CGT (n = 74) or IPT (n = 77) delivered approximately weekly.

153 ry 7, 2013, and randomized to receive CGT or IPT.

154 Of 264 women randomly assigned to the CMX or IPT-SP group, 126 of 132 and 124 of 132, respectively, w

155 omly assigned to daily 800 mg/160 mg CMX, or IPT-SP.

156 n women were randomised to receive IST-DP or IPT-SP.

157 to receive daily treatment with proguanil or IPT with either MQAS or SPAQ once every 2 months at rout

158 eening for TB, and providing TB treatment or IPT in adults testing HIV positive in Sub-Saharan Africa

159 h protein-protein interaction sites on other IPT domains but that it is completely different from the

160 who require the addition of pharmacotherapy, IPT monotherapy represents a significantly less efficaci

161 2 weeks, daily iron and IPT with SP placebo, IPT and daily iron placebo, or daily iron placebo and IP

162 ccording to WHO criteria), deferred ART plus IPT, early ART (immediate ART initiation), or early ART

163 immediate ART initiation), or early ART plus IPT.

164 venlafaxine, 22.4 [3.1]; and posttreatment: IPT, 16.2 [7.1], and venlafaxine, 10.9 [8.6]).

165 entive therapy against malaria in pregnancy (IPT) with sulfadoxine-pyrimethamine (SP) in Malawi, the

166 ine (mean [SD] HAM-D scores at pretreatment: IPT, 22.7 [2.7], and venlafaxine, 22.4 [3.1]; and posttr

167 with BCG after IPT (n = 33) or without prior IPT (n = 39).

168 rth hotspot revealed a region across the PSI-IPT 1 domains not previously associated with HGF binding

169 directed against SEMA blades 2-3 and the PSI-IPT 1 region inhibited brain invasion and prolonged surv

170 Interpersonal psychotherapy (IPT) has been developed for the treatment of depression

171 Interpersonal psychotherapy (IPT) has been shown to reduce binge eating but its long-

172 Interpersonal psychotherapy (IPT) is an effective specialty treatment for binge eatin

173 drochloride and interpersonal psychotherapy (IPT) might each alter brain blood flow in some or all of

174 er frequency of interpersonal psychotherapy (IPT) sessions during maintenance treatment has a greater

175 authors tested interpersonal psychotherapy (IPT), which has demonstrated antidepressant efficacy and

176 ink-strength, we identified several putative IPT genes using a bioinformatics approach.

177 mptomatic older children who did not receive IPT.

178 n Patients were randomly assigned to receive IPT-A (n = 34) or TAU (n = 29) from school-based health

179 tly greater proportion of women who received IPT recovered from their depressive episode based on HRS

180 nt illness episodes in children who received IPT than those who received proguanil.

181 Women who received IPT were less likely to experience poor pregnancy outcom

182 y number was similar between women receiving IPT-SP and IPTp-MQ.

183 The signaling events that regulate IPT axon pruning are not known.

184 known pregnancy outcomes; 69 (46%) reported IPT initiation during pregnancy.

185 nia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

186 was induced under drought stress in P SARK ::IPT plants.

187 f transgenic rice plants expressing P SARK ::IPT, validated by qPCR, indicated that OsWRKY47 expressi

188 We investigated the effects of P(SARK)IPT (for Senescence-Associated Receptor KinaseIsopenteny

189 leaves from wild-type and transgenic P(SARK)-IPT plants grown under optimal or restricted watering.

190 rbon assimilation in the transgenic P(SARK)::IPT plants was well correlated with enhanced nitrate con

191 ffected by stress in the transgenic P(SARK)::IPT plants.

192 ed annual follow-up and continuous secondary IPT beyond the first year after treatment would avert an

193 costs) by strategies that included secondary IPT.

194 pletion combined with 12 months of secondary IPT would avert 2472 DALYs (95% UI -888 to 7801) over a

195 Strategies of follow-up without secondary IPT were dominated (ie, expected to result in lower heal

196 SP-IPT in infants and pregnant women is reported to have fa

197 tionship between resistance mutations and SP-IPT within target populations in the context of monitori

198 super resistant areas prompting review of SP-IPT use in affected areas.

199 21 in Papua) were randomly assigned to SST, IPT, or IST clusters (26 clusters each).

200 more in multigravidae receiving IST-DP than IPT-SP.

201 Combined treatment was more effective than IPT alone (g=0.24).

202 ontrol groups, and there is no evidence that IPT was less effective than CBT.

203 The authors hypothesized that IPT would be no more than minimally inferior (a differen

204 These results provide some reassurance that IPT can be safely used in the second or third trimester

205 se results may provide some reassurance that IPT can be safely used in the second or third trimester

206 We showed that IPT are genetically associated with substance use and AD

207 The IPT group also showed a decrease in total and LDL choles

208 The IPT reduced placental malaria (relative risk [RR], 0.48;

209 ART and early-ART strategies and between the IPT and no-IPT strategies.

210 dL (95% CI, -0.15-0.49 g/dL) greater for the IPT group.

211 terval [CI], 0.82-1.47 g/dL) greater for the IPT+iron group, 0.79 g/dL (95% CI, 0.46-1.10 g/dL) great

212 showed that compared with the TAU group, the IPT-A group showed significantly fewer clinician-reporte

213 ted alleles in CFH, CFB, and 10q loci in the IPT cohort were similar to those in the ethnically match

214 of anaemia at 12 months averaged 6.3% in the IPT group and 12.6% in the placebo group (adjusted risk

215 2604 children in the IPT group and 2302 in the placebo group were included in

216 d within 28 days of any treatment (19 in the IPT group and four in the placebo group); the main side-

217 35.2%] in the CGT group vs 41 [64.1%] in the IPT group were still at least moderately ill [P = .001])

218 al malaria in the CMX group vs. 24.6% in the IPT-SP group (not significant).

219 mia was 16.7% in the CMX group vs 28% in the IPT-SP group (P = .02).

220 the CMX group and 105 of 124 (84.7%) in the IPT-SP group remained malaria-free during their pregnanc

221 the CMX group, and 19 among 19 women in the IPT-SP group.

222 in transgenic plants, the expression of the IPT gene under control of senescence-associated promoter

223 artemisinin-piperaquine, on the basis of the IPT intervention received by the woman during pregnancy:

224 Adherence to the IPT regimens was excellent, but 57% of patients took <75

225 cause of symptoms at or death related to the IPT.

226 basal ganglia activation (P =.01), while the IPT group had limbic right posterior cingulate and right

227 ard (SPT) and intensive periodontal therapy (IPT) on serum inflammatory markers and cholesterol level

228 duals, where isoniazid preventative therapy (IPT) is given to those screening negative, and use value

229 olled trial of isoniazid preventive therapy (IPT) before revaccination with bacillus Calmette-Guerin

230 ion recommends isoniazid preventive therapy (IPT) for HIV-positive contacts and those younger than 5

231 Isoniazid preventive therapy (IPT) for HIV-TB coinfected individuals reduces the react

232 Trials of isoniazid preventive therapy (IPT) for people living with HIV in southern Africa have

233 mens for isoniazid-based preventive therapy (IPT) for tuberculosis (TB) in HIV-infected individuals h

234 ) who received isoniazid preventive therapy (IPT) had developed disease compared with 4 of 149 (2.6%)

235 ng or prior to isoniazid preventive therapy (IPT) in patients infected with human immunodeficiency vi

236 Isoniazid preventive therapy (IPT) is recommended as preventive therapy in HIV-infecte

237 Isoniazid preventive therapy (IPT) is widely used to protect against tuberculosis (TB)

238 othesized that isoniazid preventive therapy (IPT) may revert LTBI diagnoses because of its sterilizin

239 Isoniazid preventive therapy (IPT) reduces mortality among HIV-infected individuals in

240 Isoniazid preventive therapy (IPT) reduces mortality among individuals living with HIV

241 Isoniazid preventive therapy (IPT) was prescribed to <1% of ART enrollees not taking T

242 ) benefit from isoniazid preventive therapy (IPT) whereas those testing TST-negative do not.

243 and secondary isoniazid preventive therapy (IPT), alone and in combination, among individuals comple

244 (ART), 6-month isoniazid preventive therapy (IPT), or both among HIV-infected adults with high CD4+ c

245 apy (ART), and isoniazid preventive therapy (IPT).

246 ed nets and intermittent preventive therapy (IPT).

247 B treatment or isoniazid preventive therapy (IPT).

248 B treatment or isoniazid preventive therapy (IPT).

249 he-2) and removal of the isopropyl-thiazole (IPT) moiety affect affinity, inhibitory potency, and the

250 s mediated by a transcription factor Ig (TIG/IPT) domain, a fold found in the NF-kappaB family of tra

251 se significantly more than those assigned to IPT (P<.01 for both).

252 ychiatric treatment and randomly assigned to IPT-MOMS (N=26) or treatment as usual (N=21).

253 usual, the offspring of mothers assigned to IPT-MOMS showed significantly lower levels of depression

254 to treatment as usual, subjects assigned to IPT-MOMS showed significantly lower levels of depression

255 Assignment to IPT-MOMS was associated with reduced levels of maternal

256 es higher in IPT-unexposed women compared to IPT-exposed women after controlling for maternal age, CD

257 gned (1:1:1) via computer-generated lists to IPT, IST, or SST clusters.

258 Daily CMX was not noninferior to IPT-SP for preventing maternal malaria but safe and at l

259 d be prudent to do a sputum culture prior to IPT where this is feasible.

260 ART and on ART undergoing screening prior to IPT.

261 survival (OS) and minor morbidity related to IPT requiring hospitalization, transfusion, or nonsurgic

262 , perforation, bleeding, or death related to IPT.

263 tients (14%) with major morbidity related to IPT: 10 required surgery (eight, obstruction; one, perfo

264 ) and extend along the infrapyramidal tract (IPT) occurs during postnatal murine development by neuri

265 ANCE STATEMENT Impulsive personality traits (IPTs) are heritable traits that are governed by frontal-

266 okinin-synthesizing isopentenyl transferase (IPT) enzyme under the control of the Arabidopsis senesce

267 s, the discovery of isopentenyl transferase (IPT) genes in plants has shed light on the CK biosynthes

268 n with homology to isopentenyl transferases (IPTs), also causes CK-specific effects when expressed in

269 Intermittent preventive treatment (IPT) for malaria is used in infants, children, adults, a

270 effect of intermittent preventive treatment (IPT) in reducing anaemia and improving classroom attenti

271 Intermittent preventive treatment (IPT) in schoolchildren offers a promising option for mal

272 Intermittent preventive treatment (IPT) of malaria has recently been shown to be a highly e

273 Intermittent preventive treatment (IPT) of malaria with dihydroartemisinin-piperaquine is a

274 frica for intermittent preventive treatment (IPT) of malaria, but resistance threatens its efficacy.

275 t monthly intermittent preventive treatment (IPT) or intermittent screening and treatment (IST) with

276 t whether intermittent preventive treatment (IPT) with a fixed-dose combination of mefloquine-artesun

277 by either intermittent preventive treatment (IPT) with SP at 4 and 8 weeks and daily iron for 12 week

278 Intermittent preventive treatment (IPT) with sulphadoxine-pyrimethamine in vulnerable popul

279 methamine intermittent preventive treatment (IPT-SP) on malaria risk in HIV-positive pregnant women i

280 g with an asymptomatic intact primary tumor (IPT) and synchronous yet unresectable metastatic disease

281 proportional hazards model with time-updated IPT exposure.

282 indirectly, through hormone regulation using IPT and ESR1, has improved rates of stable transformatio

283 .05; odds ratios: BWL vs CBTgsh, 2.3; BWL vs IPT, 2.6; and CBTgsh vs IPT, 1.2).

284 CBTgsh, 2.3; BWL vs IPT, 2.6; and CBTgsh vs IPT, 1.2).

285 ticipants had achieved remission with weekly IPT or, if required, with weekly IPT plus antidepressant

286 with weekly IPT or, if required, with weekly IPT plus antidepressant pharmacotherapy, they were rando

287 We conclude that community-wide IPT in areas of emerging HIV and drug-resistant TB shoul

288 We found that community-wide IPT will reduce the incidence of TB in the short-term bu

289 zed that preclearance of latent bacilli with IPT modulates BCG immunogenicity following revaccination

290 ment option for most patients with BED, with IPT (or full cognitive behavior therapy) used for patien

291 morbid major depression may fare better with IPT than with prolonged exposure.

292 higher in IPT-unexposed women compared with IPT-exposed women after controlling for maternal age, CD

293 on has shown limbic blood flow increase with IPT yet not venlafaxine, while both treatments demonstra

294 , 0.56; 95% CI, 0.33 to 0.94) and lower with IPT than with no IPT (adjusted hazard ratio, 0.65; 95% C

295 xis for women who can achieve remission with IPT alone.

296 Among participants who remitted with IPT alone and entered maintenance treatment (N=99), 19 (

297 78-.87]); this association strengthened with IPT started after the first trimester compared with none

298 Adolescents treated with IPT-A compared with TAU showed greater symptom reduction

299 week with CGT and 0.39 points per week with IPT [t503 = 2.87; P = .004]).

300 Without IPT, projected life expectancy was 136.1 months at a lif