Emergence of childhood psychiatric disorders: a multivariate probit analysis.

Abstract:

:We applied a computationally practical form of probit analysis for multiple response variables to data on early childhood development of four psychiatric disorders: disruptive disorders (DD-attention deficit disorders, oppositional defiant disorder, conduct disorder); adjustment disorders (ADJ); emotional disorders (ED-all anxiety disorders, depression); and other DSM-III-R Axis I disorders (OTHER). In addition to estimating the intercept slope and higher order polynomial terms for each age versus diagnosis regression, we estimated simultaneously the correlation among the four diagnostic categories. We then took into account the correlation found among these four diagnostic categories when testing the hypothesis of no age effect, which would have been ignored in a piecemeal univariate approach. Regression lines for diagnostic prevalence indicate a linear increase for OTHER disorders, and a curvilinear increase for ED. We then used expected frequencies of individual response patterns (that is, the 2(4) = 16 possible diagnostic combinations) in obtaining more precise estimates of diagnostic comorbidity and its relation to age. We further generalize the Bock and Gibbons model to alternative specification of the random-effects distribution (that is, they assumed multivariate normality), illustrate how one can estimate the random-effects distribution empirically, and study the robustness of parameter estimates to specification of the random-effects distribution.

journal_name

Stat Med

journal_title

Statistics in medicine

authors

Gibbons RD,Lavigne JV

doi

10.1002/(sici)1097-0258(19981115)17:21<2487::aid-s

subject

Has Abstract

pub_date

1998-11-15 00:00:00

pages

2487-99

issue

21

eissn

0277-6715

issn

1097-0258

pii

10.1002/(SICI)1097-0258(19981115)17:21<2487::AID-S

journal_volume

17

pub_type

杂志文章
  • Comparison of trends in HIV infection for two risk categories.

    abstract::Sensible plans for health-care needs and determination of priorities for expenditure require regular assessment of trends in HIV incidences. In particular, trends in the relative HIV incidences of different risk categories are useful when assessing whether current control strategies are working equally well for all ri...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/(SICI)1097-0258(19960830)15:16<1779::AID-S

    authors: Becker NG,Cui JS

    更新日期:1996-08-30 00:00:00

  • Evaluating the cost-effectiveness of vaccination programmes: a dynamic perspective.

    abstract::Although there are many models which are used to calculate the health benefits (and thus the cost-effectiveness) of vaccination programmes, they can be divided into two groups: those which assume a constant force of infection, that is a constant per-susceptible rate of infection; and those which assume that the force ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-0258(19991215)18:23<3263::aid-s

    authors: Edmunds WJ,Medley GF,Nokes DJ

    更新日期:1999-12-15 00:00:00

  • Power analyses for longitudinal study designs with missing data.

    abstract::Existing methods for power analysis for longitudinal study designs are limited in that they do not adequately address random missing data patterns. Although the pattern of missing data can be assessed during data analysis, it is unknown during the design phase of a study. The random nature of the missing data pattern ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.2773

    authors: Tu XM,Zhang J,Kowalski J,Shults J,Feng C,Sun W,Tang W

    更新日期:2007-07-10 00:00:00

  • Analyzing longitudinal data to characterize the accuracy of markers used to select treatment.

    abstract::With the increasing availability of detailed clinical information, there is optimism that treatment choices can be selectively directed to those individuals most likely to benefit. While standard clinical trials can establish whether a treatment appears to be effective on average, subsequent work is needed to determin...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.6138

    authors: Sitlani CM,Heagerty PJ

    更新日期:2014-07-30 00:00:00

  • A joint modeling and estimation method for multivariate longitudinal data with mixed types of responses to analyze physical activity data generated by accelerometers.

    abstract::A mixed effect model is proposed to jointly analyze multivariate longitudinal data with continuous, proportion, count, and binary responses. The association of the variables is modeled through the correlation of random effects. We use a quasi-likelihood type approximation for nonlinear variables and transform the prop...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.7401

    authors: Li H,Zhang Y,Carroll RJ,Keadle SK,Sampson JN,Matthews CE

    更新日期:2017-11-10 00:00:00

  • Assessing local influence in principal component analysis with application to haematology study data.

    abstract::In many medical and health studies, high-dimensional data are often encountered. Principal component analysis (PCA) is a commonly used technique to reduce such data to a few components that includes most of the information provided by the original data. However, PCA is known to be very sensitive to some abnormal obser...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.2747

    authors: Fung WK,Gu H,Xiang L,Yau KK

    更新日期:2007-06-15 00:00:00

  • Two-stage sampling in pharmaceutical applications.

    abstract::In the pharmaceutical industry, some tests for quality assurance before, during and after the manufacture of a drug product involve a two-stage sampling technique. We propose statistical testing procedures in a two-stage sampling problem with large within-class sample sizes. We also derive a two-stage sampling plan by...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4780122104

    authors: Shao J,Chow SC

    更新日期:1993-11-15 00:00:00

  • Model selection techniques for the covariance matrix for incomplete longitudinal data.

    abstract::In longitudinal studies with incomplete data, where the number of time points can become numerous, it is often advantageous to model the covariance matrix. We describe several covariance models (for example, mixed models, compound symmetry, AR(1)-type models, and combination models) that offer parsimonious alternative...

    journal_title:Statistics in medicine

    pub_type: 杂志文章,评审

    doi:10.1002/sim.4780141302

    authors: Grady JJ,Helms RW

    更新日期:1995-07-15 00:00:00

  • Subject allocation and study curtailment for fixed event comparative Poisson trials.

    abstract::Comparative Poisson trials of prophylactic interventions, such as vaccines, can be lengthy and costly. We evaluate two easily implemented approaches to reduce numbers of disease cases and person years of follow up (N(u+t)) for comparative Poisson trials with fixed numbers of cases (T); (i) altering k the portion of N(...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.1724

    authors: Hoover DR

    更新日期:2004-04-30 00:00:00

  • The power to detect differences in average rates of change in longitudinal studies.

    abstract::With considerable current interest in longitudinal epidemiologic studies, little is available regarding sample size requirements. This paper considers a method for analysis of longitudinal data, where one compares the mean rates of change for two or more groups, and proposes a statistic for use in determining sample s...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4780090414

    authors: Lefante JJ

    更新日期:1990-04-01 00:00:00

  • Dynamic Cox modelling based on fractional polynomials: time-variations in gastric cancer prognosis.

    abstract::The most popular model used for survival analysis is the proportional hazards regression model proposed by Cox. This is mainly due to its exceptional simplicity. Nevertheless the fundamental assumption of the Cox model is the proportionality of the hazards. For many applications, however, this assumption is doubtful. ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.1411

    authors: Berger U,Schäfer J,Ulm K

    更新日期:2003-04-15 00:00:00

  • Latent transition analysis: inference and estimation.

    abstract::Parameters for latent transition analysis (LTA) are easily estimated by maximum likelihood (ML) or Bayesian method via Markov chain Monte Carlo (MCMC). However, unusual features in the likelihood can cause difficulties in ML and Bayesian inference and estimation, especially with small samples. In this study we explore...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.3130

    authors: Chung H,Lanza ST,Loken E

    更新日期:2008-05-20 00:00:00

  • A joint modeling approach to data with informative cluster size: robustness to the cluster size model.

    abstract::In many biomedical and epidemiological studies, data are often clustered due to longitudinal follow up or repeated sampling. While in some clustered data the cluster size is pre-determined, in others it may be correlated with the outcome of subunits, resulting in informative cluster size. When the cluster size is info...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4239

    authors: Chen Z,Zhang B,Albert PS

    更新日期:2011-07-10 00:00:00

  • Surveillance of clustering near point sources.

    abstract::Health authorities are often alerted to suspected cancer clusters near the vicinity of potential point sources by members of the public. A surveillance system, where administrative regions around the potential point sources are regularly monitored for high disease rates, would allow for responses which are easier to o...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-0258(19960415)15:7/9<727::aid-s

    authors: Le ND,Petkau AJ,Rosychuk R

    更新日期:1996-04-15 00:00:00

  • An extension of the continual reassessment method using decision theory.

    abstract::The primary goal of a phase I trial is to find the maximally tolerated dose (MTD) of a treatment. The MTD is usually defined in terms of a tolerable probability, q(*), of toxicity. Our objective is to find the highest dose with toxicity risk that does not exceed q(*), a criterion that is often desired in designing pha...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.970

    authors: Leung DH,Wang YG

    更新日期:2002-01-15 00:00:00

  • A note on sample size calculations for cluster randomised crossover trials with a fixed number of clusters.

    abstract::Girardeau, Ravaud and Donner in 2008 presented a formula for sample size calculations for cluster randomised crossover trials, when the intracluster correlation coefficient, interperiod correlation coefficient and mean cluster size are specified in advance. However, in many randomised trials, the number of clusters is...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.8191

    authors: Kelly TL,Pratt N

    更新日期:2019-08-15 00:00:00

  • A general frailty model to accommodate individual heterogeneity in the acquisition of multiple infections: An application to bivariate current status data.

    abstract::The analysis of multivariate time-to-event (TTE) data can become complicated due to the presence of clustering, leading to dependence between multiple event times. For a long time, (conditional) frailty models and (marginal) copula models have been used to analyze clustered TTE data. In this article, we propose a gene...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.8506

    authors: Tran TMP,Abrams S,Braekers R

    更新日期:2020-05-30 00:00:00

  • Computational methods in medical decision making: to screen or not to screen?

    abstract::Screening for a disease such as cancer is often regarded as a beneficial and successful strategy for reducing mortality. However, as with any clinical treatment or intervention, benefit cannot be assumed, and screening can entail both costs and harms, so the screening as a 'treatment' must undergo evaluation. An evalu...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.2037

    authors: Kafadar K,Prorok PC

    更新日期:2005-02-28 00:00:00

  • Minimum sample size for developing a multivariable prediction model: PART II - binary and time-to-event outcomes.

    abstract::When designing a study to develop a new prediction model with binary or time-to-event outcomes, researchers should ensure their sample size is adequate in terms of the number of participants (n) and outcome events (E) relative to the number of predictor parameters (p) considered for inclusion. We propose that the mini...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.7992

    authors: Riley RD,Snell KI,Ensor J,Burke DL,Harrell FE Jr,Moons KG,Collins GS

    更新日期:2019-03-30 00:00:00

  • Bayesian clinical trials in action.

    abstract::Although the frequentist paradigm has been the predominant approach to clinical trial design since the 1940s, it has several notable limitations. Advancements in computational algorithms and computer hardware have greatly enhanced the alternative Bayesian paradigm. Compared with its frequentist counterpart, the Bayesi...

    journal_title:Statistics in medicine

    pub_type: 杂志文章,评审

    doi:10.1002/sim.5404

    authors: Lee JJ,Chu CT

    更新日期:2012-11-10 00:00:00

  • The analysis of incomplete data in the three-period two-treatment cross-over design for clinical trials.

    abstract::The additional time to complete a three-period two-treatment (3P2T) cross-over trial may cause a greater number of patient dropouts than with a two-period trial. This paper develops maximum likelihood (ML), single imputation and multiple imputation missing data analysis methods for the 3P2T cross-over designs. We use ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/(SICI)1097-0258(19960130)15:2<127::AID-SIM

    authors: Richardson BA,Flack VF

    更新日期:1996-01-30 00:00:00

  • The probability of a cancer cluster due to chance alone.

    abstract::We propose to use a very simple model to test whether a cancer cluster is due to chance alone. We focus on the acute childhood leukaemia cluster in Columbus, Ohio. In 1975, 12 leukaemia cases were observed in Columbus while the expected number is 6 cases per year. According to our simple model, the probability of such...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/1097-0258(20000830)19:16<2195::aid-sim522>

    authors: Schinazi RB

    更新日期:2000-08-30 00:00:00

  • Box-Cox transformation of left-censored data with application to the analysis of coronary artery calcification and pharmacokinetic data.

    abstract::Box-Cox transformation is investigated for regression models for left-censored data. Examples are provided using coronary calcification data from the Multi-Ethnic Study of Atherosclerosis and pharmacokinetic data of a nicotine nasal spray. ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.1925

    authors: Han C,Kronmal R

    更新日期:2004-12-15 00:00:00

  • An immigration-death model to estimate the duration of malaria infection when detectability of the parasite is imperfect.

    abstract::Immigration-death models are proposed to analyse the infection dynamics in longitudinal studies of panels of heavily parasitized human hosts where parasites have been typed at regular intervals by PCR. Immigration refers to the acquisition of a new parasitic genotype, occurring at rate lambda, and death refers to the ...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.2189

    authors: Sama W,Owusu-Agyei S,Felger I,Vounatsou P,Smith T

    更新日期:2005-11-15 00:00:00

  • The statistical analysis of treatment effects in 24-hour ambulatory blood pressure recordings.

    abstract::This paper presents a statistical analysis of treatment effects in 24-hour ambulatory blood pressure recordings. The statistical models account for circadian rhythms, subject effects, and the effects of treatment with drugs or relaxation therapy. In view of the heterogeneity of the subjects, we fit a separate linear m...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4780070608

    authors: Marler MR,Jacob RG,Lehoczky JP,Shapiro AP

    更新日期:1988-06-01 00:00:00

  • Identifying representative trees from ensembles.

    abstract::Tree-based methods have become popular for analyzing complex data structures where the primary goal is risk stratification of patients. Ensemble techniques improve the accuracy in prediction and address the instability in a single tree by growing an ensemble of trees and aggregating. However, in the process, individua...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4492

    authors: Banerjee M,Ding Y,Noone AM

    更新日期:2012-07-10 00:00:00

  • Reflecting on "A Statistician in Medicine" in 2020.

    abstract::In this commentary, we revisit Sir Austin Bradford Hill's seminal Alfred Watson Memorial Lecture in 1962 through the eyes of two practicing biostatisticians of the current era. We summarize some eternal takeaway messages from Hill's lecture regarding observations and experiments translated through the modern lexicon o...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.8830

    authors: Dempsey W,Mukherjee B

    更新日期:2021-01-15 00:00:00

  • Sample size to test for interaction between a specific exposure and a second risk factor in a pair-matched case-control study.

    abstract::We discuss a sample size calculation for a pair-matched case-control study to test for interaction between a specific exposure and a second risk factor. The second risk factor could be either binary or continuous. An algorithm for the calculation of sample size is suggested which is based on a logistic regression mode...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-0258(20000415)19:7<923::aid-sim

    authors: Qiu P,Moeschberger ML,Cooke GE,Goldschmidt-Clermont PJ

    更新日期:2000-04-15 00:00:00

  • Robust Bayesian sample size determination in clinical trials.

    abstract::This article deals with determination of a sample size that guarantees the success of a trial. We follow a Bayesian approach and we say an experiment is successful if it yields a large posterior probability that an unknown parameter of interest (an unknown treatment effect or an effects-difference) is greater than a c...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.3175

    authors: Brutti P,De Santis F,Gubbiotti S

    更新日期:2008-06-15 00:00:00

  • Subgroup identification from randomized clinical trial data.

    abstract::We consider the problem of identifying a subgroup of patients who may have an enhanced treatment effect in a randomized clinical trial, and it is desirable that the subgroup be defined by a limited number of covariates. For this problem, the development of a standard, pre-determined strategy may help to avoid the well...

    journal_title:Statistics in medicine

    pub_type: 杂志文章

    doi:10.1002/sim.4322

    authors: Foster JC,Taylor JM,Ruberg SJ

    更新日期:2011-10-30 00:00:00