Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Statistical power analysis”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 739 records · Page 41Linked to original sources

Optimal allele-sharing statistics for genetic mapping using affected relatives.

The choice of allele-sharing statistics can have a great impact on the power of robust affected relative methods. Similarly, when allele-sharing statistics from several pedigrees are combined, the weight applied to each pedigree's statistic can affect power. Here we describe the direct connection between the affected relative methods and traditional parametric linkage analysis, and we use this connection to give explicit formulae for the optimal sharing statistics and weights, applicable to all pedigree types. One surprising consequence is that under any single gene model, the value of the optimal allele-sharing statistic does not depend on whether observed sharing is between more closely or more distantly related affected relatives. This result also holds for any multigene model with loci unlinked, additivity between loci, and all loci having small effect. For specific classes of two-allele models, we give the most powerful statistics and optimal weights for arbitrary pedigrees. When the effect size is small, these also extend to multigene models with additivity between loci. We propose a useful new statistic, S(rob dom), which performs well for dominant and additive models with varying phenocopy rates and varying predisposing allele frequency. We find that the statistic S(_#alleles), performs well for recessive models with varying phenocopy rates and varying redisposing allele frequency. We also find that for models with large deviation from null sharing, the correspondence between allele-sharing statistics and the models for which they are optimal may also depend on which method is used to test for linkage.

Alleles↗

Analyses of multinomial mixture distributions: new tests for stochastic models of cognition and action.

Mixture distributions are formed from a weighted linear combination of 2 or more underlying basis distributions [g(x) = sigma j alpha j fj(x); sigma alpha j = 1]. They arise frequently in stochastic models of perception, cognition, and action in which a finite number of discrete internal states are entered probabilistically over a series of trials. This article reviews various distributional properties that have been examined to test for the presence of mixture distributions. A new multinomial maximum likelihood mixture (MMLM) analysis is discussed for estimating the mixing probabilities alpha j and the basis distributions fj(x) of a hypothesized mixture distribution. The analysis also generates a maximum likelihood goodness-of-fit statistic for testing various mixture hypotheses. Stochastic computer simulations characterize the statistical power of such tests under representative conditions. Two empirical studies of mental processes hypothesized to involve mixture distributions are summarized to illustrate applications of the MMLM analysis.

Arousal↗

Cerebrospinal fluid tau protein shows a better discrimination in young old (<70 years) than in old old patients with Alzheimer's disease compared with controls.

Tau protein is consistently reported to be elevated in cerebrospinal fluid (CSF) of patients with Alzheimer's disease (AD). CSF tau alone, however, is not a clinically useful diagnostic marker due to its relatively low diagnostic specificity. Therefore, efforts are under way to combine tau measurements with other criteria in order to improve diagnostic applicability. We investigated whether age could serve as an useful criterion to increase diagnostic accuracy. CSF levels of tau were measured in young old (<70 years) and old old (> or =70 years) patients with probable AD, elderly patients with major depression (MD), and age-matched healthy controls (HC). In AD patients, CSF tau levels were significantly elevated compared with MD patients and HC (P < 0.001). Based on a previously established cut-off of 260 pg/ml, the discriminative power was higher in the young old than in the old old subjects. Similarly, receiver operating characteristics analysis revealed a statistically significant higher correct classification rate in the young old. Our findings indicate that the discriminative power of CSF tau is higher in the young than in the old old. We suggest that the effect of age should be considered in studies investigating CSF tau as a diagnostic marker for neurodegenerative disorders.

Age Distribution↗

EEG nonstationarity during intracranially recorded seizures: statistical and dynamical analysis.

OBJECTIVE: The investigation of nonstationarity in complex, multivariable signals, such as electroencephalographic (EEG) recordings, requires the application of different and novel approaches to analysis. In this study, we have divided the EEG recordings during epileptic seizures into sequential stages using spectral and statistical analysis, and have as well reconstructed discrete-time models (maps) that reflect dynamical (deterministic) properties of the EEG voltage time series. METHODS: Intracranial human EEG recordings with epileptic seizures from three different subjects with medically intractable temporal lobe epilepsy were studied. The methods of statistical (power spectra, wavelet spectra, and one-dimensional probability distribution functions) and dynamical (comparison of dynamical models) nonstationarity analysis were applied. RESULTS: Dynamical nonstationarity analysis revealed more detailed inner structure within the seizures than the statistical analysis. Three or four stages with different dynamics are typically present within seizures. The difference between interictal activity and seizure events was also more evident through dynamical analysis. CONCLUSIONS: Nonstationarity analysis can reveal temporal structure within an epileptic seizure, which could further understanding of how seizures evolve. The method could also be used for identification of seizure onset. SIGNIFICANCE: Our approach reveals new information about the temporal structure of seizures, which is inaccessible using conventional methods.

Electroencephalography↗

[HRV analysis system based on Windows 95 and its preliminary application].

Objective. To provide a real useful application system for the HRV research. Method. The acquisition, detection and analysis system of HRV signal was set up based on Windows 95. The system analyzes the HRV signal with statistic method in time domain and power spectrum in frequency domain. And the power spectrum array was also introduced into the analysis. HRV signals of some healthy persons and some patients were detected and analyzed. Result. The HRV characteristic is much more obvious in the diabetics patients. Conclusion. The system is useful in HRV signal analysis and cardiovascular research.

Aerospace Medicine↗

Analysis and design issues for studies using censored biomarker measurements with an example of viral load measurements in HIV clinical trials.

For many biomarkers, the range (L,R) over which they can be quantified is restricted by technical limitations, leading to some measurements that are left or right censored. However, despite the widespread availability of statistical methods for the analysis of censored data, many studies use an imputed value for censored measurements (for example, replacing a value <L by L, or by L/2). Commonly, an analysis that ignores such imputation is then used. In clinical trials, this leads to bias and a loss of power in evaluating treatment effects. In this paper, a review of appropriate statistical methods for parametric and non-parametric analysis of such measurements is presented. This includes methods for situations in which baseline measurements are available. New results concerning design issues such as sample size determination are also presented. The paper is illustrated using two examples of studies that included censored measurements of viral load in HIV-infected subjects.

Biomarkers↗

Phosphatidylserine: quantitative EEG effects in healthy volunteers.

Eight healthy paid male volunteers (age: 21-28 years, mean: 24.5 +/- 1.7 years; weight 62-79 kg) were administered via intravenous infusion (3 min) acute 25-, 50-, and 75-mg doses of phosphatidylserine, or matching placebo in a latin-square design. Multichannel EEG recordings were performed in baseline conditions, during intravenous infusion, and 10, 30, 90, 180, and 360 min after drug/placebo administration. Blood pressure, heart rate, critical flicker-fusion frequency, and the subjects' performance at immediate and short-term retention tests were assessed after each electroencephalographic (EEG) recording. The EEG signal was quantified off-line by power spectral analysis, and bidimensional scalp maps were produced for each EEG variable. Descriptive statistical comparisons among subjects and between pre- and postdrug EEG recordings allowed the detection of systematic EEG changes (notably increment of the power on the 'alpha' frequency, which was restricted to the anterior electrode deviations at the 50-mg dose and the widespread to the whole scalp at the highest dose, and increase of the signal total power) in the absence of significant modifications of the subjects' neuropsychological status.

Adult↗

Power analysis: Part II.

Explore the source record for details and available documents.

Data Interpretation, Statistical↗

IOLSTAT--a program for comprehensive intraocular lens equation comparison with statistical analysis.

A computer program that will simultaneously solve five of the major intraocular lens (IOL) equations predicting the primary implant power required for emmetropia or ametropia is presented. The program can, alternatively, predict the degree of ametropia given the power of an IOL. The resultant predictions are analyzed using weighted and unweighted statistics, predicting a mean and a standard deviation. The results are displayed in a table which lists the prediction and the percent deviation from the weighted mean for each equation. The program features automatic averaging of keratometer readings, ultrasound axial length corrections, and an algorithm for estimating postoperative anterior chamber depth.

Algorithms↗

1,1-Dichloro-2,2-bis(p-chlorophenyl)ethylene and polychlorinated biphenyls and breast cancer: combined analysis of five U.S. studies.

BACKGROUND: Environmental exposure to organochlorines has been examined as a potential risk factor for breast cancer. In 1993, five large U.S. studies of women located mainly in the northeastern United States were funded to evaluate the association of levels of 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene (DDE) and polychlorinated biphenyls (PCBs) in blood plasma or serum with breast cancer risk. We present a combined analysis of these results to increase precision and to maximize statistical power to detect effect modification by other breast cancer risk factors. METHODS: We reanalyzed the data from these five studies, consisting of 1400 case patients with breast cancer and 1642 control subjects, by use of a standardized approach to control for confounding and assess effect modification. We calculated pooled odds ratios (ORs) and 95% confidence intervals (CIs) by use of the random-effects model. All statistical tests were two-sided. RESULTS: When we compared women in the fifth quintile of lipid-adjusted values with those in the first quintile, the multivariate pooled OR for breast cancer associated with PCBs was 0.94 (95% CI = 0.73 to 1.21), and that associated with DDE was 0.99 (95% CI = 0.77 to 1.27). Although in the original studies there were suggestions of elevated breast cancer risk associated with PCBs in certain groups of women stratified by parity and lactation, these observations were not evident in the pooled analysis. No statistically significant associations were observed in any other stratified analyses, except for an increased risk with higher levels of PCBs among women in the middle tertile of body mass index (25-29.9 kg/m(2)); however, the risk was statistically nonsignificantly decreased among heavier women. CONCLUSIONS: Combined evidence does not support an association of breast cancer risk with plasma/serum concentrations of PCBs or DDE. Exposure to these compounds, as measured in adult women, is unlikely to explain the high rates of breast cancer experienced in the northeastern United States.

Body Weight↗

The analysis of repeated 'direct' measures of change illustrated with an application in longitudinal imaging.

The use of repeated measures of an outcome variable to improve statistical power and precision in randomized clinical trials and cohort studies is well documented. Linear mixed models have great utility in the analysis of such studies in many medical applications including imaging. However, in imaging studies and other applications the basic outcome can be a 'direct' measure of change in a variable, as opposed to a difference calculated by subtraction of one measured value from another. The correlation structure of such repeated measures of 'direct' change, in particular the non-independence of within-person consecutive measures, adds complexity to the analysis. In this paper, we present a family of hierarchical mixed models for the analysis of such data and explain how to implement them using standard statistical software. We illustrate the use of our models with data from a cohort of patients with Alzheimer's disease.

Alzheimer Disease↗

EEG mapping in patients with social phobia.

Recent studies have suggested an information-processing bias in social phobia (SP). Little is known about the electrophysiological correlates of anxiety in SP. The aim of the present study was to investigate the quantitative electroencephalogram (EEG) in 25 drug-free patients with SP as compared with age- and sex-matched normal controls and to correlate anxiety and depressive symptoms with EEG data. EEG was recorded under vigilance-controlled and resting conditions. The Spielberger State and Trait Anxiety Scale (STAI) and the Beck Depression Inventory (BDI) were administered to assess anxiety and depression levels. Multivariate analysis of variance revealed significant differences between patients and controls, specifically frontopolarly and right centrally. Statistical analysis demonstrated a decrease in absolute and relative delta, theta power, alpha-adjacent slow-beta and fast beta power and an increase in absolute and relative intermediate beta power, as well as an acceleration of the total centroid and a slowing in beta centroid and its variability. Trait anxiety and depression scores correlated positively with the dominant alpha frequency and the alpha centroid, and negatively with absolute theta and slow alpha power as well as with the centroid of the delta/theta frequency band. In conclusion, EEG mapping in patients with SP revealed significant differences from normal controls suggesting a hyperarousal as a pathogenetic factor of anxiety.

Adult↗

An integrated in silico gene mapping strategy in inbred mice.

In recent years in silico analysis of common laboratory mice has been introduced and subsequently applied, in slightly different ways, as a methodology for gene mapping. Previously we have demonstrated some limitation of the methodology due to sporadic genetic correlations across the genome. Here, we revisit the three main aspects that affect in silico analysis. First, we report on the use of marker maps: we compared our existing 20,000 SNP map to the newly released 140,000 SNP map. Second, we investigated the effect of varying strain numbers on power to map QTL. Third, we introduced a novel statistical approach: a cladistic analysis, which is well suited for mouse genetics and has increased flexibility over existing in silico approaches. We have found that in our examples of complex traits, in silico analysis by itself does fail to uniquely identify quantitative trait gene (QTG)-containing regions. However, when combined with additional information, it may significantly help to prioritize candidate genes. We therefore recommend using an integrated work flow that uses other genomic information such as linkage regions, regions of shared ancestry, and gene expression information to obtain a list of candidate genes from the genome.

Algorithms↗

Sample size estimation for the sorcerer's apprentice. Guide for the uninitiated and intimidated.

OBJECTIVE: To review the importance of and practical application of sample size determination for clinical studies in the primary care setting. QUALITY OF EVIDENCE: A MEDLINE search was performed from January 1966 to January 1998 using the MeSH headings and text words "sample size," "sample estimation," and "study design." Article references, medical statistics texts, and university colleagues were also consulted for recommended resources. Citations that offered a clear and simple approach to sample size estimation were accepted, specifically those related to statistical analyses commonly applied in primary care research. MAIN MESSAGE: The chance of committing an alpha statistical error, or finding that there is a difference between two groups when there really is none, is usually set at 5%. The probability of finding no difference between two groups, when, in actuality, there is a difference, is commonly accepted at 20%, and is called the beta error. The power of a study, usually set at 80% (i.e., 1 minus beta), defines the probability that a true difference will be observed between two groups. Using these parameters, we provide examples for estimating the required sample size for comparing two means (t test), comparing event rates between two groups, calculating an odds ratio or a correlation coefficient, or performing a meta-analysis. Estimation of sample size needed before initiation of a study enables statistical power to be maximized and bias minimized, increasing the validity of the study. CONCLUSION: Sample size estimation can be done by any novice researcher who wishes to maximize the quality of his or her study.

Humans↗

Progressive electroencephalogram frequency deceleration despite constant depth of propofol-induced sedation.

OBJECTIVE: To investigate a possible time-dependent effect of propofol sedation on electroencephalographic activity, we analyzed the electroencephalogram frequency behavior while keeping patients at a constant level of sedation. DESIGN: Prospective, controlled trial. SETTING: Intensive care unit of a university hospital. PATIENTS: Twenty patients without neurologic or metabolic disorders. MEASUREMENTS AND MAIN RESULTS: During sedation with propofol (1-4 mg x kg(-1) x hr(-1)), a bifrontally recorded processed electroencephalogram was obtained. For 48 hrs, sedation was kept constant at a level according to Ramsay Scale 3 while we adjusted the dosage of propofol given per hour. At hours 6, 18, 30, and 42, blood samples were taken to assess the plasma concentration of propofol. The electroencephalogram values of 60 mins obtained during 1 hr before blood sampling were taken for further calculation. From the data, relative band power of the beta-, alpha-, theta, and delta-bands, spectral median frequency, and spectral edge frequency 90 and 95 were computed. For statistical analysis, a polynomial three-factorial repeated-measures analysis of variance with covariates was performed. Relative power of beta- and alpha-wavebands showed a constant and significant decrease over time (beta, 15.5%, 10.3%, 10.3%, 7.6%; alpha, 14.8%, 13.4%, 10.0%, 8.3%), whereas relative delta power increased (delta, 56.4%, 63.4%, 70.7%, 72.3%). The theta-waveband remained unchanged. Accordingly, spectral edge frequency 90 and 95 and spectral median frequency decreased significantly. From hours 6 to 18, a significant increase of the plasma propofol concentration was found. Subsequently, the level remained constant. CONCLUSION: Despite constant sedation, a longer period of propofol application induces a time-dependent electroencephalogram frequency deceleration. The use of electroencephalogram derivatives to monitor depth of sedation in the intensive care unit thus should be regarded cautiously.

Adult↗

The usefulness of matched pair randomization for medical practice-based research.

To be feasible, study designs for most intervention research in primary care settings must limit the number of participating physicians, without sacrificing the statistical power required to test the research hypotheses. A model was developed to examine sample size and statistical power requirements when using the physicians' practice as the unit of analysis. Randomized designs using either matched or unmatched samples of practices were compared under varying conditions. When baseline variability is small or the number of practice pairs is large, matching at best marginally increases power. However, in the typical case when baseline variability is large or the number of practice pairs is small, matching substantially increases the power to find intervention effects with a smaller sample. Thus, matching prior to randomization could improve the design of many intervention studies in primary care settings.

Humans↗

Standardizing outcome data in program evaluation.

Procedures are described for standardizing outcomes in evaluations of service delivery systems. Accounting for the variability of a given device, client gains across services can be expressed in a standard metric of change. Standardized gains take on a common meaning of change regardless of the original scale and variability of the raw data. In return, a wide range of common statistical analyses can be applied with individual client gains as the units of analysis, powerfully delineating influences on outcome variability. Implications and limitations are discussed.

Community Mental Health Services↗