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Article

A New Extended Weibull Distribution with Application to Influenza and Hepatitis Data

by
Gauss M. Cordeiro
1,*,
Elisângela C. Biazatti
2 and
Luís H. de Santana
3
1
Department of Statistics, Federal University of Pernambuco, Recife 50670-901, Brazil
2
Department of Mathematics and Statistics, Federal University of Rondônia, Ji-Paraná 76900-726, Brazil
3
Department of Technology, State University of Maringá, Umuarama 87506-370, Brazil
*
Author to whom correspondence should be addressed.
Stats 2023, 6(2), 657-673; https://doi.org/10.3390/stats6020042
Submission received: 29 April 2023 / Revised: 13 May 2023 / Accepted: 17 May 2023 / Published: 19 May 2023
(This article belongs to the Section Regression Models)

Abstract

:
The Weibull is a popular distribution that models monotonous failure rate data. In this work, we introduce the four-parameter Weibull extended Weibull distribution that presents greater flexibility, thus modeling data with bathtub-shaped and unimodal failure rate. Some of its mathematical properties such as quantile function, linear representation and moments are provided. The maximum likelihood estimation is adopted to estimate its parameters, and the log-Weibull extended Weibull regression model is presented. In addition, some simulations are carried out to show the consistency of the estimators. We prove the greater flexibility and performance of this distribution and the regression model through applications to influenza and hepatitis data. The new models perform much better than some of their competitors.

1. Introduction

The Weibull is a traditional distribution for positive real data. However, it does not accommodate data with unimodal hazard function or bathtub shape. Several modifications of the Weibull appeared to model non-monotone hazard rates, including the extended Weibull (EW) model [1]. There are also many references regarding extensions in which one seeks to obtain hazard functions that are unimodal or bathtub shaped (see [2,3,4], which provide a survey of the modified Weibull distributions). Most recently, refs. [5,6] defined the Maxwell-Weibull and the alpha power Kumaraswamy Weibull, respectively.
Two papers on EW distribution  [7,8] have been most seminal in that they pioneered the development of distributions for bathtub-shaped hazard rates. Since the publication of these papers, many distributions and in particular other generalizations of the two-parameter Weibull distribution have been proposed, each allowing for non-monotone and bathtub-shaped hazard rates. It has been proven in the literature that the EW distribution provides significantly better fits than traditional models based on the exponential, gamma, Weibull and lognormal distributions. Thus, this is a central point to choose this distribution for the baseline model in this article.
The Weibull-G (W-G) class [9] is still little explored when compared to other competitors. Some recently proposed distributions within this class are: Weibull–Dagum [10], Weibull–Kumaraswamy [11], Weibull Birnbaum–Saunders [12], Weibull inverse Lomax [13] and Weibull–Power Lomax [14]. Recently, ref. [15] addressed the Weibull–Beta Prime distribution.
Some works using influenza data are studied from a non-parametric point of view [16] or by using logistic regression [17] and functional data analysis [18]. On the other hand, spatial regression [19], machine learning models [20], Markov chains [21], and epidemiological models involving the fractal–fractional Caputo category [22] have been used in studies with hepatitis data. Our main idea with applications to real data is to show the flexibility of the new distribution that adds one more parameter in the EW distribution as well as to the new log-Weibull extended Weibull (LWEW) regression model. As examples of the application of these models, we use time data (in days), which comprises the date of hospitalization until cure of influenza patients. To apply the LWEW regression model, a data set obtained from the literature of a study with hepatitis patients is used, in which the variable of interest is the time until death from hepatitis. The result “time until the occurrence of an event of interest” is the variable of interest in survival analysis studies, and one of the main characteristics of this type of study is censoring, i.e., the partial observation of the response. Furthermore, when considering the regression structure, we can analyze possible influences of characteristics of individuals in the sample under study on the response variable.
The three-parameter EW probability density function (pdf) of the random variable X is
g ( x ) = λ β x β 1 ( 1 + α λ x β ) 1 α 1 , α > 0 , λ β x β 1 e λ x β , α = 0 ,
where α 0 and β > 0 are the shapes, and λ > 0 is the scale. The support of the EW distribution is R + , and its rth ordinary moment becomes
E ( X r ) = λ r / β α r / β 1 B ( r / β + 1 , 1 / α r / β ) , α > 0 and r < β / α , λ r / β Γ ( r / β + 1 ) , α = 0 ,
where Γ ( · ) and B ( · , · ) are the gamma and beta functions, respectively.
For lifetime models, it is of interest to know the rth incomplete moment of X, say T r ( x ) = 0 x u r f ( u ) d u , which has the form
T r ( x ) = λ β x r + β r + β 2 F 1 ( 1 / α + 1 , r / β + 1 ; r / β + 2 , α λ x β ) , α > 0 , λ r / β γ ( r / β + 1 , λ x β ) , α = 0 ,
where 2 F 1 is the hypergeometric function defined by
2 F 1 ( a 1 , a 2 ; a 3 , x ) = Γ ( a 3 ) Γ ( a 1 ) Γ ( a 2 ) j = 0 Γ ( a 1 + j ) Γ ( a 2 + j ) Γ ( a 3 + j ) x j j ! ,
and γ ( s , x ) = 0 x t s 1 e t d t , s > 0 , is the incomplete gamma function.
We define the Weibull extended Weibull (WEW) distribution in Section 2. The quantile function (qf) and linear representation are reported in Section 3. Estimation by the maximum likelihood method is discussed in Section 4. A simulation and a misspecification study are presented in Section 5. We define the log-Weibull extended Weibull (LWEW) regression in Section 6 and perform a simulation study for this model. Applications to influenza and hepatitis data are reported in Section 7. Some conclusions are summarized in Section 8.

2. The WEW Distribution

Consider the W-G class of distributions [9] with scale a = 1 and shape b > 0 . By taking the pdf (1) for the baseline in this class, the cumulative distribution function (cdf) and pdf of the WEW distribution become (for x > 0 )
F ( x ) = 1 exp ( 1 + α λ x β ) 1 α 1 b , α > 0 , 1 exp e λ x β 1 b , α = 0 ,
f ( x ) = b λ β x β 1 ( 1 + α λ x β ) 1 α 1 ( 1 + α λ x β ) 1 α 1 b 1 × exp ( 1 + α λ x β ) 1 α 1 b , α > 0 , b λ β x β 1 e λ x β e λ x β 1 b 1 exp e λ x β 1 b , α = 0 ,
respectively.
Henceforth, we change the notation and let X W E W ( b , α , β , λ ) have pdf (5). The WEW distribution has some special cases: the EW when b = 1 , W-Weibull (WW) when α = 0 , W-exponential (WE) when α = 0 and β = 1 .
Figure 1 and Figure 2 report the densities and hazard rate functions (hrfs) for fixed parameters, respectively. Plots of the WEW hrf can be inverted bathtub, bathtub, monotonically increasing, and monotonically decreasing.

3. Properties

3.1. Quantile Function

By inverting (4) (for u ( 0 , 1 ) ), the qf of X (for α > 0 ) has the form
x = F 1 ( u ) = α 1 λ 1 log ( 1 u ) 1 / b + 1 α 1 1 / β .
Plots of the Bowley skewness (b) [23] and Moors kurtosis (M) [24] of X (based on quantiles) are displayed in Figure 3 and Figure 4, respectively.
In Figure 3a, the skewness B decreases (for fixed β ) when b grows. In Figure 3b, B increases to β = 0.5 when α increases, but for larger values of β fixed, it tends to become constant. In Figure 3c, B decreases (for any α ) when β grows.
In Figure 4a, the kurtosis M decreases for β = 1 if b grows. For high values of β (fixed), M drops drastically when b grows, and after that, this curvature will be reversed, and then, M increases when b grows. In Figure 4b, as the parameter α increases, M is increasing for β = 0.3 , β = 0.5 and β = 1 , and it tends to become constant for β = 2 . In Figure 4c, M decreases for any α when β grows.

3.2. Linear Representation

In Appendix A, it is given a linear representation for the WEW pdf, namely
f ( x ) = i = 0 e i ( b ) g ( x ; α i , β , λ i ) , if α > 0 , i = 0 e i ( b ) g ( x ; β , λ i ) , if α = 0 ,
where (for i 0 ) α i = ( i + 1 ) 1 α , λ i = ( i + 1 ) λ ,
e i ( b ) = ( 1 ) i ( i + 1 ) j , k = 0 [ ( k + 1 ) b + j ] ( k + 1 ) b + j 1 i p j , k ( b )
and
p j , k ( b ) = ( 1 ) j + k b [ ( k + 1 ) b + j ] k ! [ ( k + 1 ) b + 1 ] j .
In conclusion, this representation is important since complete and incomplete moments, generating function, mean deviations, and reliability of X can be determined from those of the EW distribution.

3.3. Moments

We can study some important characteristics of the distribution through moments.
It follows from Equations (2), (A5) and (A6)
μ r = E ( X r ) = 1 λ r / β α r / β + 1 i = 0 ( i + 1 ) e i ( b ) B ( r / β + 1 , 1 + i / α r / β ) , if α > 0 and r < β / α , Γ ( r / β + 1 ) λ r / β i = 0 e i ( b ) ( i + 1 ) r / β , if α = 0 .
It is simple to verify from Equations (3), (A5) and (A6) that T r ( x ) can be expressed as
T r ( x ) = β x r + β r + β i = 0 e i ( b ) λ i 2 F 1 ( 1 / α i + 1 , r / β + 1 ; r / β + 2 , α i λ i x β ) , if α > 0 , λ r / β i = 0 e i ( b ) ( i + 1 ) r / β γ ( r / β + 1 , ( i + 1 ) λ x β ) , if α = 0 .
We can obtain the mean deviations and Lorenz and Bonferroni curves from the first incomplete moment.

4. Estimation

Let x 1 , , x n be a sample of size n from (5). The log-likelihood function for θ = ( b , α , β , λ ) from this sample reduces to
l ( θ ) = n ln b λ β + ( β 1 ) i = 1 n ln ( x i ) + 1 a 1 i = 1 n ln ( 1 + α λ x i β ) + ( b 1 ) i = 1 n ln ( 1 + α λ x i β ) 1 α 1 i = 1 n ( 1 + α λ x i β ) 1 α 1 b , α > 0 , n ln b λ β + ( β 1 ) i = 1 n ln ( x i ) + λ i = 1 n x i β + ( b 1 ) i = 1 n ln e λ x β 1 i = 1 n e λ x β 1 b , α = 0 .
Equation (10) for α = 0 gives the log-likelihood for the WW distribution. The maximum likelihood estimates (MLEs) can be found by maximizing l ( θ ) using the AdequecyModel library [25] of the R software; another option is the maxLik function via the maxLik library that provides a convenient interface for the MLEs [26], or by the optim function by selecting an optimization method, for example, BFGS, CG, and SANN, and still finding the Hessian matrix. We also can maximize (10) numerically using SAS (PROCNLMIXED) or the Ox program (sub-routine MaxBFGS), among others. The score components in U ( θ ) = ( U b , U α , U β , U λ ) (for α > 0 ) are reported in Appendix A.

5. Simulation Study

5.1. Simulations for the WEW Distribution

A Monte Carlo simulation study was conducted, using the BFGS algorithm in R software, to examine the accuracy of the MLEs of the parameters of X. Here, 1000 replications (for n = 50 , 100 and 300) were generated from Equation (6), where u U ( 0 , 1 ) . The scenarios under study were: b = 2 , α = 3 , β = 0.2 and λ = 2 (Setup 1—decreasing density curve; see Figure 1a); b = 1.2 , α = 0.5 , β = 1.5 and λ = 2 (Setup 2—unimodal density curve; see Figure 1d); and b = 1.5 , α = 0.2 , β = 2 and λ = 0.2 (Setup 3—platykurtic unimodal density curve; see Figure 1c).
We calculated the average estimates, biases and mean squared errors (MSEs) in Table 1. The biases and MSEs decrease when n grows. Thus, the estimators are consistent.

5.2. Misspecification Study

We investigated the behavior of the MLEs of the parameters in the WEW distribution when it was poorly specified by carrying out Monte Carlo simulations based on 1000 replications (for n = 100). The observations were simulated by taking b = 0.8 , α = 3 , β = 2 and λ = 3 . We used the maxLik library with the SANN method for each generated data set. In Table 2, the observed values are generated from the Gamma Extended Weibull (GEW) distribution [27] by taking a = 0.8 , α = 3 , β = 2 , and λ = 3 . In Table 3, the observed values are generated from the EW distribution by setting α = 3 , β = 2 , and λ = 3 . Further, in Table 4, the observed values are generated from the WW distribution with b = 0.8 , β = 2 , and λ = 3 .
In addition to the average estimates (AEs), the relative biases (RB), and MSEs, we present the mean measures of global deviance (GD), say G D = 2 l ( θ ^ ) , where l ( θ ^ ) is the maximized log-likelihood function (10), AIC and BIC. They indicate that there are small sample biases in the parameter estimation. The average measures of GD, AIC and BIC for the estimated WEW distribution are very close to those values obtained from the true distributions used in the generation of the observed values. Hence, the WEW distribution provides consistent MLEs even when the data are generated from different distributions.
Clearly, the goodness-of-fit measures (GD, AIC, and BIC) are lower for the distribution from which the data are generated.

6. The LWEW Regression Model

If X has the WEW pdf (5), then Y = l o g ( X ) has the log-Weibull extended Weibull (LWEW) pdf (with real support) reparameterized in terms of σ = β 1 and μ = σ log ( λ ) , which can be expressed as (for y R )
f ( y ) = b σ exp y μ σ 1 + α exp y μ σ 1 α 1 1 + α exp y μ σ 1 / α 1 b 1 × exp 1 + α exp y μ σ 1 / α 1 b , , if α > 0 , b σ exp y μ σ + exp y μ σ e e y μ σ 1 b e e y μ σ 1 b 1 , if α = 0 ,
where b , α , σ > 0 and μ R . For α = 0 , we obtain the log-Weibull Weibull (LWW) model, where μ is a location and σ is a scale.
The survival function of Y has the form
S ( y ) = exp 1 + α exp y μ σ 1 / α 1 b , α > 0 , exp e e y μ σ 1 b , α = 0 .
The density of Z = ( Y μ ) / σ (for z R ) can be expressed as
π ( z ) = b exp z 1 + α exp z 1 α 1 1 + α exp z 1 / α 1 b 1 × exp 1 + α exp z 1 / α 1 b , if α > 0 , b exp z + exp z e e z 1 b e e z 1 b 1 , if α = 0 .
We construct a regression based on the LWEW distribution
y i = v i γ + σ z i , i = 1 , , n ,
where z i has pdf (13), γ = ( γ 1 , , γ p ) is the vector of coefficients, and v i = ( v i 1 , , v i p ) is the vector of covariates for the ith response y i , which models the location parameter μ i = v i γ .
Consider that F and C are groups of individuals that failed and are censored, respectively. The log-likelihood for θ = ( b , α , σ , γ ) can be found from (13) and (14) as
l ( θ ) = q [ ln ( b ) ln ( σ ) ] + i F z i + ( 1 α 1 ) i F ln [ 1 + α exp ( z i ) ] + ( b 1 ) i F ln { [ 1 + α exp ( z i ) ] 1 a 1 } i F 1 + α exp z i 1 a 1 b ( n q ) i C 1 + α exp z i 1 a 1 b , if α > 0 , q [ ln ( b ) ln ( σ ) ] + i F z i + i F exp ( z i ) + ( b 1 ) i F e e z i 1 i F e e z i 1 b ( n q ) i C e e z i 1 b , if α = 0 ,
where q is the number of failures, and z i = ( y i v i γ ) / σ . The MLE θ ^ of θ can be found by maximizing (15).

Regression Simulation Study

A simulation study was conducted using the BFGS algorithm in R to examine the accuracy of the MLEs of the LWEW regression model with parameters: γ 0 = 2.2 , γ 1 = 1.2 , σ = 1.5 , b = 2 and α = 5 . We considered 1000 Monte Carlo replications for n = 30 , 50, and 100, and censoring percentages 0%, 10%, 30%, and 66% generated using the inverse transformation method. Occurrences of the Bernoulli distribution with success probability ( 1 p ) are generated to obtain the censored observations, where p is the percentage of censoring. The location parameter is μ = γ 0 + γ 1 v i 1 , where v i 1 U ( 0 , 1 ) .
The AEs, biases, and MSEs are reported in Table 5. The biases and MSEs usually decrease when n grows. By increasing the percentage of censoring for a fixed sample size, the biases and MSEs decrease for most AEs. Thus, an improvement in the accuracy of the estimators occurs.
Clearly, it is not possible to note the same behavior for b. This can be explained, probably, because the estimators are naturally biased since the likelihood function in the presence of censoring has the contribution of the survival function.

7. Applications

7.1. The WEW Distribution

Consider a data set from the City of São Paulo (Brazil) obtained from the Severe Acute Respiratory Syndrome on the platform of the Ministry of Health (BD-SRAG at https://opendatasus.saude.gov.br/dataset/srag-2021-a-2023, accessed on: 26 May 2022), which comprises events from 31 December 2021 to March 2022. The data set passed for a filter process to obtain the 162 times (measured in days) of influenza patients from the date of admission to the hospital until cure.
In this application, we fit the WEW distribution and compared it with some special cases and competitive four-parameter distributions: GEW [27], KwW [28], BW [29], Beta Exponentiated Exponential (BEE) [30], Kumaraswamy–Gama (KwGa) [31], and Beta–Gama (BGa) [32].
The MLEs and their standard errors (SEs between parentheses) found via the SANN method (with AdequacyModel, GenSA and MASS libraries from R software) are reported in Table 6. We adopted the well-known W * , A * and KS statistics (with abbreviations in place of full names) to compare the WEW distribution with some competitive distributions. We used AIC, CAIC, and BIC to compare the new distribution with some special cases. The findings are reported in Table 7. Further, the likelihood ratio (LR) in Table 6 confirms the superiority of the WEW distribution for these data.
Further, we compared the proposed distribution with the previous models via the generalized likelihood ratio (GLR) test [33]. The results in Table 8 indicate that the WEW distribution is the most suitable model. The histogram and the best four fitted pdfs are displayed in Figure 5a. Figure 5b reports the empirical and estimated cdfs. They also reveal the superiority of the WEW distribution.

7.2. The LWEW Regression Model

We used a data set from a randomized clinical trial carried out to investigate the effect of therapy with steroids in the treatment of acute viral hepatitis [34]. Twenty-nine patients with this disease were randomized to receive either a placebo (lactose) or the steroid (Methylprednisolone) treatment. Each patient was followed for 16 weeks or until death (event of interest) or even loss of follow-up (censoring). The observed survival times, in weeks, for the two groups are reported in Table 9. The explanatory variable in this work is taken as: ( v 1 ): treatment (placebo = 1, steroid = 2).
We fit the LWEW regression model
y i = γ 0 + γ 1 v i 1 + σ z i ,
where z i has pdf (13).
Some competing models for the regression modeling are: log-gamma extended Weibull (LGEW) [27], log-beta Weibull (LBW) [35], and log-Kumaraswamy–Weibull or Kumaraswamy Gumbel (KwGu) [36].
Table 10 provides the MLEs for the fitted LWEW, LEW, LWW, LGEW, LBW and KwGu regressions via the maxLik function and the BFGS method in R software. The codes can be accessed at https://github.com/elisangelacbiazatti/WEW (accessed on 28 April 2023). This table shows that the LWEW is the best model. The LR statistic confirms the superiority of the LWEW model for both its sub-models at the 1% level of significance. Further, control treatment and steroids are statistically different. Thus, patients who received control treatment had a shorter time to death than patients who received steroids, since the estimate of the coefficient of the treatment variable ( v 1 ) is negative.
The plots of the Kaplan–Meier and estimated survival functions in Figure 6 support that the LWEW model is the best among the fitted models.
The plot of the deviance residuals randomized around zero is reported in Figure 7a. A normal plot with an envelope is shown in Figure 7b. The model fits the data reasonably well.

8. Conclusions

We introduced the Weibull extended Weibull density and provided some of its properties. The consistency of the maximum likelihood estimators is proven by a simulation study. An application to real influenza data revealed its flexibility. We constructed a regression model log-Weibull extended Weibull and performed some simulations to study the behavior of the estimators in small and large samples. We compared the fit to acute viral hepatitis data with other existing models and performed a residual analysis study for the final model. Overall, the two applications showed the utility of the new models for symmetric and asymmetric data, censored or uncensored. In future works, we can, for example, select other systematic components for the regression model and, as an alternative method, present the estimation of the model parameters from the Bayesian approach.

Author Contributions

Conceptualization, G.M.C. and E.C.B.; methodology, G.M.C., E.C.B. and L.H.d.S.; software, E.C.B.; validation, G.M.C. and E.C.B.; formal analysis, G.M.C. and E.C.B.; investigation, G.M.C. and E.C.B.; data curation, G.M.C. and E.C.B.; writing—original draft preparation, G.M.C., E.C.B. and L.H.d.S.; writing—review and editing, G.M.C., E.C.B. and L.H.d.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Stated in the text.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A. Linear Representation

By the exponential power series, we have
exp G ( x ) G ¯ ( x ) b = k = 0 ( 1 ) k k ! G ( x ) k b G ¯ ( x ) k b .
Substituting (A1) in the W-G pdf (with a = 1 ) [9]
f ( x ) = b g ( x ) k = 0 ( 1 ) k k ! G ( x ) ( k + 1 ) b 1 G ¯ ( x ) [ ( k + 1 ) b + 1 ] .
The generalized binomial theorem holds (for any real c)
( 1 + z ) c = j = 0 c j z j , | z | < 1 ,
where c 0 = 1 and c j = 1 j ! n = 1 j ( c n + 1 ) , j 1 . Thus,
G ¯ ( x ) [ ( k + 1 ) b + 1 ] = j = 0 ( 1 ) j [ ( k + 1 ) b + 1 ] j G ( x ) j .
Inserting (A3) in Equation (A2) gives
f ( x ) = j , k = 0 p j , k ( b ) h ( k + 1 ) b + j ( x ) ,
where h p ( x ) = p g ( x ) G ( x ) p 1 ( p > 0 ) and
p j , k ( b ) = ( 1 ) j + k b [ ( k + 1 ) b + j ] k ! [ ( k + 1 ) b + 1 ] j .
For α > 0 ,
1 ( 1 + α λ x β ) 1 α ( k + 1 ) b + j 1 = i = 0 ( 1 ) i ( k + 1 ) b + j 1 i ( 1 + α λ x β ) i α ,
we have
h ( k + 1 ) b + j ( x ) = i = 0 ( 1 ) i i + 1 [ ( k + 1 ) b + j ] ( k + 1 ) b + j 1 i g ( x ; α i , β , λ i ) ,
where α i = ( i + 1 ) 1 α and λ i = ( i + 1 ) λ .
Thus,
f ( x ) = i = 0 e i ( b ) g ( x ; α i , β , λ i ) ,
where
e i ( b ) = ( 1 ) i ( i + 1 ) j , k = 0 p j , k ( b ) [ ( k + 1 ) b + j ] ( k + 1 ) b + j 1 i .
Similarly, for α = 0 , we obtain
f ( x ) = i = 0 e i ( b ) g ( x ; β , λ i ) .

Appendix A. Score Vector

The score components in U ( θ ) = ( U b , U α , U β , U λ ) (for α > 0 ) are
U b = n b + i = 1 n ln 1 + α λ x i β 1 α 1 i = 1 n 1 + α λ x i β 1 α 1 b ln 1 + α λ x i β 1 α 1 ,
U α = 1 α 2 + i = 1 n λ x i β 1 + α λ x i β + ( b 1 ) i = 1 n 1 + α λ x i β 1 α 1 + α λ x i β 1 α 1 λ x i β α 1 + α λ x i β ln 1 + α λ x i β α 2 i = 1 n b λ x i β 1 + α λ x i β 1 α 1 1 + α λ x i β 1 α 1 b 1 α b 1 + α λ x i β 1 α 1 + α λ x i β 1 α 1 b 1 ln 1 + α λ x i β α 2 ,
U β = n β + i = 1 n ln x i + 1 a 1 i = 1 n α λ x i β ln x i 1 + α λ x i β + ( b 1 ) i = 1 n λ x i β ln x i 1 + α λ x i β 1 α 1 1 + α λ x i β 1 α 1 b i = 1 n λ x i β ln x i 1 + α λ x i β 1 α 1 1 + α λ x i β 1 α 1 b 1 ,
U λ = n λ + 1 α 1 i = 1 n α x i β 1 + α λ x i β + ( b 1 ) i = 1 n x i β 1 + α λ x i β 1 α 1 1 + α λ x i β 1 α 1 b i = 1 n x i β 1 + α λ x i β 1 α 1 1 + α λ x i β 1 α 1 b 1 .

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Figure 1. The pdf of X.
Figure 1. The pdf of X.
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Figure 2. The hrf of X.
Figure 2. The hrf of X.
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Figure 3. Skewness of X.
Figure 3. Skewness of X.
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Figure 4. Kurtosis of X.
Figure 4. Kurtosis of X.
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Figure 5. (a) Estimated densities. (b) Empirical and estimated cdfs.
Figure 5. (a) Estimated densities. (b) Empirical and estimated cdfs.
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Figure 6. Kaplan–Meier and estimated survival functions.
Figure 6. Kaplan–Meier and estimated survival functions.
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Figure 7. Deviance residuals. (a) Index plot. (b) Normal plot with envelope.
Figure 7. Deviance residuals. (a) Index plot. (b) Normal plot with envelope.
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Table 1. Monte Carlo results from the WEW distribution.
Table 1. Monte Carlo results from the WEW distribution.
SetupnMeasuresParameter Estimates
b ^ α ^ β ^ λ ^
Setup 150Average2.032672.981790.202992.02287
Bias0.03267−0.018210.002990.02287
MSE0.049410.049320.000450.06756
100Average2.015582.990280.201512.01283
Bias0.01558−0.009720.001510.01283
MSE0.024650.025890.000230.03369
300Average2.006962.996870.200692.00307
Bias0.00696−0.003130.000690.00307
MSE0.007440.008040.000070.01034
Setup 250Average1.219480.476491.513712.02313
Bias0.01948−0.023510.013710.02313
MSE0.017770.024420.021990.03930
100Average1.209340.488181.505552.01248
Bias0.00934−0.011820.005550.01248
MSE0.008880.012740.011100.01989
300Average1.204250.496391.503272.00351
Bias0.00425−0.003610.003270.00351
MSE0.002680.003910.003430.00607
Setup 350Average1.524510.200462.011780.20156
Bias0.024510.000460.011780.00156
MSE0.027810.010190.006690.00019
100Average1.511580.198262.006180.20091
Bias0.01158−0.001740.006180.00091
MSE0.013860.006290.003450.00010
300Average1.505320.197382.002100.20024
Bias0.00532−0.002620.002100.00024
MSE0.004180.002580.001050.00003
Table 2. Simulation results for the GEW distribution when n = 100 , a = 0.8 , α = 3 , β = 2 and λ = 3 .
Table 2. Simulation results for the GEW distribution when n = 100 , a = 0.8 , α = 3 , β = 2 and λ = 3 .
MeasuresGEWWEW
a ^ α ^ β ^ λ ^ b ^ α ^ β ^ λ ^
AE0.872102.707811.901172.832930.450193.571552.562221.93563
RB0.09013−0.09739−0.04942−0.05569−0.437270.190520.28111−0.35479
MSE0.071440.763180.153220.700720.130511.208971.240622.55440
GD = 317.80AIC = 325.80BIC = 336.23 GD = 324.63AIC = 332.63BIC = 343.05
Table 3. Simulation results for the EW distribution when n = 100 , α = 3 , β = 2 and λ = 3 .
Table 3. Simulation results for the EW distribution when n = 100 , α = 3 , β = 2 and λ = 3 .
MeasuresEWWEW
α ^ β ^ λ ^ b ^ α ^ β ^ λ ^
AE2.786191.928862.701980.427193.680452.664190.96509
RB−0.07127−0.03557−0.09934−0.466010.226820.33209−0.67830
MSE0.359060.069430.672970.149122.064552.128036.32109
GD = 403.81AIC = 409.81BIC = 417.62GD = 413.92AIC = 421.92BIC = 432.34
Table 4. Simulation results for the WW distribution when n = 100 , b = 0.8 , β = 2 and λ = 3 .
Table 4. Simulation results for the WW distribution when n = 100 , b = 0.8 , β = 2 and λ = 3 .
MeasuresWW WEW
b ^ β ^ λ ^ b ^ α ^ β ^ λ ^
AE0.971811.871952.86490 0.885280.089211.976423.11492
RB0.21476−0.06402−0.04503 0.10660−0.97026−0.011790.03831
MSE0.216040.246480.60125 0.077888.502490.095830.22338
GD = −51.86948AIC = −45.86948BIC = −38.05397 GD = −51.78366AIC = −43.78366BIC = −33.36298
Table 5. Simulation from the LWEW regression.
Table 5. Simulation from the LWEW regression.
0%10%30%66%
n θ AEBiasMSEAEBiasMSEAEBiasMSEAEBiasMSE
30 γ 0 1.98554−0.214460.109582.09407−0.105930.038492.16869−0.031300.007692.209600.009600.00148
γ 1 1.06941−0.130590.051711.12913−0.070870.017661.16661−0.033390.006931.19417−0.005840.00250
σ 1.39258−0.107420.023251.42713−0.072870.013761.46657−0.033430.005071.500630.000630.00039
b2.187270.187270.149732.149120.149120.153422.085670.085670.166141.80592−0.194080.24300
α 4.69906−0.300940.189244.82055−0.179450.089544.92641−0.073590.027584.99624−0.003760.00266
50 γ 0 2.02365−0.176350.072612.10670−0.093290.028542.18128−0.018720.005402.217260.017260.00119
γ 1 1.06815−0.131850.048921.12879−0.071200.017461.16988−0.030120.005971.200950.000950.00186
σ 1.41518−0.084820.014621.44859−0.051410.007181.48528−0.014720.001471.505120.005120.00024
b2.131620.131620.099152.085220.085220.088431.98223−0.017770.093531.69623−0.303770.20879
α 4.77274−0.227260.110734.87189−0.128110.046764.96244−0.037560.009815.009890.009890.00159
100 γ 0 2.07334−0.126660.038792.13691−0.063090.014872.18932−0.010680.003392.225470.025470.00118
γ 1 1.07318−0.126820.039521.13136−0.068640.015661.17634−0.023660.004601.208020.008020.00148
σ 1.44380−0.056190.006981.46945−0.030550.003121.49265−0.007350.000841.508460.008460.00019
b2.072020.072020.046542.012710.012710.039181.94392−0.056080.047441.61877−0.381230.20287
α 4.84402−0.155980.054674.91633−0.083670.021334.97571−0.024290.005635.020500.020500.00127
Table 6. Estimation results.
Table 6. Estimation results.
DistributionMLEs and SEs
WEWb α β λ
1.7043896.7358531.0326010.76439
(0.099237)( 8.4 × 10 6 )(0.08398)(0.00049)
EW *b α β λ
1201.770181.914290.05117
(-)(0.89550)(0.08389)( 8.4 × 10 6 )
WW **b α β λ
10000.008380.68115
(0.08579)(-)(0.00018)( 2.6 × 10 6 )
WE ***b α β λ
0.78267010.06627
(0.04885)(-)(-)(0.00425)
GEWa α β λ
14.966570.497192.1987990.77049
(0.00805)(0.00503)(0.00304)( 5.9 × 10 5 )
KwWab β λ
4.39908102.11870.3339198.50308
(0.28679)(0.00061)(0.03279)( 6.2 × 10 6 )
BWab β λ
0.52781185.91651.90579211.1240
(0.07526)( 8.4 × 10 6 )(0.07965)( 2.9 × 10 6 )
BEEab λ α
7.902320.332140.509620.24477
(1.22239)(0.02937)(0.00034)(0.00008)
KwGaab α β
8.034690.244790.438130.60068
(0.16546)(0.01926)( 1.8 × 10 5 )( 1.8 × 10 5 )
BGaab α β
0.031000.1916840.771952.31482
( 2.8 × 10 6 )( 6.3 × 10 6 )( 7.7 × 10 7 )( 1.8 × 10 6 )
* L R = 29.373; (p-value ≤ 0.0001); ** L R = 35.165; (p-value ≤ 0.0001); *** L R = 83.863; (p-value ≤ 0.0001).
Table 7. GoF statistics for some fitted models.
Table 7. GoF statistics for some fitted models.
DistributionAICCAICBIC W * A * K-SK-S p-Value
WEW945.8351946.0899958.18550.157211.216190.087240.1698
EW973.2082973.3601982.47100.406383.328980.24370 8.8 × 10 9
WW979.0003979.1522988.26310.501823.088370.118980.02038
WE1025.6981025.7731031.8731.016946.033060.18871 1.9 × 10 5
GEW952.3737952.6284964.72410.166841.324910.099820.07925
KwW972.5957972.8505984.94610.400592.482400.114190.02927
BW1011.9771012.2321024.3280.916355.489420.164000.00033
BEE960.2507960.5055972.60110.258111.640870.123400.01439
KwGa958.1527958.4075970.50310.233301.491630.131830.00717
BGa977.6345977.8893989.98490.359832.223110.163330.00035
Table 8. GLR tests for some fitted models.
Table 8. GLR tests for some fitted models.
Distribution GLR StatisticDecision
WEW × GEW7.70553WEW is chosen
WEW × KwW18.80256WEW is chosen
WEW × BW6.01989WEW is chosen
WEW × BEE9.14457WEW is chosen
WEW × KwGa10.50785WEW is chosen
WEW × BGa11.25128WEW is chosen
Table 9. Survival times in weeks from hepatitis study.
Table 9. Survival times in weeks from hepatitis study.
Placebo: 1+, 2+, 3, 3, 3+, 5+, 5+, 16+, 16+, 16+, 16+, 16+, 16+,16+, 16+.
Steroid: 1, 1, 1, 1+, 4+, 5, 7, 8, 10, 10+, 12+, 16+, 16+, 16+.
Note: + indicates censoring.
Table 10. Estimation results [p values] and adequacy measures for some regressions.
Table 10. Estimation results [p values] and adequacy measures for some regressions.
ModelMLEs, SEs and p ValuesAICCAICBIC
LWEWb α σ γ 0 γ 1 52.32954.93859.166
0.58060150.906030.033822.34490−1.10239
(0.18658)(4.08123)(0.01369)(0.147361)(0.08117)
[<0.0001][<0.0001]
LEW *b α σ γ 0 γ 1 107.135108.802112.604
1 7.7 × 10 7 23.4613711.7190613.90735
(-)(0.03386)(0.07149)(0.02771)0.03222
[<0.0001][<0.0001]
LWW **b α σ γ 0 γ 1 61.04162.70766.509
0.1098200.133286.63796−1.86159
(0.02451)(-)(0.00076)(0.00074)(0.00025)
[<0.0001][<0.0001]
LGEWa α σ γ 0 γ 1 53.22555.83460.061
0.73631169.030100.034572.32548−1.10290
(0.18543)(4.20435)(0.01646)(0.18200)(0.09769)
[<0.0001][<0.0001]
LBWab σ γ 0 γ 1 92.83495.44399.671
0.084110.733090.130384.41069−0.81134
(0.01656)(0.30395)(0.00364)(0.00221)(0.00113)
[<0.0001][<0.0001]
KwGuab σ γ 0 γ 1 72.91775.52679.754
0.045220.346450.088712.81745−0.10872
(0.01634)(0.09152)(0.00002)(0.04302)(0.04298)
[<0.0001][0.01143]
* L R = 56.806; (p-value = 4.8 × 10 14 ); ** L R = 10.711; (p value = 0.00106).
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Cordeiro, G.M.; Biazatti, E.C.; de Santana, L.H. A New Extended Weibull Distribution with Application to Influenza and Hepatitis Data. Stats 2023, 6, 657-673. https://doi.org/10.3390/stats6020042

AMA Style

Cordeiro GM, Biazatti EC, de Santana LH. A New Extended Weibull Distribution with Application to Influenza and Hepatitis Data. Stats. 2023; 6(2):657-673. https://doi.org/10.3390/stats6020042

Chicago/Turabian Style

Cordeiro, Gauss M., Elisângela C. Biazatti, and Luís H. de Santana. 2023. "A New Extended Weibull Distribution with Application to Influenza and Hepatitis Data" Stats 6, no. 2: 657-673. https://doi.org/10.3390/stats6020042

APA Style

Cordeiro, G. M., Biazatti, E. C., & de Santana, L. H. (2023). A New Extended Weibull Distribution with Application to Influenza and Hepatitis Data. Stats, 6(2), 657-673. https://doi.org/10.3390/stats6020042

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