词条 | Gompertz function |
释义 |
The Gompertz curve or Gompertz function, is a type of mathematical model for a time series and is named after Benjamin Gompertz (1779-1865). It is a sigmoid function which describes growth as being slowest at the start and end of a given time period. The right-hand or future value asymptote of the function is approached much more gradually by the curve than the left-hand or lower valued asymptote. This is in contrast to the simple logistic function in which both asymptotes are approached by the curve symmetrically. It is a special case of the generalised logistic function. The function was originally designed to describe human mortality, but since has been modified to be applied in biology, with regards to detailing populations. HistoryBenjamin Gompertz originally designed the function to detail his law of human mortality for the Royal Society in 1825. The law rests upon an a priori assumption that a person's resistance to death decreases as his age increases. The model can be written in this way: where:
N(t) represents the number of individuals in the given time period, t. The letters c and a are constants. This model is a modification of a demographic model of Robert Malthus. It was commonly used by insurance companies to calculate the cost of life insurance. This equation is known as a Gompertz function. Formulawhere
PropertiesThe halfway point is found by solving for t. The point of maximum rate of increase () is found by solving for t. The increase at is DerivationThe function curve can be derived from a Gompertz law of mortality, which states the rate of absolute mortality (decay) falls exponentially with current size. Mathematically, where
Example usesExamples of uses for Gompertz curves include:
ApplicationsGompertz CurvePopulation biology is especially concerned with the Gompertz Function. This function is especially useful in describing the rapid growth of a certain population of organisms while also being able to account for the eventual horizontal asymptote, once the carrying capacity is determined (plateau cell/population number). It is modeled as follows: where:
This function consideration of the plateau cell number makes it useful in accurately mimicking real-life population dynamics. The function also adheres to the sigmoid function, which is the most widely accepted convention of generally detailing a population's growth. Moreover, the function makes use of initial growth rate, which is commonly seen in populations of bacterial and cancer cells, which undergo the log phase and grow rapidly in numbers. Despite its popularity, the function initial rate of tumor growth is difficult to predetermine given the varying microcosms present with a patient, or varying environmental factors in the case of population biology. In cancer patients, factors such as age, diet, ethnicity, genetic pre-dispositions, metabolism, lifestyle and origin of metastasis play a role in determining the tumor growth rate. The carrying capacity is also expected to change based on these factors, and so describing such phenomena is difficult. Metabolic CurveThe metabolic function is particularly concerned with accounting for the rate of metabolism within an organism. This function can be applied to monitor tumor cells; metabolic rate is dynamic and is greatly flexible, making it more precise in detailing cancer growth.The metabolic curve takes in to consideration the energy the body provides in maintaining and creating tissue. This energy can be considered as metabolism and follows a specific pattern in cellular division. Energy conservation can be used to model such growth, irrespective of differing masses and development times. All taxon
The differentiation between energy used at rest and metabolic rate work allows for the model to more precisely determine the rate of growth. The energy at rest is lower than the energy used to maintain a tissue, and together represent the energy required to maintain the existing tissue. The use of these two factors, alongside the energy required to create new tissue, comprehensively map the rate of growth, and moreover, lead in to an accurate representation of the lag phase. Growth of tumorsIn the 1960s A.K. Laird[4] for the first time successfully used the Gompertz curve to fit data of growth of tumors. In fact, tumors are cellular populations growing in a confined space where the availability of nutrients is limited. Denoting the tumor size as X(t) it is useful to write the Gompertz Curve as follows: where:
independently on X(0)>0. Note that, in absence of therapies etc.. usually it is X(0)
It is easy to verify that the dynamics of X(t) is governed by the Gompertz differential equation: i.e. is of the form when broken down: F(X) is the instantaneous proliferation rate of the cellular population, whose decreasing nature is due to the competition for the nutrients due to the increase of the cellular population, similarly to the logistic growth rate. However, there is a fundamental difference: in the logistic case the proliferation rate for small cellular population is finite: whereas in the Gompertz case the proliferation rate is unbounded: As noticed by Steel[5] and by Wheldon,[6] the proliferation rate of the cellular population is ultimately bounded by the cell division time. Thus, this might be an evidence that the Gompertz equation is not good to model the growth of small tumors. Moreover, more recently it has been noticed[7] that, including the interaction with immune system, Gompertz and other laws characterized by unbounded F(0) would preclude the possibility of immune surveillance. Gompertz growth and logistic growthThe Gompertz differential equation is the limiting case of the generalized logistic differential equation (where is a positive real number) since . In addition, there is an inflection point in the graph of the generalized logistic function when and one in the graph of the Gompertz function when . Gomp-ex law of growthBased on the above considerations, Wheldon[6] proposed a mathematical model of tumor growth, called the Gomp-Ex model, that slightly modifies the Gompertz law. In the Gomp-Ex model it is assumed that initially there is no competition for resources, so that the cellular population expands following the exponential law. However, there is a critical size threshold such that for . The assumption that there is no competition for resources holds true in most scenarios. It can however be affected by limiting factor the growth follows the Gompertz Law: so that: Here there are some numerical estimates[6] for :
See also
References1. ^{{citation | last1 = Islam | first1 = Towhidul | last2 = Fiebig | first2 = Denzil G. | last3 = Meade | first3 = Nigel | doi = 10.1016/S0169-2070(02)00073-0 | issue = 4 | journal = International Journal of Forecasting | pages = 605–624 | title = Modelling multinational telecommunications demand with limited data | volume = 18 | year = 2002}}. 2. ^{{citation | last1 = Zwietering | first1 = M. H. | last2 = Jongenburger | first2 = I. | last3 = Rombout | first3 = F. M. | last4 = van 't Riet | first4 = K. | issue = 6 | journal = Applied and Environmental Microbiology | pages = 1875–1881 | title = Modeling of the Bacterial Growth Curve | url = http://aem.asm.org/content/56/6/1875 | volume = 56 | year = 1990}}. 3. ^{{citation | last1 = Caravelli | first1 = F. | last2 = Sindoni | first2 = L. | last3 = Caccioli | first3 = F. | last4 = Ududec | first4 = C. | title = Optimal leverage trajectories in presence of market impact | arxiv = 1510.05123| year = 2015| bibcode = 2016PhRvE..94b2315C| doi = 10.1103/PhysRevE.94.022315}}. 4. ^{{cite journal | author= Laird A. K. | title= Dynamics of tumor growth | journal= Br J Cancer | volume= 18 |year=1964 | pages=490–502 | doi= 10.1038/bjc.1964.55 | issue= 3}} 5. ^{{cite book |last=Steel |first=G.G. |coauthors= |title= Growth Kinetics of Tumors |year=1977 |publisher=Clarendon Press |location= Oxford |isbn=0-19-857388-X |pages= |chapter= }} 6. ^1 2 {{cite book |last=Wheldon |first=T.E. |coauthors= |title= Mathematical Models in Cancer Research |year=1988 |publisher=Adam Hilger |location= Bristol |isbn=0-85274-291-6 |pages= |chapter= }} 7. ^{{cite journal | author= d'Onofrio A. | title= A general framework for modeling tumor-immune system competition and immunotherapy: Mathematical analysis and biomedical inferences | journal= Physica D | volume= 208 |year=2005 | pages=220–235 | doi= 10.1016/j.physd.2005.06.032 | issue= 3–4| arxiv= 1309.3337 | bibcode= 2005PhyD..208..220D }} External links
3 : Demography|Time series models|Growth curves |
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