Standardizing estimates of the Plasmodium falciparum parasite rate

Abstract

David L Smith1,5, Carlos A Guerra2,3, Robert W Snow3,4 and Simon I Hay2,3

1Fogarty International Center, National Institutes of Health, Building 16, 16 Center Drive, Bethesda, Maryland 20892, USA

2Spatial Ecology and Epidemiology Group, Tinbergen Building, Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK

3Malaria Public Health & Epidemiology Group, Centre for Geographic Medicine, KEMRI-Wellcome Trust-Collaborative Programme, Kenyatta National Hospital Grounds, PO Box 43640-00100 Nairobi, Kenya

4Centre for Tropical Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DS, UK

5Department of Zoology & Emerging Pathogens Institute, University of Florida, 223 Bartram Hall, PO Box 118525 Gainesville FL, USA

Background

The Plasmodium falciparum parasite rate (PfPR) is a commonly reported index of malaria transmission intensity. PfPR rises after birth to a plateau before declining in older children and adults. Studies of populations with different age ranges generally report average PfPR, so age is an important source of heterogeneity in reported PfPR data. This confounds simple comparisons of PfPR surveys conducted at different times or places.

Methods

Several algorithms for standardizing PfPR were developed using 21 studies that stratify in detail PfPR by age. An additional 121 studies were found that recorded PfPR from the same population over at least two different age ranges; these paired estimates were used to evaluate these algorithms. The best algorithm was judged to be the one that described most of the variance when converting the PfPR pairs from one age-range to another.

Results

The analysis suggests that the relationship between PfPR and age is predictable across the observed range of malaria endemicity. PfPR reaches a peak after about two years and remains fairly constant in older children until age ten before declining throughout adolescence and adulthood. The PfPR pairs were poorly correlated; using one to predict the other would explain only 5% of the total variance. By contrast, the PfPR predicted by the best algorithm explained 72% of the variance.

Conclusion

The PfPR in older children is useful for standardization because it has good biological, epidemiological and statistical properties. It is also historically consistent with the classical categories of hypoendemic, mesoendemic and hyperendemic malaria. This algorithm provides a reliable method for standardizing PfPR for the purposes of comparing studies and mapping malaria endemicity. The scripts for doing so are freely available to all.

◊ An open access article from Malaria Journal 2007, 6:131 distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), viewed from Biology-Online.org.


Background

The intensity of malaria transmission by its anopheline vectors varies enormously [1], and this affects most quantitative aspects of malaria epidemiology [2]. A commonly used index of malaria transmission intensity is the Plasmodium falciparum parasite rate (PfPR), the proportion of the population found to carry asexual blood-stage parasites. In mathematical models, PfPR is related to the entomological inoculation rate (EIR), the number of bites on a person by sporozoite positive vectors, at the steady state [3,4]. The notion of a steady state has limited application for PfPR, however, because PfPR follows a well-established pattern as a function of age and transmission intensity; PfPR rises during infancy and early childhood [5,6], settles to a plateau in older children, and declines in adolescents and adults as malaria immunity develops [7-10]. This pattern has been known for decades [11,12], but there are no established standards for reporting PfPR, so thousands of studies have reported crude PfPR, without stratifying by age [13]. As a result, the different age-ranges over which studies have reported PfPR make it difficult to compare prevalence estimates at different times and places. Assemblies of PfPR data aimed at describing the current global distribution of malaria endemicity [13], therefore, need a mechanism to standardize these data to a consistent age-grouping in order to be meaningfully summarized.

Mathematical models with slowly acquired immunity qualitatively reproduce the empirical relationships between age and PfPR [14-17]. The models suggest that EIR (or the force of infection) determines both the rate that PfPR rises in children and the level of the plateau, so either measure would provide a reliable index of transmission intensity. The PfPR in children is correlated with EIR [4], and the PfPR in children aged 2–10 has provided a basis for the classical categorical measures of malaria transmission: hypoendemic (<10%), mesoendemic (10–50%), and hyperendemic (50–75%) [18]. Holoendemicity refers to PfPR >75% in those less than 12 months old [18].

The variable way of reporting PfPR also limits the number of studies where PfPR can be used to index transmission intensity, which poses a particular problem for recent approaches aimed at using empirical PfPR data to model the spatial distributions of malaria transmission intensity at regional [19-21] or potentially at global scales [22]. For example, maps of transmission intensity in Africa are often based on studies of PfPR that include only children [23,21,25]. The evidence base for mapping malaria, the geographical extent and coverage of places where PfPR has been measured directly, could all be greatly expanded if it were possible to standardize crude PfPR in studies that include adults. The consistent pattern apparent in age-stratified PfPR data suggests that it is amenable to mathematical or statistical modeling. A set of candidate algorithms was derived and evaluated in an attempt to provide a single evidence-based method for converting crude estimates of PfPR to a standard age range for improving future global comparisons of malaria risk using existing extensive PfPR data [13].


Methods

Experimental approach and data

This analysis has the distinctive purpose of developing an algorithm to age-standardize PfPR data or, in other words, the purpose is to find a function, F, that transforms an estimate of PfPR over any age range [x,y), into a PfPR over a standard age range [L,U), i.e. F: PR[x,y)PR[L,U). This principle was achieved for a number of candidate statistical and biological deterministic models developed from 21 studies that report very detailed PfPR by age (the training set). The skill of the models was then evaluated by inter-conversion of 121 pairs of crude PfPR estimates, where both were taken from the same population but aggregated over different age ranges (the testing set).

The data selection criteria and summary details are given in Additional File 1 and Additional File 2 for the training and testing sets, respectively. Briefly, the data spanned all potential P. falciparum transmission intensity categories [18]. The algorithms developed from the training set were validated against the 121 pairs of the testing dataset by comparing the conversions from one age group to the other, usually from adults to children, and vice versa. A selection was made of the best performing algorithm using the goodness of fit, measured as the proportion of the variance explained, and defined as the ratio of the variance in residual error divided by the error in the observed PfPR subtracted from one.

The algorithms all differ from each other in significant ways. The linear regression algorithm was based only on the testing set. The other algorithms were based on only the training set, and did not use the testing set for their development. The linear regression algorithm does not predict a relationship between age and PfPR. The interpolation algorithm predicts PfPR in the testing set based on direct interpolation of the training set data; it does not predict an age-PfPR relationship. The two parametric algorithms were fitted to the training set, but they were used only for prediction on the testing set, so parsimony is not an important concern. The most important measure of performance is their skill – a more complicated model that did better at standardizing PfPR would be preferred regardless of the level of complexity, as long as the algorithm had not been fitted to the testing set. Since the linear regression algorithm is a statistical description of the testing set, it sets a standard for judging the skill of the other algorithms. The predictions based on linear regression of the testing set, on the other hand, do raise important issues of parsimony. Because the statistical analysis was one of the candidate algorithms, the analysis was repeated on a sub-sample of the testing set: two-thirds of the data pairs were used for fitting and one-third for validation. Based on these rules, one algorithm was selected as the most appropriate evidence-based method to age-standardize PfPR for future comparisons between studies reporting parasite prevalence across different age ranges.

Statistical candidate algorithms

Linear regression

Linear regression was used to describe the relationship between the pairs of PfPR estimates from the testing set. It differs from the other algorithms in that it is based on a statistical analysis of the testing set; it does not predict a relationship between PfPR and age, and it does not rely on the training set. Let PR1 and PR2 denote the two estimates made on the intervals [L1, U1) and [L2, U2), respectively. The full regression included the age limits: (i.e. PR1 = c0 PR2 + c1 L1 + c2 U1 + c3 L2 + c4 U2 + ε). This formula sometimes returns values for predicted PR1 that are outside the interval (0,1), so the analysis was repeated as non-linear regression where the points outside this range were forced to be either 0 or 1. The regression analysis included each pair twice; each member was both PR1 once and PR2 once. Linear regression of the full testing set provided a standard for the other algorithms, and the predicted values from the linear regression were also evaluated as a potential algorithm.

Interpolation

A general class of interpolation algorithms was based on the training set: (i) given the PfPR from a focal study, PRf[x,y), compute the PfPR for the training sets over the same interval, PRi[x,y), i = 1...21; (ii) let Wi = | PRf[x,y) - PRi[x,y) | -z, and let ωi = Wi/∑iWi denote the weight of the ith PfPR estimate and (iii) the standardized PfPR is then ∑iωiPRi [L,U). Linear interpolation was also considered and was very similar to the general interpolation algorithm with z = 6.

Pull & Grab-based Algorithm

Let P(A) denote the true prevalence and F(A) the sensitivity of the microscopy, a standard method for estimating PfPR, as a function of age. The function F(A) was motivated by the notion that sensitivity declines with age as blood-stage immunity reduces parasite densities to a point where they are often below the detection thresholds of microscopy [26,27]. Therefore, the apparent PfPR, the one that a study would find using microscopy, is p(A) = P(A) F(A). Crude PfPR estimates also depend on the age-distribution of the sampled population, S(A); when PfPR is reported crudely, the age-distribution is generally not reported, so it must also be inferred. Given p(A) and S(A), an estimate of crude PfPR would be PRf[x,y) = ∫xyp(A) S(A) dA/∫xyS(A) dA. The standardized estimate would be PRf[L,U) = ∫LUp(A) S(A) dA/∫LUS(A) dA.

The estimate of S(A) was based on the age-distributions in the training set (Figure 1). Each of the 21 studies reports the number of people sampled by age or by age class. Typically, ages were binned by year through childhood, then by 5-year age classes up to age 65, and finally the elderly, which was arbitrarily truncated at age 85. When a study binned several age classes, the observations for each year were proportional to the total observed for that class. For example, the sample for 27 year olds was counted as 1/5 of the total observations for 25–30 year olds. In sum, to get an estimate of S(A): (i) for each study, the proportion of all people sampled that belonged to each one-year age class was computed and (ii) the proportion for each age class was the average for all the studies, where each study was weighted equally.

To generate p(A), the curves P(A) and F(A) were generated separately. P(A) was based on Pull & Grab's equations [28], which were motivated by the Ross model [29] and previous work by Muench [30]. The change in PfPR with age is described by the equation:

dP/dA = h (1-P) - r P;

where h denotes the force of infection (i.e., the "happenings" rate), and r is the rate at which infections clear. When P(0) = 1, this equation has the solution:

P(A) = P' (1 - e-bA ).

Here, P' = h/(h+r) is the PfPR at equilibrium, and b = h+r describes the rate at which PfPR approaches equilibrium.

A three-parameter function was used for F(A): 1 - s [1 - min (1, e-c(A-α)) ]. Beginning at age a, this function declines from 1, to 1-s; the parameter c describes the decline from 1 to 1-s as a function of age. Conceptually, this function can be thought of as the decline in the probability of detecting an active infection, although the real reason for the decline in PfPR might be that immunity leads to real declines in h or real increases in r. For the purposes of standardization, the biological reasons for the decline are not relevant.

The modified Pull & Grab model was fitted to all 21 datasets using maximum likelihood estimation (Figure 2). The algorithm used the average estimates of b, α, s, and c. The 21 best-fit parameter values for α, b, c, and s were uncorrelated with P' (a scatter plot of the slope, b, is plotted against the plateau, P', Figure 3). A few of the parameter values were clearly extreme, but a careful examination of the extreme values suggested that they were irrelevant (i.e. changing their values by a factor of 10 did not change the shape of the fitted curve because of the other fitted parameters), so the influence of these extreme but irrelevant values was removed by taking the trimmed means. This generated a family of age-PR curves that depended only on P'.

The modified Pull & Grab equations each generate a curve that describes PfPR as a function of age for each value of P'. To turn this function into a standardization algorithm, the function need only be inverted. In other words, the algorithm found a value P* such that PRf[x,y) = ∫xyp(A|P*) S(A) dA/∫xyS(A) dA. The standardized value was then PRf[L,U) = ∫LUp(A|P*) S(A) dA/∫LUS(A) dA.

The Garki model

Another parametric method was based on the Garki model [14], using parameter values that were fitted during the Garki project [31]. This model is based on a system of seven coupled difference equations [14]. Here, P(A) was computed using an analogue of the Garki equation with seven coupled ordinary differential equations. To convert the parameter values, -log(1-x), was used instead of the parameter x. Instead of a fixed delay for the pre-patent periods – the pre-patent period was assumed to be distributed exponentially, but with the same mean time as in the Garki model (i.e. 1/N). The differences between the ordinary differential equation and difference equations are negligible and are available upon request. Births and deaths were ignored (i.e. δ = 0) because the quantity of interest was prevalence in the survivors; the initial value of x1 was set to 1, and all other variables were initially set to 0. The equations were:

dx1/dA = R1 y2 - h x1

dx2/dA = h x1 - x2/N

dy1/dA = x2/N - α1 y1

dy2/dA = α1 y1 - (α2 + R1) y2

dx3/dA = R2 y3 - h x3

dx4/dA = h x3 - x4/N

dy3/dA = α2 y2 + x4/N - R2 y3

The function p(A) = q1y1(A) + q2y2(A) + q3y3(A), where yi(A) were found by choosing a value for h and then numerically solving the system of equations. The algorithm used the age distribution from the training set, S(A). All other parameters except h were taken from the original paper (note that the values of R1 and R2 are fixed by h and other parameters). To turn this function into a standardization algorithm, the function again, need only be inverted. In other words, the algorithm found a value h* such that PRf[x,y) = ∫xyp(A|h*) S(A) dA/∫xyS(A) dA. The standardized value was then PRf[L,U) = ∫LUp(A|h*) S(A) dA/∫LUS(A) dA.

All the routines described were written in R [32], and are available upon request.


Results

Overall, the Pull & Grab-based algorithm ranked highest; it explained 72% of the variance in the testing set, despite being calibrated only on the training set. Linear regression ranked second-best; it explained 68% of the variance. Interpolation (with z = 1.5) ranked third; it explained 64% of the variance. The Garki model explained 58% of the variance. The results are plotted in Figure 4, summarized in Table 1, and discussed in detail in the following sections. Because the algorithm based on Pull & Grab ranked highest, and because it was never fitted to the testing set, the issue of parsimony was not relevant. Had the algorithm based on linear regression ranked highest, the issue of parsimony would have been an important concern.

Linear regression

By itself, PR2 explained only 5% of the variance in PR1 (i.e. r2 = 0.05). Linear regression using the formula PR1 = a + b PR2 improved the r2 to 26%. Linear regression with the formula PR1 = a + b PR2 + c L1 + d L2 + e U1 + f U2 improved the r2 to 68%, the same as with the slightly non-linear version that always returned a value between 0 and 1. All of the coefficients were statistically significant at the 95% level except for c, the coefficient corresponding to L1.

Interpolation

Several different values of z were evaluated including z = 0.5, 1, 1.5, 2, 3, 4, 6, 10. Of these values, z = 1.5 minimized the sum of squared errors and explained 65% of the variance.

Pull & Grab

The trimmed mean value for α corresponded to a decline in PfPR beginning around age 9.5. The trimmed mean value for s corresponded to a decline in sensitivity to approximately 36% of P', but the trimmed mean value of c was low and implied that PfPR declines slowly, so that the apparent PfPR is not close to 36% of the PfPR in children between two and ten years of age until late in life. There was substantial variability in b, but by the trimmed mean, PfPR was within 90% of P' by age two. The parameter names, interpretations, and values are summarized in Table 2. Some of the individual datasets differed from this pattern, but the majority were within this value by age two. The family of curves described by the algorithm is illustrated in Figure 5. This algorithm explained 72% of the variance.

Garki

The algorithm based on the Garki model [14] and calibrated during the Garki Project [31] was recently used to generate endemicity maps [20]. The algorithm was therefore included as a candidate for comparison; the relationship between age and PR is qualitatively very similar to the modified Pull & Grab model. It was, therefore, used as-is, without further fitting to the training set or the testing set. It explained 58% of the variance, the lowest of the four algorithms considered.

Analysis of the sub-sampled data

To evaluate the algorithms further, and to enable the linear regression analysis to be assessed as an algorithm, the testing set was sub-sampled 100 times. The Pull-and-Grab -based algorithm ranked 1st 80% of the time, 2nd or better 94% of the time, and 3rd or better 99% of the time. The similar ranking vector for linear regression was 17%, 70% and 95%, for interpolation 3%, 28%, and 50%. The Garki-based algorithm ranked in the top three only 5% of the time.

The algorithms were developed and evaluated for standardizing PfPR from any age range to any other; it is possible that they have different skill at standardizing to the PfPR in 2–10 year olds. To further evaluate the algorithm for standardization specifically to the 2–10 year old age classes, 87 datasets were identified in which the age limits were between two and 10 (Figure 6). The PfPR pairs were, again, used as a standard for comparison. When PR1 was used instead of its paired PfPR estimate, PR2, the categorical description was wrong in 38% of the cases; virtually all of the hyperendemic populations were misclassified as mesoendemic, and many mesoendemic areas were misclassified as hypoendemic. By way of contrast, the standardized PfPR gave the wrong categorical description in 18% of the cases. Standardization reduced the number of mesoendemic populations that would have been classified as hypoendemic, but it also misclassified two populations as mesoendemic that were actually hypoendemic. Standardization correctly classified most, but not all, of the misclassified hyperendemic populations, but two mesoendemic populations were misclassified as hyperendemic. Given the natural scatter in the estimates, errors are inevitable when continuous data are placed into categories. All other candidate algorithms performed more poorly (Table 1).


Discussion

Four methods were developed and evaluated as potential candidates for an algorithm that is suitable for standardizing crude PfPR data. Of the four methods, the selected algorithm based on a modified version of Pull & Grab's equations [28] was clearly superior to all others. The algorithm explained 72% of the variance in PfPR estimates on a set of independent data, and it was superior to the predictions obtained through linear regression of that data. The mathematical model on which the algorithm was based was biologically motivated and fitted to a set of highly stratified PfPR data that spanned the range of P. falciparum transmission intensity. The analysis suggests that the relationship between age and PfPR is fairly consistent across the range of P. falciparum transmission intensity and that it is strongly determined by the underlying biology. The algorithm works better than regression because it captures more information about the general patterns in PfPR-age relationships than the 121 averaged PfPR pairs.

While the algorithm permits age-standardization of PfPR for the heterogeneous way of reporting it, this would be unnecessary if minimum standards were followed for reporting PfPR data. Because PfPR varies by age, published estimates of PfPR should always be stratified by age; the 21 training sets listed here have set a reasonable bar, with some important caveats. This analysis suggests that reporting the average PfPR for the 2–10 year old age classes can often be done without loss of information, but the data should first be checked for the typical pattern. For example, PfPR did not reach the plateau until age 5 in some studies. The PfPR begins to decline in older children sometime after age 10 because of blood stage immunity, except possibly at very low PfPR, so PfPR data should be stratified by age in older children and adults. A sensible rule would be to bin by year at least through age 15, and then to bin by at most 5-year age groups after age 20.

For children younger than 2, the PfPR should be reported at a grain that is fine enough to describe changes in PfPR, subject to the social, logistic and ethical concerns of recruiting sufficient infants and young children to the survey. PfPR increases with age in very young children as they acquire their first infections, develop clinical malaria, and then either clear the infections with antimalarial drugs and await reinfection, or recover from symptoms and maintain an asymptomatic infection. Reinfection and clinical malaria continue throughout life, but the frequency and severity of clinical malaria decline as clinical immunity develops [33]. As a consequence, so does the rate at which parasites are cleared by antimalarial drugs. Thus, the expected time to clinical malaria gets longer as children grow older, and this can affect the use of antimalarial drugs. The rate at which children are bitten also increases as their body size increases, and they thus absorb a greater proportion of the bites in the household [34]. Thus, the expectation is that PfPR increases rapidly during these years.

This analysis suggests that after the first few years of life, PfPR settles to a plateau where it remains fairly constant until the onset of adolescence. The plateau reflects the original steady state that was the motivation for using PfPR to index transmission intensity, a population dynamic equilibrium at which parasite clearance is balanced by new infections, and simultaneously not biased by detection issues associated with immunity and microscopy [26,27]. The rise in PfPR with age has been suggested as an alternative index of transmission intensity [35], but this analysis found substantial variability in the slope that was uncorrelated with the PfPR in 2–10 year olds (Figure 3). The discrepancy between the two raises the question of which measure provides a better index of transmission intensity.

For practical and epidemiological reasons, the PfPR in older children provides a good index of transmission intensity, and the age limits from the classical categories are appropriate for standardizing PfPR. There are three justifications for standardizing reported PfPR to 2–10 year olds for use as an index of transmission intensity. First, because PfPR remains relatively constant between the ages of about two and 10, the average is therefore meaningful. Second, because the frequency of clinical malaria declines in older children, the PfPR over these ages may be least influenced by drug treatment [36]. PfPR in older children is also relatively unaffected by immunity, so it can be argued that the PfPR in older children comes closest to reflecting the steady state relationship predicted by mathematical models. It is, therefore, most likely to provide a good index of transmission intensity. Third, it is consistent with the historical approaches to defining endemicity [18].

Using the rise in PfPR in very young children to index transmission has some advantages, but it also has several disadvantages. Although young children are of great interest for malaria control, the slope of PfPR, not the average PfPR in young children, is an index of transmission intensity. From a practical point of view, it is more difficult to measure a slope than an average. The ideal measure of transmission intensity would be the infant conversion rate, characterized by the waiting time to a patent infection in uninfected children. A slightly less direct measure of the force of infection would be any exposure to malaria vs. age, a measure that would be found in an appropriately designed study of seroprevalence [37,38]. PfPR is a distant third because it reflects a balance between exposure and clearance, including natural clearance and radical curative therapy with antimalarial drugs. The frequency of clinical malaria is highest in young children, before they develop functional immunity, so the need for antimalarial drugs is also likely to be correlated with age. The rise in PfPR reflects both exposure and clearance, so it can be quite a volatile measure. For example, the rise in PfPR in young children would dramatically underestimate transmission intensity in populations where effective antimalarial drugs had been used frequently and properly to clear infections. Because gametocytes clear slowly, it has also been argued that measuring gametocyte prevalence directly is a more appropriate measure of exposure, but considerable technical difficulties still limit its wider application [39].

The relationship between age and PR follows a fairly consistent pattern across the natural range of malaria transmission intensity that can be described by a relatively simple, biologically motivated mathematical model. The model, fitted to age-stratified data, accurately describes the rise and fall in PfPR with age, but it does not resolve any questions about the biological causes of this pattern, since it was not designed to do so. The algorithm based on this model can be used to reliably standardize crude estimates, but some important residual variance remains unexplained. This could be due to a variety of factors that were not considered here, including sampling, seasonality, heterogeneous biting, the prevalence of P. vivax, and variable use of effective anti-malarial drugs. These will be the focus of future research effort. Despite these caveats, the algorithm explained 72% of the variance, suggesting that age is a dominant source of heterogeneity in PfPR estimates from places with similar transmission intensity. The algorithm thus provides a useful way of standardizing PfPR to 2–10 year olds for comparing studies and ultimately for the mapping of malaria risk.


Acknowledgements

We are extremely grateful to all those individuals who contributed PfPR data and who are acknowledged on the Malaria Atlas Project (MAP) website [40]. We additionally thank those who have supplied (directly to the authors or indirectly through exemplary documentation in publication) very high resolution age-stratified PfPR data: Waqar Butt, Verena Carrara, Helen Guyatt, Marie Claire Henry, Akira Kaneko, Kojo Koram, Akiko Matsumto, Bruno Moonen, D. Müller, Tabitha Mwangi, François Nosten, Christophe Rogier, Dennis Shanks, David Sintasath, Tom Smith, Jean-François Trape and Dejan Zurovac. We also thank F. Ellis McKenzie, Andy Tatem, Anand Patil, and three anonymous reviewers for their helpful comments and suggestions.

DLS conducted this research at the Fogarty International Center, National Institutes of Health, and at the Emerging Pathogens Institute, University of Florida. CAG is supported by a Wellcome Trust Project grant (#076951) and also acknowledges support from the Fundación para la Ciencia y Tecnología (FUNDACYT), Quito, Ecuador. RWS is a Wellcome Trust Principal Research Fellow (#079080). SIH is funded by a Senior Research Fellowship from the Wellcome Trust (#079091). RWS and SIH acknowledge the support of the Kenyan Medical Research Institute (KEMRI). This paper is published with the permission of the director of KEMRI. This work forms part of the output of the MAP, principally funded by the Wellcome Trust, UK.


References

  1. Smith DL, McKenzie FE, Snow RW, Hay SI: Revisiting the basic reproductive number for malaria and its implications for malaria control.

    PLoS Biol 2007, 5:e42.

  2. Snow RW, Marsh K: The consequences of reducing transmission of Plasmodium falciparum in Africa.

    Adv Parasitol 2002, 52:235-264.

  3. Dietz K: Mathematical models for transmission and control of malaria. In Malaria, Principles and Practice of Malariology. Edited by: Wernsdorfer WH, McGregor I. Edinburgh: Churchill Livingstone; 1988:1091-1133.

  4. Smith DL, Dushoff J, Snow RW, Hay SI: The entomological inoculation rate and Plasmodium falciparum infection in African children.

    Nature 2005, 438:492-495.

  5. Gupta S, Snow RW, Donnelly C, Newbold C: Acquired immunity and postnatal clinical protection in childhood cerebral malaria.

    Proc R Soc Lond Ser B-Biol Sci 1999, 266:33-38.

  6. Gupta S, Snow RW, Donnelly CA, Marsh K, Newbold C: Immunity to non-cerebral severe malaria is acquired after one or two infections.

    Nat Med 1999, 5:340-343.

  7. Baird JK, Jones TR, Danudirgo EW, Annis BA, Bangs MJ, Basri H, Purnomo , Masbar S: Age-dependent acquired protection against Plasmodium falciparum in people having two years exposure to hyperendemic malaria.

    The American Journal of Tropical Medicine and Hygiene 1991, 45:65-76.

  8. Baird JK, Purnomo , Basri H, Bangs MJ, Andersen EM, Jones TR, Masbar S, Harjosuwarno S, Subianto B, Arbani PR: Age-specific prevalence of Plasmodium falciparum among six populations with limited histories of exposure to endemic malaria.

    The American Journal of Tropical Medicine and Hygiene 1993, 49:707-719.

  9. Trape JF, Rogier C, Konate L, Diagne N, Bouganali H, Canque B, Legros F, Badji A, Ndiaye G, Ndiaye P, et al.: The Dielmo project: a longitudinal study of natural malaria infection and the mechanisms of protective immunity in a community living in a holoendemic area of Senegal.

    The American Journal of Tropical Medicine and Hygiene 1994, 51:123-137.

  10. Baird JK: Host age as a determinant of naturally acquired-immunity to Plasmodium falciparum.

    Parasitol Today 1995, 11:105-111.

  11. Bagster-Wilson D: Malaria incidence in central and south Africa. In Malariology A comprehensive survey of all aspects of this group of diseases from a global standpoint. Volume II. Edited by: Boyd MF. Philadelphia and London: W. B. Saunders Company; 1949:800-809.

  12. Garnham PCC: Malaria immunity in Africans: effects in infancy and early childhood.

    Ann Trop Med Parasitol 1949, 43:47-61.

  13. Guerra CA, Hay SI, Lucioparedes LS, Gikandi P, Tatem AJ, Noor AM, Snow RW: Assembling a global database of malaria parasite prevalence for the Malaria Atlas Project.

    Malar J 2007, 6:17.

  14. Dietz K, Molineaux L, Thomas A: A malaria model tested in the African savannah.

    Bull World Health Organ 1974, 50:347-357.

  15. Aron JL, May RM: The population dynamics of malaria. In Population dynamics and infectious disease. Edited by: Anderson RM. London: Chapman and Hall; 1982:139-179.

  16. Aron JL: Mathematical modeling of immunity to malaria.

    Mathematical Biosciences 1988, 90:385-396.

  17. Smith T, Hii JL, Genton B, Muller I, Booth M, Gibson N, Narara A, Alpers MP: Associations of peak shifts in age-prevalence for human malarias with bednet coverage.

    Trans R Soc Trop Med Hyg 2001, 95:1-6.

  18. Metselaar D, van Thiel PH: Classification of malaria.

    Trop Geog Med 1959, 11:157-161.

  19. Gemperli A, Sogoba N, Fondjo E, Mabaso M, Bagayoko M, Briet OJ, Anderegg D, Liebe J, Smith T, Vounatsou P: Mapping malaria transmission in West and Central Africa.

    Trop Med Int Health 2006, 11:1032-1046.

  20. Gemperli A, Vounatsou P, Sogoba N, Smith T: Malaria mapping using transmission models: application to survey data from Mali.

    Am J Epidemiol 2006, 163:289-297.

  21. Omumbo JA, Hay SI, Snow RW, Tatem AJ, Rogers DJ: Modelling malaria risk in East Africa at high-spatial resolution.

    Trop Med Int Health 2005, 10:557-566.

  22. Hay SI, Snow RW: The Malaria Atlas Project: developing global maps of malaria risk.

    PLoS Med 2006, 3:e473.

  23. Kleinschmidt I, Bagayoko M, Clarke GPY, Craig M, Le Sueur D: A spatial statistical approach to malaria mapping.

    Int J Epidemiol 2000, 29:355-361.

  24. Kleinschmidt I, Omumbo J, Briet O, van de Giesen N, Sogoba N, Mensah NK, Windmeijer P, Moussa M, Teuscher T: An empirical malaria distribution map for West Africa.

    Trop Med Int Health 2001, 6:779-786.

  25. Kazembe LN, Kleinschmidt I, Holtz TH, Sharp BL: Spatial analysis and mapping of malaria risk in Malawi using point-referenced prevalence of infection data.

    Int J Health Geogr 2006, 5:41.

  26. Mayor A, Aponte JJ, Fogg C, Saute F, Greenwood B, Dgedge M, Menendez C, Alonso PL: The epidemiology of malaria in adults in a rural area of southern Mozambique.

    Malar J 2007, 6:3.

  27. McKenzie FE, Sirichaisinthop J, Miller RS, Gasser RA Jr, Wongsrichanalai C: Dependence of malaria detection and species diagnosis by microscopy on parasite density.

    The American Journal of Tropical Medicine and Hygiene 2003, 69:372-376.

  28. Pull JH, Grab B: A simple epidemiological model for evaluating the malaria inoculation rate and the risk of infection in infants.

    Bull World Health Organ 1974, 51:507-516.

  29. Ross R: The prevention of malaria. London: John Murray; 1910.

  30. Muench H: Catalytic models in epidemiology. Cambridge: Harvard University Press; 1959.

  31. Molineaux L, Storey J, Cohen JE, Thomas A: A longitudinal study of human malaria in the West African Savanna in the absence of control measures: relationships between different Plasmodium species, in particular P. falciparum and P. malariae.

    The American Journal of Tropical Medicine and Hygiene 1980, 29:725-737.

  32. R Development Core Team: R: a language and environment for statistical computing. In Book R: a language and environment for statistical computing. City: R Foundation for Statistical Computing; 2006.

  33. Snow RW, Omumbo JA, Lowe B, Molyneux CS, Obiero JO, Palmer A, Weber MW, Pinder M, Nahlen B, Obonyo C, et al.: Relation between severe malaria morbidity in children and level of Plasmodium falciparum transmission in Africa.

    Lancet 1997, 349:1650-1654.

  34. Port GR, Boreham PFL, Bryan JH: The relationship of host size to feeding by mosquitoes of the Anopheles gambiae Giles complex (Diptera: Culicidae).

    Bulletin of Entomological Research 1980, 70:133-144.

  35. Smith T, Beck HP, Kitua A, Mwankusye S, Felger I, Fraser-Hurt N, Irion A, Alonso P, Teuscher T, Tanner M: Age dependence of the multiplicity of Plasmodium falciparum infections and of other malariological indices in an area of high endemicity.

    Trans R Soc Trop Med Hyg 1999, 93:15-20.

  36. al-Yaman F, Genton B, Reeder JC, Anders RF, Smith T, Alpers MP: Reduced risk of clinical malaria in children infected with multiple clones of Plasmodium falciparum in a highly endemic area: a prospective community study.

    Trans R Soc Trop Med Hyg 1997, 91:602-605.

  37. Snow RW, Molyneux CS, Warn PA, Omumbo J, Nevill CG, Gupta S, Marsh K: Infant parasite rates and immunoglobulin M seroprevalence as a measure of exposure to Plasmodium falciparum during a randomized controlled trial of insecticide-treated bed nets on the Kenyan coast.

    The American Journal of Tropical Medicine and Hygiene 1996, 55:144-149.

  38. Snow RW, Shenton FC, Lindsay SW, Greenwood BM, Bennett S, Wheeler J, Delgiudice G, Verdini AS, Pessi A: Sporozoite antibodies and malaria in children in a rural area of The Gambia.

    Ann Trop Med Parasitol 1989, 83:559-568.

  39. Drakeley C, Sutherland C, Bouserna JT, Sauerwein RW, Targett GAT: The epidemiology of Plasmodium falciparum gametocytes: weapons of mass dispersion.

    Trends Parasitol 2006, 22:424-430.

  40. Malaria Access Project (MAP) [http://www.map.ox.ac.uk]


Figures

 

mcith_Standardizing_f01.JPG
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Figure 1   The average distribution of sample sizes, S(A), from 21 studies that report PfPR by age, A. The lines show, by age, the mean (blue), the trimmed mean (red, with 10% of extreme values eliminated), the median (thick black), the interquartile range (thin black), and the 5th and 95th quantiles (dashed lines).

mcith_Standardizing_f02.JPG
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Figure 2 The 21 training sets, ordered by peak PfPR. The PfPR data (black) have been plotted against the root of age in years, along with the confidence limits by the exact test for each proportion (grey). The maximum likelihood best-fit for the modified Pull & Grab model (orange) was also plotted; the plateau (horizontal dashed red line) and the age when PfPR begins to decline (vertical dashed red line) are indicated and the other fitted parameters are reported on each graph. The algorithm (blue) fitted to the data (i.e. four parameters were fixed at their trimmed mean values and the fifth parameter was fitted).  

mcith_Standardizing_f03.JPG
Click to enlarge image

Figure 3   Theory predicts that the slope of PfPR in young children (i.e. b) and the PfPR in older children (i.e. the plateau, P') should be correlated. The best-fit parameters describing these two quantities are plotted here. Two extreme values were excluded from this plot. There was no correlation with (p = 0.23) or without (p = 0.56) the extreme values.

mcith_Standardizing_f04.JPG
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Figure 4   Predicted PfPR plotted against observed PfPR for the four candidate algorithms for the testing set.

mcith_Standardizing_f05.JPG
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Figure 5    The age-PR relationship as generated by the algorithm. Holoendemic areas are colored dark green, hyper-endemic areas green, meso-endemic areas light green, and hypoendemic olive.

mcith_Standardizing_f06.JPG
Click to enlarge image

Figure 6   The graphs plot a subset of 87 PfPR estimates (i.e. PR1) in the testing set that were already standard (i.e. L1 ≥ 2 and U1 ≤ 10) and the predicted PfPR using either the PfPR pair (i.e. PR2, left) or the selected standardization algorithm (right). The dashed lines show the cutoffs for the classical categories [18]. The colors highlight properly classified hypoendemic (blue), mesoendemic (grey), and hyperendemic (orange) populations, as well as misclassified populations. Some mesoendemic populations were misclassified as hypoendemic (green) and some hyperendemic populations were misclassified as mesoendemic (orange). After standardizing, a few populations were mistakenly misclassified moved from hypoendemic to mesoendemic (cyan), or from mesoendemic to hyperendemic (tan). In sum, the PfPR would have been misclassified by the paired estimate (i.e. PR2) in 33/87 cases (38%). Using the selected Pull & Grab modified algorithm, the standardized values were misclassified in 16/87 cases (18%).

 


Table 01

Comparing Algorithms

Data Subset
All (n = 242)
Random (n = 160/82)
L1 2–10 U1 (n = 87)

r2
1st
2nd
3rd
r2 (n=87)
Cat. Err.
Pull & Grab
0.72
80%
94%
99%
0.71
18%
Regression
0.68
17%
70%
95%
0.68
31%
Interpolation
0.64
3%
28%
50%
0.57
22%
Garki
0.58
0%
0%
5%
0.46
25%
PR2
0.05
0%
0%
0%
0.21
38%

A summary of the skill of the four candidate standardization algorithms. The columns summarize the proportion of variance explained (r2), for the full data, the rankings of the four algorithms fitted to 100 random sub-samples of the testing set (n = 160) and tested on the remainder (n = 82), and the r2 and the proportion of categorical errors for the subset of the testing set that was within the standardization range. The table also includes an evaluation of the paired PfPR estimate (PR2).


Table 02

Algorithm Parameters

b
The slope, the rate that PfPR approaches the plateau (1.8 y-1)
P'
PfPR in older children; the plateau (Variable)
α
The age when PfPR begins to decline (≈ 9.5 years)
1-s
The asymptotic sensitivity of microscopy (1-s ≈ 36%)
c
The rate that PfPR declines with age, after age α (0.07 y-1)

The parameter names and interpretations in the algorithm based on the modified Pull & Grab equations.


Additional Files

Additional file 1.The training set. A description of the age-stratified PfPR data from 21 studies.

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Additional file 2.The testing set. A description of the pairs of PfPR estimates from 121 studies. The estimates were taken from the same population over different age-ranges.

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http://www.biology-online.org/articles/standardizing-estimates-plasmodium-falciparum-parasite.html