The Prostate Cancer Road Map Hypothesis in 49 Countries; from Iron-Defi- ciency Anemia (IDA) to Death

Background: During the follow up analysis of the San Valentino (Italy) screening of cardiovascular diseases of death due to prostate cancer (PCa) in 2016 had in common iron deficiency anemia (IDA) in 2000. Methods: An analysis was conducted in 49 countries to determine the relationship between PCa, IDA and other 16 variables possibly connected with IDA. Data were retrieved from the WHO records (2018) using the ASDRs (Age-Standardized Death Rate x 100000 population) in 49 countries limited to the years 2000, 2010 and 2016. The 49 selected countries (SC) were those considered by WHO “with high completeness and quality of cause-of-death assignment” and “may be used for priority setting and policy evaluation”. PCa, IDA, and 16 diseases: tuberculosis, gonorrhea, syphilis, chlamydia in females, other sexually transmitted diseases (STDs in both genders), diarrheal diseases, gastric ulcers, cirrhosis, IDA, HIV, digestive diseases, respiratory infections, alcohol, and drugs addictions. The correlations with PCa were calculated using the Cluster analysis followed by the Multivariate analysis and the Residual Normal Quantile Plot. Results: IDA, HIV, chlamydia in females, and digestive diseases were significantly correlated with PCa. All the other variables resulted not correlated. Conclusions: The road map of PCa seems to be IDA, immune depression, followed by infections caused by chlamydia. Digestive diseasesother than gastric ulcers and cirrhosisare only minimally predictive. Chlamydia vaccination is suggested as a possible solution to protect from PCa. Prospective, long-term studies should be considered


Introduction
The epidemiological study in San Valentino (Italy) started in 1997 aimed at the screening of cardiovascular diseases [1,2]. During the follow up of the participants in 2016 the attention was focused on 3 males who died for prostate cancer (PCa).
Going back to their records, the only observation common to these patients was the presence of IDA beginning in 2000, without any infection or hematuria in the urines. These subjects partially recovered their hematocrit after 2000 with an appropriate diet (including an increase of meat intake and vitamin C supplementation). However, full recovery was not observed in the following years (2003 and 2004). These subjects were within the normal range for other blood tests including glucose, lipids and for clinical observations. The IDA recovery was managed at GP level. In 2010 a diagnosis of PCa was made and they eventually died in 2016.
The PCa is the fifth leading cause of death in man summing up about 300,000 cases in 2015 [3]. The pathogenesis has been studied [4][5][6] but still is unclear. The suggestion about foods and genetic trait characteristics [7] had emerged and the screening of Prostate-Specific Antigen (PCA) was suggested as an effective tool for earlier diagnosis with the aim of reducing deaths [8].
Age is considered the major risk factor [9], with race, socioeconomic status; PCa is more frequent in the underdeveloped countries [10,11] and death is related to the stage of cancer, the possible management, and its affordability, metastatic conditions, and type of therapy [12,13]. Preliminary studies concerning sexually transmitted infections (STDs) or prostatitis showed that their influence on PCa is unclear [14]. Some studied ruled out a possible role for gonorrhea and syphilis [15].
However, a systematic analysis of 47 studies concluded that gonorrhea was associated with PCa, whereas any other STDs, either bacterial or viral, were excluded [16]. IDA was never considered as a connecting or facilitating factor for PCa and the observation made in the San Valentino epidemiological study suggested investigating possible correlations of PCa with some of the most common diseases possibly causing IDA.
The analysis was conducted on all available data within the WHO records concerning total mortality for PCa in term of ASDRs (Age-Standardized-Death Rate x 100000 population) compared to ASDRs of IDA and diseases possibly causing IDA considering the year 2000 [17].

Criteria of choice for the variables and period of time
The Age-Standardized Death Rate x 100000 population (ASDRs), and Crude Death Rate x 100000 population (CDR) for PCa were considered. ASDRs were chosen as main variables because -unlike CDR prevalence/incidence measures -are free of the bias related to age.
The ASDRs data listed as Global Health Estimates 2016 published in 2018 were used [17]; PCa values were compared to IDA and other diseases known to cause IDA. Data regarding males were considered for all the variables, whereas for females the research was limited to STDs and chlamydia only.

Data collection
The values up to the fourth decimal place were taken from the WHO records relative to the selected ASDRs for 2000,

Criteria of choice of the countries
The data used for correlations were relative to the 49 countries (selected countries or SC) considered by WHO "with high completeness and quality of cause-of-death assignment" that "may be compared and time series may be used for priority setting and policy evaluation" (see Table 1). For the calculation of the CDR were considered all the 185 countries as listed in the WHO report. The male population in the respective years was taken from the same report.

Statistical evaluation
A five steps analysis was followed [18][19][20][21]. The first was the calculation of the averages ± SD for all the variables in order to obtain a general picture, followed by the % increase for each

Population, CRD, and ASDRs
In the 185 countries, the total male population is re- Comparing data of 2016 and 2000 almost all the ASDRs considered showed a reduction (see Table 2). For the rarer diseases with ASDRs <, 1 the most evident reduction was shown for gonorrhea (-66.7 %) and parasitic and vectorial diseases (-45.5 %).
In females, the only ASDRs considered were STDs and Chlamydia both showing a reduction of ≥50 %.

Cluster analysis
The Cluster analysis identified four clusters and the most represented variables are reported in Table 4. The variables within each cluster were similar to each other, but the difference from those included in the closest clusters. Using all of them in a multiple regression process was possible to adjust the comparison for any confounder since two or more related variables contained the same information.
IDA and five other variables were selected corresponding to the highest R squared values for PCa within the correspondent cluster as reported in Table 5 Table 7 Despite the time needed for PCa development up to death is not known, the period of 16 years was considered sufficient by other authors [8]. The choice of ASDRs as the main variable can be a further limitation because the values sometimes represent a cluster of diseases. In particular, IDA could be more consistent as a symptom within other illnesses determining death. This is also true for some of the other variables (e.g. chlamydia or gonorrhea) which can be concomitant with other severe diseases (e.g. cardiovascular, metabolic). However, as declared by WHO, the cause of death allows us to compare the mortalities among countries, and ASDRs is a reliable measure for the "diseases dimen- The WHO records do not differentiate the type of chlamydia (e.g. C. trachomatis or pneumoniae) and IDA can be a protective mechanism against infection since iron is needed for bacterial growth and survival [25]. Our findings confirm a possible statistical connection between IDA and chlamydia and indicate IDA as a possible concomitant cause and not as a consequence.

The ASDRs of the diseases correlated with PCA
Other infectious diseases such as TBC, syphilis, gonorrhea, were never correlated and most of the other infections (e.g. trichomoniasis) were rarely represented in the 49 SC countries.
The digestive diseases listed by WHO consists of many illnesses being a gastric ulcer and cirrhosis the most represented in the 49 SC, whereas all the other diseases (appendicitis, gastroduodenal diseases, paralytic ileus and intestinal obstructions, inflammatory bowel diseases, gallbladder, and biliary diseases, pancreatitis) are much less represented. Gastric-duodenal ulcer and cirrhosis were analyzed separately and no correlation with PCa was shown indicating that these diseases can be ruled out.
The relationship of PCa with other digestive diseases remains obscure, and no reliable hypothesis can be drawn because in the Prediction profile analysis their importance was minimal.
HIV is a disease associated with immune depression [26], characterized by a chronic inflammation that persists even during antiretroviral therapy (ART). This condition can be the ground for the development of PCa. IDA was shown to be prevalent in HIV patients [27] and even following active ART is associated with a higher risk of mortality [28]. However, anemia of different types could be determined by therapies for PCa. In this instance, it could "concentrate" the cases acting as a filter. Because of this, IDA could be considered a "consequence" and not a "cause". In the case of PCa, one of the most common therapies is the androgen deprivation therapy (ADT) which is recognized to cause a temporally normochromic normocytic anemia and not IDA [30,31]. In about 90 % of the cases, anemia due to ADT can be corrected with the use of recombinant erythropoietin; the condition is reversible after discontinuation of hormonal therapy [32][33][34]. Furthermore, altered lipid profile and insulin resistance are also common adverse effects [35]. Anemia, in general, has been described by approximately 30 % of PCa patients with metastases to the bone marrow at the time of the diagnosis [36]. A part of ADT, several other factors causing anemia have to be considered consisting of hematuria, radiotherapy, inflammatory cytokines, chronic diseases, poor nutritional status, and orchiectomy. All these conditions may cause mainly a leucoerythroblastic anemia.
However, IDA is classically defined as hypochromic microcytic anemia, and because of this, the impact of ATD can be disregarded. Furthermore, in our patients of the San Valentino epidemiological study, IDA could not have been caused by drugs (they were free of any therapy). Despite this, in the case of PCa one may not rule out completely the influence of other therapies (e.g. radiation, chemotherapy) causing IDA.
A large part of the world male population is affected by IDA (about 7-8 % of the males), and many chronic diseases are characterized by this symptom [37], particularly in those countries where foods are not sufficient either in terms of quantity and quality to ensure an appropriate iron intake.
Lack of food was not the case of most 49 SC, whereas the dietary intake (e.g. meat, vegetables, cereals, beverages) could be one of the causes of iron deficiency.
Iron is important for blood-red cell production that will be reduced in case of an impaired inflow of iron from storage sites into the transporting pool red cells [29]. The lack of iron does not affected cells alone since in general is consistent with the reduction of cellular proliferation, DNA synthesis, and the activity of iron-containing/dependent enzymes involved in the microbial killing.
As a rule, bacterial infections are followed by serum iron reduction which predisposes to infection morbidity and mortality [38]. In experimentally induced IDA, morbidity and mortality due to bacterial challenge increase several times [39] due to the impairment of cell-mediated immunity, and the intracellular bacterial killing capacity of polymorphonuclear cells (PMNs).
It is believed that viruses, unlike bacteria do not require iron as a growth factor [40]. Conversely, the availability of the free iron is a critical determinant for bacterial multiplication, such that pathogen and host compete for iron [41,42] and the host defense mechanism is aimed to deprive microbes of iron.
The problem that can arise is the influence of iron on viral growth. The PMNs, also in case of immune depression, continue to collect old erythrocytes and use their iron to replicate.
However, in the case of viral infection, they may also contain a virus, which takes an indirect advantage from PMNs replication to spread the infection. The consequence is that viruses will take an indirect advantage from IDA which was shown to be an independent predictive marker for an unfavorable HIV prognosis [43]. On the other hand, iron was also considered to favor neoplastic growth [44] and in this case, IDA could have a favorable aspect to counteract PCa.
This "Janus", two faces behavior of iron indicates that IDA could be considered as a protective mechanism against cancer but at the same time it may favor the pathogen micro-organism invasion which can trigger PCa development. However, considering the complexity of the present analysis, IDA seems to be more prominent as cause than as effect.

Conclusions
From the analysis of the data based on the WHO record concerning the 49 SC, three diseases were found correlated with PCa: IDA, HIV, and chlamydia in females. A sort of "road map" for PCa can be hypothesized.
The starting point can be IDA which allows the infective invasion caused by chlamydia or viruses such as HIV. This is the first time that chlamydia is considered one of the conditions responsible for PCa. The competence of the immune system may be compromised by IDA and the consequence is a reduction of the defense against the PCa. The increase of immunological capacity opens an avenue for specific vaccination against chlamydia (particularly for males). In the end, the presence of IDA in males stimulates a deeper and specific analysis of the patients.

Author contributions
Cornelli U conceived the trial, retrieved some of the WHO data and wrote the article; Belcaro G retrieved part of the WHO data; Martino Recchia was responsible for the statistical analysis. All the authors read and approved the final manuscript.