Dietary intake of P and the serum P concentration are important spects in patients with renal disease. During the course of CKD, many substances, which are normally excreted by the kidney, are retained in the body. Serum P concentration is usually maintained within the normal range of 2.5 to 4.5 mg/dL, by a variety of compensatory mechanisms, until renal disease has progressed to approximately stage 4 - 5 CKD (
15). An effective mechanism is the reduction in renal tubular absorption of phosphate (PO4), i.e. increased fractional excretion of P regulated by parathyroid hormone (PTH) and by the phosphatonin fibroblast growth factor 23 (
16,
17). In advanced stages of CKD, these mechanisms become inadequate to remove the P load, causing hyperphosphatemia (
18,
19). The Kidney Disease Outcomes Quality Initiative (Clinical Practice Guidelines for Bone Metabolism and Disease recommend that serum P levels should be maintained between 2.7 and 4.6 mg/dL in patients with CKD stages 3 and 4, and between 3.5 and 5.5 mg/dL in dialysis patients (
20).
Different therapeutic approaches are today available in clinical practice, to treat P balance disorders, such as dietary restrictions, adequate dialysis schedule and oral phosphate binders administration (
21).
Despite these approaches, normalization of serum P levels is often difficult and frequently not obtained. Recent data suggest that less than 50% of patients meet target levels for serum P (
22). Excessive dietary intake of P is one of the key factors. Our study showed that the majority of HD patients (50%) made use of pre-cooked foods from four to six times a week.
The PO4 additives can dramatically increase the amount of P consumed in the daily diet, especially because P is more easily absorbed in its inorganic form. In contrast, plant food, seeds and legumes that are rich in P, are usually associated with lower intestinal P absorption because of phytates in these foods. Moreover, the P load from the food additives in fast food, soft drinks and processed cheese and snacks is disproportionately high, in relation to their dietary P content, compared to natural P sources from animal-based (excluding dairy products) and plant-derived foods.
In these products, information on the P content and the type of preparation of food is often unavailable or misleading (
11). Therefore, the increased use of food additives rich in P, together with the growing popularity of ready meals and attendance of fast food restaurants, has greatly increased the amount of P consumed by both the general population and patients with CKD (
23).
In a recent randomized controlled trial, Sullivan et al. (
16) have shown that the inorganic P in processed foods contributed significantly to the P load of dialysis patients and educating patients with ESRD to avoid P containing food additives, leads to improvements in hyperphosphatemia.
Several studies have highlighted the contribution of socio-economic inequalities in health and mortality (
24-
26). Lower socio-economic status was independently associated with higher serum phosphate concentrations and higher likelihood of hyperphosphatemia among a diverse cohort of individuals participating in the CRIC Study (
27).
Gutierrez et al. (
27) shown that increasing poverty was independently associated with higher serum P levels and greater likelihood of hyperphosphatemia in a cohort of over 14,000 adults with largely preserved kidney function. Compared with participants in the highest quartile (income more than 300% of the federal poverty level), participants in the lowest quartile (income less than the federal poverty level) had more than twice the odds of hyperphosphatemia (≥ 4.4 mg/dL) (
27).
In another study, Gutierrez et al. (
28) performed a cross-sectional analysis of race, socio-economic status, and serum P among 2879 participants in the Chronic Renal Insufficiency Cohort. Low socioeconomic status was associated with higher serum P concentrations, irrespective of race (
28).
These data suggest that a low socio-economic status is a novel risk factor for increased serum P concentrations in CKD. We studied patients on HD and we have shown that elderly subjects, in middle-class regarding socio-economic and cultural status, represent the majority of this population. Patients living in lower socio-economic conditions had higher levels of P (P = 0.003). In this group, patients used to consume foods with highly absorbable and indeterminate P additives, explaining their higher likelihood of hyperphosphoremia. Indeed, the intake of pre-cooked food significantly increased serum P level (P = 0.002).
These results confirm and strengthen evidences emerging from previous studies (
16,
29). We also evaluated drug compliance of HD patients and observed that 55% of them individually reduce the dosage of the medications prescribed as P binders. The most frequent limitation in taking these drugs is low palatability and the high frequency of administration. These drugs are associated with gastrointestinal intolerance side effects (nausea, vomiting, abdominal pain, bloating, diarrhea, and constipation) that represent the most common reason for drugs discontinuation in CKD patients (
21).
The poor compliance, combined with the high consumption of convenience food, makes very difficult to control P levels in these patients. Whereas, as already mentioned, increased serum P is associated with cardiovascular disease, kidney disease progression, and death (
1-
10). Keeping the values of P in the normal range becomes a fundamental objective in patients with CKD. The increase in P, through promoting vascular calcification, endothelial dysfunction, and renal injury, suggests a causal link between elevated serum P and adverse health outcomes (
30-
33).
A thorough nutritional assessment and an adequate diet are crucial in HD patients. It would be useful to sensitize patients to follow a diet with a low load of P. A mixed composition of food from plant and food from animal origin should be encouraged, while the intake of processed foods should be limited. More detailed information of the P content of foods, described by manufacturers, can lead to better control of phosphorus intake with the diet. Finally, considering that patients show reduced compliance, in respect of drugs acting on the calcium-phosphorus balance, diet therapy plays an even more important role in the management of patients with ESRD.
In conclusion, we observed that the food containing hidden P is preferred for people who, besides having a low socio-economic status, also live alone, and, for this reason, consume unhealthy food. This is one of the firsts studies that correlate poverty and the condition of living alone (very often associated with depression) with serum P levels. Because of the strong association of these conditions with the diet quality, we wanted to stress the interventions that consider the population with low socio-economic situation, to deliver important messages on foods with the least amount of P and adequate protein content, and this may be a successful strategy in targeting patients at a higher risk of hyperphosphoremia.