Obesity Clinical Trial
Official title:
The Links Between Water and Salt Intake, Body Weight, Hypertension and Kidney Stones: a Difficult Puzzle
Nephrolithiasis is a disease that strikes roughly 10% of the Italian population and its
incidence in industrialized countries is on the increase. The most common form of the
disease (80%) is Idiopathic Calcium Nephrolithiasis (ICN) with calcium-oxalate (CaOx) and/or
calcium-phosphate (CaP) stones. The etiopathogenesis involves both genetic and acquired
factors, the interplay of which leads to urinary biochemical anomalies at the root of stone
formation. The elements and urinary compounds involved are known as "urinary stone risk
factors". The risk factors for CaOx stones consist of low urine volume, hypercalciuria,
hyperoxaluria, hyperuricosuria, hypocitraturia and hypomagnesuria. In the case of CaP
stones, the hyperphosphaturia and pH parameters are of particular importance; a pH>7
promotes the formation of stones prevalently composed of phosphates, while a pH of between 6
and 7, associated with a volume <1l/day, can raise CaP supersaturation to a dangerously high
level and lead to the formation of mixed CaOx and CaP stones. For uric acid stones, the
elements involved are hyperuricosuria and pH<5.5. In general, the most prevalent alteration
in ICN is hypercalciuria (50%). Hypertension and obesity are also social diseases with
important epidemiological similarities to nephrolithiasis. These affinities have led to the
search for a common pathogenic moment. As far as hypertension is concerned, various studies
have demonstrated high calciuria in hypertensives with a linear relationship between 24-h
calciuria and arterial blood pressure. The incidence of stone disease is greater in
hypertensives than in normotensives and, by the same token, the incidence of hypertension is
greater in stone formers than in non stone formers, but it is not clear whether
nephrolithiasis is a risk factor for hypertension or vice versa. Moreover, a linear
relationship exists between calciuria and natriuria, where the calcium is the dependent
variable, with a much steeper slope of the straight line in stone formers and hypertensives
compared to controls. It has, in fact, been demonstrated that to reduce calcium, it is more
efficacious to reduce sodium intake as opposed to calcium intake. Finally, BMI and body
weight are independently associated with an increase in stone risk even though, due to a
number of bias (limited weight categories, low number of obese persons in the study
populations, no control group, no recording of food intake) the studies published failed to
be conclusive. In the final analysis, stone disease, arterial hypertension and excess
weight/obesity prove to be closely interconnected and it is possible to intervene with
targeted diets aimed at reducing the risk of illness and death from these diseases. Among
such dietary approaches, the reduction of sodium chloride in food, increased hydration and
an increased intake of foods with an alkaline potential seem to play an important role.
For many years now, the investigators research unit has been involved in projects, partially
financed by the Italian Ministry of University and Research (MIUR), geared towards studying
the effects induced by dietary changes in patients with calcium stone disease. The aim of
the present project is to analyse in depth the relationship between stone disease,
hypertension, body weight and water and salt intake both in the general population of the
area of Parma (where historically and by gastronomic tradition, the usual diet tends to have
a high salt content) and in a selected population of stone formers and hypertensives not
under treatment. A representative sample of the population of the area of Parma will be
studied, divided on the basis of weight category, in order to assess water and salt intake
and relationships with the presence of hypertension, and a sample of normal and hypertensive
stone formers randomized to receive for one year either water therapy+low salt diet or water
therapy alone.
Background and rationale
Nephrolithiasis is a disease that could be defined as social, due to its widespread
distribution and its continually increasing incidence in industrialized countries with a
high standard of living (1). In Italy, it strikes just under 10% of the population, leading
to expenditure of approx. 200 million euro/year for hospital admissions alone (2).
Idiopathic Calcium Nephrolithiasis (ICN) with the formation of calcium oxalate stones,
sometimes mixed with calcium phosphate ones, is the most common form, having an incidence of
roughly 80% (3,4). As regards distribution in the two sexes, a slightly higher incidence in
males has been observed. The pathogenesis of ICN involves both genetic and acquired factors
(5), the combining of which leads to urinary biochemical anomalies which lie at the root of
stone formation. A high rate of calcium-oxalate and/or calcium-phosphate supersaturation
leads to the formation of nests of crystals that can then grow and aggregate to form a
stone. The elements and urine compounds involved in the process of crystallization, whether
they be inhibitors or promoters, are known as urinary stone risk factors. For Ca-oxalate
they are: low urine volume (<2 l/day), hypercalciuria (>250mg/day), hyperoxaluria (>40
mg/day), hyperuricosuria (>600 mg/day), hypocitraturia (<320 mg/day) and hypomagnesuria (<50
mg/day). For Ca-phosphate, in addition to the above-mentioned factors, hyperphosphaturia
(>1000 mg/day) and urinary pH also acquire considerable importance: a pH>7 promotes the
formation of stones prevalently composed of phosphates, while a pH of between 6 and 7
associated with a urine volume <1l/day, can dangerously raise Ca-phosphate supersaturation
and lead to the formation of mixed Ca-oxalate and Ca-phosphate stones. Finally, for uric
acid stone disease the elements involved are hyperuricosuria and pH < 5.5. Among the stone
risk factors, the most common found in the urine of patients affected by ICN is
hypercalciuria with an incidence of around 50%. With regard to age of onset, there are two
peaks, one between 20 and 30 years of age and one between 50 and 60.
Hypertension and obesity are also widespread social diseases with important epidemiological
similarities to nephrolithiasis. These affinities have, over the years, led investigators to
seek interconnections between the three diseases in order to find a common pathogenic
moment. As far as hypertension is concerned, various studies have demonstrated that urinary
excretion of calcium is greater in hypertensives than in normotensives. A linear association
between the excretion of 24-h calcium and arterial blood pressure has been demonstrated in
numerous studies, including INTERSALT (6). In 1999, after following up 132 hypertensives and
135 controls for 5 years, our group published a paper which reported the onset of stone
disease in the hypertensives in significantly higher percentages compared to the controls,
with an RR of 5.5 (7). Moreover, a year earlier, Madore and Curhan published two studies
(8,9) conducted on a large cohort of Americans in which they demonstrated that patients with
a past history of nephrolithiasis without hypertension were more prone to become
hypertensive during the follow-up than non stone formers. These results, further confirmed
by many subsequent studies, did not however succeed in clarifying the doubt as to whether it
is the hypercalciuria of hypertensives that predisposes them to the development of stone
disease or whether it is the renal damage, albeit microscopic, caused by stone disease that
triggers the development of hypertension. Scientific literature has, however, identified,
for hypertensives, stone formers and controls alike, a linear relationship between the
excretion of calcium and the excretion of sodium, where calcium is the dependent variable
and where the slope of the straight line, i.e. the increase of calcium for each mmol of
sodium, is much greater in both stone formers and hypertensives than in controls. Moreover,
as far back as the '80s, it was demonstrated that a reduction in kitchen salt intake from 10
g to 4 g per day, has the capacity to reduce calciuria more than a reduction in calcium
intake from 1000 mg to 500 mg (10,11).
In 2002, we confirmed this experimental data with a paper published in the New England
Journal of Medicine in which we demonstrated in recurrent male hypercalciuric stone formers
followed up for 5 years, that a normal calcium, low-salt, low-protein diet had the power to
reduce both the calciuria and the stone recurrences much more significantly than a
low-calcium diet (12). Obviously it was not possible to separate the effect of the
restriction of sodium from the restriction of protein. Both diets were accompanied by the
recommendation to drink water, the effectiveness of which had already been demonstrated in
first-episode stone formers in a previous study randomized with a follow-up of 5 years
conducted on 199 stone formers and 101 controls (13).
The central role of body weight in determining stone risk is clearly described in scientific
literature. BMI, weight, abdominal circumference are independently associated with kidney
stone risk (14). Nevertheless, the mechanisms underlying this relation are still unknown.
Data exist in literature to suggest that body weight can affect the excretion of many
promoters or inhibitors of crystalline aggregation. For example, some population studies in
the United States have demonstrated how urine pH is inversely correlated to body weight and
how urinary excretion of calcium, oxalate and uric acid increase as body weight increases
(15,16). Notwithstanding these data, the effects of body weight on the excretion of many
urinary stone risk factors remains partly unknown; this is due to the limited weight
categories, the low number of obese people in the study populations, the absence of a
control group with "non stone formers" and the failure to record food intake in the studies
published. In addition to this, as regards urinary excretion, the evaluation of excess
weight solely on the basis of BMI values and abdominal circumference may seem somewhat
reductive. It would appear to be more useful to assess body composition, lean mass, fat
tissue mass and mineral mass. In this way, by better stratifying obesity classes, it might
become simpler to understand the intricate endocrine/metabolic changes that occur in obesity
(hyperinsulinism, hyperestrogenism etc.) and establish better correlations with the urinary
excretion of stone risk factors. In fact, some studies (16) have demonstrated a slight
increase in the total incidence of stone disease in female obese patients compared to males,
with a slightly higher mean age in the females and, in any case, ages being equal, with a
lower number of recurrences in the females compared to the males. These phenomena are
probably affected by the concentration of serum estrogens and by the transformation in the
fatty tissue of the adrenal androgens into estrogens; nonetheless the effects of serum
estrogens on the urinary excretion of calcium are unknown. Finally, some studies have
demonstrated that body weight also affects the composition of the stones. In fact, it has
been demonstrated how the incidence of uric acid stones is higher in overweight/obese
patients than in normal weight patients; some studies have highlighted that patients with
idiopathic uric acid nephrolithiasis have a higher BMI than hyperuricosuric patients who
form calcium oxalate stones. The pathophysiological link should be sought in
hyperinsulinism: in fact insulin resistance is associated with a decrease in the production
of renal ammonia leading to a consequent decrease in urinary pH, characteristic of uric acid
stone disease (17). This theory is indirectly corroborated by the aforementioned indirect
relationship between BMI and 24-h urine pH and the finding that also age-related reduced
urinary acidification capacity increases the risk of uric stone disease, irrespective of
body weight. On the basis of the above, it is clear how the presence of excess
weight/obesity, uric acid or mixed stone disease could raise suspicions of a Metabolic
Syndrome: there are, however, no conclusive studies on this, and neither have the effects on
stone risk and arterial blood pressure of water therapy and a low-salt diet in a population
of overweight/obese stone formers been sufficiently studied.
In the final analysis, nephrolithiasis, arterial hypertension and excess weight/obesity
prove to be closely interconnected and it is possible to develop targeted diets aimed at
reducing the risk of illness and death from this disease. Among such dietary approaches, the
reduction of sodium chloride in food, increased hydration and an increased intake of foods
with an alkaline potential (18) seem to play an important role.
For many years now, our research unit has been involved in projects, partially financed by
the Italian Ministry of University and Research (MIUR), geared towards studying the effects
induced by dietary changes in patients with calcium stone disease. The aim of the present
project is to deepen our knowledge on the relationship between stone disease, hypertension,
body weight and water and salt intake both in the general population of the area of Parma,
where historically and by gastronomic tradition the normal diet tends to have a high salt
content, and in a selected population of stone formers and hypertensives.
Experimental design/description of methodologies
As already mentioned, the aim of this project is to attempt to clarify the relationship
between idiopathic calcium stone disease, salt and water intake, hypertension and body
weight.
The study will be divided into two sub-projects:
1. Assessment of the salt and water intake in the general population of the area of Parma
(duration 24 months)
2. Assessment of the effects of a low salt + water therapy diet vs water therapy alone for
one year in patients with idiopathic calcium stone disease, both male and female,
normal- and hypertensive without treatment (duration 12 months)
At least 350 healthy controls, 100 hypertensive non stone formers without treatment, 150
normotensive stone formers and 100 hypertensive stone formers without treatment will be
enrolled in the study. Both the controls and the stone formers will be subdivided according
to a 4-class BMI scale. The classes will have the following characteristics: Class 1 BMI £
18.9 (underweight condition); Class 2 BMI between 19 and 24.9 (normal weight condition);
Class 3 BMI between 25 and 29.9 (excess weight condition); Class 4 BMI > 30 (obesity). The
patients enrolled will have their medical history recorded after which they will be
subjected to the measurement of anthropometric parameters and arterial blood pressure, and a
stone risk mini-profile will be drawn up including volume, creatinine, sodium, potassium and
calcium measured according to the methods published. As is well-known, 24-h urinary sodium
is considered the "gold standard" for the assessment of food-related salt intake, creatinine
is a sensitive marker of lean mass, potassium is an index of the body's alkaline potential
and calcium has the important pathophysiological role described above.
The stone formers will be randomized to receive a low salt+water therapy diet or water
therapy alone, for one year. The term "water therapy" refers to an abundant intake of water
with a low mineral and low sodium content (at least 2 litres in winter and 3 in summer). For
stone formers only, at the end of the 12 month period of therapy, anthropometric parameters
and arterial blood pressure will be measured once more and the urinary mini-profile will be
repeated.
Objectives
Sub-project 1) "Assessment of the salt and water intake in the general population of the
area of Parma"
Primary objective To assess the consumption of kitchen salt (NaCl) and the water intake in
the general population of the area of Parma after adjustment for the BMI, and to study any
possible relationships with the presence of arterial hypertension.
Secondary objectives
1. To study the urinary sodium-calcium relationship in the general normo- and hypertensive
population without treatment.
2. To confirm the described relationship between 24-h calciuria and arterial blood
pressure.
3. To identify any correlations between BMI and urinary solutes.
4. To stratify the salt and water intake by age category.
5. To assess the stone risk in the general normo- and hypertensive population without
treatment.
6. To define urinary sodium-potassium-volume relationships in the general normo- and
hypertensive population without treatment.
Sub-project 2) "Assessment of the effects of a low salt + water therapy diet vs water
therapy alone for one year in patients with idiopathic calcium stone disease, both male and
female, normal- and hypertensive without treatment (duration 12 months)"
Primary objective To assess the effects of a low-salt diet + water therapy vs water therapy
alone, maintained for one year, on calciuria, arterial blood pressure and body weight in
normo- and hypertensive stone formers.
Secondary objectives
1. To study the urinary sodium-calcium relationship in normo- and hypertensive stone
formers without treatment and compare it with matched non stone formers.
2. To study the relationship between 24-h calciuria and arterial blood pressure in stone
formers and compare it with matched non stone formers.
3. To identify any correlations between BMI and urinary solutes and evaluate the
differences with matched non stone formers.
4. To stratify the salt and water intake by age category and recurrence rate in recurrent
stone formers.
5. To assess the compliance with the low salt diet after one year.
6. To define the urinary sodium-potassium-volume relationships in normo- and hypertensive
stone formers without treatment and compare them with matched non stone formers.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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