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ORIGINAL RESEARCH COMMUNICATION |
1 From the Department of Public Health and Primary Care, University of Cambridge, Strangeways Site, Cambridge, United Kingdom (AAW); Medical Research Council Dunn Human Nutrition Unit, Cambridge, United Kingdom (SAB); and the Strangeways Research Laboratory (JR) and Clinical Gerontology Unit (KTK), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
2 Supported by program grants from the Medical Research Council UK and Cancer Research UK and by the European Union, Stroke Association, British Heart Foundation, the UK Department of Health, Food Standards Agency, and the Wellcome Trust.
3 Reprints not available. Address correspondence to AAW Welch, Department of Public Health and Primary Care, University of Cambridge, Strangeways Site, Wort's Causeway, Cambridge, CB1 8RN United Kingdom. E-mail: ailsa.welch{at}phpc.cam.ac.uk.
| ABSTRACT |
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Objective: We investigated the relation between a measure of dietary acid-base load, potential renal acid load (PRAL), and calcaneal broadband ultrasound attenuation (BUA) after adjustment for confounders and also compared the results with different estimates of acid-base load.
Design: A cross-sectional study was conducted in 14 563 men and women aged 4282 y living in Norfolk, United Kingdom, in which measures of calcaneal BUA and dietary PRAL were estimated by using the European Prospective Investigation into Cancer and Nutrition Norfolk (EPIC-Norfolk) food-frequency questionnaire.
Results: A more acidic dietary intake (high PRAL) was significantly associated with lower calcaneal BUA in women but not in men; there was a difference of
2% in BUA between the highest and lowest quintiles of PRAL, independent of age, body mass index, smoking habit, physical activity, diagnosed osteoporosis, and history of fracture, and (in women) hormone replacement therapy. No relation was observed between history of fracture or incident fracture and PRAL. Those with the greatest PRAL had higher intakes of meat, fish, eggs, and cereal and cereal products and lower intakes of fruit and vegetables, tea, and coffee.
Conclusion: PRAL was inversely associated with bone ultrasound measures in women, but the magnitude of the association was relatively small compared with other known risk factors. Further longitudinal studies are required to establish whether, in the long term, these small effects are important in overall fracture risk in populations.
Key Words: Acid-base balance diet broadband ultrasound attenuation BUA bone density potential renal acid load PRAL European Prospective Investigation into Cancer and Nutrition Norfolk EPIC-Norfolk
| INTRODUCTION |
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The acid-base balance in the body is important to bone health and is modifiable by diet (3-5). The organic acids that are produced during metabolism and the hepatic oxidation of sulfur-containing amino acids (cysteine and methionine) lower blood pH through increased production of hydrogen ions (5, 6). Alkaline dietary salts contain the cations (potassium, calcium, and magnesium) and act as buffers for organic acids that have the potential to raise pH. If insufficient levels of buffering capacity are available from alkaline salts, mild metabolic acidosis develops, even in healthy persons (5, 7, 8). In healthy persons in whom acid production is increased experimentally, acid production increases more than does renal net acid excretion, so that acid balances become positive (8).
The suggested mechanism for the negative effect of increased metabolic acidosis on bone is bone resorption (8-12). Mature osteoclasts are activated, and osteoclastic calcium mobilization is stimulated so that bone matrix mineralization is inhibited (10, 13, 14). Because bone provides a large reservoir of buffering capacity from the content of carbonate and hydroxyapatite salts, mobilization of this reservoir ameliorates acidosis (13-15). The release of CaCO3 is stimulated by acidosis, and increased excretion of calcium and markers of bone resorption has been found during metabolic acidosis (5, 8, 16, 17), which indicates that buffering by bone is a mechanism by which large changes in pH are avoided in the body (8, 13). Although indirect evidence is available for the effect of metabolic acidosis on bone from in vivo intervention studies and in vitro experiments, studies of bone density in general populations are limited2 in women, 1 in children, and none in men (18-20). The dietary potential renal acid load (PRAL) is one measure of acid-base load. It is calculated by taking into account the mineral and protein composition of foods, the average intestinal absorption rates of nutrients, sulfur metabolism, and urinary excretion of organic acids (21, 22).
The purpose of the present study was to investigate the cross-sectional relation between a dietary measure of acid-base load (PRAL), calcaneal broadband ultrasound attenuation (BUA; a measure of bone density), and incident fracture risk in a general population of men and women aged 42-82 y in the Norfolk area of the United Kingdom. Second, because adequate intakes of calcium and protein were shown to determine bone density, we investigated whether a relation existed between intakes of calcium and protein and the effect of dietary acid-base load (23-25). Third, because different methods of calculating dietary acid-base load are available, we wanted to compare the effect of different methods of estimation, specifically the net rate of noncarbonic endogenous acid production (NEAP) and the protein-to-potassium ratio (protein:potassium), on BUA (4, 7).
| SUBJECTS AND METHODS |
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All participants gave written informed consent and then were asked to complete a self-administered food-frequency questionnaire (FFQ) and a detailed health and lifestyle questionnaire (29, 30). The FFQ was designed to estimate habitual intake during the previous year, and nutrients were computed with the use of an in-house program, the CAFE (Compositional Analyses from Frequency Estimates) program (29). Ethical permission was granted by the Norfolk and Norwich Ethics Committee.
History of fracture was established from the answers to the question, "Has your doctor ever told you that you have any of the following? " The question was followed by a list of conditions that included osteoporosis, hip fracture, wrist fracture after age 20 y, and vertebral fracture (spinal fractures). Participants were followed for health events and the number of incident fractures by site (hip, wrist, spine, and other). The number of incident fractures was obtained between date of entry to the study (19972000) and mid-2005 for participants admitted to the hospital with the use of the unique National Health Service number by linking to the East Norfolk Health Authority database (ENCORE), which identifies all hospital contacts throughout England and Wales for Norfolk residents.
Quantitative ultrasound scanning was used to measure BUA and velocity of sound of the calcaneum with the use of the CUBA clinical machine (McCue Ultrasonics, Winchester, United Kingdom) at least twice on each foot, as described elsewhere (27, 28). Five machines were used, and each was calibrated daily with its physical phantom and monthly with a roving phantom and on one operator's calcaneum. We previously examined the data for evidence of systematic differences in temperature and machine by using multivariate regression models of BUA on age, weight, height, body mass index (BMI; in kg/m2), smoking habit, use of hormone replacement therapy (HRT) for women, and previous fracture history. We found that no further adjustments for temperature, machine, or machine drift informed the fit of the data; therefore, the data are presented unadjusted for temperature (27). Height and weight were measured to the nearest 0.1 cm and 0.2 kg, respectively, while participants were wearing light clothing and no shoes (26, 27).
The PRAL index was calculated by using individual nutrients derived from the FFQ by using the following formula (22, 29):
![]() | (1) |
Because previous studies also used other measures of acid-base load and because it was indicated that protein:potassium is the main determinant of PRAL, protein:potassium was calculated (protein g/d divided by potassium mEq/d), and renal net acid excretion, hereafter referred to as NEAP, was also calculated according to equations determined by Frassetto et al (7) (unadjusted for energy). The analyses were repeated with the use of these 2 measures, as in the following equation:
![]() | (2) |
We compared mean BUA in men and women in the different quintiles of PRAL before and after adjustment for age, BMI, smoking status, physical activity, and previously diagnosed osteoporosis and for HRT status in women; these factors were previously established as having a significant relation to calcaneal BUA within this population (27, 32). Men and women were studied separately because we previously found important sex differences in age-related bone loss in this population (21). Because the effect of acid-base load may be expected to differ depending on adequate intakes of calcium and because protein could also affect bone health independently of acid-base load, the analyses were repeated and additionally adjusted for calcium and protein. Analyses were also repeated and included adjustment for total energy intake. We also repeated the analyses with the use of velocity of sound. However, because the results did not differ substantially from those for BUA, only data for BUA are presented here.
Because the effect of HRT on bone density in postmenopausal women is well established, the analyses were repeated after excluding women currently taking HRT and after adjustment for total energy intake. Because a history of fracture is also known to affect BUA, the analyses were repeated after the exclusion of persons with a history of fracture. Mean PRAL was calculated according to incident fracture status and was adjusted for age, BMI, total energy intake, previously diagnosed osteoporosis, physical activity, and smoking status and (in women) the use of HRT.
Intakes of nutrients and food types were stratified by quintiles of PRAL. In the United Kingdom, the main sources of potassium are potatoes and savory snacks, fruit and vegetables, and meat and meat products (33). The main sources of magnesium are cereals and cereal products, fruit and vegetables, and beverages (33). The main sources of protein and phosphorus are meat and meat products, milk and milk products, and cereals and cereal products (33).
Statistical analysis
Statistical analyses were performed with STATA statistical software (version 7.0; Stata Corp, College Station, TX). All analyses were stratified by sex. Mean BUA, adjusted for covariates, was calculated by analysis of covariance. Analysis of variance was used to test for differences among quintiles of PRAL for all variables except physical activity, smoking, and HRT status, for which chi-square tests were performed. Relative risks were calculated with the use of single-variable and multivariate logistic regressions.
In a further analysis to compare the relative magnitude of effect of PRAL with other known osteoporotic risk factors, the continuous variables were standardized and run in a multivariable regression. PRAL was analyzed by SD (z score), BMI by 3-unit groups, and age by 10-y groups. The inactive and moderately active categories of exercise were compared with the moderately active and active categories; current smoking was compared with no smoking; and the use of HRT medication was compared with no use of HRT medication.
To quantify the effects of dietary acid-base load on urinary acid-base excretion, a further analysis of urine pH in a subsample of 363 men and women aged 4379 y was conducted with the use of a pH meter (model 3310; Jenway, Dunmow, United Kingdom) in 24-h urine collections. The pH was regressed against quintiles of PRAL.
| RESULTS |
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When classified by quintiles of PRAL, the trends for the nutrients comprising PRAL and also NEAP and protein:potassium were significant (P < 0.001) (Table 2
). Men and women in the top quintile of PRAL (most acidic) consumed approximately twice as much meat, approximately one-quarter as much fish, and
40% more cereals and cereal products than did those in the bottom quintile (Table 3
). Intakes of fruit and vegetables and of tea and coffee in the top quintile of PRAL were
60% and
80%, respectively, of those in the lowest quintile. Trends in intake of food types associated with quintile of PRAL were significant (P < 0.001).
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When the analyses were repeated with NEAP and protein:potassium, the results did not differ significantly (data not shown). The correlation between the different measures of acid-base load was 0.93 (P < 0.001) for the relation between PRAL and protein-potassium and for that between PRAL and NEAP.
In the comparative regression analysis that used standardized variables all variables except smoking status were significant in women (Table 5
). Age and the use of HRT were the variables most strongly associated with BUA in women, followed by BMI, physical activity, smoking status, and PRAL, whereas, in men, the effects were all much smaller but differed significantly from those in women for age and BMI.
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| DISCUSSION |
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PRAL is a measure of the relative consumption of foodstuffs supplying the nutrients included in the acid load. The foods contributing the most to the acid load are meat, fish, milk and milk products, and eggs; cereal grains and foods are also main contributors (34). In the present study, there were significant (P < 0.001) trends of all food groups with PRAL, with higher intakes of meat, fish, eggs, and cereal and cereal products and lower intakes of fruit and vegetables, tea, and coffee between the highest quintile of PRAL and the lowest.
Mean PRAL was more alkaline in our study (3.68 ± 10.51 mEq/d; range: 46.284.9 mEq/d) than in another UK study (7.60 mEq/d; range: 119.7168.18 mEq/d; (35). The PRAL index does not include the contribution from organic acids, and, in populations with relatively alkaline intake, organic acids could be more important (13). However, because organic acids are calculated from body size and because BMI is the main determinant of BUA, we wanted to determine the effect of dietary acid-base load independent of body weight. Although the diet in the present study was more alkaline than that in another UK study, our average estimate of NEAP was 46 mEq/d, which is similar to that in the United States (48 mEq/d) (34).
The size of association between BUA and dietary acid-base load in women between quintiles 1 and 5 of PRALthe most alkaline and most acidic, respectivelywas
2% after adjustment for known factors that affect BUA (ie, BMI, age, smoking status, exercise behaviors, previously diagnosed osteoporosis, and use of HRT medication in women) and after exclusion of subjects taking HRT medication and subjects with a history of fracture. When protein and calcium intakes were accounted for, there was little difference in the results. However, compared with other known risk factors, the effect of PRAL is small. In addition, no association was found with either a history of fracture or incident fracture.
The magnitude of the associations found are similar to those in another UK study, in which a 24% reduction in lumbar spine and hip bone density between quartiles 1 and 4 of dietary NEAP was found (1056 premenopausal and perimenopausal women aged 4554 y) (19). In further analyses of premenopausal, perimenopausal, and postmenopausal women, no significant difference was observed in the bone mineral density of the lumbar spine or femoral neck with NEAP; however, in menstruating women, significant associations were observed with energy-adjusted NEAP at the femoral neck (P = 0.04) and with NEAP (P = 0.026) and energy-adjusted NEAP (P = 0.014) at the lumbar spine (18). In a study with children aged 618 y, those with a higher PRAL had significantly less cortical area (P < 0.05) and bone mineral content (P < 0.01) after adjustment for protein intake (20). PRAL accounted for 2% of the variation in bone indexes.
The correlations between the different dietary indexes of acidityPRAL, NEAP, and protein:potassiumwere high and were similar to those in another study (35). The results of analyses with the use of these indexes also did not differ significantly, which indicated that they capture the same elements of dietary acid-base load.
We found no association between dietary intake of PRAL and BUA in men in this population. It is well documented that bone density and BUA decrease with age in women. Although our previous study confirmed these findings in women, we found only small age-related differences in BUA in men (27, 36-43). Why women should be more sensitive than men to the effects of dietary acid load remains an open question. Bone loss in women is related to reduced production of circulating estrogen during and after menopause. It is possible that the effects of mild metabolic acidosis induced by diet could interact with the effects of estrogen withdrawal in women. Although the relation between PRAL and BUA in women was small, because there is an age-related decline in renal function that leads to development of low-grade diet-dependent metabolic acidosis, the effect of excess dietary acid could have a greater effect as people age (44).
The present study has several limitations. The cross-sectional associations limit the causal inferences that can be made, although there are biologically plausible mechanisms for the relation between dietary acid load and bone metabolism. It is unlikely that persons with different bone measures across the normal range would change their dietary intake. Of course, we cannot exclude confounding, although the associations in women were independent of known factors that influence bone health, such as smoking and BMI. The study could have lacked power to detect associations or could have underestimated any associations because of measurement errors in assessment of diet and bone health or because of the range of dietary intake or bone measures. Measurements with BUA were made of the calcaneum and not of the spine or hip. Nevertheless, previous associations with known osteoporotic risk factors and increased risk of incident fracture with BUA were shown in this population (27, 28). As with other studies reporting associations, we used an FFQ to measure diet; in a substudy, we found significant relations with PRAL and urinary pH, which indicated that the dietary measurement reflects the acid-base balance in the body.
Evidence that mild metabolic acidosis is detrimental to bone health has been available for some time (3, 4, 8, 45, 46), although the present study is the largest population study to show an association between a more acidic dietary load and bone health in women. Our findings concur with previous small-scale human intervention and animal studies that found measurable effects of dietary interventions designed to modify the acid-base load on measures of blood and urine pH and bone turnover (5, 8, 16, 17). Supplementation studies with alkaline salts have found effects on markers of bone turnover and urinary pH and net acid excretion (8, 16, 47). In addition, animal and in vitro studies have elucidated the mechanisms for the effect of metabolic acidosis on bone metabolism (10-12, 45, 48, 49) and have also established that metabolicnot respiratoryacidosis is responsible for the effect of modified (blood) pH on bone cells and that this effect is mediated by prostaglandin E2 (12, 49).
In conclusion, we found that a more acidic PRAL was associated with a significantly lower calcaneal BUA in women but not in men. We also found no evidence that risk of history of fracture or incident fracture was affected in either men or women. Although the association in women was independent of other known factors that influence bone, the magnitude of these associations was relatively small compared with other known risk factors. However, longitudinal studies are required to establish whether, in the long term, these small effects are important to overall fracture risk in populations.
| ACKNOWLEDGMENTS |
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| REFERENCES |
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