Renal Net Acid Excretion Capacity Is Comparable in Prepubescence, Adolescence, and Young Adulthood but Falls with Aging

OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. DESIGN: Cross‐sectional observational study. SETTING: Community‐based. PARTICIPANTS: Young participants were from the DOrtmund Nutritiona...

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Published inJournal of the American Geriatrics Society (JAGS) Vol. 56; no. 8; pp. 1442 - 1448
Main Authors Berkemeyer, Shoma, Vormann, Jürgen, Günther, Anke L. B., Rylander, Ragnar, Frassetto, Lynda A., Remer, Thomas
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.08.2008
Blackwell
Wiley Subscription Services, Inc
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ISSN0002-8614
1532-5415
1532-5415
DOI10.1111/j.1532-5415.2008.01799.x

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Abstract OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. DESIGN: Cross‐sectional observational study. SETTING: Community‐based. PARTICIPANTS: Young participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden. MEASUREMENTS: Twenty‐four‐hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55–75; n=85), young adults (aged 18–22; n=117), adolescents (aged 13–14; n=112), and prepubescent children (aged 6–7; n=217). NAEC was determined as 24‐hour NAE adjusted for urine pH using the residual method. RESULTS: In elderly participants 24‐hour urinary pH (5.9±0.53) was lower (P<.05) and NAE (60±27 mEq/d) higher (P<.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants (P<.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults. CONCLUSION: The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.
AbstractList To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people.OBJECTIVESTo evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people.Cross-sectional observational study.DESIGNCross-sectional observational study.Community-based.SETTINGCommunity-based.Young participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden.PARTICIPANTSYoung participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden.Twenty-four-hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55-75; n=85), young adults (aged 18-22; n=117), adolescents (aged 13-14; n=112), and prepubescent children (aged 6-7; n=217). NAEC was determined as 24-hour NAE adjusted for urine pH using the residual method.MEASUREMENTSTwenty-four-hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55-75; n=85), young adults (aged 18-22; n=117), adolescents (aged 13-14; n=112), and prepubescent children (aged 6-7; n=217). NAEC was determined as 24-hour NAE adjusted for urine pH using the residual method.In elderly participants 24-hour urinary pH (5.9+/-0.53) was lower (P<.05) and NAE (60+/-27 mEq/d) higher (P<.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants (P<.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults.RESULTSIn elderly participants 24-hour urinary pH (5.9+/-0.53) was lower (P<.05) and NAE (60+/-27 mEq/d) higher (P<.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants (P<.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults.The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.CONCLUSIONThe capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.
OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. DESIGN: Cross‐sectional observational study. SETTING: Community‐based. PARTICIPANTS: Young participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden. MEASUREMENTS: Twenty‐four‐hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55–75; n=85), young adults (aged 18–22; n=117), adolescents (aged 13–14; n=112), and prepubescent children (aged 6–7; n=217). NAEC was determined as 24‐hour NAE adjusted for urine pH using the residual method. RESULTS: In elderly participants 24‐hour urinary pH (5.9±0.53) was lower ( P <.05) and NAE (60±27 mEq/d) higher ( P <.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants ( P <.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults. CONCLUSION: The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.
OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. DESIGN: Cross‐sectional observational study. SETTING: Community‐based. PARTICIPANTS: Young participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden. MEASUREMENTS: Twenty‐four‐hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55–75; n=85), young adults (aged 18–22; n=117), adolescents (aged 13–14; n=112), and prepubescent children (aged 6–7; n=217). NAEC was determined as 24‐hour NAE adjusted for urine pH using the residual method. RESULTS: In elderly participants 24‐hour urinary pH (5.9±0.53) was lower (P<.05) and NAE (60±27 mEq/d) higher (P<.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants (P<.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults. CONCLUSION: The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.
To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. Cross-sectional observational study. Community-based. Young participants were from the DOrtmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden. Twenty-four-hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55-75; n=85), young adults (aged 18-22; n=117), adolescents (aged 13-14; n=112), and prepubescent children (aged 6-7; n=217). NAEC was determined as 24-hour NAE adjusted for urine pH using the residual method. In elderly participants 24-hour urinary pH (5.9+/-0.53) was lower (P<.05) and NAE (60+/-27 mEq/d) higher (P<.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants (P<.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults. The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses.
To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people. Cross-sectional observational study. Community-based. Young participants were from the Dortmund Nutritional and Anthropometric Longitudinally Designed Study, Dortmund, Germany; elderly participants were from Gothenburg, Sweden. Twenty-four-hour urine pH, net acid excretion (NAE), urinary phosphorus, total nitrogen excretion, and anthropometric data were measured in healthy elderly people (aged 55-75; n=85), young adults (aged 18-22; n=117), adolescents (aged 13-14; n=112), and prepubescent children (aged 6-7; n=217). NAEC was determined as 24-hour NAE adjusted for urine pH using the residual method. In elderly participants 24-hour urinary pH (5.9±0.53) was lower ( P <.05) and NAE (60±27 mEq/d) higher ( P <.05) than in the three other groups. In a regression model adjusted for age, sex, and body surface area, NAEC showed a clear decrease with age, with highest values in prepubescents and lowest in elderly participants. However, NAEC remained significantly lower only in elderly participants ( P <.001) after the inclusion of total nitrogen excretion, a protein intake index, which was included because protein intake is known to modulate renal function. NAEC was approximately 8 mEq/d lower in healthy elderly participants than in young adults. The capacity to excrete net endogenous acid does not vary markedly from childhood to young adulthood but falls significantly with age, implying that elderly people may require higher daily alkalizing mineral intake to compensate for renal function losses. [PUBLICATION ABSTRACT]
Author Rylander, Ragnar
Vormann, Jürgen
Günther, Anke L. B.
Berkemeyer, Shoma
Remer, Thomas
Frassetto, Lynda A.
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  fullname: Berkemeyer, Shoma
  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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  fullname: Günther, Anke L. B.
  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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  fullname: Rylander, Ragnar
  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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  givenname: Lynda A.
  surname: Frassetto
  fullname: Frassetto, Lynda A.
  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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  givenname: Thomas
  surname: Remer
  fullname: Remer, Thomas
  organization: From theResearch Institute of Child Nutrition, Dortmund, Germany†Institute for Prevention and Nutrition, Ismaning, Germany‡BioFact Environmental Health Research Center, Lerum, Sweden§Department of Medicine, University of California at San Francisco, San Francisco, California
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IsPeerReviewed true
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Issue 8
Keywords Human
Kidney disease
Excretion
Senescence
Urinary system disease
Renal function
Healthy subject
healthy subjects
Ageing
net acid excretion capacity
Base
Protein
Kidney
Urinary system
Acids
Capacity
Adolescent
Young adult
Fall
Pharmacokinetics
acid-base
Elderly
Geriatrics
Language English
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PublicationCentury 2000
PublicationDate August 2008
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  text: August 2008
PublicationDecade 2000
PublicationPlace Malden, USA
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PublicationTitle Journal of the American Geriatrics Society (JAGS)
PublicationTitleAlternate J Am Geriatr Soc
PublicationYear 2008
Publisher Blackwell Publishing Inc
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Wiley Subscription Services, Inc
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References Hayton WL. Maturation and growth of renal function: Dosing renally cleared drugs in children. AAPS PharmSci 2000;2:E3.
Manz F, Wentz A, Lange S. Factors affecting renal hydrogen ion excretion capacity in healthy children. Pediatr Nephrol 2001;16:443-445.
Molnar D, Schutz Y. Fat oxidation in nonobese and obese adolescents: Effect of body composition and pubertal development. J Pediatr 1998;132:98-104.
Jehle S, Zanetti A, Muser J et al. Partial neutralization of the acidogenic Western diet with potassium citrate increases bone mass in postmenopausal women with osteopenia. J Am Soc Nephrol 2006;17:3213-3222.
Fliser D, Ritz E, Franek E. Renal reserve in the elderly. Semin Nephrol 1995;15:463-467.
Adler S, Lindeman RD, Yiengst MJ et al. Effect of acute acid loading on urinary acid excretion by the aging human kidney. J Lab Clin Med 1968;72:278-289.
Remer T, Manz F. Potential renal acid load of foods and its influence on urine pH. J Am Diet Assoc 1995;95:791-797.
Manz F, Wentz A. Renal net acid excretion related to body surface area in children and adolescents. DONALD (DOrtmund Nutritional and Anthropometric Longitudinally Designed) Study. Pediatr Nephrol 2000;15:101-104.
Remer T, Berkemeyer S, Rylander R et al. Muscularity and adiposity in addition to net acid excretion as predictors of 24-h urinary pH in young adults and elderly. Eur J Clin Nutr 2007;61:605-609.
Schurch MA, Rizzoli R, Slosman D et al. Protein supplements increase serum insulin-like growth factor-I levels and attenuate proximal femur bone loss in patients with recent hip fracture. A randomized, double-blind, placebo-controlled trial. Ann Intern Med 1998;128:801-809.
Remer T, Neubert A, Maser-Gluth C. Anthropometry-based reference values for 24-h urinary creatinine excretion during growth and their use in endocrine and nutritional research. Am J Clin Nutr 2002;75:561-569.
Bingham SA. Urine nitrogen as a biomarker for the validation of dietary protein intake. J Nutr 2003;133 (Suppl 3):921S-924S.
Wang Y, Moss J, Thisted R. Predictors of body surface area. J Clin Anesth 1992;4:4-10.
Tasevska N, Runswick SA, Bingham SA. Urinary potassium is as reliable as urinary nitrogen for use as a recovery biomarker in dietary studies of free living individuals. J Nutr 2006;136:1334-1340.
Sebastian A. Dietary protein content and the diet's net acid load: Opposing effects on bone health. Am J Clin Nutr 2005;82:921-922.
Rowe JW, Andres R, Tobin JD et al. The effect of age on creatinine clearance in men: A cross-sectional and longitudinal study. J Gerontol 1976;31:155-163.
Goodman AD, Lemann J Jr, Lennon EJ et al. Production, excretion, and net balance of fixed acid in patients with renal acidosis. J Clin Invest 1965;44:495-506.
Hirschberg R, Rottka H, Von Herrath D et al. Effect of an acute protein load on the creatinine clearance in healthy vegetarians. Klin Wochenschr 1985;63:217-220.
Remer T, Manz F. Dietary protein as a modulator of the renal net acid excretion capacity: Evidence that an increased protein intake improves the capability of the kidney to excrete ammonium. Nutr Biochem 1995;6:431-437.
Manz F, Remer T, Decher-Spliethoff E et al. Effects of a high protein intake on renal acid excretion in bodybuilders. Z Ernahrungswiss 1995;34:10-15.
Poortmans JR, Ouchinsky M. Glomerular filtration rate and albumin excretion after maximal exercise in aging sedentary and active men. J Gerontol A Biol Sci Med Sci 2006;61:1181-1185.
Rylander R, Remer T, Berkemeyer S et al. Acid-base status affects renal magnesium losses in healthy, elderly persons. J Nutr 2006;136:2374-2377.
Kalhoff H, Manz F, Diekmann L et al. Decreased growth rate of low-birth-weight infants with prolonged maximum renal acid stimulation. Acta Paediatr 1993;82:522-527.
Berkemeyer S, Remer T. Anthropometrics provide a better estimate of urinary organic acid anion excretion than a dietary mineral intake-based estimate in children, adolescents, and young adults. J Nutr 2006;136:1203-1208.
Hostetter TH. Human renal response to meat meal. Am J Physiol 1986;250:F613-F618.
O'Donnell MP, Kasiske BL, Raij L et al. Age is a determinant of the glomerular morphologic and functional responses to chronic nephron loss. J Lab Clin Med 1985;106:308-313.
Gonick HC, Kleeman CR, Rubini ME et al. Functional impairment in chronic renal disease. II. Studies of acid excretion. Nephron 1969;6:28-49.
Manz F, Kalhoff H, Remer T. Renal acid excretion in early infancy. Pediatr Nephrol 1997;11:231-243.
Lüthy C, Moser C, Oetliker O. Three-phasic acid/base titration in urine. Med Lab 1977;30:174-181.
Bartels H, Cikes M. Chromogens in the creatinine determination of Jaffe [Ueber Chromegene der Keatininbestimmung nach Jaffe]. Clin Chim Acta 1969;26:1-10.
Alexy U, Remer T, Manz F et al. Long-term protein intake and dietary potential renal acid load are associated with bone modeling and remodeling at the proximal radius in healthy children. Am J Clin Nutr 2005;82:1107-1114.
Laing CM, Unwin RJ. Renal tubular acidosis. J Nephrol 2006;19 (Suppl 9):S46-S52.
Buemi M, Nostro L, Aloisi C et al. Kidney aging: From phenotype to genetics. Rejuvenat Res 2005;8:101-109.
Rubin MI, Bruck E, Rapoport M et al. Maturation of renal function in childhood: Clearance Studies. J Clin Invest 1949;28:1144-1162.
Kildeberg P. Disturbances of hydrogen ion balance occurring in premature infants. II. Late metabolic acidosis. Acta Paediatr 1964;53:517-526.
Watkin DM, Schock NW. Age-wise standard value for CIN, CPAH, and TmPAH in adult males. J Clin Invest 1955;34:969.
Remer T, Fonteyn N, Alexy U et al. Longitudinal examination of 24-h urinary iodine excretion in schoolchildren as a sensitive, hydration status-independent research tool for studying iodine status. Am J Clin Nutr 2006;83:639-646.
Frassetto LA, Morris RC Jr, Sebastian A. Effect of age on blood acid-base composition in adult humans: Role of age-related renal functional decline. Am J Physiol 1996;271:F1114-F1122.
Frassetto LA, Todd KM, Morris RC Jr et al. Worldwide incidence of hip fracture in elderly women: Relation to consumption of animal and vegetable foods. J Gerontol A Biol Sci Med Sci 2000;55:M585-M592.
1995; 95
2002; 75
1993; 82
1995; 15
1995; 34
2006; 17
1986; 250
2006; 19
2000; 2
1985; 106
1985; 63
2005; 82
1998; 132
1995; 6
2003; 133
2006; 136
1976; 31
1965; 44
2006; 61
2006; 83
1997; 11
2000; 15
2005; 8
2000; 55
1969; 6
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1996; 271
1964; 53
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Hayton WL. (e_1_2_6_11_2) 2000; 2
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Remer T (e_1_2_6_26_2) 1995; 6
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Frassetto LA (e_1_2_6_2_2) 1996; 271
Adler S (e_1_2_6_8_2) 1968; 72
Laing CM (e_1_2_6_9_2) 2006; 19
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Fliser D (e_1_2_6_33_2) 1995; 15
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Watkin DM (e_1_2_6_7_2) 1955; 34
Lüthy C (e_1_2_6_21_2) 1977; 30
Sebastian A. (e_1_2_6_37_2) 2005; 82
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Buemi M (e_1_2_6_10_2) 2005; 8
Molnar D (e_1_2_6_23_2) 1998; 132
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O'Donnell MP (e_1_2_6_27_2) 1985; 106
Frassetto LA (e_1_2_6_36_2) 2000; 55
Rowe JW (e_1_2_6_6_2) 1976; 31
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References_xml – reference: Alexy U, Remer T, Manz F et al. Long-term protein intake and dietary potential renal acid load are associated with bone modeling and remodeling at the proximal radius in healthy children. Am J Clin Nutr 2005;82:1107-1114.
– reference: Manz F, Wentz A. Renal net acid excretion related to body surface area in children and adolescents. DONALD (DOrtmund Nutritional and Anthropometric Longitudinally Designed) Study. Pediatr Nephrol 2000;15:101-104.
– reference: Rowe JW, Andres R, Tobin JD et al. The effect of age on creatinine clearance in men: A cross-sectional and longitudinal study. J Gerontol 1976;31:155-163.
– reference: Poortmans JR, Ouchinsky M. Glomerular filtration rate and albumin excretion after maximal exercise in aging sedentary and active men. J Gerontol A Biol Sci Med Sci 2006;61:1181-1185.
– reference: Manz F, Remer T, Decher-Spliethoff E et al. Effects of a high protein intake on renal acid excretion in bodybuilders. Z Ernahrungswiss 1995;34:10-15.
– reference: Molnar D, Schutz Y. Fat oxidation in nonobese and obese adolescents: Effect of body composition and pubertal development. J Pediatr 1998;132:98-104.
– reference: Rylander R, Remer T, Berkemeyer S et al. Acid-base status affects renal magnesium losses in healthy, elderly persons. J Nutr 2006;136:2374-2377.
– reference: O'Donnell MP, Kasiske BL, Raij L et al. Age is a determinant of the glomerular morphologic and functional responses to chronic nephron loss. J Lab Clin Med 1985;106:308-313.
– reference: Laing CM, Unwin RJ. Renal tubular acidosis. J Nephrol 2006;19 (Suppl 9):S46-S52.
– reference: Lüthy C, Moser C, Oetliker O. Three-phasic acid/base titration in urine. Med Lab 1977;30:174-181.
– reference: Frassetto LA, Morris RC Jr, Sebastian A. Effect of age on blood acid-base composition in adult humans: Role of age-related renal functional decline. Am J Physiol 1996;271:F1114-F1122.
– reference: Remer T, Neubert A, Maser-Gluth C. Anthropometry-based reference values for 24-h urinary creatinine excretion during growth and their use in endocrine and nutritional research. Am J Clin Nutr 2002;75:561-569.
– reference: Remer T, Manz F. Dietary protein as a modulator of the renal net acid excretion capacity: Evidence that an increased protein intake improves the capability of the kidney to excrete ammonium. Nutr Biochem 1995;6:431-437.
– reference: Jehle S, Zanetti A, Muser J et al. Partial neutralization of the acidogenic Western diet with potassium citrate increases bone mass in postmenopausal women with osteopenia. J Am Soc Nephrol 2006;17:3213-3222.
– reference: Buemi M, Nostro L, Aloisi C et al. Kidney aging: From phenotype to genetics. Rejuvenat Res 2005;8:101-109.
– reference: Schurch MA, Rizzoli R, Slosman D et al. Protein supplements increase serum insulin-like growth factor-I levels and attenuate proximal femur bone loss in patients with recent hip fracture. A randomized, double-blind, placebo-controlled trial. Ann Intern Med 1998;128:801-809.
– reference: Frassetto LA, Todd KM, Morris RC Jr et al. Worldwide incidence of hip fracture in elderly women: Relation to consumption of animal and vegetable foods. J Gerontol A Biol Sci Med Sci 2000;55:M585-M592.
– reference: Tasevska N, Runswick SA, Bingham SA. Urinary potassium is as reliable as urinary nitrogen for use as a recovery biomarker in dietary studies of free living individuals. J Nutr 2006;136:1334-1340.
– reference: Hirschberg R, Rottka H, Von Herrath D et al. Effect of an acute protein load on the creatinine clearance in healthy vegetarians. Klin Wochenschr 1985;63:217-220.
– reference: Fliser D, Ritz E, Franek E. Renal reserve in the elderly. Semin Nephrol 1995;15:463-467.
– reference: Watkin DM, Schock NW. Age-wise standard value for CIN, CPAH, and TmPAH in adult males. J Clin Invest 1955;34:969.
– reference: Remer T, Fonteyn N, Alexy U et al. Longitudinal examination of 24-h urinary iodine excretion in schoolchildren as a sensitive, hydration status-independent research tool for studying iodine status. Am J Clin Nutr 2006;83:639-646.
– reference: Goodman AD, Lemann J Jr, Lennon EJ et al. Production, excretion, and net balance of fixed acid in patients with renal acidosis. J Clin Invest 1965;44:495-506.
– reference: Kildeberg P. Disturbances of hydrogen ion balance occurring in premature infants. II. Late metabolic acidosis. Acta Paediatr 1964;53:517-526.
– reference: Remer T, Manz F. Potential renal acid load of foods and its influence on urine pH. J Am Diet Assoc 1995;95:791-797.
– reference: Hayton WL. Maturation and growth of renal function: Dosing renally cleared drugs in children. AAPS PharmSci 2000;2:E3.
– reference: Adler S, Lindeman RD, Yiengst MJ et al. Effect of acute acid loading on urinary acid excretion by the aging human kidney. J Lab Clin Med 1968;72:278-289.
– reference: Bingham SA. Urine nitrogen as a biomarker for the validation of dietary protein intake. J Nutr 2003;133 (Suppl 3):921S-924S.
– reference: Manz F, Wentz A, Lange S. Factors affecting renal hydrogen ion excretion capacity in healthy children. Pediatr Nephrol 2001;16:443-445.
– reference: Rubin MI, Bruck E, Rapoport M et al. Maturation of renal function in childhood: Clearance Studies. J Clin Invest 1949;28:1144-1162.
– reference: Kalhoff H, Manz F, Diekmann L et al. Decreased growth rate of low-birth-weight infants with prolonged maximum renal acid stimulation. Acta Paediatr 1993;82:522-527.
– reference: Berkemeyer S, Remer T. Anthropometrics provide a better estimate of urinary organic acid anion excretion than a dietary mineral intake-based estimate in children, adolescents, and young adults. J Nutr 2006;136:1203-1208.
– reference: Remer T, Berkemeyer S, Rylander R et al. Muscularity and adiposity in addition to net acid excretion as predictors of 24-h urinary pH in young adults and elderly. Eur J Clin Nutr 2007;61:605-609.
– reference: Sebastian A. Dietary protein content and the diet's net acid load: Opposing effects on bone health. Am J Clin Nutr 2005;82:921-922.
– reference: Gonick HC, Kleeman CR, Rubini ME et al. Functional impairment in chronic renal disease. II. Studies of acid excretion. Nephron 1969;6:28-49.
– reference: Wang Y, Moss J, Thisted R. Predictors of body surface area. J Clin Anesth 1992;4:4-10.
– reference: Hostetter TH. Human renal response to meat meal. Am J Physiol 1986;250:F613-F618.
– reference: Manz F, Kalhoff H, Remer T. Renal acid excretion in early infancy. Pediatr Nephrol 1997;11:231-243.
– reference: Bartels H, Cikes M. Chromogens in the creatinine determination of Jaffe [Ueber Chromegene der Keatininbestimmung nach Jaffe]. Clin Chim Acta 1969;26:1-10.
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Snippet OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly...
OBJECTIVES: To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly...
To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly people....
To evaluate whether renal net acid excretion capacity (NAEC) varies across different age groups and, specifically, whether it falls in elderly...
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SubjectTerms acid-base
Acid-Base Equilibrium - physiology
Adolescent
Adult
Aged
Aging
Aging - physiology
Anthropometry
Biological and medical sciences
Child
Creatinine - urine
Cross-Sectional Studies
Female
General aspects
Germany
healthy subjects
Humans
Hydrogen-Ion Concentration
Kidney Function Tests
Kidneys
Male
Medical disorders
Medical sciences
Middle Aged
Miscellaneous
Nephrology
net acid excretion capacity
Nitrogen - urine
Older people
Phosphorus - urine
protein
Public health. Hygiene
Public health. Hygiene-occupational medicine
renal function
Sweden
Title Renal Net Acid Excretion Capacity Is Comparable in Prepubescence, Adolescence, and Young Adulthood but Falls with Aging
URI https://api.istex.fr/ark:/67375/WNG-QJD50H3K-F/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1532-5415.2008.01799.x
https://www.ncbi.nlm.nih.gov/pubmed/18808599
https://www.proquest.com/docview/210382725
https://www.proquest.com/docview/69589604
Volume 56
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