The negative effect of unloading exceeds the bone-sparing effect of alkaline supplementation: a bed rest study

Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali sal...

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Veröffentlicht in:Osteoporosis international 2019-02, Vol.30 (2), p.431-439
Hauptverfasser: Frings-Meuthen, P., Bernhardt, G., Buehlmeier, J., Baecker, N., May, F., Heer, M.
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container_end_page 439
container_issue 2
container_start_page 431
container_title Osteoporosis international
container_volume 30
creator Frings-Meuthen, P.
Bernhardt, G.
Buehlmeier, J.
Baecker, N.
May, F.
Heer, M.
description Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali salts appears to positively influence calcium and bone metabolism and, thus, could be a countermeasure for population groups with an increased risk for bone loss. However, the extent to which alkalization counteracts acid-induced bone resorption or whether it merely has a calcium and bone maintenance effect is still not completely understood. In the present study, we hypothesized that additional alkalization to an already alkaline diet can further counteract bed rest-induced bone loss. Methods Seven healthy male subjects completed two parts of a crossover designed 21-day bed rest study: bed rest only (control) and bed rest supplemented with 90 mmol potassium bicarbonate (KHCO 3 ) daily. Results KHCO 3 supplementation during bed rest resulted in a more alkaline status compared to the control intervention, demonstrated by the increase in pH and buffer capacity level (pH p  = 0.023, HCO 3 p  = 0.02, ABE p  = 0.03). Urinary calcium excretion was decreased during KHCO 3 supplementation (control 6.05 ± 2.74 mmol/24 h; KHCO 3 4.87 ± 2.21 mmol/24 h, p  = 0.03); whereas, bone formation was not affected by additional alkalization (bAP p  = 0.58; PINP p  = 0.60). Bone resorption marker UCTX tended to be lower during alkaline supplementation (UCTX p  = 0.16). Conclusions The more alkaline acid-base status, achieved by KHCO 3 supplementation, reduced renal calcium excretion during bed rest, but was not able to prevent immobilization-induced bone resorption. However, advantages of alkaline salts on bone metabolism may occur under acidic metabolic conditions or with respect to the positive effect of reduced calcium excretion within a longer time frame. Trial registration Trial number: NCT01509456
doi_str_mv 10.1007/s00198-018-4703-6
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Introduction Supplementation with alkali salts appears to positively influence calcium and bone metabolism and, thus, could be a countermeasure for population groups with an increased risk for bone loss. However, the extent to which alkalization counteracts acid-induced bone resorption or whether it merely has a calcium and bone maintenance effect is still not completely understood. In the present study, we hypothesized that additional alkalization to an already alkaline diet can further counteract bed rest-induced bone loss. Methods Seven healthy male subjects completed two parts of a crossover designed 21-day bed rest study: bed rest only (control) and bed rest supplemented with 90 mmol potassium bicarbonate (KHCO 3 ) daily. Results KHCO 3 supplementation during bed rest resulted in a more alkaline status compared to the control intervention, demonstrated by the increase in pH and buffer capacity level (pH p  = 0.023, HCO 3 p  = 0.02, ABE p  = 0.03). Urinary calcium excretion was decreased during KHCO 3 supplementation (control 6.05 ± 2.74 mmol/24 h; KHCO 3 4.87 ± 2.21 mmol/24 h, p  = 0.03); whereas, bone formation was not affected by additional alkalization (bAP p  = 0.58; PINP p  = 0.60). Bone resorption marker UCTX tended to be lower during alkaline supplementation (UCTX p  = 0.16). Conclusions The more alkaline acid-base status, achieved by KHCO 3 supplementation, reduced renal calcium excretion during bed rest, but was not able to prevent immobilization-induced bone resorption. However, advantages of alkaline salts on bone metabolism may occur under acidic metabolic conditions or with respect to the positive effect of reduced calcium excretion within a longer time frame. Trial registration Trial number: NCT01509456</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-018-4703-6</identifier><identifier>PMID: 30255228</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Acid-base status ; Adult ; Bed Rest - adverse effects ; Bicarbonates ; Bicarbonates - pharmacology ; Bicarbonates - therapeutic use ; Biomarkers - metabolism ; Bone growth ; Bone loss ; Bone resorption ; Bone Resorption - etiology ; Bone Resorption - metabolism ; Bone Resorption - prevention &amp; control ; Bone turnover ; Calcium (urinary) ; Calcium - urine ; Calcium metabolism ; Cross-Over Studies ; Dietary Supplements ; Endocrinology ; Excretion ; Humans ; Hydrogen-Ion Concentration - drug effects ; Immobilization ; Immobilization - adverse effects ; Immobilization - physiology ; Male ; Medicine ; Medicine &amp; Public Health ; Metabolism ; Original Article ; Orthopedics ; Osteogenesis ; Osteogenesis - drug effects ; pH effects ; Potassium ; Potassium Compounds - pharmacology ; Potassium Compounds - therapeutic use ; Renal function ; Rheumatology ; Salts ; Unloading ; Weight-Bearing - physiology ; Young Adult</subject><ispartof>Osteoporosis international, 2019-02, Vol.30 (2), p.431-439</ispartof><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2018</rights><rights>Osteoporosis International is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-343b79117b12e4db3c342361693c0f0511a2310f35e382a2e27dc30b7bf30a653</citedby><cites>FETCH-LOGICAL-c372t-343b79117b12e4db3c342361693c0f0511a2310f35e382a2e27dc30b7bf30a653</cites><orcidid>0000-0001-5291-4419</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00198-018-4703-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00198-018-4703-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30255228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frings-Meuthen, P.</creatorcontrib><creatorcontrib>Bernhardt, G.</creatorcontrib><creatorcontrib>Buehlmeier, J.</creatorcontrib><creatorcontrib>Baecker, N.</creatorcontrib><creatorcontrib>May, F.</creatorcontrib><creatorcontrib>Heer, M.</creatorcontrib><title>The negative effect of unloading exceeds the bone-sparing effect of alkaline supplementation: a bed rest study</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><description>Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali salts appears to positively influence calcium and bone metabolism and, thus, could be a countermeasure for population groups with an increased risk for bone loss. However, the extent to which alkalization counteracts acid-induced bone resorption or whether it merely has a calcium and bone maintenance effect is still not completely understood. In the present study, we hypothesized that additional alkalization to an already alkaline diet can further counteract bed rest-induced bone loss. Methods Seven healthy male subjects completed two parts of a crossover designed 21-day bed rest study: bed rest only (control) and bed rest supplemented with 90 mmol potassium bicarbonate (KHCO 3 ) daily. Results KHCO 3 supplementation during bed rest resulted in a more alkaline status compared to the control intervention, demonstrated by the increase in pH and buffer capacity level (pH p  = 0.023, HCO 3 p  = 0.02, ABE p  = 0.03). Urinary calcium excretion was decreased during KHCO 3 supplementation (control 6.05 ± 2.74 mmol/24 h; KHCO 3 4.87 ± 2.21 mmol/24 h, p  = 0.03); whereas, bone formation was not affected by additional alkalization (bAP p  = 0.58; PINP p  = 0.60). Bone resorption marker UCTX tended to be lower during alkaline supplementation (UCTX p  = 0.16). Conclusions The more alkaline acid-base status, achieved by KHCO 3 supplementation, reduced renal calcium excretion during bed rest, but was not able to prevent immobilization-induced bone resorption. However, advantages of alkaline salts on bone metabolism may occur under acidic metabolic conditions or with respect to the positive effect of reduced calcium excretion within a longer time frame. Trial registration Trial number: NCT01509456</description><subject>Acid-base status</subject><subject>Adult</subject><subject>Bed Rest - adverse effects</subject><subject>Bicarbonates</subject><subject>Bicarbonates - pharmacology</subject><subject>Bicarbonates - therapeutic use</subject><subject>Biomarkers - metabolism</subject><subject>Bone growth</subject><subject>Bone loss</subject><subject>Bone resorption</subject><subject>Bone Resorption - etiology</subject><subject>Bone Resorption - metabolism</subject><subject>Bone Resorption - prevention &amp; control</subject><subject>Bone turnover</subject><subject>Calcium (urinary)</subject><subject>Calcium - urine</subject><subject>Calcium metabolism</subject><subject>Cross-Over Studies</subject><subject>Dietary Supplements</subject><subject>Endocrinology</subject><subject>Excretion</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration - drug effects</subject><subject>Immobilization</subject><subject>Immobilization - adverse effects</subject><subject>Immobilization - physiology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; 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Public Health</topic><topic>Metabolism</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Osteogenesis</topic><topic>Osteogenesis - drug effects</topic><topic>pH effects</topic><topic>Potassium</topic><topic>Potassium Compounds - pharmacology</topic><topic>Potassium Compounds - therapeutic use</topic><topic>Renal function</topic><topic>Rheumatology</topic><topic>Salts</topic><topic>Unloading</topic><topic>Weight-Bearing - physiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frings-Meuthen, P.</creatorcontrib><creatorcontrib>Bernhardt, G.</creatorcontrib><creatorcontrib>Buehlmeier, J.</creatorcontrib><creatorcontrib>Baecker, N.</creatorcontrib><creatorcontrib>May, F.</creatorcontrib><creatorcontrib>Heer, M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; 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Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Osteoporosis international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frings-Meuthen, P.</au><au>Bernhardt, G.</au><au>Buehlmeier, J.</au><au>Baecker, N.</au><au>May, F.</au><au>Heer, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The negative effect of unloading exceeds the bone-sparing effect of alkaline supplementation: a bed rest study</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>30</volume><issue>2</issue><spage>431</spage><epage>439</epage><pages>431-439</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali salts appears to positively influence calcium and bone metabolism and, thus, could be a countermeasure for population groups with an increased risk for bone loss. However, the extent to which alkalization counteracts acid-induced bone resorption or whether it merely has a calcium and bone maintenance effect is still not completely understood. In the present study, we hypothesized that additional alkalization to an already alkaline diet can further counteract bed rest-induced bone loss. Methods Seven healthy male subjects completed two parts of a crossover designed 21-day bed rest study: bed rest only (control) and bed rest supplemented with 90 mmol potassium bicarbonate (KHCO 3 ) daily. Results KHCO 3 supplementation during bed rest resulted in a more alkaline status compared to the control intervention, demonstrated by the increase in pH and buffer capacity level (pH p  = 0.023, HCO 3 p  = 0.02, ABE p  = 0.03). Urinary calcium excretion was decreased during KHCO 3 supplementation (control 6.05 ± 2.74 mmol/24 h; KHCO 3 4.87 ± 2.21 mmol/24 h, p  = 0.03); whereas, bone formation was not affected by additional alkalization (bAP p  = 0.58; PINP p  = 0.60). Bone resorption marker UCTX tended to be lower during alkaline supplementation (UCTX p  = 0.16). Conclusions The more alkaline acid-base status, achieved by KHCO 3 supplementation, reduced renal calcium excretion during bed rest, but was not able to prevent immobilization-induced bone resorption. However, advantages of alkaline salts on bone metabolism may occur under acidic metabolic conditions or with respect to the positive effect of reduced calcium excretion within a longer time frame. Trial registration Trial number: NCT01509456</abstract><cop>London</cop><pub>Springer London</pub><pmid>30255228</pmid><doi>10.1007/s00198-018-4703-6</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5291-4419</orcidid></addata></record>
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subjects Acid-base status
Adult
Bed Rest - adverse effects
Bicarbonates
Bicarbonates - pharmacology
Bicarbonates - therapeutic use
Biomarkers - metabolism
Bone growth
Bone loss
Bone resorption
Bone Resorption - etiology
Bone Resorption - metabolism
Bone Resorption - prevention & control
Bone turnover
Calcium (urinary)
Calcium - urine
Calcium metabolism
Cross-Over Studies
Dietary Supplements
Endocrinology
Excretion
Humans
Hydrogen-Ion Concentration - drug effects
Immobilization
Immobilization - adverse effects
Immobilization - physiology
Male
Medicine
Medicine & Public Health
Metabolism
Original Article
Orthopedics
Osteogenesis
Osteogenesis - drug effects
pH effects
Potassium
Potassium Compounds - pharmacology
Potassium Compounds - therapeutic use
Renal function
Rheumatology
Salts
Unloading
Weight-Bearing - physiology
Young Adult
title The negative effect of unloading exceeds the bone-sparing effect of alkaline supplementation: a bed rest study
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