Skeletal dynamics in man measured by nonradioactive strontium
Skeletal dynamics were calculated by usual dilution formulas, using stable strontium as a tracer, in 25 normal subjects, 14 athletes, 26 patients with postmenopausal osteoporosis, 28 with primary hyperparathyroidism, 3 with hyperadrenocorticism 8 with acromegaly, 7 with thyrotoxicosis, 11 with urcli...
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Veröffentlicht in: | Journal of Clinical Investigation (U.S.) 1961-10, Vol.40, p.1809-1825 |
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creator | EISENBERG, E GORDAN, G S |
description | Skeletal dynamics were calculated by usual dilution formulas, using
stable strontium as a tracer, in 25 normal subjects, 14 athletes, 26 patients
with postmenopausal osteoporosis, 28 with primary hyperparathyroidism, 3 with
hyperadrenocorticism 8 with acromegaly, 7 with thyrotoxicosis, 11 with
urclithiasis, 5 with Paget's disease of bone. and 1 with vitamin D poisoning.
The technic requires that 10 mEq of strontium gluconate be injected intravenously
and blood and urine concentrations be measured for 4 to 6 days. In normal
subjects the rapidly miscible pool was equivalent to 42.7 + 1.1 L of serum,
turning over at a rate of 13.5 plus or minus 0.6 L daily, of which 3.9 + 0.2 L
was excreted by the kidney and 9.6 + 0.4 L went to bone. Since only
approximately 2.5% of the pool is excreted in the feces daily, fecal excretion
was not measured routinely. Good reproducibility was found in 21 duplicate
studies. Intense muscular exercise (athletes) was found to expand the pool
greatly and to accelerate the rate of deposition in bone. Kinetically, two
divergent types of osteoporosis were differentiated. A small pool and low rate
of bone deposition were found in postmenopausal osteoporosis and Cushing's
disease of long duration. The large pool and rapid rate of bone deposition in
thyrotoxicosis was confirmed and also found in acromegaly. In these two,
excessive bone resorption is postulated. Urinary excretion rate was excessive in
Cushing's disease, thyrotoxicosis, and acromegaly. In hyperparathyroidism with
clinically evident osteitis, expanded pools, greatly increased turnover, urinary
excretion, and bone deposition rates were confirmed. In patients with normal
roentgenographic appearance and phosphatase, bone involvement was shown by slight
increase in bone deposition rate and microscopic foci of resorption on iliac
crest biopsy. In seven patients without histological foci of resorption, the
bone deposition rate was not increased. (auth) |
doi_str_mv | 10.1172/JCI104405 |
format | Article |
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stable strontium as a tracer, in 25 normal subjects, 14 athletes, 26 patients
with postmenopausal osteoporosis, 28 with primary hyperparathyroidism, 3 with
hyperadrenocorticism 8 with acromegaly, 7 with thyrotoxicosis, 11 with
urclithiasis, 5 with Paget's disease of bone. and 1 with vitamin D poisoning.
The technic requires that 10 mEq of strontium gluconate be injected intravenously
and blood and urine concentrations be measured for 4 to 6 days. In normal
subjects the rapidly miscible pool was equivalent to 42.7 + 1.1 L of serum,
turning over at a rate of 13.5 plus or minus 0.6 L daily, of which 3.9 + 0.2 L
was excreted by the kidney and 9.6 + 0.4 L went to bone. Since only
approximately 2.5% of the pool is excreted in the feces daily, fecal excretion
was not measured routinely. Good reproducibility was found in 21 duplicate
studies. Intense muscular exercise (athletes) was found to expand the pool
greatly and to accelerate the rate of deposition in bone. Kinetically, two
divergent types of osteoporosis were differentiated. A small pool and low rate
of bone deposition were found in postmenopausal osteoporosis and Cushing's
disease of long duration. The large pool and rapid rate of bone deposition in
thyrotoxicosis was confirmed and also found in acromegaly. In these two,
excessive bone resorption is postulated. Urinary excretion rate was excessive in
Cushing's disease, thyrotoxicosis, and acromegaly. In hyperparathyroidism with
clinically evident osteitis, expanded pools, greatly increased turnover, urinary
excretion, and bone deposition rates were confirmed. In patients with normal
roentgenographic appearance and phosphatase, bone involvement was shown by slight
increase in bone deposition rate and microscopic foci of resorption on iliac
crest biopsy. In seven patients without histological foci of resorption, the
bone deposition rate was not increased. (auth)</description><identifier>ISSN: 0021-9738</identifier><identifier>DOI: 10.1172/JCI104405</identifier><identifier>PMID: 13889673</identifier><language>eng</language><publisher>United States</publisher><subject>BIOLOGY AND MEDICINE ; BLOOD SERUM ; Bone and Bones - metabolism ; BONES ; DISEASES ; ENZYMES ; GLANDS ; HORMONES ; Humans ; KIDNEYS ; Male ; MAN ; METABOLISM ; Old Medline ; POISONING ; QUANTITY RATIO ; STRONTIUM ; Strontium - metabolism ; TRACER TECHNIQUES ; URINE ; VITAMIN D ; VITAMINS</subject><ispartof>Journal of Clinical Investigation (U.S.), 1961-10, Vol.40, p.1809-1825</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/13889673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/4839351$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>EISENBERG, E</creatorcontrib><creatorcontrib>GORDAN, G S</creatorcontrib><creatorcontrib>Univ. of California School of Medicine, San Francisco</creatorcontrib><title>Skeletal dynamics in man measured by nonradioactive strontium</title><title>Journal of Clinical Investigation (U.S.)</title><addtitle>J Clin Invest</addtitle><description>Skeletal dynamics were calculated by usual dilution formulas, using
stable strontium as a tracer, in 25 normal subjects, 14 athletes, 26 patients
with postmenopausal osteoporosis, 28 with primary hyperparathyroidism, 3 with
hyperadrenocorticism 8 with acromegaly, 7 with thyrotoxicosis, 11 with
urclithiasis, 5 with Paget's disease of bone. and 1 with vitamin D poisoning.
The technic requires that 10 mEq of strontium gluconate be injected intravenously
and blood and urine concentrations be measured for 4 to 6 days. In normal
subjects the rapidly miscible pool was equivalent to 42.7 + 1.1 L of serum,
turning over at a rate of 13.5 plus or minus 0.6 L daily, of which 3.9 + 0.2 L
was excreted by the kidney and 9.6 + 0.4 L went to bone. Since only
approximately 2.5% of the pool is excreted in the feces daily, fecal excretion
was not measured routinely. Good reproducibility was found in 21 duplicate
studies. Intense muscular exercise (athletes) was found to expand the pool
greatly and to accelerate the rate of deposition in bone. Kinetically, two
divergent types of osteoporosis were differentiated. A small pool and low rate
of bone deposition were found in postmenopausal osteoporosis and Cushing's
disease of long duration. The large pool and rapid rate of bone deposition in
thyrotoxicosis was confirmed and also found in acromegaly. In these two,
excessive bone resorption is postulated. Urinary excretion rate was excessive in
Cushing's disease, thyrotoxicosis, and acromegaly. In hyperparathyroidism with
clinically evident osteitis, expanded pools, greatly increased turnover, urinary
excretion, and bone deposition rates were confirmed. In patients with normal
roentgenographic appearance and phosphatase, bone involvement was shown by slight
increase in bone deposition rate and microscopic foci of resorption on iliac
crest biopsy. In seven patients without histological foci of resorption, the
bone deposition rate was not increased. (auth)</description><subject>BIOLOGY AND MEDICINE</subject><subject>BLOOD SERUM</subject><subject>Bone and Bones - metabolism</subject><subject>BONES</subject><subject>DISEASES</subject><subject>ENZYMES</subject><subject>GLANDS</subject><subject>HORMONES</subject><subject>Humans</subject><subject>KIDNEYS</subject><subject>Male</subject><subject>MAN</subject><subject>METABOLISM</subject><subject>Old Medline</subject><subject>POISONING</subject><subject>QUANTITY RATIO</subject><subject>STRONTIUM</subject><subject>Strontium - metabolism</subject><subject>TRACER TECHNIQUES</subject><subject>URINE</subject><subject>VITAMIN D</subject><subject>VITAMINS</subject><issn>0021-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1961</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo10L1OwzAUBWAPIFoKAy-AIga2gK_tJL4DA6r4KarEAMyR49wIQ2KX2EHq21OpZTg6y6czHMYugN8AVOL2ZbkCrhQvjticcwE5VlLP2GmMX5yDUoU6YTOQWmNZyTm7e_umnpLps3brzeBszJzPBrMLmTiN1GbNNvPBj6Z1wdjkfimLaQw-uWk4Y8ed6SOdH3rBPh4f3pfP-fr1abW8X-dBSJXyxqAAJOSFKJTU1BE3JTSEiGBLWYHoUBdlU5ZoteFKIJjWaotl2ykhrVywq_1uiMnV0bpE9tMG78mmWmmJsoAdut6jzRh-JoqpHly01PfGU5hirQVyEFW1g5cHODUDtfVmdIMZt_X_K_IPvspf4Q</recordid><startdate>196110</startdate><enddate>196110</enddate><creator>EISENBERG, E</creator><creator>GORDAN, G S</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>196110</creationdate><title>Skeletal dynamics in man measured by nonradioactive strontium</title><author>EISENBERG, E ; GORDAN, G S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-o234t-ba9219e90525438efe0a61be9991c63712f9856b669c8a04291adc8c96df423c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1961</creationdate><topic>BIOLOGY AND MEDICINE</topic><topic>BLOOD SERUM</topic><topic>Bone and Bones - metabolism</topic><topic>BONES</topic><topic>DISEASES</topic><topic>ENZYMES</topic><topic>GLANDS</topic><topic>HORMONES</topic><topic>Humans</topic><topic>KIDNEYS</topic><topic>Male</topic><topic>MAN</topic><topic>METABOLISM</topic><topic>Old Medline</topic><topic>POISONING</topic><topic>QUANTITY RATIO</topic><topic>STRONTIUM</topic><topic>Strontium - metabolism</topic><topic>TRACER TECHNIQUES</topic><topic>URINE</topic><topic>VITAMIN D</topic><topic>VITAMINS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EISENBERG, E</creatorcontrib><creatorcontrib>GORDAN, G S</creatorcontrib><creatorcontrib>Univ. of California School of Medicine, San Francisco</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Journal of Clinical Investigation (U.S.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EISENBERG, E</au><au>GORDAN, G S</au><aucorp>Univ. of California School of Medicine, San Francisco</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skeletal dynamics in man measured by nonradioactive strontium</atitle><jtitle>Journal of Clinical Investigation (U.S.)</jtitle><addtitle>J Clin Invest</addtitle><date>1961-10</date><risdate>1961</risdate><volume>40</volume><spage>1809</spage><epage>1825</epage><pages>1809-1825</pages><issn>0021-9738</issn><abstract>Skeletal dynamics were calculated by usual dilution formulas, using
stable strontium as a tracer, in 25 normal subjects, 14 athletes, 26 patients
with postmenopausal osteoporosis, 28 with primary hyperparathyroidism, 3 with
hyperadrenocorticism 8 with acromegaly, 7 with thyrotoxicosis, 11 with
urclithiasis, 5 with Paget's disease of bone. and 1 with vitamin D poisoning.
The technic requires that 10 mEq of strontium gluconate be injected intravenously
and blood and urine concentrations be measured for 4 to 6 days. In normal
subjects the rapidly miscible pool was equivalent to 42.7 + 1.1 L of serum,
turning over at a rate of 13.5 plus or minus 0.6 L daily, of which 3.9 + 0.2 L
was excreted by the kidney and 9.6 + 0.4 L went to bone. Since only
approximately 2.5% of the pool is excreted in the feces daily, fecal excretion
was not measured routinely. Good reproducibility was found in 21 duplicate
studies. Intense muscular exercise (athletes) was found to expand the pool
greatly and to accelerate the rate of deposition in bone. Kinetically, two
divergent types of osteoporosis were differentiated. A small pool and low rate
of bone deposition were found in postmenopausal osteoporosis and Cushing's
disease of long duration. The large pool and rapid rate of bone deposition in
thyrotoxicosis was confirmed and also found in acromegaly. In these two,
excessive bone resorption is postulated. Urinary excretion rate was excessive in
Cushing's disease, thyrotoxicosis, and acromegaly. In hyperparathyroidism with
clinically evident osteitis, expanded pools, greatly increased turnover, urinary
excretion, and bone deposition rates were confirmed. In patients with normal
roentgenographic appearance and phosphatase, bone involvement was shown by slight
increase in bone deposition rate and microscopic foci of resorption on iliac
crest biopsy. In seven patients without histological foci of resorption, the
bone deposition rate was not increased. (auth)</abstract><cop>United States</cop><pmid>13889673</pmid><doi>10.1172/JCI104405</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | BIOLOGY AND MEDICINE BLOOD SERUM Bone and Bones - metabolism BONES DISEASES ENZYMES GLANDS HORMONES Humans KIDNEYS Male MAN METABOLISM Old Medline POISONING QUANTITY RATIO STRONTIUM Strontium - metabolism TRACER TECHNIQUES URINE VITAMIN D VITAMINS |
title | Skeletal dynamics in man measured by nonradioactive strontium |
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