Variations in Hematologic Responses to Increased Lead Absorption in Young Children

In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been...

Full description

Saved in:
Bibliographic Details
Published inEnvironmental health perspectives Vol. 7; pp. 7 - 12
Main Authors Chisolm, J. Julian, Mellits, E. David, Keil, Julian E., Barrett, Maureen B.
Format Journal Article
LanguageEnglish
Published United States National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare 01.05.1974
Subjects
Online AccessGet full text
ISSN0091-6765
1552-9924
DOI10.1289/ehp.7477

Cover

Abstract In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been associated with differing risks of toxicity for groups, it is not a precise index of adverse effect per se, even at elevated levels. Within the red blood cell itself there is not a close association between the concentration of lead and such adverse metabolic effects as the increased loss of potassium caused by lead. Above the apparent "threshold zone" of approximately 30-50 μg Pb/100 ml whole blood, equivalent metabolic effects on heme synthesis may be seen over an interval of at least 20 μg Pb/100 ml whole blood. This variation will be examined with particular reference to the interrelationship between the concentrations of lead and protoporphyrin in peripheral blood. The data indicate that limitations in both precision and accuracy of measurement account for a relatively small fraction of the observed variations. Together with other experimental and clinical information, they suggest that concurrent dietary deficiency of iron may be one of the important modifying factors in the responses of subjects with increased lead absorption. It is suggested that suspected adverse effects upon the various organ systems associated with increased lead absorption be measured directly and that the CaEDTA mobilization test for lead should be more fully explored as a measure of the "metabolically active" fraction of the total body lead burden.
AbstractList In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been associated with differing risks of toxicity for groups, it is not a precise index of adverse effect per se, even at elevated levels. Within the red blood cell itself there is not a close association between the concentration of lead and such adverse metabolic effects as the increased loss of potassium caused by lead. Above the apparent "threshold zone" of approximately 30-50 mug Pb/100 ml whole blood, equivalent metabolic effects on heme synthesis may be seen over an interval of at least 20 mug Pb/100 ml whole blood. This variation will be examined with particular reference to the interrelationship between the concentrations of lead and protoporphyrin in peripheral blood. The data indicate that limitations in both precision and accuracy of measurement account for a relatively small fraction of the observed variations. Together with other experimental and clinical information, they suggest that concurrent dietary deficiency of iron may be one of the important modifying factors in the responses of subjects with increased lead absorption. It is suggested that suspected adverse effects upon the various organ systems associated with increased lead absorption be measured directly and that the CaEDTA mobilization test for lead should be more fully explored as a measure of the "metabolically active" fraction of the total body lead burden.
In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been associated with differing risks of toxicity for groups, it is not a precise index of adverse effect per se, even at elevated levels. Within the red blood cell itself there is not a close association between the concentration of lead and such adverse metabolic effects as the increased loss of potassium caused by lead. Above the apparent "threshold zone" of approximately 30-50 mug Pb/100 ml whole blood, equivalent metabolic effects on heme synthesis may be seen over an interval of at least 20 mug Pb/100 ml whole blood. This variation will be examined with particular reference to the interrelationship between the concentrations of lead and protoporphyrin in peripheral blood. The data indicate that limitations in both precision and accuracy of measurement account for a relatively small fraction of the observed variations. Together with other experimental and clinical information, they suggest that concurrent dietary deficiency of iron may be one of the important modifying factors in the responses of subjects with increased lead absorption. It is suggested that suspected adverse effects upon the various organ systems associated with increased lead absorption be measured directly and that the CaEDTA mobilization test for lead should be more fully explored as a measure of the "metabolically active" fraction of the total body lead burden.In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been associated with differing risks of toxicity for groups, it is not a precise index of adverse effect per se, even at elevated levels. Within the red blood cell itself there is not a close association between the concentration of lead and such adverse metabolic effects as the increased loss of potassium caused by lead. Above the apparent "threshold zone" of approximately 30-50 mug Pb/100 ml whole blood, equivalent metabolic effects on heme synthesis may be seen over an interval of at least 20 mug Pb/100 ml whole blood. This variation will be examined with particular reference to the interrelationship between the concentrations of lead and protoporphyrin in peripheral blood. The data indicate that limitations in both precision and accuracy of measurement account for a relatively small fraction of the observed variations. Together with other experimental and clinical information, they suggest that concurrent dietary deficiency of iron may be one of the important modifying factors in the responses of subjects with increased lead absorption. It is suggested that suspected adverse effects upon the various organ systems associated with increased lead absorption be measured directly and that the CaEDTA mobilization test for lead should be more fully explored as a measure of the "metabolically active" fraction of the total body lead burden.
In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence which indicates that this measurement reflects recent and current assimilation of lead. While broad ranges in blood lead concentration have been associated with differing risks of toxicity for groups, it is not a precise index of adverse effect per se, even at elevated levels. Within the red blood cell itself there is not a close association between the concentration of lead and such adverse metabolic effects as the increased loss of potassium caused by lead. Above the apparent “threshold zone” of approximately 30–50 μg Pb/100 ml whole blood, equivalent metabolic effects on heme synthesis may be seen over an interval of at least 20 μg Pb/100 ml whole blood. This variation will be examined with particular reference to the interrelationship between the concentrations of lead and protoporphyrin in peripheral blood. The data indicate that limitations in both precision and accuracy of measurement account for a relatively small fraction of the observed variations. Together with other experimental and clinical information, they suggest that concurrent dietary deficiency of iron may be one of the important modifying factors in the responses of subjects with increased lead absorption. It is suggested that suspected adverse effects upon the various organ systems associated with increased lead absorption be measured directly and that the CaEDTA mobilization test for lead should be more fully explored as a measure of the “metabolically active” fraction of the total body lead burden.
Author Mellits, E. David
Barrett, Maureen B.
Chisolm, J. Julian
Keil, Julian E.
Author_xml – sequence: 1
  givenname: J. Julian
  surname: Chisolm
  fullname: Chisolm, J. Julian
– sequence: 2
  givenname: E. David
  surname: Mellits
  fullname: Mellits, E. David
– sequence: 3
  givenname: Julian E.
  surname: Keil
  fullname: Keil, Julian E.
– sequence: 4
  givenname: Maureen B.
  surname: Barrett
  fullname: Barrett, Maureen B.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/4831151$$D View this record in MEDLINE/PubMed
BookMark eNptUUtrGzEQFiUldZJC_kBgD6Xksq60klarSyGYvMBQCE2hJ6GVRrbCWtpK60L_feXYhKSUOYjR95hhvhN0FGIAhM4JnpOmk19gPc4FE-IdmhHOm1rKhh2hGcaS1K1o-Qd0kvMTxph0bXuMjllHCeFkhh5-6OT15GPIlQ_VHWz0FIe48qZ6gDyWb8jVFKv7YBLoDLZagrbVVZ9jGneynepn3IZVtVj7wSYIZ-i900OGj4f3FD3eXH9f3NXLb7f3i6tlbSjtRF32xpZaZpzk0GvuGtq3gmFne9Y7xox0opfcOd4SLUsRY2XpeC-Y5ULSU_R17ztu-w1YA2FKelBj8hud_qiovXqLBL9Wq_hbESY4obgYfD4YpPhrC3lSG58NDIMOELdZdQ3tCpEX4sXrSS8jDlcs-OUeNynmnMC9MAhWu3xUyUft8inU-T9U46fn-5cV_fA_wae94ClPMb02bigWirJGyK6jfwEhjZ_a
CitedBy_id crossref_primary_10_3390_ijerph110606314
crossref_primary_10_1016_0048_9697_84_90369_3
crossref_primary_10_1016_S0022_3476_75_80130_2
crossref_primary_10_1016_S0315_5463_80_73396_5
crossref_primary_10_1136_oem_50_12_1123
crossref_primary_10_1080_15287397709529572
crossref_primary_10_3109_10408447909113048
ContentType Journal Article
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOI 10.1289/ehp.7477
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Public Health
EISSN 1552-9924
EndPage 12
ExternalDocumentID PMC1475130
4831151
10_1289_ehp_7477
3427988
Genre Journal Article
GeographicLocations South Carolina
GeographicLocations_xml – name: South Carolina
GroupedDBID ---
-~X
04C
29G
2WC
5GY
5RE
5VS
6PF
85S
9K5
AACGO
AAFWJ
AANCE
AAWTL
ABBHK
ABOCM
ABPLY
ABPPZ
ABTLG
ABXSQ
ACGFO
ACHIC
ACIHN
ACIWK
ACNCT
ACPRK
ADBBV
ADOJX
ADQXQ
ADRAZ
ADULT
AEAQA
AENEX
AEUPB
AEXZC
AFPKN
AFRAH
AHDLI
AHMBA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ANHSF
AOIJS
AQVQM
AS~
AXR
BAWUL
BCNDV
C1A
CS3
DCCCD
DIK
DU5
E3Z
EBS
ECF
EHB
EJD
EMB
ESX
F5P
F8P
GROUPED_DOAJ
GX1
H13
HGD
HQ3
HTVGU
HYE
IAO
IEA
IHR
INH
INR
IOF
IPO
IPSME
JAAYA
JBMMH
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JSG
JST
KQ8
M48
O5R
O5S
OK1
OVT
P2P
PGMZT
QN7
REH
RGD
RPM
SA0
SJN
TAN
TR2
U5U
UGJ
WH7
WOQ
WOW
XSB
YR5
ZGI
~02
~KM
.GJ
2XV
36B
3O-
42X
4P2
53G
7RV
7WY
7X7
7XC
88E
8AO
8C1
8FE
8FG
8FH
8FI
8FJ
8FL
8G5
8R4
8R5
AAYXX
ABDBF
ABJCF
ABUWG
ACUHS
AEUYN
AFKRA
AGNAY
AN0
ATCPS
AZQEC
B0M
BENPR
BES
BEZIV
BGLVJ
BHPHI
BKEYQ
BKNYI
BMSDO
BNQBC
BPHCQ
BVXVI
CCPQU
CITATION
DWQXO
EAD
EAP
EAS
EBC
EBD
EBX
ECGQY
ECT
EDH
EHC
EHE
EHN
EIHBH
EMK
EMOBN
EPL
EPT
EX3
FRNLG
FYUFA
GNUQQ
GUQSH
HCIFZ
HMCUK
I-F
IAG
IEP
IER
IHW
IOV
ISR
ITC
K60
K6~
K9-
L6V
M0C
M0R
M1P
M2O
M7S
NAPCQ
NEJ
PATMY
PCD
PHGZM
PHGZT
PIMPY
PQBIZ
PQBZA
PQQKQ
PROAC
PSQYO
PTHSS
PV9
PYCSY
Q2X
QF4
QM9
QO4
Q~Q
RNS
RWL
RZL
S0X
SV3
TAE
TUS
UDP
UKHRP
WQ9
ZAC
ZE2
~8M
3V.
ADZLD
CGR
CUY
CVF
DOOOF
ECM
EIF
EQZMY
JSODD
M~E
NPM
PKN
7X8
5PM
ID FETCH-LOGICAL-c3387-1280d3d4cf95eba5f23b6740fdb4bf44c9f7b95ff561a9a9a1cd9ff55b74d5793
IEDL.DBID M48
ISSN 0091-6765
IngestDate Thu Aug 21 13:43:40 EDT 2025
Thu Sep 04 19:46:34 EDT 2025
Wed Feb 19 02:43:37 EST 2025
Tue Jul 01 03:09:57 EDT 2025
Thu Apr 24 22:55:22 EDT 2025
Thu Jul 03 21:14:17 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3387-1280d3d4cf95eba5f23b6740fdb4bf44c9f7b95ff561a9a9a1cd9ff55b74d5793
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1289/ehp.7477
PMID 4831151
PQID 82385135
PQPubID 23479
PageCount 6
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_1475130
proquest_miscellaneous_82385135
pubmed_primary_4831151
crossref_primary_10_1289_ehp_7477
crossref_citationtrail_10_1289_ehp_7477
jstor_primary_10_2307_3427988
ProviderPackageCode CITATION
AAYXX
PublicationCentury 1900
PublicationDate 19740501
PublicationDateYYYYMMDD 1974-05-01
PublicationDate_xml – month: 5
  year: 1974
  text: 19740501
  day: 1
PublicationDecade 1970
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Environmental health perspectives
PublicationTitleAlternate Environ Health Perspect
PublicationYear 1974
Publisher National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare
Publisher_xml – name: National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare
References 4633129 - J Med Primatol. 1972;1(3):142-55
5007557 - J Lab Clin Med. 1972 Jan;79(1):128-36
4695860 - Pediatrics. 1973 Feb;51(2):254-9
13752197 - J R Inst Public Health. 1961 Aug;24:177-203
5935989 - Br J Haematol. 1966 May;12(3):326-30
5473751 - Am Ind Hyg Assoc J. 1970 Jul-Aug;31(4):412-29
4683366 - Clin Chem. 1973 Jan;19(1):49-57
4643025 - J Pediatr. 1972 Dec;81(6):1088-91
4969284 - J Pediatr. 1968 Jul;73(1):1-38
5073013 - Pediatrics. 1972 Oct;50(4):625-31
13494075 - Pediatrics. 1958 Jan;21(1):40-6
5488694 - Br J Ind Med. 1970 Oct;27(4):352-5
4744314 - Biochem Med. 1973 Aug;8(1):135-48
6017110 - Arch Environ Health. 1967 Feb;14(2):309-12
5485382 - J Lab Clin Med. 1970 Dec;76(6):933-42
References_xml – reference: 4969284 - J Pediatr. 1968 Jul;73(1):1-38
– reference: 5073013 - Pediatrics. 1972 Oct;50(4):625-31
– reference: 5007557 - J Lab Clin Med. 1972 Jan;79(1):128-36
– reference: 4633129 - J Med Primatol. 1972;1(3):142-55
– reference: 5488694 - Br J Ind Med. 1970 Oct;27(4):352-5
– reference: 4643025 - J Pediatr. 1972 Dec;81(6):1088-91
– reference: 5935989 - Br J Haematol. 1966 May;12(3):326-30
– reference: 6017110 - Arch Environ Health. 1967 Feb;14(2):309-12
– reference: 13752197 - J R Inst Public Health. 1961 Aug;24:177-203
– reference: 4683366 - Clin Chem. 1973 Jan;19(1):49-57
– reference: 4695860 - Pediatrics. 1973 Feb;51(2):254-9
– reference: 5473751 - Am Ind Hyg Assoc J. 1970 Jul-Aug;31(4):412-29
– reference: 13494075 - Pediatrics. 1958 Jan;21(1):40-6
– reference: 5485382 - J Lab Clin Med. 1970 Dec;76(6):933-42
– reference: 4744314 - Biochem Med. 1973 Aug;8(1):135-48
SSID ssj0001866
Score 1.2354193
Snippet In the study of human populations, much emphasis is placed on the concentration of lead in whole peripheral blood. There is a considerable body of evidence...
SourceID pubmedcentral
proquest
pubmed
crossref
jstor
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 7
SubjectTerms Blood
Child, Preschool
Children
Erythrocytes
Excretion
Hematocrit
Housing
Humans
Lead
Lead - blood
Lead poisoning
Lead Poisoning - blood
Pediatrics
Porphyrins - blood
Preschool children
Protoporphyrins
Regression Analysis
South Carolina
Title Variations in Hematologic Responses to Increased Lead Absorption in Young Children
URI https://www.jstor.org/stable/3427988
https://www.ncbi.nlm.nih.gov/pubmed/4831151
https://www.proquest.com/docview/82385135
https://pubmed.ncbi.nlm.nih.gov/PMC1475130
Volume 7
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3dS8MwED-mvggifuL8jCD4VG2bpGkfRESUoSgoTnwrTZqyweh0m6D_vXdNNzfZgxQKbdKQ3jWX-6WX3wGc-BpBQCy4J2WYe0SA5WXGci9PbJRxSnFsqijfx6jVFndv8q0B42ybtQCHc6Ed5ZNqD3pnXx_flzjgLypuhDg5t533M_SK1QIs4XwUEQR7EL-c4UTp5rgoAy9SkawpaKefnJmUXFziPI_zb-Dk1Ex0uwartQvJrpzO16Fhyw1YcetvzG0r2oTnVwTBbjWOdUu8jZ6ps3Ps2YXF2iEb9RnaBwpLtzmjZJvsSg_7g8qK0FOVKWDX9X7vLWjf3rxct7w6f4JnOFHm4iv6Oc-FKRJpdSaLkOtICb_ItdCFECYplE5kUaAPlSV4BCZP8EpqJXKJA3cbFst-aXeAhSqzmW9j4oMTkUl0Zo1FbBsqKwzXQRNOxwJMTU0uTjkueimBDBR1iqJOSdRNOJ7UfHeEGnPqHFQ6mK5AAespFyHxqzXhaKybFEcD_eLIStv_HKYxeiAy4LIJ205TkyZETLxC2FE1o8JJOdFsz5aU3U5Ftx0IhU36u__o-B4sBwjQXEDkPiyOBp_2AJ2WkT6swD6e75_iw-r7_AFZ9u7J
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Variations+in+Hematologic+Responses+to+Increased+Lead+Absorption+in+Young+Children&rft.jtitle=Environmental+health+perspectives&rft.au=Chisolm%2C+J.+Julian&rft.au=Mellits%2C+E.+David&rft.au=Keil%2C+Julian+E.&rft.au=Barrett%2C+Maureen+B.&rft.date=1974-05-01&rft.issn=0091-6765&rft.eissn=1552-9924&rft.volume=7&rft.spage=7&rft.epage=12&rft_id=info:doi/10.1289%2Fehp.7477&rft.externalDBID=n%2Fa&rft.externalDocID=10_1289_ehp_7477
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0091-6765&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0091-6765&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0091-6765&client=summon