Maternal Inflammation at Delivery Affects Assessment of Maternal Iron Status

Pregnant adolescents (aged ≤18 y, n = 253) were followed from ≥12 wk of gestation to delivery to assess longitudinal changes in anemia and iron status and to explore associations between iron status indicators, hepcidin, and inflammatory markers. Hemoglobin, soluble transferrin receptor (sTfR), ferr...

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Veröffentlicht in:The Journal of nutrition 2014-10, Vol.144 (10), p.1524-1532
Hauptverfasser: Lee, Sunmin, Guillet, Ronnie, Cooper, Elizabeth M., Westerman, Mark, Orlando, Mark, Pressman, Eva, O'Brien, Kimberly O.
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container_end_page 1532
container_issue 10
container_start_page 1524
container_title The Journal of nutrition
container_volume 144
creator Lee, Sunmin
Guillet, Ronnie
Cooper, Elizabeth M.
Westerman, Mark
Orlando, Mark
Pressman, Eva
O'Brien, Kimberly O.
description Pregnant adolescents (aged ≤18 y, n = 253) were followed from ≥12 wk of gestation to delivery to assess longitudinal changes in anemia and iron status and to explore associations between iron status indicators, hepcidin, and inflammatory markers. Hemoglobin, soluble transferrin receptor (sTfR), ferritin, serum iron, erythropoietin (EPO), hepcidin, C-reactive protein, interleukin-6 (IL-6), folate, and vitamin B-12 were measured, and total body iron (TBI) (milligrams per kilogram) was calculated using sTfR and ferritin values. Anemia prevalence increased from trimesters 1 and 2 (3–5%, 8.5 mg/L) doubled from pregnancy to delivery (7% to 14%, P = 0.04). Ferritin and hepcidin concentrations at delivery may have been elevated as a consequence of inflammation because IL-6 concentrations at delivery were 1.6-fold higher than those obtained at 26.1 ± 3.3 wk of gestation (P < 0.0001), and a positive association was found between IL-6 and both hepcidin and ferritin at delivery (P < 0.01). EPO was consistently correlated with hemoglobin (r = −0.36 and −0.43, P < 0.001), ferritin (r = −0.37 and −0.32, P < 0.0001), sTfR (r = 0.35 and 0.25, P < 0.001), TBI (r = −0.44 and −0.37, P < 0.0001), and serum iron (r = −0.22 and −0.16, P < 0.05) at mid-gestation and at delivery, respectively. EPO alone explained the largest proportion of variance in hemoglobin at 26.0 ± 3.3 wk of gestation (R2 = 0.13, P = 0.0001, n = 113) and at delivery (R2 = 0.19, P < 0.0001, n = 192). Pregnant adolescents are at high risk of anemia. EPO is a sensitive indicator of iron status across gestation, is not affected by systemic inflammation, and may better predict risk of anemia at term. The trial was registered at >clinicaltrials.gov as NCT01019902.
doi_str_mv 10.3945/jn.114.191445
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Hemoglobin, soluble transferrin receptor (sTfR), ferritin, serum iron, erythropoietin (EPO), hepcidin, C-reactive protein, interleukin-6 (IL-6), folate, and vitamin B-12 were measured, and total body iron (TBI) (milligrams per kilogram) was calculated using sTfR and ferritin values. Anemia prevalence increased from trimesters 1 and 2 (3–5%, <28 wk) to trimester 3 (25%, 33.2 ± 3.7 wk, P < 0.0001). The prevalence of iron deficiency (sTfR > 8.5 mg/L) doubled from pregnancy to delivery (7% to 14%, P = 0.04). Ferritin and hepcidin concentrations at delivery may have been elevated as a consequence of inflammation because IL-6 concentrations at delivery were 1.6-fold higher than those obtained at 26.1 ± 3.3 wk of gestation (P < 0.0001), and a positive association was found between IL-6 and both hepcidin and ferritin at delivery (P < 0.01). EPO was consistently correlated with hemoglobin (r = −0.36 and −0.43, P < 0.001), ferritin (r = −0.37 and −0.32, P < 0.0001), sTfR (r = 0.35 and 0.25, P < 0.001), TBI (r = −0.44 and −0.37, P < 0.0001), and serum iron (r = −0.22 and −0.16, P < 0.05) at mid-gestation and at delivery, respectively. EPO alone explained the largest proportion of variance in hemoglobin at 26.0 ± 3.3 wk of gestation (R2 = 0.13, P = 0.0001, n = 113) and at delivery (R2 = 0.19, P < 0.0001, n = 192). Pregnant adolescents are at high risk of anemia. EPO is a sensitive indicator of iron status across gestation, is not affected by systemic inflammation, and may better predict risk of anemia at term. 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Hemoglobin, soluble transferrin receptor (sTfR), ferritin, serum iron, erythropoietin (EPO), hepcidin, C-reactive protein, interleukin-6 (IL-6), folate, and vitamin B-12 were measured, and total body iron (TBI) (milligrams per kilogram) was calculated using sTfR and ferritin values. Anemia prevalence increased from trimesters 1 and 2 (3–5%, <28 wk) to trimester 3 (25%, 33.2 ± 3.7 wk, P < 0.0001). The prevalence of iron deficiency (sTfR > 8.5 mg/L) doubled from pregnancy to delivery (7% to 14%, P = 0.04). Ferritin and hepcidin concentrations at delivery may have been elevated as a consequence of inflammation because IL-6 concentrations at delivery were 1.6-fold higher than those obtained at 26.1 ± 3.3 wk of gestation (P < 0.0001), and a positive association was found between IL-6 and both hepcidin and ferritin at delivery (P < 0.01). EPO was consistently correlated with hemoglobin (r = −0.36 and −0.43, P < 0.001), ferritin (r = −0.37 and −0.32, P < 0.0001), sTfR (r = 0.35 and 0.25, P < 0.001), TBI (r = −0.44 and −0.37, P < 0.0001), and serum iron (r = −0.22 and −0.16, P < 0.05) at mid-gestation and at delivery, respectively. EPO alone explained the largest proportion of variance in hemoglobin at 26.0 ± 3.3 wk of gestation (R2 = 0.13, P = 0.0001, n = 113) and at delivery (R2 = 0.19, P < 0.0001, n = 192). Pregnant adolescents are at high risk of anemia. EPO is a sensitive indicator of iron status across gestation, is not affected by systemic inflammation, and may better predict risk of anemia at term. The trial was registered at >clinicaltrials.gov as NCT01019902.]]></description><subject>Adolescent</subject><subject>Anemia, Iron-Deficiency - blood</subject><subject>Anemia, Iron-Deficiency - epidemiology</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cross-Sectional Studies</subject><subject>Delivery, Obstetric</subject><subject>Dietary Supplements</subject><subject>Erythropoietin - blood</subject><subject>Female</subject><subject>Ferritins - blood</subject><subject>Folic Acid - blood</subject><subject>Hemoglobins - metabolism</subject><subject>Hepcidins - blood</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Inflammation - epidemiology</subject><subject>Interleukin-6 - blood</subject><subject>Iron, Dietary - administration &amp; dosage</subject><subject>Iron, Dietary - blood</subject><subject>Longitudinal Studies</subject><subject>Multivariate Analysis</subject><subject>Nutrition Assessment</subject><subject>Nutritional Status</subject><subject>Pregnancy</subject><subject>Prevalence</subject><subject>Receptors, Transferrin - blood</subject><subject>Regression Analysis</subject><subject>Surveys and Questionnaires</subject><subject>Vitamin B 12 - blood</subject><issn>0022-3166</issn><issn>1541-6100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10DtPwzAUhmELgWgpjKwoI0vKOY6TxmNVbpWKGIDZcpxjKVUuxXYq9d8TlAITk5fHn3Rexq4R5okU6d22nSOKOUoUIj1hU0wFxhkCnLIpAOdxglk2YRfebwEAhczP2YSnkEMqYMo2LzqQa3UdrVtb66bRoeraSIfonupqT-4QLa0lE3y09J68b6gNUWejv39u8G9Bh95fsjOra09Xx3fGPh4f3lfP8eb1ab1abmKT5BBiURa5Riux5JAZTLgueC6LVCRJuSgWIDOOFlID1miNIjPSaiJjbJmRtmCSGbsdd3eu--zJB9VU3lBd65a63itMs0RKLng-0HikxnXeO7Jq56pGu4NCUN8B1bZVQ0A1Bhz8zXG6Lxoqf_VPsQEsRkDDgfuKnPKmotZQWbkhkyq76p_pL5vDfpE</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Lee, Sunmin</creator><creator>Guillet, Ronnie</creator><creator>Cooper, Elizabeth M.</creator><creator>Westerman, Mark</creator><creator>Orlando, Mark</creator><creator>Pressman, Eva</creator><creator>O'Brien, Kimberly O.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20141001</creationdate><title>Maternal Inflammation at Delivery Affects Assessment of Maternal Iron Status</title><author>Lee, Sunmin ; Guillet, Ronnie ; Cooper, Elizabeth M. ; Westerman, Mark ; Orlando, Mark ; Pressman, Eva ; O'Brien, Kimberly O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-4db8a1f91d206c132ab289b5433d7b709621f05c0fcaa146c9faeeccfd6eaf0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Anemia, Iron-Deficiency - blood</topic><topic>Anemia, Iron-Deficiency - epidemiology</topic><topic>C-Reactive Protein - metabolism</topic><topic>Cross-Sectional Studies</topic><topic>Delivery, Obstetric</topic><topic>Dietary Supplements</topic><topic>Erythropoietin - blood</topic><topic>Female</topic><topic>Ferritins - blood</topic><topic>Folic Acid - blood</topic><topic>Hemoglobins - metabolism</topic><topic>Hepcidins - blood</topic><topic>Humans</topic><topic>Inflammation - blood</topic><topic>Inflammation - epidemiology</topic><topic>Interleukin-6 - blood</topic><topic>Iron, Dietary - administration &amp; dosage</topic><topic>Iron, Dietary - blood</topic><topic>Longitudinal Studies</topic><topic>Multivariate Analysis</topic><topic>Nutrition Assessment</topic><topic>Nutritional Status</topic><topic>Pregnancy</topic><topic>Prevalence</topic><topic>Receptors, Transferrin - blood</topic><topic>Regression Analysis</topic><topic>Surveys and Questionnaires</topic><topic>Vitamin B 12 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Sunmin</creatorcontrib><creatorcontrib>Guillet, Ronnie</creatorcontrib><creatorcontrib>Cooper, Elizabeth M.</creatorcontrib><creatorcontrib>Westerman, Mark</creatorcontrib><creatorcontrib>Orlando, Mark</creatorcontrib><creatorcontrib>Pressman, Eva</creatorcontrib><creatorcontrib>O'Brien, Kimberly O.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Sunmin</au><au>Guillet, Ronnie</au><au>Cooper, Elizabeth M.</au><au>Westerman, Mark</au><au>Orlando, Mark</au><au>Pressman, Eva</au><au>O'Brien, Kimberly O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal Inflammation at Delivery Affects Assessment of Maternal Iron Status</atitle><jtitle>The Journal of nutrition</jtitle><addtitle>J Nutr</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>144</volume><issue>10</issue><spage>1524</spage><epage>1532</epage><pages>1524-1532</pages><issn>0022-3166</issn><eissn>1541-6100</eissn><abstract><![CDATA[Pregnant adolescents (aged ≤18 y, n = 253) were followed from ≥12 wk of gestation to delivery to assess longitudinal changes in anemia and iron status and to explore associations between iron status indicators, hepcidin, and inflammatory markers. Hemoglobin, soluble transferrin receptor (sTfR), ferritin, serum iron, erythropoietin (EPO), hepcidin, C-reactive protein, interleukin-6 (IL-6), folate, and vitamin B-12 were measured, and total body iron (TBI) (milligrams per kilogram) was calculated using sTfR and ferritin values. Anemia prevalence increased from trimesters 1 and 2 (3–5%, <28 wk) to trimester 3 (25%, 33.2 ± 3.7 wk, P < 0.0001). The prevalence of iron deficiency (sTfR > 8.5 mg/L) doubled from pregnancy to delivery (7% to 14%, P = 0.04). Ferritin and hepcidin concentrations at delivery may have been elevated as a consequence of inflammation because IL-6 concentrations at delivery were 1.6-fold higher than those obtained at 26.1 ± 3.3 wk of gestation (P < 0.0001), and a positive association was found between IL-6 and both hepcidin and ferritin at delivery (P < 0.01). EPO was consistently correlated with hemoglobin (r = −0.36 and −0.43, P < 0.001), ferritin (r = −0.37 and −0.32, P < 0.0001), sTfR (r = 0.35 and 0.25, P < 0.001), TBI (r = −0.44 and −0.37, P < 0.0001), and serum iron (r = −0.22 and −0.16, P < 0.05) at mid-gestation and at delivery, respectively. EPO alone explained the largest proportion of variance in hemoglobin at 26.0 ± 3.3 wk of gestation (R2 = 0.13, P = 0.0001, n = 113) and at delivery (R2 = 0.19, P < 0.0001, n = 192). Pregnant adolescents are at high risk of anemia. EPO is a sensitive indicator of iron status across gestation, is not affected by systemic inflammation, and may better predict risk of anemia at term. The trial was registered at >clinicaltrials.gov as NCT01019902.]]></abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25080540</pmid><doi>10.3945/jn.114.191445</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Anemia, Iron-Deficiency - blood
Anemia, Iron-Deficiency - epidemiology
C-Reactive Protein - metabolism
Cross-Sectional Studies
Delivery, Obstetric
Dietary Supplements
Erythropoietin - blood
Female
Ferritins - blood
Folic Acid - blood
Hemoglobins - metabolism
Hepcidins - blood
Humans
Inflammation - blood
Inflammation - epidemiology
Interleukin-6 - blood
Iron, Dietary - administration & dosage
Iron, Dietary - blood
Longitudinal Studies
Multivariate Analysis
Nutrition Assessment
Nutritional Status
Pregnancy
Prevalence
Receptors, Transferrin - blood
Regression Analysis
Surveys and Questionnaires
Vitamin B 12 - blood
title Maternal Inflammation at Delivery Affects Assessment of Maternal Iron Status
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