Instant Coffee Acutely Affects Glucose Tolerance in University Students: Early Findings

Coffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population. Healthy par...

Full description

Saved in:
Bibliographic Details
Published inCurrent developments in nutrition Vol. 4; no. Supplement_2; p. nzaa045_095
Main Authors Rowlands, Tessa, Danhoff, Laura, Gainer, Bryce, Dolan, Kevin, Green, Natasha, Smith, Jenna, Thombs, Emma, Lowery, Lonnie
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Inc 01.06.2020
Oxford University Press
Subjects
Online AccessGet full text
ISSN2475-2991
2475-2991
DOI10.1093/cdn/nzaa045_095

Cover

Abstract Coffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population. Healthy participants (N = 10, 18–35 y, HbA1c = 5.2%) of varied habitual coffee intakes were free of glycemia-affecting medications and were recreationally active. In a randomized, double-blind, crossover design, each pre-breakfast participant consumed Starbucks Via® decaffeinated instant coffee (DCF), an identically tasting regular instant coffee (VIA), or water (WTR, unblinded) over 25 minutes. Subsequently, 48 g carbohydrate was provided as four pieces of commercial white bread. Whole blood glucose measures were taken in duplicate each 30 min. for two hours. For glucose concentrations (mg/dl), a 3 × 5 repeated measures factorial ANOVA revealed a non-significant trend in the statistical interaction (P ≤ 0.10), with DCF quantitatively increasing the most at 30 minutes (150.4 ± 21.4 mg/dl) compared to VIA (137.3 ± 17.7 mg/dl) and WTR (140.2 ± 16.3 mg/dl). This peak was followed by the steepest quantitative decline for DCF in the second half of testing. (The non-significant interaction prevented post hoc statistical analyses). More robustly, an interaction (P ≤ 0.05) during incremental area under the curve analysis (AUC, mg/dl * min), when followed up by SNK post hoc testing, revealed that the peak AUC for DCF at 30–60 min. was 14.4% above baseline (P ≤ 0.05) and declined significantly at both the 60–90 segment and the 90–120 min segment (both P ≤ 0.05). VIA induced an AUC peak at 30–60 min. 17.1% above baseline (P ≤ 0.05) with a less-steep decline by the 60–90 min. segment (NS) and the 90–120 min. segment (P ≤ 0.05). Comparatively, the WTR AUC peak of 15.6% did not decline significantly in later stages of the OGTT (P ≥ 0.05). These early data support the hypothesis, suggesting instant coffees, both decaffeinated and regularly caffeinated, cause a mild but observably greater glucose disposal compared to water during the late stages of an OGTT in young, healthy participants. Future research should include insulin measures to elucidate the benefits of coffee on glycemia in university students. University of Mount Union Inter-Science Research Club.
AbstractList Coffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population. Healthy participants (N = 10, 18–35 y, HbA1c = 5.2%) of varied habitual coffee intakes were free of glycemia-affecting medications and were recreationally active. In a randomized, double-blind, crossover design, each pre-breakfast participant consumed Starbucks Via® decaffeinated instant coffee (DCF), an identically tasting regular instant coffee (VIA), or water (WTR, unblinded) over 25 minutes. Subsequently, 48 g carbohydrate was provided as four pieces of commercial white bread. Whole blood glucose measures were taken in duplicate each 30 min. for two hours. For glucose concentrations (mg/dl), a 3 × 5 repeated measures factorial ANOVA revealed a non-significant trend in the statistical interaction (P ≤ 0.10), with DCF quantitatively increasing the most at 30 minutes (150.4 ± 21.4 mg/dl) compared to VIA (137.3 ± 17.7 mg/dl) and WTR (140.2 ± 16.3 mg/dl). This peak was followed by the steepest quantitative decline for DCF in the second half of testing. (The non-significant interaction prevented post hoc statistical analyses). More robustly, an interaction (P ≤ 0.05) during incremental area under the curve analysis (AUC, mg/dl * min), when followed up by SNK post hoc testing, revealed that the peak AUC for DCF at 30–60 min. was 14.4% above baseline (P ≤ 0.05) and declined significantly at both the 60–90 segment and the 90–120 min segment (both P ≤ 0.05). VIA induced an AUC peak at 30–60 min. 17.1% above baseline (P ≤ 0.05) with a less-steep decline by the 60–90 min. segment (NS) and the 90–120 min. segment (P ≤ 0.05). Comparatively, the WTR AUC peak of 15.6% did not decline significantly in later stages of the OGTT (P ≥ 0.05). These early data support the hypothesis, suggesting instant coffees, both decaffeinated and regularly caffeinated, cause a mild but observably greater glucose disposal compared to water during the late stages of an OGTT in young, healthy participants. Future research should include insulin measures to elucidate the benefits of coffee on glycemia in university students. University of Mount Union Inter-Science Research Club.
ObjectivesCoffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population.MethodsHealthy participants (N = 10, 18–35 y, HbA1c = 5.2%) of varied habitual coffee intakes were free of glycemia-affecting medications and were recreationally active. In a randomized, double-blind, crossover design, each pre-breakfast participant consumed Starbucks Via® decaffeinated instant coffee (DCF), an identically tasting regular instant coffee (VIA), or water (WTR, unblinded) over 25 minutes. Subsequently, 48 g carbohydrate was provided as four pieces of commercial white bread. Whole blood glucose measures were taken in duplicate each 30 min. for two hours.ResultsFor glucose concentrations (mg/dl), a 3 × 5 repeated measures factorial ANOVA revealed a non-significant trend in the statistical interaction (P ≤ 0.10), with DCF quantitatively increasing the most at 30 minutes (150.4 ± 21.4 mg/dl) compared to VIA (137.3 ± 17.7 mg/dl) and WTR (140.2 ± 16.3 mg/dl). This peak was followed by the steepest quantitative decline for DCF in the second half of testing. (The non-significant interaction prevented post hoc statistical analyses). More robustly, an interaction (P ≤ 0.05) during incremental area under the curve analysis (AUC, mg/dl * min), when followed up by SNK post hoc testing, revealed that the peak AUC for DCF at 30–60 min. was 14.4% above baseline (P ≤ 0.05) and declined significantly at both the 60–90 segment and the 90–120 min segment (both P ≤ 0.05). VIA induced an AUC peak at 30–60 min. 17.1% above baseline (P ≤ 0.05) with a less-steep decline by the 60–90 min. segment (NS) and the 90–120 min. segment (P ≤ 0.05). Comparatively, the WTR AUC peak of 15.6% did not decline significantly in later stages of the OGTT (P ≥ 0.05).ConclusionsThese early data support the hypothesis, suggesting instant coffees, both decaffeinated and regularly caffeinated, cause a mild but observably greater glucose disposal compared to water during the late stages of an OGTT in young, healthy participants. Future research should include insulin measures to elucidate the benefits of coffee on glycemia in university students.Funding SourcesUniversity of Mount Union Inter-Science Research Club.
ObjectivesCoffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population.MethodsHealthy participants (N = 10, 18–35 y, HbA1c = 5.2%) of varied habitual coffee intakes were free of glycemia-affecting medications and were recreationally active. In a randomized, double-blind, crossover design, each pre-breakfast participant consumed Starbucks Via® decaffeinated instant coffee (DCF), an identically tasting regular instant coffee (VIA), or water (WTR, unblinded) over 25 minutes. Subsequently, 48 g carbohydrate was provided as four pieces of commercial white bread. Whole blood glucose measures were taken in duplicate each 30 min. for two hours.ResultsFor glucose concentrations (mg/dl), a 3 × 5 repeated measures factorial ANOVA revealed a non-significant trend in the statistical interaction (P ≤ 0.10), with DCF quantitatively increasing the most at 30 minutes (150.4 ± 21.4 mg/dl) compared to VIA (137.3 ± 17.7 mg/dl) and WTR (140.2 ± 16.3 mg/dl). This peak was followed by the steepest quantitative decline for DCF in the second half of testing. (The non-significant interaction prevented post hoc statistical analyses). More robustly, an interaction (P ≤ 0.05) during incremental area under the curve analysis (AUC, mg/dl * min), when followed up by SNK post hoc testing, revealed that the peak AUC for DCF at 30–60 min. was 14.4% above baseline (P ≤ 0.05) and declined significantly at both the 60–90 segment and the 90–120 min segment (both P ≤ 0.05). VIA induced an AUC peak at 30–60 min. 17.1% above baseline (P ≤ 0.05) with a less-steep decline by the 60–90 min. segment (NS) and the 90–120 min. segment (P ≤ 0.05). Comparatively, the WTR AUC peak of 15.6% did not decline significantly in later stages of the OGTT (P ≥ 0.05).ConclusionsThese early data support the hypothesis, suggesting instant coffees, both decaffeinated and regularly caffeinated, cause a mild but observably greater glucose disposal compared to water during the late stages of an OGTT in young, healthy participants. Future research should include insulin measures to elucidate the benefits of coffee on glycemia in university students.Funding SourcesUniversity of Mount Union Inter-Science Research Club.
AbstractObjectivesCoffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We hypothesized that acute glucose disposal effects will be: Decaffeinated coffee > regular coffee > water in this population. MethodsHealthy participants ( N = 10, 18–35 y, Hb A1c = 5.2%) of varied habitual coffee intakes were free of glycemia-affecting medications and were recreationally active. In a randomized, double-blind, crossover design, each pre-breakfast participant consumed Starbucks Via® decaffeinated instant coffee (DCF), an identically tasting regular instant coffee (VIA), or water (WTR, unblinded) over 25 minutes. Subsequently, 48 g carbohydrate was provided as four pieces of commercial white bread. Whole blood glucose measures were taken in duplicate each 30 min. for two hours. ResultsFor glucose concentrations (mg/dl), a 3 × 5 repeated measures factorial ANOVA revealed a non-significant trend in the statistical interaction ( P ≤ 0.10), with DCF quantitatively increasing the most at 30 minutes (150.4 ± 21.4 mg/dl) compared to VIA (137.3 ± 17.7 mg/dl) and WTR (140.2 ± 16.3 mg/dl). This peak was followed by the steepest quantitative decline for DCF in the second half of testing. (The non-significant interaction prevented post hoc statistical analyses). More robustly, an interaction ( P ≤ 0.05) during incremental area under the curve analysis (AUC, mg/dl * min), when followed up by SNK post hoc testing, revealed that the peak AUC for DCF at 30–60 min. was 14.4% above baseline ( P ≤ 0.05) and declined significantly at both the 60–90 segment and the 90–120 min segment (both P ≤ 0.05). VIA induced an AUC peak at 30–60 min. 17.1% above baseline ( P ≤ 0.05) with a less-steep decline by the 60–90 min. segment (NS) and the 90–120 min. segment ( P ≤ 0.05). Comparatively, the WTR AUC peak of 15.6% did not decline significantly in later stages of the OGTT ( P ≥ 0.05). ConclusionsThese early data support the hypothesis, suggesting instant coffees, both decaffeinated and regularly caffeinated, cause a mild but observably greater glucose disposal compared to water during the late stages of an OGTT in young, healthy participants. Future research should include insulin measures to elucidate the benefits of coffee on glycemia in university students. Funding SourcesUniversity of Mount Union Inter-Science Research Club.
ArticleNumber nzaa045_095
Author Thombs, Emma
Green, Natasha
Lowery, Lonnie
Gainer, Bryce
Danhoff, Laura
Smith, Jenna
Dolan, Kevin
Rowlands, Tessa
AuthorAffiliation University of Mount Union
AuthorAffiliation_xml – name: University of Mount Union
Author_xml – sequence: 1
  givenname: Tessa
  surname: Rowlands
  fullname: Rowlands, Tessa
  organization: University of Mount Union
– sequence: 2
  givenname: Laura
  surname: Danhoff
  fullname: Danhoff, Laura
  organization: University of Mount Union
– sequence: 3
  givenname: Bryce
  surname: Gainer
  fullname: Gainer, Bryce
  organization: University of Mount Union
– sequence: 4
  givenname: Kevin
  surname: Dolan
  fullname: Dolan, Kevin
  organization: University of Mount Union
– sequence: 5
  givenname: Natasha
  surname: Green
  fullname: Green, Natasha
  organization: University of Mount Union
– sequence: 6
  givenname: Jenna
  surname: Smith
  fullname: Smith, Jenna
  organization: University of Mount Union
– sequence: 7
  givenname: Emma
  surname: Thombs
  fullname: Thombs, Emma
  organization: University of Mount Union
– sequence: 8
  givenname: Lonnie
  surname: Lowery
  fullname: Lowery, Lonnie
  organization: University of Mount Union
BookMark eNqNUs9rFDEUDlLBWnv2GvAmrPsyM5nM81BYlrYWCh7a4jFkkzc1dZqsyczC9q8365ZSBYunJLzvx8v73lt2EGIgxt4L-CQA67l1YR4ejIFGakD5ih1WjZKzClEcPLu_Ycc53wGAQMQW8JB9uwh5NGHky9j3RHxhp5GGLV-Ulx0zPx8mGzPx6zhQMsES94HfBL-hlP245Vfj5CiM-TM_NanwznxwPtzmd-x1b4ZMx4_nEbs5O71efpldfj2_WC4uZ7aWlZw5MNb1pFYrg3WLLfUghaiNaqyTLQmFAp0TYAEkVQTOiJUylaSm7RrVYX3ETva662l1T86WXpIZ9Dr5e5O2Ohqv_6wE_13fxo1WlVSIUAQ-PAqk-HOiPOq7OKVQeta1aFF2VffbZr5H2RRzTtQ_OQjQuwR0SUA_S6AwPu4ZcVr_Bxj3YCqj2nhKOltPZdrOpxKDdtG_wD35i2sHH7w1ww_aUn76jdC50qCvdsuw24WqBoUd7ATUvwVetP4Fr6fH9A
ContentType Journal Article
Copyright 2020 American Society for Nutrition.
American Society for Nutrition.
Copyright © The Author(s) on behalf of the American Society for Nutrition 2020. 2020
Copyright © The Author(s) on behalf of the American Society for Nutrition 2020.
Copyright_xml – notice: 2020 American Society for Nutrition.
– notice: American Society for Nutrition.
– notice: Copyright © The Author(s) on behalf of the American Society for Nutrition 2020. 2020
– notice: Copyright © The Author(s) on behalf of the American Society for Nutrition 2020.
DBID 6I.
AAFTH
AAYXX
CITATION
3V.
7RV
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
K9.
KB0
M0S
NAPCQ
PHGZM
PHGZT
PIMPY
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
5PM
DOI 10.1093/cdn/nzaa045_095
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
ProQuest Central (Corporate)
Nursing & Allied Health Database
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials - QC
ProQuest Central
ProQuest One
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
ProQuest Health & Medical Collection
Nursing & Allied Health Premium
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central China
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Central (New)
ProQuest One Academic Eastern Edition
ProQuest Nursing & Allied Health Source
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest Nursing & Allied Health Source (Alumni)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
DatabaseTitleList
Publicly Available Content Database



Database_xml – sequence: 1
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
DocumentTitleAlternate NUTRITION 2020 LIVE ONLINE Abstracts
EISSN 2475-2991
EndPage nzaa045_095
ExternalDocumentID PMC7257990
10_1093_cdn_nzaa045_095
10.1093/cdn/nzaa045_095
S2475299123079805
1_s2_0_S2475299123079805
GroupedDBID .1-
.FO
0R~
7RV
7X7
8FI
8FJ
AAFWJ
AAHBH
AALRI
AAPXW
AAVAP
AAXUO
AAYWO
ABPTD
ABUWG
ABXVV
ACGFS
ACVFH
ADBBV
ADCNI
ADVLN
AEUPX
AFJKZ
AFKRA
AFPKN
AFPUW
AFRHN
AIGII
AITUG
AJUYK
AKBMS
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMNDL
AMRAJ
AOIJS
APXCP
BAYMD
BCNDV
BENPR
CCPQU
EBS
EJD
EMOBN
FDB
FYUFA
GROUPED_DOAJ
H13
HMCUK
HYE
IAO
IHR
INH
ITC
KSI
M~E
NAPCQ
O9-
OK1
PHGZM
PHGZT
PIMPY
PPXIY
PUEGO
RPM
UKHRP
Z5R
6I.
AAFTH
ABDBF
ABEJV
AFULF
BTTYL
ROX
TOX
AAYXX
CITATION
3V.
7XB
8FK
AZQEC
DWQXO
K9.
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
5PM
ID FETCH-LOGICAL-c3525-d0acdfe7bba93696ef05113a74cd56e17919dd10c005e2e0da1b7a25e46847893
IEDL.DBID 7X7
ISSN 2475-2991
IngestDate Thu Aug 21 18:11:50 EDT 2025
Fri Jul 25 22:03:59 EDT 2025
Wed Aug 06 19:27:10 EDT 2025
Tue Nov 19 12:02:23 EST 2024
Sat Aug 30 17:16:51 EDT 2025
Fri Aug 08 06:00:38 EDT 2025
Tue Aug 26 16:33:05 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue Supplement_2
Language English
License http://creativecommons.org/licenses/by-nc-nd/4.0
This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3525-d0acdfe7bba93696ef05113a74cd56e17919dd10c005e2e0da1b7a25e46847893
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
OpenAccessLink https://www.proquest.com/docview/3169582889?pq-origsite=%requestingapplication%
PQID 3169582889
PQPubID 7121353
PageCount 1
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_7257990
proquest_journals_3169582889
crossref_primary_10_1093_cdn_nzaa045_095
oup_primary_10_1093_cdn_nzaa045_095
elsevier_sciencedirect_doi_10_1093_cdn_nzaa045_095
elsevier_clinicalkeyesjournals_1_s2_0_S2475299123079805
elsevier_clinicalkey_doi_10_1093_cdn_nzaa045_095
PublicationCentury 2000
PublicationDate 20200601
PublicationDateYYYYMMDD 2020-06-01
PublicationDate_xml – month: 06
  year: 2020
  text: 20200601
  day: 01
PublicationDecade 2020
PublicationPlace Oxford
PublicationPlace_xml – name: Oxford
PublicationTitle Current developments in nutrition
PublicationYear 2020
Publisher Elsevier Inc
Oxford University Press
Publisher_xml – name: Elsevier Inc
– name: Oxford University Press
SSID ssj0001999609
Score 2.108035
Snippet Coffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university students. We...
AbstractObjectivesCoffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy...
ObjectivesCoffee has been shown to enhance glucose disposal in middle-aged insulin-resistant subjects but less research has been done on healthy university...
SourceID pubmedcentral
proquest
crossref
oup
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage nzaa045_095
SubjectTerms Coffee
Dietary Bioactive Components
Gastroenterology and Hepatology
Glucose
University students
Title Instant Coffee Acutely Affects Glucose Tolerance in University Students: Early Findings
URI https://www.clinicalkey.com/#!/content/1-s2.0-S2475299123079805
https://www.clinicalkey.es/playcontent/1-s2.0-S2475299123079805
https://dx.doi.org/10.1093/cdn/nzaa045_095
https://www.proquest.com/docview/3169582889
https://pubmed.ncbi.nlm.nih.gov/PMC7257990
Volume 4
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1JT-swELZYLu-CWPXYKksgxCWqkzhxzAUVRFkkEGLR681y7KmoBCmQcoBfz9hJWirx4ByN4zizfB6PvyFkFyNcGhnLA2kZBFyHaHOcx4EGwAca4sTzFlxepWf3_KKX9OqEW1mXVTY-0TtqOzQuR96Ow1S6I55MHj6_BK5rlDtdrVtozJJ5T12G-ix6YpJjcWieyYbRR8ZtY4t28aE1AhnFXE-J74PR1F03BzmnCya_RKDuIlmooSPtVP96icxAsUxWOgVum5_e6R71xZw-S75C_p172Deix8N-H4B2zNsIHt9ppyrfoKdVpTq9Gz6Ca60BdFDQSZEGva0oL8sD6hmQaXfgb7-Uq-S-e3J3fBbUPRQC44hOA8u0sX0Qea596z7ooxWGsRbc2CQFR04qrQ2ZQWuECJjVYS50lABPMW4hmFkjc8WwgL-EunAf6yzPTK65TlKpc8E0B5mlJpUZrJP9ZjHVc0WVoaoj7ljhuqsv675OWLPYqrkBij5LoRv_v4j4TgTK2uZKFaoyUkzdRlwkGGRDV-IuM4aS0ViyhhUVXPj5dTuoA79_x1ajI2o8j4mm4pyn9GY8nOP0nn5SDB48t7dAF4oAYePngTfJn8jt-302aIvMjV7fYBvB0ShveQtokfmjk6vrm5ZPMXwCO9MUtA
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LbxMxELaq9FAuiFIQhQKWWhCXVbxe78OVKhRK04S2EaKp6M147YmIVDalmwqFH8VvZOzdTRqplFPPK-9jdh6fxzPfELKDES7hxopAWgaB0CHanBBRoAHwgoYo9rwFJ4OkdyY-ncfnK-RP0wvjyiobn-gdtZ0YlyNvR2Ei3RFPJt9f_gzc1Ch3utqM0KjU4ghmv3DLVu71P-L_fcN592C43wvqqQKBcdSfgWXa2BGkea79MDsYoV6GkU6FsXECjq5TWhsyg_oJHJjVYZ5qHoNI0JNnjnwJXf6qcB2tLbL64WDw-csiq-P2D0w2HEIyahtbtIvfWiN0UsxNsbg9_C111zmQu1yieSPmdR-RhzVYpZ1Ku9bJChSPyUanwI36jxl9S335qM_Lb5CvfQ80p3R_MhoB0I65nsLFjHaqghF6WNXG0-HkAtwwD6Djgi7KQuhpRbJZ7lLPuUy7Y99vUz4hZ_ci36ekVUwKeEaoAxiRzvLM5FroOJE6T5kWILPEJDKDTfKuEaa6rMg5VHWoHimUu7oh903CGmGrpucUvaTCwPHvJeltS6CsrbxUoSq5YuqUizTGsB66onqZMVzJ5ytrIFMBlLsft4068P_v2Gp0RM3fY2Eb-M5LejO_nWMRX75SjL97NvEUnTZCkud33_g1WesNT47VcX9w9II84C7r4HNRW6Q1vbqGlwjNpvmr2h4o-XbfJvgXL11QCg
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=Instant+Coffee+Acutely+Affects+Glucose+Tolerance+in+University+Students%3A+Early+Findings&rft.jtitle=Current+developments+in+nutrition&rft.au=Rowlands%2C+Tessa&rft.au=Danhoff%2C+Laura&rft.au=Gainer%2C+Bryce&rft.au=Dolan%2C+Kevin&rft.date=2020-06-01&rft.pub=Elsevier+Inc&rft.issn=2475-2991&rft.eissn=2475-2991&rft.volume=4&rft_id=info:doi/10.1093%2Fcdn%2Fnzaa045_095&rft.externalDocID=S2475299123079805
thumbnail_m http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F24752991%2FS2475299120X04148%2Fcov150h.gif