Tea consumption and risk of type 2 diabetes mellitus: a systematic review and meta-analysis update

Objective Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to con...

Full description

Saved in:
Bibliographic Details
Published inBMJ open Vol. 4; no. 7; p. e005632
Main Authors Yang, Jian, Mao, Qun-Xia, Xu, Hong-Xia, Ma, Xu, Zeng, Chun-Yu
Format Journal Article
LanguageEnglish
Published England BMJ Publishing Group LTD 22.07.2014
BMJ Publishing Group
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Objective Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM. Design Systematic review and meta-analysis. Methods We performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea. Results Overall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses. Conclusions The results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.
AbstractList Objective Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM. Design Systematic review and meta-analysis. Methods We performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea. Results Overall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses. Conclusions The results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.
Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM.OBJECTIVETea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM.Systematic review and meta-analysis.DESIGNSystematic review and meta-analysis.We performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea.METHODSWe performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea.Overall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses.RESULTSOverall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses.The results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.CONCLUSIONSThe results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.
ObjectiveTea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM.DesignSystematic review and meta-analysis.MethodsWe performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea.ResultsOverall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses.ConclusionsThe results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.
Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed inconsistent results for the association between tea consumption and type 2 diabetes mellitus (T2DM) risk. The aim of this study was to conduct a meta-analysis to further explore the association between tea consumption and incidence of T2DM. Systematic review and meta-analysis. We performed a systematic literature search up to 30 August 2013 in PubMed, EMBASE, Chinese Wanfang Database and CNKI database. Pooling relative risks (RRs) were estimated by random-effect models. Two kinds of subgroup analyses (according to sex and regions) were performed. Sensitive analyses were performed according to types of tea. Overall, no statistically significant relationship between tea consumption and risk of T2DM was found based on 12 eligible studies (pooling RR 0.99, 95% CI 0.95 to 1.03). Compared with the lowest/non-tea group, daily tea consumption (≥3 cups/day) was associated with a lower T2DM risk (RR 0.84, 95% CI 0.73 to 0.97). Subgroup analyses showed a difference between men and women. Overall, the RRs (95% CI) were 0.92 (0.84 to 1.00) for men, and 1.00 (0.96 to 1.05) for women, respectively. Tea consumption of ≥3 cups/day was associated with decreased T2DM risk in women (RR 0.84, 95% CI 0.71 to 1.00). Overall, the RRs (95% CIs) were 0.84 (0.71 to 1.00) for Asians, and 1.00 (0.97 to 1.04) for Americans and Europeans, respectively. No obvious change was found in sensitivity analyses. The results suggest that daily tea consumption (≥3 cups/day) is associated with a lower T2DM risk. However, further studies are needed to enrich related evidence, especially with regard to types of tea or sex.
Author Mao, Qun-Xia
Yang, Jian
Ma, Xu
Xu, Hong-Xia
Zeng, Chun-Yu
AuthorAffiliation 4 National Research Institute for Family Planning , Beijing , People's Republic of China
2 Department of Cardiology , Daping Hospital, The Third Military Medical University , Chongqing , People's Republic of China
1 Department of Nutrition , Daping Hospital, The Third Military Medical University , Chongqing , People's Republic of China
3 Social Medical Science Research Centre, National Research Institute for Family Planning , Beijing , People's Republic of China
AuthorAffiliation_xml – name: 3 Social Medical Science Research Centre, National Research Institute for Family Planning , Beijing , People's Republic of China
– name: 4 National Research Institute for Family Planning , Beijing , People's Republic of China
– name: 1 Department of Nutrition , Daping Hospital, The Third Military Medical University , Chongqing , People's Republic of China
– name: 2 Department of Cardiology , Daping Hospital, The Third Military Medical University , Chongqing , People's Republic of China
Author_xml – sequence: 1
  givenname: Jian
  surname: Yang
  fullname: Yang, Jian
  email: chunyuzeng01@163.com, genetic@263.net.cn
  organization: Department of Cardiology, Daping Hospital, The Third Military Medical University, Chongqing, People's Republic of China
– sequence: 2
  givenname: Qun-Xia
  surname: Mao
  fullname: Mao, Qun-Xia
  email: chunyuzeng01@163.com, genetic@263.net.cn
  organization: Social Medical Science Research Centre, National Research Institute for Family Planning, Beijing, People's Republic of China
– sequence: 3
  givenname: Hong-Xia
  surname: Xu
  fullname: Xu, Hong-Xia
  email: chunyuzeng01@163.com, genetic@263.net.cn
  organization: Department of Nutrition, Daping Hospital, The Third Military Medical University, Chongqing, People's Republic of China
– sequence: 4
  givenname: Xu
  surname: Ma
  fullname: Ma, Xu
  email: chunyuzeng01@163.com, genetic@263.net.cn
  organization: National Research Institute for Family Planning, Beijing, People's Republic of China
– sequence: 5
  givenname: Chun-Yu
  surname: Zeng
  fullname: Zeng, Chun-Yu
  email: chunyuzeng01@163.com, genetic@263.net.cn
  organization: Department of Cardiology, Daping Hospital, The Third Military Medical University, Chongqing, People's Republic of China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25052177$$D View this record in MEDLINE/PubMed
BookMark eNqNkU9rFTEUxYNUbK39BIIE3HQzNX9n5rkQSqlaKLip63BnckfznEnGJNPyvn3zfK9Suyhmk8D9ncO5Oa_JgQ8eCXnL2Rnnsv7QTeswo68E46piTNdSvCBHgilV1Uzrg0fvQ3KS0pqVo_RKa_GKHArNtOBNc0S6GwTaB5-Wac4ueAre0ujSLxoGmjczUkGtgw4zJjrhOLq8pI8UaNqkjBNk19OItw7v_ignzFCBh3GTXKLLbCHjG_JygDHhyf4-Jt8_X95cfK2uv325uji_rjot21xx3jesa7kQllsxqIFZrUA3jbRtVyuLgtUcu6ZuSprVoKFmkmkEwKHhSrbymHza-c5LN6Ht0ecIo5mjmyBuTABn_p1499P8CLdGccGkUsXgdG8Qw-8FUzaTS33ZGTyGJRmuVctXsnxcQd8_QddhiWXvQjWtlluIF-rd40R_ozx8fwFWO6CPIaWIg-ldhm0PJaAbDWdm27bZt222bZtd20Urn2gf7J9Xne1UZfhfgnsc276w
CitedBy_id crossref_primary_10_1080_19393210_2024_2304233
crossref_primary_10_3390_nu11040841
crossref_primary_10_1016_j_nutres_2023_08_002
crossref_primary_10_1021_acs_jafc_8b05242
crossref_primary_10_1002_mnfr_202000353
crossref_primary_10_2337_dc18_2655
crossref_primary_10_1038_s41598_021_03153_7
crossref_primary_10_3389_fnut_2024_1428445
crossref_primary_10_1155_2020_1860452
crossref_primary_10_3390_antiox11020283
crossref_primary_10_2147_DMSO_S238483
crossref_primary_10_1080_03067319_2024_2343104
crossref_primary_10_3390_foods7020017
crossref_primary_10_1186_s12890_023_02762_4
crossref_primary_10_1016_j_fct_2017_09_015
crossref_primary_10_1093_ajcn_nqy083
crossref_primary_10_1016_j_freeradbiomed_2018_09_037
crossref_primary_10_1111_1541_4337_12479
crossref_primary_10_1093_jn_nxz031
crossref_primary_10_3390_antiox8060170
crossref_primary_10_1016_j_numecd_2019_11_015
crossref_primary_10_1093_jn_nxz156
crossref_primary_10_1142_S0192415X22500628
crossref_primary_10_3390_antiox7040056
crossref_primary_10_1021_acs_jafc_3c08492
crossref_primary_10_1016_j_jnutbio_2020_108478
crossref_primary_10_1136_bmjdrc_2022_003266
crossref_primary_10_1016_j_conctc_2019_100495
crossref_primary_10_13005_bpj_2718
crossref_primary_10_2174_1573401316666200514224433
crossref_primary_10_3389_fgene_2022_835917
crossref_primary_10_1142_S2575900020300088
crossref_primary_10_1111_jgs_16467
crossref_primary_10_3390_ijms18061188
crossref_primary_10_3945_jn_115_222414
crossref_primary_10_1007_s13410_018_0675_5
crossref_primary_10_1039_D1FO04209B
crossref_primary_10_1093_ije_dyy173
crossref_primary_10_1186_s13148_015_0095_z
crossref_primary_10_3390_nu13041144
crossref_primary_10_7762_cnr_2024_13_3_201
crossref_primary_10_1038_s41430_018_0218_7
crossref_primary_10_1152_ajpheart_00376_2019
crossref_primary_10_3390_molecules22050849
crossref_primary_10_3390_nu15061448
crossref_primary_10_1080_07315724_2020_1827082
crossref_primary_10_1093_advances_nmz038
crossref_primary_10_1007_s10654_024_01165_x
crossref_primary_10_1038_s41430_020_00710_7
crossref_primary_10_1016_j_phyplu_2020_100001
crossref_primary_10_1016_j_tifs_2018_05_026
crossref_primary_10_1007_s00394_024_03341_x
crossref_primary_10_1007_s12603_017_0898_z
crossref_primary_10_1016_j_ctim_2019_08_019
crossref_primary_10_1371_journal_pone_0194127
crossref_primary_10_29219_fnr_v68_10458
crossref_primary_10_1111_dom_15839
crossref_primary_10_3390_nu8010017
crossref_primary_10_1016_j_pharmthera_2025_108828
crossref_primary_10_1186_s12916_024_03736_x
crossref_primary_10_1080_09637486_2017_1362690
crossref_primary_10_1016_j_fbio_2024_103716
Cites_doi 10.1016/j.ajog.2010.02.008
10.1080/07315724.2009.10718097
10.1038/sj.ijo.0802999
10.1001/archinte.166.12.1311
10.1007/s00125-009-1516-3
10.1002/mnfr.200700437
10.1017/S1368980010002004
10.1080/01635589809514635
10.1093/ajcn/77.3.622
10.1001/jama.2011.812
10.1016/0091-7435(92)90041-F
10.2337/dc11-0891
10.1093/ajcn/88.4.979
10.1002/jemt.20721
10.1038/sj.ijo.0803341
10.1007/s00125-004-1590-5
10.1007/BF02976881
10.1016/j.envres.2006.11.002
10.1017/S0007114508944135
10.1017/S1368980010000170
10.3349/ymj.2009.50.1.31
10.1136/bmj.f5001
10.1371/journal.pone.0036910
10.1001/archinternmed.2009.439
10.1080/07315724.2005.10719488
10.7326/0003-4819-140-1-200401060-00005
10.2337/diacare.26.7.2211
10.1210/jc.2011-0118
10.1016/1047-2797(92)90011-E
10.1016/S0278-6915(02)00066-2
10.1021/jf0300801
10.1021/jf2024819
10.1093/carcin/bgm171
10.1093/aje/kwf111
10.3945/ajcn.2009.28741
10.3945/ajcn.2010.29598
10.1007/s11606-009-0929-5
10.1371/journal.pone.0026725
10.7326/0003-4819-144-8-200604180-00005
10.1093/jn/136.12.3039
10.7326/0003-4819-159-8-201310150-00007
10.1017/S0007114510004824
10.1089/jmf.2010.1396
10.1017/S0007114509991966
10.2337/diacare.29.02.06.dc05-1512
10.2337/dc08-9017
10.1111/j.1464-5491.2011.03239.x
10.2337/db10-1193
10.7326/0003-4819-138-1-200301070-00005
10.1093/carcin/bgi028
ContentType Journal Article
Copyright Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2014 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2014
Copyright_xml – notice: Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
– notice: Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
– notice: Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2014 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2014
DBID 9YT
ACMMV
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7RV
7X7
7XB
88E
88G
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
BTHHO
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
K9-
K9.
KB0
M0R
M0S
M1P
M2M
NAPCQ
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
PSYQQ
Q9U
7X8
5PM
DOI 10.1136/bmjopen-2014-005632
DatabaseName BMJ Open Access Journals
BMJ Journals:Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Nursing & Allied Health Database
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Psychology Database (Alumni)
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
ProQuest Central
BMJ Journals
ProQuest One Community College
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
Consumer Health Database (Alumni Edition)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
ProQuest Family Health
ProQuest Health & Medical Collection
Medical Database
Psychology Database
Nursing & Allied Health Premium
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest Health & Medical Research Collection
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
ProQuest One Psychology
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest One Psychology
ProQuest Central Student
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 Family Health (Alumni Edition)
ProQuest Central China
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Central Basic
ProQuest Family Health
ProQuest One Academic Eastern Edition
ProQuest Nursing & Allied Health Source
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Psychology Journals (Alumni)
ProQuest Hospital Collection (Alumni)
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest Psychology Journals
ProQuest One Academic UKI Edition
BMJ Journals
ProQuest Nursing & Allied Health Source (Alumni)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
Publicly Available Content Database
MEDLINE
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
– sequence: 3
  dbid: ACMMV
  name: BMJ Journals:Open Access
  url: https://journals.bmj.com/
  sourceTypes: Publisher
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2044-6055
ExternalDocumentID PMC4120344
4039206051
25052177
10_1136_bmjopen_2014_005632
bmjopen
Genre Meta-Analysis
Research Support, Non-U.S. Gov't
Systematic Review
Journal Article
GroupedDBID ---
4.4
53G
5VS
7RV
7X7
7~R
88E
8FI
8FJ
9YT
ABUWG
ACGFS
ACMMV
ADBBV
ADRAZ
AENEX
AFKRA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BCNDV
BENPR
BKNYI
BPHCQ
BTFSW
BTHHO
BVXVI
CCPQU
DIK
DWQXO
EBS
EJD
FYUFA
GNUQQ
GROUPED_DOAJ
GX1
H13
HMCUK
HYE
HZ~
K9-
KQ8
M0R
M1P
M2M
M48
M~E
NAPCQ
O9-
OK1
PGMZT
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
PSYQQ
RHI
RMJ
RPM
UKHRP
AAYXX
CITATION
PHGZM
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
3V.
7XB
8FK
K9.
PKEHL
PQEST
PQUKI
PRINS
Q9U
7X8
5PM
ID FETCH-LOGICAL-b538t-11c70b8122d1d2f4f0d54a5773d8b64de2061eb767abe9f5a60305eaaef714383
IEDL.DBID 9YT
ISSN 2044-6055
IngestDate Thu Aug 21 18:16:51 EDT 2025
Fri Jul 11 07:23:08 EDT 2025
Fri Jul 25 02:58:36 EDT 2025
Wed Jul 30 01:46:57 EDT 2025
Tue Jul 01 01:06:23 EDT 2025
Thu Apr 24 23:09:55 EDT 2025
Thu Apr 24 23:02:52 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords Epidemiology
Language English
License This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-b538t-11c70b8122d1d2f4f0d54a5773d8b64de2061eb767abe9f5a60305eaaef714383
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ObjectType-Undefined-4
JY and Q-XM contributed equally.
OpenAccessLink http://dx.doi.org/10.1136/bmjopen-2014-005632
PMID 25052177
PQID 1785332171
PQPubID 2040975
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4120344
proquest_miscellaneous_1548193217
proquest_journals_1785332171
pubmed_primary_25052177
crossref_citationtrail_10_1136_bmjopen_2014_005632
crossref_primary_10_1136_bmjopen_2014_005632
bmj_primary_10_1136_bmjopen_2014_005632
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20140722
PublicationDateYYYYMMDD 2014-07-22
PublicationDate_xml – month: 7
  year: 2014
  text: 20140722
  day: 22
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
– name: BMA House, Tavistock Square, London, WC1H 9JR
PublicationTitle BMJ open
PublicationTitleAlternate BMJ Open
PublicationYear 2014
Publisher BMJ Publishing Group LTD
BMJ Publishing Group
Publisher_xml – name: BMJ Publishing Group LTD
– name: BMJ Publishing Group
References Grøntved, Hu 2011; 305
Montonen, Knekt, Järvinen 2003; 77
Nagata, Kabuto, Shimizu 1998; 30
Odegaard, Pereira, Koh 2008; 88
Salazar-Martinez, Willett, Ascherio 2004; 140
Muraki, Imamura, Manson 2013; 347
Iso, Date, Wakai 2006; 144
Boggs, Rosenberg, Ruiz-Narvaez 2010; 92
Yamaji, Mizoue, Tabata 2004; 47
2008; 31
Satoh, Sakamoto, Ogata 2002; 40
Jing, Han, Hu 2009; 24
Steinbrecher, Erber, Grandinetti 2011; 14
Pereira, Parker, Folsom 2006; 166
Hu, Jousilahti, Peltonen 2006; 30
Graham 1992; 21
Yasui, Miyoshi, Tababe 2011; 14
van Dam, Willett, Manson 2006; 29
Oba, Nagata, Nakamura 2010; 103
Goto, Song, Chen 2011; 60
Sun, Yuan, Koh 2007; 28
Lin, Lin 2008; 52
van Dieren, Uiterwaal, van der Schouw 2009; 52
Song, Manson, Buring 2005; 24
Panagiotakos, Lionis, Zeimbekis 2009; 50
Cabrera, Giménez, López 2003; 51
Wu, Arakawa, Stanczyk 2005; 26
Huxley, Lee, Barzi 2009; 169
Grossmann 2011; 96
Saremi, Tulloch-Reid, Knowler 2003; 26
Yang, Li 2010; 203
Everett, Frithsen, Diaz 2007; 103
Yang, Han, Sun 2011; 59
Manson, Rimm, Colditz 1992; 2
Kanaya, Herrington, Vittinghoff 2003; 138
Manikandan, Sundaram, Thiagarajan 2009; 72
Fu, Zhen, Yuskavage 2011; 105
Persson, Persson, Hägg 2010; 13
Romaguera, Guevara, Norat 2011; 34
Song, Hur, Han 2003; 26
Greenberg, Axen, Schnoll 2005; 29
Golozar, Khademi, Kamangar 2011; 6
Hininger-Favier, Benaraba, Coves 2009; 28
Hamer, Witte, Mosdøl 2008; 100
Schellenberg, Dryden, Vandermeer 2013; 159
2012; 7
Nettleton, Harnack, Scrafford 2006; 136
Sartorelli, Fagherazzi, Balkau 2010; 91
Saydah, Eberhardt, Loria 2002; 156
Hayashino, Fukuhara, Okamura 2011; 28
2024051512291918000_4.7.e005632.34
2024051512291918000_4.7.e005632.32
2024051512291918000_4.7.e005632.39
2024051512291918000_4.7.e005632.38
2024051512291918000_4.7.e005632.36
Song (2024051512291918000_4.7.e005632.17) 2005; 24
2024051512291918000_4.7.e005632.31
2024051512291918000_4.7.e005632.30
Persson (2024051512291918000_4.7.e005632.45) 2010; 13
2024051512291918000_4.7.e005632.23
2024051512291918000_4.7.e005632.22
2024051512291918000_4.7.e005632.21
2024051512291918000_4.7.e005632.28
2024051512291918000_4.7.e005632.27
2024051512291918000_4.7.e005632.25
Fu (2024051512291918000_4.7.e005632.11) 2011; 105
Odegaard (2024051512291918000_4.7.e005632.20) 2008; 88
2024051512291918000_4.7.e005632.6
2024051512291918000_4.7.e005632.5
2024051512291918000_4.7.e005632.8
2024051512291918000_4.7.e005632.7
2024051512291918000_4.7.e005632.2
2024051512291918000_4.7.e005632.1
2024051512291918000_4.7.e005632.4
2024051512291918000_4.7.e005632.3
2024051512291918000_4.7.e005632.29
2024051512291918000_4.7.e005632.12
Golozar (2024051512291918000_4.7.e005632.24) 2011; 6
2024051512291918000_4.7.e005632.10
Nettleton (2024051512291918000_4.7.e005632.33) 2006; 136
Hu (2024051512291918000_4.7.e005632.35) 2006; 30
2024051512291918000_4.7.e005632.16
2024051512291918000_4.7.e005632.14
Hayashino (2024051512291918000_4.7.e005632.26) 2011; 28
2024051512291918000_4.7.e005632.52
2024051512291918000_4.7.e005632.51
2024051512291918000_4.7.e005632.50
Hininger-Favier (2024051512291918000_4.7.e005632.9) 2009; 28
Yang (2024051512291918000_4.7.e005632.15) 2010; 203
Yang (2024051512291918000_4.7.e005632.13) 2011; 59
2024051512291918000_4.7.e005632.19
2024051512291918000_4.7.e005632.18
2024051512291918000_4.7.e005632.46
2024051512291918000_4.7.e005632.44
Manson (2024051512291918000_4.7.e005632.42) 1992; 2
2024051512291918000_4.7.e005632.43
2024051512291918000_4.7.e005632.48
2024051512291918000_4.7.e005632.47
2024051512291918000_4.7.e005632.41
2024051512291918000_4.7.e005632.40
Everett (2024051512291918000_4.7.e005632.37) 2007; 103
Montonen (2024051512291918000_4.7.e005632.49) 2003; 77
References_xml – volume: 30
  start-page: 1742
  year: 2006
  article-title: Joint association of coffee consumption and other factors to the risk of type 2 diabetes: a prospective study in Finland
  publication-title: Int J Obes (Lond)
– volume: 51
  start-page: 4427
  year: 2003
  article-title: Determination of tea components with antioxidant activity
  publication-title: J Agric Food Chem
– volume: 96
  start-page: 2341
  year: 2011
  article-title: Low testosterone in men with type 2 diabetes: significance and treatment
  publication-title: J Clin Endocrinol Metab
– volume: 34
  start-page: 1913
  year: 2011
  article-title: Mediterranean diet and type 2 diabetes risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) study: the InterAct project
  publication-title: Diabetes Care
– volume: 6
  start-page: e26725
  year: 2011
  article-title: Diabetes mellitus and its correlates in an Iranian adult population
  publication-title: PLoS ONE
– volume: 169
  start-page: 2053
  year: 2009
  article-title: Coffee, decaffeinated coffee, and tea consumption in relation to incident type 2 diabetes mellitus: a systematic review with meta-analysis
  publication-title: Arch Intern Med
– volume: 26
  start-page: 2211
  year: 2003
  article-title: Coffee consumption and the incidence of type 2 diabetes
  publication-title: Diabetes Care
– volume: 47
  start-page: 2145
  year: 2004
  article-title: Coffee consumption and glucose tolerance status in middle-aged Japanese men
  publication-title: Diabetologia
– volume: 24
  start-page: 557
  year: 2009
  article-title: Tea consumption and risk of type 2 diabetes: a meta-analysis of cohort studies
  publication-title: J Gen Intern Med
– volume: 59
  start-page: 11483
  year: 2011
  article-title: (-)-Epigallocatechin gallate suppresses proliferation of vascular smooth muscle cells induced by high glucose by inhibition of PKC and ERK1/2 signalings
  publication-title: J Agric Food Chem
– volume: 60
  start-page: 269
  year: 2011
  article-title: Coffee and caffeine consumption in relation to sex hormone-binding globulin and risk of type 2 diabetes in postmenopausal women
  publication-title: Diabetes
– volume: 14
  start-page: 568
  year: 2011
  article-title: Meat consumption and risk of type 2 diabetes: the Multiethnic Cohort
  publication-title: Public Health Nutr
– volume: 7
  start-page: e36910
  year: 2012
  article-title: Tea consumption and incidence of type 2 diabetes in Europe: the EPIC-InterAct case-cohort study
  publication-title: PLoS ONE
– volume: 21
  start-page: 334
  year: 1992
  article-title: Green tea composition, consumption, and polyphenol chemistry
  publication-title: Prev Med
– volume: 100
  start-page: 1046
  year: 2008
  article-title: Prospective study of coffee and tea consumption in relation to risk of type 2 diabetes mellitus among men and women: the Whitehall II study
  publication-title: Br J Nutr
– volume: 13
  start-page: 730
  year: 2010
  article-title: Effects of green tea, black tea and Rooibos tea on angiotensin-converting enzyme and nitric oxide in healthy volunteers
  publication-title: Public Health Nutr
– volume: 103
  start-page: 413
  year: 2007
  article-title: Association of a polychlorinated dibenzo-p-dioxin, a polychlorinated biphenyl, and DDT with diabetes in the 1999–2002 National Health and Nutrition Examination Survey
  publication-title: Environ Res
– volume: 91
  start-page: 1002
  year: 2010
  article-title: Differential effects of coffee on the risk of type 2 diabetes according to meal consumption in a French cohort of women: the E3N/EPIC cohort study
  publication-title: Am J Clin Nutr
– volume: 140
  start-page: 1
  year: 2004
  article-title: Coffee consumption and risk for type 2 diabetes mellitus
  publication-title: Ann Intern Med
– volume: 28
  start-page: 805
  year: 2011
  article-title: High oolong tea consumption predicts future risk of diabetes among Japanese male workers: a prospective cohort study
  publication-title: Diabet Med
– volume: 26
  start-page: 976
  year: 2005
  article-title: Tea and circulating estrogen levels in postmenopausal Chinese women in Singapore
  publication-title: Carcinogenesis
– volume: 14
  start-page: 930
  year: 2011
  article-title: Effects of oolong tea on gene expression of gluconeogenic enzymes in the mouse liver and in rat hepatoma H4IIE cells
  publication-title: J Med Food
– volume: 50
  start-page: 31
  year: 2009
  article-title: Long-term tea intake is associated with reduced prevalence of (type 2) diabetes mellitus among elderly people from Mediterranean islands: MEDIS epidemiological study
  publication-title: Yonsei Med J
– volume: 138
  start-page: 1
  year: 2003
  article-title: Glycemic effects of postmenopausal hormone therapy: the Heart and Estrogen/progestin Replacement Study. A randomized, double-blind, placebo-controlled trial
  publication-title: Ann Intern Med
– volume: 52
  start-page: 2561
  year: 2009
  article-title: Coffee and tea consumption and risk of type 2 diabetes
  publication-title: Diabetologia
– volume: 136
  start-page: 3039
  year: 2006
  article-title: Dietary flavonoids and flavonoid-rich foods are not associated with risk of type 2 diabetes in postmenopausal women
  publication-title: J Nutr
– volume: 156
  start-page: 714
  year: 2002
  article-title: Age and the burden of death attributable to diabetes in the United States
  publication-title: Am J Epidemiol
– volume: 92
  start-page: 960
  year: 2010
  article-title: Coffee, tea, and alcohol intake in relation to risk of type 2 diabetes in African American women
  publication-title: Am J Clin Nutr
– volume: 40
  start-page: 925
  year: 2002
  article-title: Inhibition of aromatase activity by green tea extract catechins and their endocrinological effects of oral administration in rats
  publication-title: Food Chem Toxicol
– volume: 28
  start-page: 355
  year: 2009
  article-title: Green tea extract decreases oxidative stress and improves insulin sensitivity in an animal model of insulin resistance, the fructose-fed rat
  publication-title: J Am Coll Nutr
– volume: 159
  start-page: 543
  year: 2013
  article-title: Lifestyle interventions for patients with and at risk for type 2 diabetes: a systematic review and meta-analysis
  publication-title: Ann Intern Med
– volume: 52
  start-page: 930
  year: 2008
  article-title: Epigallocatechin gallate (EGCG) attenuates high glucose-induced insulin signaling blockade in human hepG2 hepatoma cells
  publication-title: Mol Nutr Food Res
– volume: 347
  start-page: f5001
  year: 2013
  article-title: Fruit consumption and risk of type 2 diabetes: results from three prospective longitudinal cohort studies
  publication-title: BMJ
– volume: 26
  start-page: 559
  year: 2003
  article-title: Epigallocatechin gallate prevents autoimmune diabetes induced by multiple low doses of streptozotocin in mice
  publication-title: Arch Pharm Res
– volume: 30
  start-page: 21
  year: 1998
  article-title: Association of coffee, green tea, and caffeine intakes with serum concentrations of estradiol and sex hormone-binding globulin in premenopausal Japanese women
  publication-title: Nutr Cancer
– volume: 105
  start-page: 1218
  year: 2011
  article-title: Epigallocatechin gallate delays the onset of type 1 diabetes in spontaneous non-obese diabetic mice
  publication-title: Br J Nutr
– volume: 203
  start-page: 75.e1
  year: 2010
  article-title: Epigallocatechin-3-gallate ameliorates hyperglycemia-induced embryonic vasculopathy and malformation by inhibition of Foxo3a activation
  publication-title: Am J Obstet Gynecol
– volume: 88
  start-page: 979
  year: 2008
  article-title: Coffee, tea, and incident type 2 diabetes: the Singapore Chinese Health Study
  publication-title: Am J Clin Nutr
– volume: 77
  start-page: 622
  year: 2003
  article-title: Whole-grain and fiber intake and the incidence of type 2 diabetes
  publication-title: Am J Clin Nutr
– volume: 103
  start-page: 453
  year: 2010
  article-title: Consumption of coffee, green tea, oolong tea, black tea, chocolate snacks and the caffeine content in relation to risk of diabetes in Japanese men and women
  publication-title: Br J Nutr
– volume: 29
  start-page: 1121
  year: 2005
  article-title: Coffee, tea and diabetes: the role of weight loss and caffeine
  publication-title: Int J Obes (Lond)
– volume: 166
  start-page: 1311
  year: 2006
  article-title: Coffee consumption and risk of type 2 diabetes mellitus: an 11-year prospective study of 28 812 postmenopausal women
  publication-title: Arch Intern Med
– volume: 29
  start-page: 398
  year: 2006
  article-title: Coffee, caffeine, and risk of type 2 diabetes: a prospective cohort study in younger and middle-aged U.S. women
  publication-title: Diabetes Care
– volume: 2
  start-page: 665
  year: 1992
  article-title: A prospective study of postmenopausal estrogen therapy and subsequent incidence of non-insulin-dependent diabetes mellitus
  publication-title: Ann Epidemiol
– volume: 305
  start-page: 2448
  year: 2011
  article-title: Television viewing and risk of type 2 diabetes, cardiovascular disease, and all-cause mortality: a meta-analysis
  publication-title: JAMA
– volume: 31
  start-page: 596
  year: 2008
  article-title: Economic costs of diabetes in the U.S. In 2007
  publication-title: Diabetes Care
– volume: 72
  start-page: 723
  year: 2009
  article-title: Effect of black tea on histological and immunohistochemical changes in pancreatic tissues of normal and streptozotocin-induced diabetic mice (Mus musculus)
  publication-title: Microsc Res Tech
– volume: 28
  start-page: 2143
  year: 2007
  article-title: Green tea and black tea consumption in relation to colorectal cancer risk: the Singapore Chinese Health Study
  publication-title: Carcinogenesis
– volume: 24
  start-page: 376
  year: 2005
  article-title: Associations of dietary flavonoids with risk of type 2 diabetes, and markers of insulin resistance and systemic inflammation in women: a prospective study and cross-sectional analysis
  publication-title: J Am Coll Nutr
– volume: 144
  start-page: 554
  year: 2006
  article-title: The relationship between green tea and total caffeine intake and risk for self-reported type 2 diabetes among Japanese adults
  publication-title: Ann Intern Med
– volume: 203
  start-page: 75.e1
  year: 2010
  ident: 2024051512291918000_4.7.e005632.15
  article-title: Epigallocatechin-3-gallate ameliorates hyperglycemia-induced embryonic vasculopathy and malformation by inhibition of Foxo3a activation
  publication-title: Am J Obstet Gynecol
  doi: 10.1016/j.ajog.2010.02.008
– volume: 28
  start-page: 355
  year: 2009
  ident: 2024051512291918000_4.7.e005632.9
  article-title: Green tea extract decreases oxidative stress and improves insulin sensitivity in an animal model of insulin resistance, the fructose-fed rat
  publication-title: J Am Coll Nutr
  doi: 10.1080/07315724.2009.10718097
– ident: 2024051512291918000_4.7.e005632.16
  doi: 10.1038/sj.ijo.0802999
– ident: 2024051512291918000_4.7.e005632.18
  doi: 10.1001/archinte.166.12.1311
– ident: 2024051512291918000_4.7.e005632.21
  doi: 10.1007/s00125-009-1516-3
– ident: 2024051512291918000_4.7.e005632.14
  doi: 10.1002/mnfr.200700437
– ident: 2024051512291918000_4.7.e005632.50
  doi: 10.1017/S1368980010002004
– ident: 2024051512291918000_4.7.e005632.43
  doi: 10.1080/01635589809514635
– volume: 77
  start-page: 622
  year: 2003
  ident: 2024051512291918000_4.7.e005632.49
  article-title: Whole-grain and fiber intake and the incidence of type 2 diabetes
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/77.3.622
– ident: 2024051512291918000_4.7.e005632.51
  doi: 10.1001/jama.2011.812
– ident: 2024051512291918000_4.7.e005632.1
  doi: 10.1016/0091-7435(92)90041-F
– ident: 2024051512291918000_4.7.e005632.8
  doi: 10.2337/dc11-0891
– volume: 88
  start-page: 979
  year: 2008
  ident: 2024051512291918000_4.7.e005632.20
  article-title: Coffee, tea, and incident type 2 diabetes: the Singapore Chinese Health Study
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/88.4.979
– ident: 2024051512291918000_4.7.e005632.10
  doi: 10.1002/jemt.20721
– volume: 30
  start-page: 1742
  year: 2006
  ident: 2024051512291918000_4.7.e005632.35
  article-title: Joint association of coffee consumption and other factors to the risk of type 2 diabetes: a prospective study in Finland
  publication-title: Int J Obes (Lond)
  doi: 10.1038/sj.ijo.0803341
– ident: 2024051512291918000_4.7.e005632.31
  doi: 10.1007/s00125-004-1590-5
– ident: 2024051512291918000_4.7.e005632.12
  doi: 10.1007/BF02976881
– volume: 103
  start-page: 413
  year: 2007
  ident: 2024051512291918000_4.7.e005632.37
  article-title: Association of a polychlorinated dibenzo-p-dioxin, a polychlorinated biphenyl, and DDT with diabetes in the 1999–2002 National Health and Nutrition Examination Survey
  publication-title: Environ Res
  doi: 10.1016/j.envres.2006.11.002
– ident: 2024051512291918000_4.7.e005632.36
  doi: 10.1017/S0007114508944135
– volume: 13
  start-page: 730
  year: 2010
  ident: 2024051512291918000_4.7.e005632.45
  article-title: Effects of green tea, black tea and Rooibos tea on angiotensin-converting enzyme and nitric oxide in healthy volunteers
  publication-title: Public Health Nutr
  doi: 10.1017/S1368980010000170
– ident: 2024051512291918000_4.7.e005632.22
  doi: 10.3349/ymj.2009.50.1.31
– ident: 2024051512291918000_4.7.e005632.48
  doi: 10.1136/bmj.f5001
– ident: 2024051512291918000_4.7.e005632.28
  doi: 10.1371/journal.pone.0036910
– ident: 2024051512291918000_4.7.e005632.38
  doi: 10.1001/archinternmed.2009.439
– volume: 24
  start-page: 376
  year: 2005
  ident: 2024051512291918000_4.7.e005632.17
  article-title: Associations of dietary flavonoids with risk of type 2 diabetes, and markers of insulin resistance and systemic inflammation in women: a prospective study and cross-sectional analysis
  publication-title: J Am Coll Nutr
  doi: 10.1080/07315724.2005.10719488
– ident: 2024051512291918000_4.7.e005632.32
  doi: 10.7326/0003-4819-140-1-200401060-00005
– ident: 2024051512291918000_4.7.e005632.30
  doi: 10.2337/diacare.26.7.2211
– ident: 2024051512291918000_4.7.e005632.39
  doi: 10.1210/jc.2011-0118
– volume: 2
  start-page: 665
  year: 1992
  ident: 2024051512291918000_4.7.e005632.42
  article-title: A prospective study of postmenopausal estrogen therapy and subsequent incidence of non-insulin-dependent diabetes mellitus
  publication-title: Ann Epidemiol
  doi: 10.1016/1047-2797(92)90011-E
– ident: 2024051512291918000_4.7.e005632.40
  doi: 10.1016/S0278-6915(02)00066-2
– ident: 2024051512291918000_4.7.e005632.2
  doi: 10.1021/jf0300801
– volume: 59
  start-page: 11483
  year: 2011
  ident: 2024051512291918000_4.7.e005632.13
  article-title: (-)-Epigallocatechin gallate suppresses proliferation of vascular smooth muscle cells induced by high glucose by inhibition of PKC and ERK1/2 signalings
  publication-title: J Agric Food Chem
  doi: 10.1021/jf2024819
– ident: 2024051512291918000_4.7.e005632.3
  doi: 10.1093/carcin/bgm171
– ident: 2024051512291918000_4.7.e005632.6
  doi: 10.1093/aje/kwf111
– ident: 2024051512291918000_4.7.e005632.47
  doi: 10.3945/ajcn.2009.28741
– ident: 2024051512291918000_4.7.e005632.25
  doi: 10.3945/ajcn.2010.29598
– ident: 2024051512291918000_4.7.e005632.4
  doi: 10.1007/s11606-009-0929-5
– volume: 6
  start-page: e26725
  year: 2011
  ident: 2024051512291918000_4.7.e005632.24
  article-title: Diabetes mellitus and its correlates in an Iranian adult population
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0026725
– ident: 2024051512291918000_4.7.e005632.19
  doi: 10.7326/0003-4819-144-8-200604180-00005
– volume: 136
  start-page: 3039
  year: 2006
  ident: 2024051512291918000_4.7.e005632.33
  article-title: Dietary flavonoids and flavonoid-rich foods are not associated with risk of type 2 diabetes in postmenopausal women
  publication-title: J Nutr
  doi: 10.1093/jn/136.12.3039
– ident: 2024051512291918000_4.7.e005632.52
  doi: 10.7326/0003-4819-159-8-201310150-00007
– volume: 105
  start-page: 1218
  year: 2011
  ident: 2024051512291918000_4.7.e005632.11
  article-title: Epigallocatechin gallate delays the onset of type 1 diabetes in spontaneous non-obese diabetic mice
  publication-title: Br J Nutr
  doi: 10.1017/S0007114510004824
– ident: 2024051512291918000_4.7.e005632.46
  doi: 10.1089/jmf.2010.1396
– ident: 2024051512291918000_4.7.e005632.23
  doi: 10.1017/S0007114509991966
– ident: 2024051512291918000_4.7.e005632.34
  doi: 10.2337/diacare.29.02.06.dc05-1512
– ident: 2024051512291918000_4.7.e005632.7
  doi: 10.2337/dc08-9017
– volume: 28
  start-page: 805
  year: 2011
  ident: 2024051512291918000_4.7.e005632.26
  article-title: High oolong tea consumption predicts future risk of diabetes among Japanese male workers: a prospective cohort study
  publication-title: Diabet Med
  doi: 10.1111/j.1464-5491.2011.03239.x
– ident: 2024051512291918000_4.7.e005632.29
– ident: 2024051512291918000_4.7.e005632.5
– ident: 2024051512291918000_4.7.e005632.27
  doi: 10.2337/db10-1193
– ident: 2024051512291918000_4.7.e005632.41
  doi: 10.7326/0003-4819-138-1-200301070-00005
– ident: 2024051512291918000_4.7.e005632.44
  doi: 10.1093/carcin/bgi028
SSID ssj0000459552
Score 2.324552
SecondaryResourceType review_article
Snippet Objective Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies...
Tea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed...
ObjectiveTea has been suggested to decrease blood glucose levels and protect pancreatic β cells in diabetic mice. However, human epidemiological studies showed...
SourceID pubmedcentral
proquest
pubmed
crossref
bmj
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e005632
SubjectTerms Diabetes and Endocrinology
Diabetes Mellitus, Type 2 - epidemiology
Diabetes Mellitus, Type 2 - etiology
Female
Humans
Male
Risk Assessment
Systematic review
Tea - adverse effects
SummonAdditionalLinks – databaseName: ProQuest Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3fSxwxEA71CuKLqPXH6VlSKPSl4S7ZbJLzRUqpiGCfFO5tSTYJWry9a2_v_3dmN7d6Fg5fdxKyzEwmk0nyfYR8NZnPtFOGKT92TEYHc85YCIalV-MAZrER6x23v9X1vbyZ5JNUcFuka5WrmNgEaj8rsUY-RBb5LIMEml_O_zJkjcLT1UShsUU-InQZerWe6K7GAunKOM9FAhvimRq66R9kpQLf4JIhDCbSjmzB1_Vl6b9c8-2VyVdr0NUe2U3JI_3RWnuffAjVAdm-Tcfjn4i7C5aWzaPKJhJQW3mKl8fpLFIstlJBV8VWOkUoznq5uKCWvuA50_YtS9NzGmrLbEItocs5FgcOyf3Vr7uf1yyRKDAHsaxmnJd65GAZF557EWUc-VzaXOvMG6ekB3soHpxWGkYfx9wqDAHB2hAbavTsiPSqWRVOCC2jNLkrYdoHI0vBrYVcyzjvjVHWyNgn30CTxbyFySia7UWmiqTzAnVetDrvE7HSdlEmLHKkxHja3Ol71-ldYwxWZizSvFwUL17UJ186McwoPCaxVZgtoQ1s4jCt5bpPjlurd-NhwggCkOg1f-gaIFr3uqR6fGhQuyUXCK94uvm3zshO65uaCTEgvfrfMpxD2lO7z41vPwPM1wJu
  priority: 102
  providerName: ProQuest
– databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3dSyMxEA_iweGL6H1o1TtyIPhyqyabTdKDQ0RO5KA-tdC3JdkkqLTbWreg_70zu9l69Yt73cmQZWYyH_n4DSH7OnWpslIn0nVtIoKFNacNOMPCya4HtZiA-x29S3kxEH-H2XCFtF1RowDvXi3tsJ_UYDY6vL99OIEF_zt2JDmy4xskgcKZSBDbMgWf_AFCk8KWBr2Y79euWWTdLOMRfegNXogy8HU5Tr1IPp_fofwnKJ1vkPWYTdLTRv2bZMWXn8jHXjwv_0xs3xta1K8sa9dATeko3iank0Bx95Vy2u6-0jFic1bzu1_U0CeAZ9o8bqk5x74yiYkwJnQ-xd2CL2Rw_qd_dpHErgqJBedWJYwV6thCXOeOOR5EOHaZMJlSqdNWCgcKksxbJRXM3g2ZkegTvDE-1L3S069ktZyUfpvQIgid2QL8gNei4MwYSL60dU5rabQIHXIAksynDW5GXtcbqcyjzHOUed7IvEN4K-28iODk2CNj9D7TzwXTf82x16oxb-0sZwrylRTqMtYhPxZkWGJ4bmJKP5nDGKjqMM9lqkO2Gq0v5sMMEghAUUv2sBiA8N3LlPL6qobxFowj3uLO-7-1S9Ya21QJ53tktZrN_TfIgyr7vbbtRxjABwo
  priority: 102
  providerName: Scholars Portal
Title Tea consumption and risk of type 2 diabetes mellitus: a systematic review and meta-analysis update
URI http://bmjopen.bmj.com/content/4/7/e005632.full
https://www.ncbi.nlm.nih.gov/pubmed/25052177
https://www.proquest.com/docview/1785332171
https://www.proquest.com/docview/1548193217
https://pubmed.ncbi.nlm.nih.gov/PMC4120344
Volume 4
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1La9wwEB7SBEovJU362DZZVCjkUtGVLEtybknIg4BDCZuwPRnJkmhL1xsa7__vSPa62ZaWXGzwSBbMaKRPI-kbgA86c5myUlPpCktFsOhz2uBgWDtZeDSLCTHeUV7JixtxOctnDy6rr-_gs0x-svPvMZEUmpMJGpkrMxxxtyIrS-zExZfpEFJBdFLkKccOnwhBEajnPc_QP_6D8wl-XZ-R_oKZf56WfDD9nG3D8x43kqPO0C9gwzc78LTsd8Z3wU69IXW6T5kGAWIaR-K5cbIIJMZZCSerOCuZRxbOdnl_SAz5TeVMumssqebct4aanrCELO9iXOAl3JydTk8uaJ8_gVocxlrKWK0mFmdw7pjjQYSJy4XJlcqctlI4NIVk3iqpsPUi5EZG7_fG-JCyomevYLNZNP4NkDoIndsaPd5rUXNmDMIsbZ3TWhotwggOUJPVXceQUaWVRSarXudV1HnV6XwEfKXtqu5pyGM2jB__r_RxqPSoNvZWZqx6l7yvmEJkkuEKjI3g_SBGZ4o7JKbxiyWWwfVbRLRMjeB1Z_WhvYgVUYAStdYfhgKRqHtd0nz7mgi7BeORWfHto5X0Dp513VRRzvdgs_259PsIflo7hidqpsap449h6-ikLG_xfXx69fl6nAIK-DyfMXyWQv8CtyIE_A
linkProvider BMJ Publishing Group Ltd
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LbxMxEB61RYJeEO8GChgJxIVVY6_XdpAQQkCV0qanVMptsde2AJFNIBsh_hS_kZl9lYBUcel1ba-teXlmbH8D8NSkPtVOmUT5kUtkdKhzxqIxLLwaBWSLjZTvmJyq8Zn8MMtmW_CrewtD1yo7m1gbar8oKEd-QFXk0xQdaP56-S2hqlF0utqV0GjE4jj8_IEh2-rV0Tvk7zMhDt9P346TtqpA4lC5q4TzQg8d7mvCcy-ijEOfSZtpnXrjlPS4QMWD00pbF0Yxs4p0IlgbYl0rPMX_bsMV3HiHFOzpme5zOugejbJMtOBGPFUHbv6FqmChLHKZEOwmlTnZxq-b2-A_vu3fVzT_2PMOb8D11lllbxrpuglbobwFVyftcfxtcNNgWVE_4qwtD7OlZ3RZnS0io-QuE6xL7rI5QX9W69VLZtk5fjRr3s7UI-ehsoltUVLYeknJiDtwdinkvQs75aIMe8CKKE3mCjQzwchCcGvRtzPOe2OUNTIO4DlSMl82sBx5Hc6kKm9pnhPN84bmAxAdtfOixT6nEhxfLx70oh_0X3Psd2zMWzuwys-ldgBP-mbUYDqWsWVYrLEPBo3kRnM9gHsN1_v5yEHFBmzRG_LQdyB08M2W8vOnGiVcckFwjvcvXtZjuDaeTk7yk6PT4wew28ipToTYh53q-zo8RJerco9qOWfw8bIV6zeBIT7v
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1faxQxEB_aKxRfxP-eVo2g-OJyTXY3yQkianu01h5FWujbmmwSbPH2Tm8P8av56ZzZzV49heJLX3eSTZjMTGYmyW8AnunUpcpKnUg3tEkWLOqcNmgMSyeHHpfFBMp3HI7l3kn24TQ_XYNf3VsYulbZ2cTGULtpSTnyAVWRT1N0oPkgxGsRRzujN7NvCVWQopPWrpxGKyIH_ucPDN_mr_d3cK2fCzHaPX6_l8QKA4lFRa8Tzku1bXGPE447EbKw7fLM5EqlTluZOZys5N4qqYz1w5AbSfrhjfGhqRue4n_XYUNRVNSDjXe746NPywwPOkvDPBcR6oincmAn51QTCyWTZwmBcFLRk3X8urop_uPp_n1h848dcHQDrkfXlb1tZe0mrPnqFmwexsP522CPvWFl86SzsUPMVI7R1XU2DYxSvUywLtXLJgQEWi_mr5hhF2jSrH1J0_Sc-NokJmKmsMWMUhN34ORKGHwXetW08veBlSHTuS3R6HidlYIbg56ets5pLY3OQh9eICeLWQvSUTTBTSqLyPOCeF60PO-D6LhdlBEJnQpyfL2808tlp_8aY6tbxiJahXlxIcN9eLokoz7TIY2p_HSBbTCEJKeaqz7ca1d9OR65q0hAilqRh2UDwgpfpVRnXxrM8IwLAnd8cPm0nsAmKlXxcX988BCutWKqEiG2oFd_X_hH6H_V9nEUdAafr1q3fgO28USK
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=Tea+consumption+and+risk+of+type+2+diabetes+mellitus%3A+a+systematic+review+and+meta-analysis+update&rft.jtitle=BMJ+open&rft.au=Yang%2C+Jian&rft.au=Qun-Xia+Mao&rft.au=Hong-Xia%2C+Xu&rft.au=Xu%2C+Ma&rft.date=2014-07-22&rft.pub=BMJ+Publishing+Group+LTD&rft.eissn=2044-6055&rft.volume=4&rft.issue=7&rft.spage=e005632&rft_id=info:doi/10.1136%2Fbmjopen-2014-005632&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=4039206051
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2044-6055&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2044-6055&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2044-6055&client=summon