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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s00380-018-1136-2.

Title:
Comparison of the effects of linagliptin and voglibose on endothelial function in patients with type 2 diabetes and coronary artery disease: a prospective, randomized, pilot study (EFFORT) | Heart and Vessels
Description:
Endothelial dysfunction contributes to poor cardiovascular prognosis in patients with type 2 diabetes mellitus (T2DM) and coronary artery disease (CAD). The effect of dipeptidyl peptidase-4 inhibitors on endothelial function remains controversial. We sought to compare the effects of linagliptin and voglibose on endothelial function, as assessed by reactive hyperemia-peripheral arterial tonometry (RH-PAT). Sixteen patients with newly diagnosed T2DM and CAD were randomized 1:1 to linagliptin (5 mg, once-daily) or voglibose (0.9 mg, thrice-daily). The RH-PAT and laboratory parameters, including 75 g oral glucose tolerance test, were measured at baseline and 3 months. Linagliptin increased serum levels of active glucagon-like peptide-1 and high-molecular-weight adiponectin. Age-, sex-, and baseline-adjusted changes in logarithmic RH-PAT index (LnRHI) after 3 months were significant between groups (linagliptin, 0.135 ± 0.097; voglibose, − 0.124 ± 0.091; P = 0.047). In the linagliptin group, change in LnRHI was positively correlated with change in high-density lipoprotein cholesterol and negatively correlated with changes in both urine albumin-to-creatinine ratio and high-sensitivity C-reactive protein. Furthermore, linagliptin treatment for 3 months reduced serum levels of both glucose and insulin at 2 h, relative to voglibose, in the age-, sex-, and baseline-adjusted model. Linagliptin improved endothelial function relative to voglibose, accompanied by amelioration of glycemic, renal, and cardiometabolic parameters, in patients with newly diagnosed T2DM and CAD. Trial registration Unique Trial Number, UMIN 000029169 ( https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012442 ).
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Social Networks

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't figure out the monetization strategy.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com has a revenue plan, but it's either invisible or we haven't found it.

Keywords {🔍}

pubmed, article, endothelial, google, scholar, cas, function, diabetes, linagliptin, patients, type, central, heart, artery, voglibose, coronary, disease, study, dysfunction, vascular, research, tanaka, cardiovasc, japan, privacy, cookies, content, randomized, node, dipeptidyl, peptidase, related, inhibitor, publish, search, vessels, effects, manuscript, inoue, cardiovascular, effect, glucose, access, lerman, diabetol, saga, mitsubishi, tanabe, boehringer, ingelheim,

Topics {✒️}

jp/cgi-open-bin/ctr_e/ctr_view high-sensitivity c-reactive protein month download article/chapter jun-ichi oyama high-density lipoprotein cholesterol high-molecular-weight adiponectin logarithmic rh-pat index full article pdf coronary artery disease dipeptidyl peptidase-4 inhibitors koichi node privacy choices/manage cookies masashi sakuma & teruo inoue research program faculty endothelial vasomotor function dipeptidyl peptidase-4 inhibitor author information authors article koyama improves endothelial dysfunction unique pharmacological profile dipeptidyl-peptidase 4 inhibition ameliorates endothelial dysfunction early endothelial dysfunction boston scientific japan diabetes mellitus serum adiponectin level vascular endothelial functions european economic area short communication published flow-mediated vasodilatation stabilises arteriosclerotic lesions flow-mediated vasodilation excellent secretarial assistance ethics declarations conflict placebo-controlled study conditions privacy policy newly diagnosed t2dm poor cardiovascular prognosis prologue study investigators article log glucose-independent improvement article heart accepting optional cookies check access fukuoka wajiro hospital instant access dokkyo medical university endothelial function baseline-adjusted model anti-inflammatory effects

Questions {❓}

  • Ceriello A (2005) Postprandial hyperglycemia and diabetes complications: is it time to treat?

Schema {🗺️}

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         headline:Comparison of the effects of linagliptin and voglibose on endothelial function in patients with type 2 diabetes and coronary artery disease: a prospective, randomized, pilot study (EFFORT)
         description:Endothelial dysfunction contributes to poor cardiovascular prognosis in patients with type 2 diabetes mellitus (T2DM) and coronary artery disease (CAD). The effect of dipeptidyl peptidase-4 inhibitors on endothelial function remains controversial. We sought to compare the effects of linagliptin and voglibose on endothelial function, as assessed by reactive hyperemia-peripheral arterial tonometry (RH-PAT). Sixteen patients with newly diagnosed T2DM and CAD were randomized 1:1 to linagliptin (5 mg, once-daily) or voglibose (0.9 mg, thrice-daily). The RH-PAT and laboratory parameters, including 75 g oral glucose tolerance test, were measured at baseline and 3 months. Linagliptin increased serum levels of active glucagon-like peptide-1 and high-molecular-weight adiponectin. Age-, sex-, and baseline-adjusted changes in logarithmic RH-PAT index (LnRHI) after 3 months were significant between groups (linagliptin, 0.135 ± 0.097; voglibose, − 0.124 ± 0.091; P = 0.047). In the linagliptin group, change in LnRHI was positively correlated with change in high-density lipoprotein cholesterol and negatively correlated with changes in both urine albumin-to-creatinine ratio and high-sensitivity C-reactive protein. Furthermore, linagliptin treatment for 3 months reduced serum levels of both glucose and insulin at 2 h, relative to voglibose, in the age-, sex-, and baseline-adjusted model. Linagliptin improved endothelial function relative to voglibose, accompanied by amelioration of glycemic, renal, and cardiometabolic parameters, in patients with newly diagnosed T2DM and CAD. Trial registration Unique Trial Number, UMIN 000029169 ( https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012442 ).
         datePublished:2018-02-09T00:00:00Z
         dateModified:2018-02-09T00:00:00Z
         pageStart:958
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            Linagliptin
            Voglibose
            Type 2 diabetes mellitus
            Coronary artery disease
            Cardiology
            Cardiac Surgery
            Vascular Surgery
            Biomedical Engineering and Bioengineering
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      headline:Comparison of the effects of linagliptin and voglibose on endothelial function in patients with type 2 diabetes and coronary artery disease: a prospective, randomized, pilot study (EFFORT)
      description:Endothelial dysfunction contributes to poor cardiovascular prognosis in patients with type 2 diabetes mellitus (T2DM) and coronary artery disease (CAD). The effect of dipeptidyl peptidase-4 inhibitors on endothelial function remains controversial. We sought to compare the effects of linagliptin and voglibose on endothelial function, as assessed by reactive hyperemia-peripheral arterial tonometry (RH-PAT). Sixteen patients with newly diagnosed T2DM and CAD were randomized 1:1 to linagliptin (5 mg, once-daily) or voglibose (0.9 mg, thrice-daily). The RH-PAT and laboratory parameters, including 75 g oral glucose tolerance test, were measured at baseline and 3 months. Linagliptin increased serum levels of active glucagon-like peptide-1 and high-molecular-weight adiponectin. Age-, sex-, and baseline-adjusted changes in logarithmic RH-PAT index (LnRHI) after 3 months were significant between groups (linagliptin, 0.135 ± 0.097; voglibose, − 0.124 ± 0.091; P = 0.047). In the linagliptin group, change in LnRHI was positively correlated with change in high-density lipoprotein cholesterol and negatively correlated with changes in both urine albumin-to-creatinine ratio and high-sensitivity C-reactive protein. Furthermore, linagliptin treatment for 3 months reduced serum levels of both glucose and insulin at 2 h, relative to voglibose, in the age-, sex-, and baseline-adjusted model. Linagliptin improved endothelial function relative to voglibose, accompanied by amelioration of glycemic, renal, and cardiometabolic parameters, in patients with newly diagnosed T2DM and CAD. Trial registration Unique Trial Number, UMIN 000029169 ( https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012442 ).
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         Endothelial function
         Linagliptin
         Voglibose
         Type 2 diabetes mellitus
         Coronary artery disease
         Cardiology
         Cardiac Surgery
         Vascular Surgery
         Biomedical Engineering and Bioengineering
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            name:Shigeru Toyoda
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                     type:PostalAddress
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            type:Person
            name:Koichi Node
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                  name:Saga University
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         name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
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         name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
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         name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
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      name:Jun-ichi Oyama
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            name:Saga University
            address:
               name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
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      name:Shigeru Toyoda
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            name:Dokkyo Medical University
            address:
               name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
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      name:Masashi Sakuma
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            name:Dokkyo Medical University
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               name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
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      name:Teruo Inoue
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            name:Dokkyo Medical University
            address:
               name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
               type:PostalAddress
            type:Organization
      name:Yoritaka Otsuka
      affiliation:
            name:Fukuoka Wajiro Hospital
            address:
               name:Department of Cardiology, Fukuoka Wajiro Hospital, Fukuoka, Japan
               type:PostalAddress
            type:Organization
      name:Koichi Node
      affiliation:
            name:Saga University
            address:
               name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
               type:PostalAddress
            type:Organization
      email:[email protected]
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      name:Department of Cardiology, Fukuoka Wajiro Hospital, Fukuoka, Japan
      name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
      name:Clinical Research Center, Saga University, Saga, Japan
      name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
      name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
      name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
      name:Department of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan
      name:Department of Cardiology, Fukuoka Wajiro Hospital, Fukuoka, Japan
      name:Department of Cardiovascular Medicine, Saga University, Saga, Japan
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External Links {🔗}(119)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.6s.