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  1. Article ; Online: Biomarkers and personalised medicine in paediatric kidney disease.

    Neuen, Brendon L / Kennedy, Sean

    The Lancet. Child & adolescent health

    2023  Volume 7, Issue 6, Page(s) 369–371

    MeSH term(s) Child ; Humans ; Precision Medicine ; Biomarkers ; Kidney Diseases/diagnosis
    Chemical Substances Biomarkers
    Language English
    Publishing date 2023-04-26
    Publishing country England
    Document type Journal Article ; Comment
    ISSN 2352-4650
    ISSN (online) 2352-4650
    DOI 10.1016/S2352-4642(23)00102-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Accelerated Risk-Based Implementation of Guideline-Directed Medical Therapy for Type 2 Diabetes and Chronic Kidney Disease.

    Neuen, Brendon L / Tuttle, Katherine R / Vaduganathan, Muthiah

    Circulation

    2024  Volume 149, Issue 16, Page(s) 1238–1240

    MeSH term(s) Humans ; Diabetes Mellitus, Type 2/diagnosis ; Diabetes Mellitus, Type 2/drug therapy ; Diabetes Mellitus, Type 2/epidemiology ; Renal Insufficiency, Chronic/diagnosis ; Renal Insufficiency, Chronic/drug therapy ; Renal Insufficiency, Chronic/epidemiology
    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.123.068524
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: SGLT2 inhibitors and finerenone: one or the other or both?

    Neuen, Brendon L / Jardine, Meg J

    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

    2022  Volume 37, Issue 7, Page(s) 1209–1211

    MeSH term(s) Canagliflozin ; Humans ; Mineralocorticoid Receptor Antagonists ; Naphthyridines ; Sodium-Glucose Transporter 2 Inhibitors/therapeutic use
    Chemical Substances Mineralocorticoid Receptor Antagonists ; Naphthyridines ; Sodium-Glucose Transporter 2 Inhibitors ; finerenone ; Canagliflozin (0SAC974Z85)
    Language English
    Publishing date 2022-02-25
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 90594-x
    ISSN 1460-2385 ; 0931-0509
    ISSN (online) 1460-2385
    ISSN 0931-0509
    DOI 10.1093/ndt/gfac046
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The authors reply.

    Heerspink, Hiddo J L / Jongs, Niels / Neuen, Brendon L

    Kidney international

    2023  Volume 104, Issue 3, Page(s) 617–618

    Language English
    Publishing date 2023-08-18
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2023.06.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Blood Pressure Effects of SGLT2 Inhibitors: Mechanisms and Clinical Evidence in Different Populations.

    Beal, Bryony / Schutte, Aletta E / Neuen, Brendon L

    Current hypertension reports

    2023  Volume 25, Issue 12, Page(s) 429–435

    Abstract: Purpose of review: Sodium glucose transporter 2 inhibitors (SGLT2 inhibitors) are increasingly prescribed due to their considerable benefits on clinical outcomes in people with diabetes, heart failure, and chronic kidney disease (CKD). Hypertension is a ...

    Abstract Purpose of review: Sodium glucose transporter 2 inhibitors (SGLT2 inhibitors) are increasingly prescribed due to their considerable benefits on clinical outcomes in people with diabetes, heart failure, and chronic kidney disease (CKD). Hypertension is a common comorbidity in each of these disease states, increasing risk of cardiovascular morbidity and mortality. We herein review the effects of SGLT2 inhibitors on blood pressure in different populations, proposed mechanisms of action, and the contribution of blood pressure lowering to end-organ protection.
    Recent findings: A recognised effect of SGLT2 inhibitors in recent clinical trials is blood pressure lowering, with multiple postulated mechanisms. This advantageous effect was first identified in populations with type 2 diabetes mellitus, prior to expansion of these trials to broader cohorts. On our review, we identified that the blood pressure lowering effect of SGLT2 inhibitors appears to be a dose-independent class-effect, with a magnitude of effect comparable to that seen with a low dose hydrochlorothiazide. There is considerable evidence demonstrating that this effect is observed across populations including those with type 2 diabetes mellitus, chronic kidney disease, and resistant hypertension.
    MeSH term(s) Humans ; Sodium-Glucose Transporter 2 Inhibitors/pharmacology ; Sodium-Glucose Transporter 2 Inhibitors/therapeutic use ; Diabetes Mellitus, Type 2/complications ; Diabetes Mellitus, Type 2/drug therapy ; Hypoglycemic Agents ; Blood Pressure/physiology ; Hypertension/drug therapy ; Renal Insufficiency, Chronic/complications ; Renal Insufficiency, Chronic/drug therapy
    Chemical Substances Sodium-Glucose Transporter 2 Inhibitors ; Hypoglycemic Agents
    Language English
    Publishing date 2023-11-10
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2057367-4
    ISSN 1534-3111 ; 1522-6417
    ISSN (online) 1534-3111
    ISSN 1522-6417
    DOI 10.1007/s11906-023-01281-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Empagliflozin in Patients with Chronic Kidney Disease.

    Neuen, Brendon L / Fletcher, Robert A / Heerspink, Hiddo J L

    The New England journal of medicine

    2023  Volume 388, Issue 24, Page(s) 2300

    MeSH term(s) Humans ; Benzhydryl Compounds/therapeutic use ; Glucosides/therapeutic use ; Patients ; Renal Insufficiency, Chronic/complications ; Renal Insufficiency, Chronic/drug therapy
    Chemical Substances empagliflozin (HDC1R2M35U) ; Benzhydryl Compounds ; Glucosides
    Language English
    Publishing date 2023-06-14
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc2301923
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Sodium-Glucose Cotransporter 2 Inhibition: Rationale and Mechanisms for Kidney and Cardiovascular Protection in People With and Without Diabetes.

    Pollock, Carol / Neuen, Brendon L

    Advances in chronic kidney disease

    2021  Volume 28, Issue 4, Page(s) 298–308

    Abstract: Large-scale randomized trials have demonstrated the remarkable capacity of sodium-glucose cotransporter 2 inhibitors to reduce the risk of cardiovascular outcomes and kidney disease progression, irrespective of the presence or absence of type 2 diabetes ... ...

    Abstract Large-scale randomized trials have demonstrated the remarkable capacity of sodium-glucose cotransporter 2 inhibitors to reduce the risk of cardiovascular outcomes and kidney disease progression, irrespective of the presence or absence of type 2 diabetes mellitus. Although the results of these trials have transformed clinical practice guidelines, the mechanisms underpinning the wide-ranging benefits of this class of agents remain incompletely understood and subject to ongoing investigation. Improvements in cardiometabolic risk factors such as glucose, blood pressure, body weight, and albuminuria likely contribute. However, other direct effects on physiological and cellular function, such as restoration of tubuloglomerular feedback, improvements in kidney and cardiac oxygenation and energy efficiency, as well as restoration of normal autophagy are also likely to be important. This review summarizes the rationale and potential mechanisms for cardiorenal protection with sodium-glucose cotransporter 2 inhibitors in people with and without diabetes, their relative importance, and the experimental and clinical lines of evidence supporting these hypotheses.
    MeSH term(s) Blood Glucose ; Cardiovascular Diseases/etiology ; Cardiovascular Diseases/prevention & control ; Diabetes Mellitus, Type 2/complications ; Diabetes Mellitus, Type 2/drug therapy ; Glucose ; Humans ; Hypoglycemic Agents/therapeutic use ; Kidney ; Sodium ; Sodium-Glucose Transporter 2 Inhibitors/therapeutic use
    Chemical Substances Blood Glucose ; Hypoglycemic Agents ; Sodium-Glucose Transporter 2 Inhibitors ; Sodium (9NEZ333N27) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2021-12-16
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 1548-5609 ; 1548-5595
    ISSN (online) 1548-5609
    ISSN 1548-5595
    DOI 10.1053/j.ackd.2021.02.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Endothelin Receptor Antagonists and Risk of Heart Failure in CKD: Balancing the Cardiorenal Axis.

    Neuen, Brendon L / Inker, Lesley A / Vaduganathan, Muthiah

    JACC. Heart failure

    2022  Volume 10, Issue 7, Page(s) 508–511

    MeSH term(s) Endothelin Receptor Antagonists/therapeutic use ; Glomerular Filtration Rate ; Heart Failure/drug therapy ; Humans ; Renal Insufficiency, Chronic/complications
    Chemical Substances Endothelin Receptor Antagonists
    Language English
    Publishing date 2022-06-08
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 2705621-1
    ISSN 2213-1787 ; 2213-1779
    ISSN (online) 2213-1787
    ISSN 2213-1779
    DOI 10.1016/j.jchf.2022.04.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Pilot Trials in Nephrology: Establishing a BASE for Large-Scale Randomized Trials.

    Neuen, Brendon L / Perkovic, Vlado

    Journal of the American Society of Nephrology : JASN

    2019  Volume 31, Issue 1, Page(s) 4–6

    MeSH term(s) Humans ; Nephrology ; Pilot Projects ; Randomized Controlled Trials as Topic ; Renal Insufficiency, Chronic ; Sodium Bicarbonate
    Chemical Substances Sodium Bicarbonate (8MDF5V39QO)
    Language English
    Publishing date 2019-12-17
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 1085942-1
    ISSN 1533-3450 ; 1046-6673
    ISSN (online) 1533-3450
    ISSN 1046-6673
    DOI 10.1681/ASN.2019111196
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Heart Failure in Patients with Diabetes and Chronic Kidney Disease: Challenges and Opportunities.

    Vijay, Kris / Neuen, Brendon L / Lerma, Edgar V

    Cardiorenal medicine

    2021  Volume 12, Issue 1, Page(s) 1–10

    Abstract: Background: Heart failure (HF), diabetes mellitus (DM), and chronic kidney disease (CKD) are commonly occurring and interlinked conditions. Approximately 25%-40% of patients with HF have DM, and approximately 40%-50% of patients with HF have CKD. Both ... ...

    Abstract Background: Heart failure (HF), diabetes mellitus (DM), and chronic kidney disease (CKD) are commonly occurring and interlinked conditions. Approximately 25%-40% of patients with HF have DM, and approximately 40%-50% of patients with HF have CKD. Both DM and CKD are associated with increased risk of incident HF. Furthermore, 40% of people with DM develop CKD, making DM the leading cause of kidney failure globally. Importantly, 16% of patients with HF have both comorbid DM and CKD, and the combination of these 3 comorbidities is associated with substantially increased risk for hospitalization and mortality. Mechanisms that underlie the relationships between HF, DM, and CKD are complex but likely relate to shared cardiovascular and metabolic risk factors, as well as downstream effects on inflammation, oxidative stress, and neurohormonal pathways.
    Summary: This review outlines the epidemiology and links between HF, DM, and CKD, as well as current clinical evidence for the treatment of individuals with a combination of these comorbidities. A case study of a patient with concomitant HF, DM, and CKD is discussed to explore potential treatment approaches for patients in whom all 3 comorbidities exist.
    Key messages: Treatment plans for patients with a combination of these 3 comorbidities should consider the available clinical evidence.
    MeSH term(s) Diabetes Mellitus/epidemiology ; Female ; Heart Failure/complications ; Heart Failure/epidemiology ; Heart Failure/therapy ; Hospitalization ; Humans ; Male ; Renal Insufficiency, Chronic/complications ; Renal Insufficiency, Chronic/drug therapy ; Renal Insufficiency, Chronic/epidemiology ; Risk Factors
    Language English
    Publishing date 2021-11-19
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2595659-0
    ISSN 1664-5502 ; 1664-3828
    ISSN (online) 1664-5502
    ISSN 1664-3828
    DOI 10.1159/000520909
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