Effects of probiotics and fibers on markers of nephropathy, inflammation, intestinal barrier dysfunction and endothelial dysfunction in individuals with type 1 diabetes and albuminuria. The ProFOS Study
To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria. Randomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks...
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Published in | Journal of diabetes and its complications Vol. 38; no. 12; p. 108892 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.12.2024
Elsevier Limited |
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Online Access | Get full text |
ISSN | 1056-8727 1873-460X 1873-460X |
DOI | 10.1016/j.jdiacomp.2024.108892 |
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Abstract | To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.
Randomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure.
Thirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63–293) mg/g, estimated GFR was 75 (30) ml/min/1.73m2. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of −3.0 (−18.4; 15.5) % in the synbiotic group and −12.0 (−29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (−25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated.
Twelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria.
•There is need for treatment of CKD in type 1 diabetes. Alterations in the gut microbiota is linked to CKD and diabetes.•Can synbiotics be an intervention to prevent development and progression of CKD in type 1 diabetes?•Treatment with synbiotics had no effect on UACR in subjects with type 1 diabetes and albuminuria.•Unfortunately our study could not find support of using synbiotics as additional treatment. |
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AbstractList | To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.
Randomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure.
Thirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63-293) mg/g, estimated GFR was 75 (30) ml/min/1.73m
. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of -3.0 (-18.4; 15.5) % in the synbiotic group and -12.0 (-29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (-25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated.
Twelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria. AimsTo estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.MethodsRandomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure.ResultsThirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63–293) mg/g, estimated GFR was 75 (30) ml/min/1.73m2. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of −3.0 (−18.4; 15.5) % in the synbiotic group and −12.0 (−29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (−25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated.ConclusionTwelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria. To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria. Randomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure. Thirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63–293) mg/g, estimated GFR was 75 (30) ml/min/1.73m2. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of −3.0 (−18.4; 15.5) % in the synbiotic group and −12.0 (−29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (−25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated. Twelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria. •There is need for treatment of CKD in type 1 diabetes. Alterations in the gut microbiota is linked to CKD and diabetes.•Can synbiotics be an intervention to prevent development and progression of CKD in type 1 diabetes?•Treatment with synbiotics had no effect on UACR in subjects with type 1 diabetes and albuminuria.•Unfortunately our study could not find support of using synbiotics as additional treatment. To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.AIMSTo estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.Randomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure.METHODSRandomized, placebo-controlled, crossover study. Forty-one participants received synbiotic (pre- and probiotics) mix or placebo for 12 weeks with 6 weeks washout. Primary endpoint was change from baseline to end-of-period in UACR. Secondary endpoints were changes in endothelial glycocalyx thickness, inflammatory and intestinal barrier dysfunction markers, glomerular filtration rate (GFR) and ambulatory systolic blood pressure.Thirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63-293) mg/g, estimated GFR was 75 (30) ml/min/1.73m2. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of -3.0 (-18.4; 15.5) % in the synbiotic group and -12.0 (-29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (-25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated.RESULTSThirty-five participants completed the study. Mean age was 58 (SD 10) years, 73 % (n = 30) were male, median UACR was 134 (IQR 63-293) mg/g, estimated GFR was 75 (30) ml/min/1.73m2. There was no significant difference in UACR with a mean relative change (CI 95 %) from baseline to end-of-treatment of -3.0 (-18.4; 15.5) % in the synbiotic group and -12.0 (-29.6; 9.6) % in the placebo group with no significant difference between treatment periods (9.37 (-25.2; 44.0) percentage points; p = 0.60). No significant beneficial difference in the secondary end points was demonstrated.Twelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria.CONCLUSIONTwelve weeks treatment with synbiotic mix had no effect on UACR or on any of the secondary endpoints in subjects with type 1 diabetes and albuminuria. |
ArticleNumber | 108892 |
Author | Sivalingam, Suvanjaa Varasteh, Soheil Steinert, Robert E. Stougaard, Elisabeth B. Tougaard, Ninna Hahn Hansen, Christian Stevns Groop, Per-Henrik Hansen, Tine Willum Frimodt-Møller, Marie Lehto, Markku J. Størling, Joachim Persson, Frederik Rossing, Peter Salmenkari, Hanne |
Author_xml | – sequence: 1 givenname: Elisabeth B. surname: Stougaard fullname: Stougaard, Elisabeth B. email: elisabeth.buur.stougaard@regionh.dk organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 2 givenname: Ninna Hahn surname: Tougaard fullname: Tougaard, Ninna Hahn organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 3 givenname: Suvanjaa surname: Sivalingam fullname: Sivalingam, Suvanjaa organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 4 givenname: Christian Stevns surname: Hansen fullname: Hansen, Christian Stevns organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 5 givenname: Joachim surname: Størling fullname: Størling, Joachim organization: Translational Type 1 Diabetes Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 6 givenname: Tine Willum surname: Hansen fullname: Hansen, Tine Willum organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 7 givenname: Marie surname: Frimodt-Møller fullname: Frimodt-Møller, Marie organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 8 givenname: Robert E. surname: Steinert fullname: Steinert, Robert E. organization: DSM-Firmenich, Health, Nutrition & Care (HNC), Kaiseraugst, Switzerland – sequence: 9 givenname: Soheil surname: Varasteh fullname: Varasteh, Soheil organization: DSM-Firmenich, Health, Nutrition & Care (HNC), Kaiseraugst, Switzerland – sequence: 10 givenname: Per-Henrik surname: Groop fullname: Groop, Per-Henrik organization: Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland – sequence: 11 givenname: Hanne surname: Salmenkari fullname: Salmenkari, Hanne organization: Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland – sequence: 12 givenname: Markku J. surname: Lehto fullname: Lehto, Markku J. organization: Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland – sequence: 13 givenname: Frederik surname: Persson fullname: Persson, Frederik organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark – sequence: 14 givenname: Peter surname: Rossing fullname: Rossing, Peter organization: Complication Research, Steno Diabetes Center Copenhagen, Denmark |
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Keywords | Kidney disease Gut microbiota Type 1 diabetes |
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Snippet | To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and albuminuria.... AimsTo estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and... To estimate whether a mix of pre- and probiotics would strengthen the gut barrier and protect the kidneys in individuals with type 1 diabetes and... |
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SubjectTerms | Adult Aged Albuminuria Antibiotics Biomarkers - analysis Blood pressure Creatinine Cross-Over Studies Diabetes Diabetes Mellitus, Type 1 - complications Diabetic Nephropathies - diagnosis Diabetic Nephropathies - physiopathology Diabetic Nephropathies - therapy Diabetic neuropathy Dietary Fiber - administration & dosage Endothelium Endothelium, Vascular - drug effects Endothelium, Vascular - physiopathology Female Gastrointestinal surgery Glomerular Filtration Rate Gut microbiota Humans Inflammation Inflammatory bowel disease Intestinal Mucosa - drug effects Intestinal Mucosa - metabolism Intestinal Mucosa - pathology Kidney disease Kidney diseases Male Microbiota Microorganisms Middle Aged Plasma Prebiotics Probiotics Probiotics - administration & dosage Probiotics - therapeutic use Questionnaires Synbiotics - administration & dosage Type 1 diabetes Urine |
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Title | Effects of probiotics and fibers on markers of nephropathy, inflammation, intestinal barrier dysfunction and endothelial dysfunction in individuals with type 1 diabetes and albuminuria. The ProFOS Study |
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