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Resolution of Microalbuminuria and Dysmetabolism Following Bariatric Surgery: Prospective Study

Resolution of Microalbuminuria and Dysmetabolism Following Bariatric Surgery: Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02068833
Enrollment
48
Registered
2014-02-21
Start date
2013-06-30
Completion date
2016-12-31
Last updated
2014-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Microalbuminuria, Gastrectomy, Biliopancreatic Diversion With Duodenal Switch

Keywords

Microalbuminuria, Gastrectomy, Biliopancreatic Diversion With Duodenal Switch

Brief summary

Favorable effects of bariatric surgery have been demonstrated in particular regarding increased insulin sensitivity, decreased blood pressure, improved blood lipids and decreased cardiovascular risk. After surgery, weight loss also leads to improvement of the chronic inflammatory state related to obesity, a strong predictor of the metabolic status. Although obese patients are often affected with type 2 diabetes and hypertension, both related to renal impairment, the existence of a distinct mechanism by which obesity would cause chronic renal insufficiency has been suggested. The mechanisms underlying obesity-related nephropathy have been proposed to involve hyperfiltration, expansion of mesangial cells, hyperperfusion leading to proteinuria and glomerulosclerosis, as noted in obese dogs. In humans, improvements in renal function may be observed following bariatric surgery, although some reported a possibility of increased nephrolithiases. Whether biliopancreatic diversion and gastrectomy alone have similar effects is uncertain. More prospective studies are needed to assess the impact of all types of weight loss surgery to reverse chronic renal insufficiency. The objective of this study is to document changes in microalbuminuria and metabolic parameters in patients with altered renal function undergoing bariatric surgery. Patients enrolled in the study will show renal function impairment as demonstrated by albumin/creatinine ratio alterations in 2 out of 3 measurements taking place before surgery. We will perform a prospective study of renal function markers (albumin/creatinine ratio) and metabolic parameters (blood lipids, glucose, insulin, inflammatory markers) before and 6, 12, 24 months after surgery in patients with microalbuminuria at study onset (albumin/creatinine ratio 2.0-20.0 mg/mmol in men and 2.8-28.0 mg/mmol in women). Data will be analysed with repeated measures analyses in both subgroup. Thereafter, a linear regression model will be created to adjust for potentially confounding factors such as hypertension and diabetes. We hypothesize that patients with severe obesity and altered renal function, whether they are diabetic or not, have improved microalbuminuria and metabolic parameters following biliopancreatic diversion with sleeve gastrectomy or sleeve gastrectomy alone. The extent of renal function recovery will correlate directly with metabolic improvements.

Interventions

PROCEDUREGastrectomy
PROCEDUREBPD-DS

Sponsors

Johnson & Johnson
CollaboratorINDUSTRY
Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec
CollaboratorOTHER
Laval University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patient showing preoperative microalbuminuria (albumine/creatinine ratio between 2.0 and 20.0 in men and between 2.8 and 28.0 in women * Men and Women between 18-60 years old; * BMI ≥ 40 kg/m2 or between 35 and 40 kg/m2 if they have high-risk comorbidities; * Subjects capable of understanding and being able to sign a consent form; * Subjects capable of following the protocol directives, including the proposed visits (timeline); * Subjects living within a reasonable distance from the hospital and capable of being present at all required visits.

Exclusion criteria

* Urinary infection; * Hematuria (2+ or more) on 2 urinary analyses performed at 1 week interval; * Hyperglycemia \> 11 mmol/L at the time of the 2 urinary analyses; * Known renal disease unrelated to hypertension or diabetes, normoalbuminuria, macroalbuminuria or proteinuria; * Pregnant women or women who plan on becoming pregnant during the study, or women in fertile age range who refuse proper contraceptive methods during the study. (Must have negative pregnancy test at moment of enrolment and use medically acceptable contraception which include; oral contraceptives, injectable or implantable contraceptives, intrauterine devices or double-barrier method ie. condoms and diaphragm); * Previous oesophagal, gastric or bariatric surgery; * Irritable bowel syndrome, unexplained intermittent vomiting, severe abdominal pain, diarrhea or chronic constipation; * History of duodenal or gastric ulcers; * History of renal disease, hepatic disease (cirrhosis) or severe cardiac or pulmonary disease; * Corticosteroid intake in the previous month; * Presence of psychiatric problems or behavioral issues that could limit subject's capacity at understanding the procedure and to conform to medical/surgical recommendations; * History of drug use or alcoholism in previous 12 months before study; * History of inflammatory diseases of the gastro-intestinal tract (Esophagitis, varices, gastric or duodenal ulcers, Crohn's disease, congenital or acquired anomalies of the digestive tract).

Design outcomes

Primary

MeasureTime frameDescription
Changes in A/C RatioBaseline, 6, 12, 24 months* A/C Ratio * Weight Loss

Countries

Canada

Contacts

Primary ContactMarc Lapointe
marc.lapointe@criucpq.ulaval.ca4186568711
Backup ContactMélanie Nadeau
melanie.nadeau@criucpq.ulaval.ca4186568711

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026