Long-term kidney and systemic effects of calorie restriction in overweight or obese type 2 diabetic patients (C.Re.S.O. 2 randomized controlled trial)

•In patients with T2D and obesity, calorie restriction ameliorated hyperfiltration.•This effect translated into a relative long-term stabilization of kidney function.•In this population calorie restriction improved many cardiovascular risk factors. In type 2 diabetic patients with obesity, hyperfilt...

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Veröffentlicht in:Diabetes research and clinical practice 2022-03, Vol.185, p.109804-109804, Article 109804
Hauptverfasser: Ruggenenti, Piero, Cortinovis, Monica, Trillini, Matias, Parvanova, Aneliya, Abbate, Manuela, Satriano, Chiara, Salvetti, Ferdinando, Bossi, Antonio C., Trevisan, Roberto, Perna, Annalisa, Peracchi, Tobia, Rubis, Nadia, Diadei, Olimpia, Martinetti, Davide, Gaspari, Flavio, Fontana, Luigi, Remuzzi, Giuseppe
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container_title Diabetes research and clinical practice
container_volume 185
creator Ruggenenti, Piero
Cortinovis, Monica
Trillini, Matias
Parvanova, Aneliya
Abbate, Manuela
Satriano, Chiara
Salvetti, Ferdinando
Bossi, Antonio C.
Trevisan, Roberto
Perna, Annalisa
Peracchi, Tobia
Rubis, Nadia
Diadei, Olimpia
Martinetti, Davide
Gaspari, Flavio
Fontana, Luigi
Remuzzi, Giuseppe
description •In patients with T2D and obesity, calorie restriction ameliorated hyperfiltration.•This effect translated into a relative long-term stabilization of kidney function.•In this population calorie restriction improved many cardiovascular risk factors. In type 2 diabetic patients with obesity, hyperfiltration is a risk factor for accelerated glomerular filtration rate (GFR) decline and is ameliorated by calorie restriction (CR). We assessed whether CR-induced amelioration of hyperfiltration could translate into slower long-term GFR decline in this population. In this academic, single-center, parallel-group, prospective, randomized, open-label, blinded endpoint trial, consenting >40-year-old patients with type 2 diabetes, BMI ≥27 kg/m2, creatinine
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In type 2 diabetic patients with obesity, hyperfiltration is a risk factor for accelerated glomerular filtration rate (GFR) decline and is ameliorated by calorie restriction (CR). We assessed whether CR-induced amelioration of hyperfiltration could translate into slower long-term GFR decline in this population. In this academic, single-center, parallel-group, prospective, randomized, open-label, blinded endpoint trial, consenting &gt;40-year-old patients with type 2 diabetes, BMI ≥27 kg/m2, creatinine &lt;1.2 mg/dL and albuminuria ≤300 mg/24 h were randomized (1:1) to two-year 25% CR (n = 53) or standard diet (SD, n = 50). Primary outcome was 6-month measured GFR. Analyses were by modified intention-to-treat. At 6 months GFR decreased by 5.16 ± 10.03 mL/min (P = 0.001) with CR, and by 0.98 ± 9.71 mL/min (P = 0.497) with SD. Between-group difference was significant (P = 0.044). GFR decline from 6 to 24 months was significant with SD (P &lt; 0.01), but not with CR (P = 0.075). Between-group difference, however, was not significant (P = 0.414). Body weight, BMI, waist circumference, systolic blood pressure, HbA1c, blood glucose, serum triglycerides decreased and ApoA-I concentration increased with CR. No changes were observed with SD. Between-group differences were significant. CR was tolerated well. In obese type 2 diabetic patients, CR ameliorated glomerular hyperfiltration and several cardiovascular risk factors, and blunted long-term GFR decline. 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In type 2 diabetic patients with obesity, hyperfiltration is a risk factor for accelerated glomerular filtration rate (GFR) decline and is ameliorated by calorie restriction (CR). We assessed whether CR-induced amelioration of hyperfiltration could translate into slower long-term GFR decline in this population. In this academic, single-center, parallel-group, prospective, randomized, open-label, blinded endpoint trial, consenting &gt;40-year-old patients with type 2 diabetes, BMI ≥27 kg/m2, creatinine &lt;1.2 mg/dL and albuminuria ≤300 mg/24 h were randomized (1:1) to two-year 25% CR (n = 53) or standard diet (SD, n = 50). Primary outcome was 6-month measured GFR. Analyses were by modified intention-to-treat. At 6 months GFR decreased by 5.16 ± 10.03 mL/min (P = 0.001) with CR, and by 0.98 ± 9.71 mL/min (P = 0.497) with SD. Between-group difference was significant (P = 0.044). GFR decline from 6 to 24 months was significant with SD (P &lt; 0.01), but not with CR (P = 0.075). Between-group difference, however, was not significant (P = 0.414). Body weight, BMI, waist circumference, systolic blood pressure, HbA1c, blood glucose, serum triglycerides decreased and ApoA-I concentration increased with CR. No changes were observed with SD. Between-group differences were significant. CR was tolerated well. In obese type 2 diabetic patients, CR ameliorated glomerular hyperfiltration and several cardiovascular risk factors, and blunted long-term GFR decline. 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Between-group difference, however, was not significant (P = 0.414). Body weight, BMI, waist circumference, systolic blood pressure, HbA1c, blood glucose, serum triglycerides decreased and ApoA-I concentration increased with CR. No changes were observed with SD. Between-group differences were significant. CR was tolerated well. In obese type 2 diabetic patients, CR ameliorated glomerular hyperfiltration and several cardiovascular risk factors, and blunted long-term GFR decline. Trial registration: NCT01930136.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>35219762</pmid><doi>10.1016/j.diabres.2022.109804</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Albuminuria - complications
Caloric Restriction
Calorie restriction
Cardiovascular risk
Diabetes Mellitus, Type 2 - complications
Diabetic Nephropathies - etiology
Female
Glomerular Filtration Rate - physiology
Humans
Kidney
Male
Nephropathy
Obesity
Obesity - complications
Overweight - complications
Prospective Studies
Type 2 diabetes
title Long-term kidney and systemic effects of calorie restriction in overweight or obese type 2 diabetic patients (C.Re.S.O. 2 randomized controlled trial)
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