B. Rasouli
Karolinska Institutet
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Featured researches published by B. Rasouli.
Diabetic Medicine | 2013
B. Rasouli; Anders Ahlbom; Tomas Andersson; Valdemar Grill; Kristian Midthjell; Lisa Olsson; Sofia Carlsson
Diabet. Med. 30, 56–64 (2013)
Diabetes Care | 2013
B. Rasouli; Valdemar Grill; Kristian Midthjell; Anders Ahlbom; Tomas Andersson; Sofia Carlsson
OBJECTIVE To investigate the association between smoking habits and risk of autoimmune diabetes in adults and of type 2 diabetes. RESEARCH DESIGN AND METHODS We used data from the three surveys of the Nord-Trøndelag Health Study, spanning 1984–2008 and including a cohort of 90,819 Norwegian men (48%) and women (52%) aged ≥20 years. Incident cases of diabetes were identified by questionnaire and classified as type 2 diabetes (n = 1,860) and autoimmune diabetes (n = 140) based on antibodies to glutamic decarboxylase (GADA) and age at onset of diabetes. Hazard ratios (HRs) adjusted for confounders were estimated by Cox proportional hazards regression models. RESULTS The risk of autoimmune diabetes was reduced by 48% (HR 0.52 [95% CI 0.30–0.89]) in current smokers and 58% in heavy smokers (0.42 [0.18–0.98]). The reduced risk was positively associated with number of pack-years. Heavy smoking was associated with lower levels of GADA (P = 0.001) and higher levels of C-peptide (964 vs. 886 pmol/L; P = 0.03). In contrast, smoking was associated with an increased risk of type 2 diabetes, restricted to overweight men (1.33 [1.10–1.61]). Attributable proportion due to an interaction between overweight and heavy smoking was estimated to 0.40 (95% CI 0.23–0.57). CONCLUSIONS In this epidemiological study, smoking is associated with a reduced risk of autoimmune diabetes, possibly linked to an inhibitory effect on the autoimmune process. An increased risk of type 2 diabetes was restricted to overweight men.
Diabetic Medicine | 2014
J.E. Löfvenborg; Tomas Andersson; Per-Ola Carlsson; Mozhgan Dorkhan; Leif Groop; Mats Martinell; B. Rasouli; Petter Storm; Tiinamaija Tuomi; Sofia Carlsson
Coffee consumption is associated with a reduced risk of Type 2 diabetes. Our aim was to investigate if coffee intake may also reduce the risk of latent autoimmune diabetes in adults, an autoimmune form of diabetes with features of Type 2 diabetes.
European Journal of Endocrinology | 2014
B. Rasouli; Tomas Andersson; Per-Ola Carlsson; Mozhgan Dorkhan; Valdemar Grill; Leif Groop; Mats Martinell; Tiinamaija Tuomi; Sofia Carlsson
Objective Moderate alcohol consumption is associated with a reduced risk of type 2 diabetes. Our aim was to investigate whether alcohol consumption is associated with the risk of latent autoimmune diabetes in adults (LADA), an autoimmune form of diabetes with features of type 2 diabetes. Design A population-based case–control study was carried out to investigate the association of alcohol consumption and the risk of LADA. Methods We used data from the ESTRID case–control study carried out between 2010 and 2013, including 250 incident cases of LADA (glutamic acid decarboxylase antibodies (GADAs) positive) and 764 cases of type 2 diabetes (GADA negative), and 1012 randomly selected controls aged ≥35. Logistic regression was used to estimate the odds ratios (ORs) of diabetes in relation to alcohol intake, adjusted for age, sex, BMI, family history of diabetes, smoking, and education. Results Alcohol consumption was inversely associated with the risk of type 2 diabetes (OR 0.95, 95% CI 0.92–0.99 for every 5-g increment in daily intake). Similar results were observed for LADA, but stratification by median GADA levels revealed that the results only pertained to LADA with low GADA levels (OR 0.85, 95% CI 0.76–0.94/5 g alcohol per day), whereas no association was observed with LADA having high GADA levels (OR 1.00, 95% CI 0.94–1.06/5 g per day). Every 5-g increment of daily alcohol intake was associated with a 10% increase in GADA levels (P=0.0312), and a 10% reduction in homeostasis model assessment of insulin resistance (P=0.0418). Conclusions Our findings indicate that alcohol intake may reduce the risk of type 2 diabetes and type 2-like LADA, but has no beneficial effects on diabetes-related autoimmunity.
Diabetes Care | 2016
B. Rasouli; Tomas Andersson; Per-Ola Carlsson; Valdemar Grill; Leif Groop; Mats Martinell; Petter Storm; Tiinamaija Tuomi; Sofia Carlsson
OBJECTIVE Smoking is an established risk factor for type 2 diabetes. In contrast, it has been proposed that smoking may reduce the risk of latent autoimmune diabetes in adults (LADA), but studies are scarce. We aimed to study the impact of smoking on LADA and type 2 diabetes risks. RESEARCH DESIGN AND METHODS We used data from a Swedish case-control study including incident case patients with LADA (GAD antibody [GADA] positive, n = 377) and type 2 diabetes (GADA negative, n = 1,188) and control subjects randomly selected from the population (n = 1,472). We calculated odds ratios (ORs) with 95% CIs by logistic regression, adjusted for age, sex, BMI, family history of diabetes, and alcohol consumption. RESULTS There was no indication of reduced risk of LADA in smokers; instead, heavy smoking was associated with an increased risk of LADA (OR 1.37, 95% CI 1.02–1.84). Heavy smokers had higher levels of HOMA of insulin resistance (9.89 vs. 4.38, P = 0.0479) and HOMA of β-cell function (55.7 vs. 42.5, P = 0.0204), but lower levels of GADA (75 vs. 250, P = 0.0445), compared with never smokers. Smokers also displayed an increased risk of type 2 diabetes (OR in ever smokers 1.53, 95% CI 1.25–1.88). CONCLUSIONS In this large population of LADA patients, we did not observe a protective effect of smoking on autoimmunity and the risk of LADA. A protective effect could possibly be masked by a smoking-induced aggravation of insulin resistance, akin to the diabetogenic effect seen in individuals with type 2 diabetes.
Diabetic Medicine | 2017
B. Rasouli; Tomas Andersson; Per-Ola Carlsson; Valdemar Grill; Leif Groop; Mats Martinell; Kristian Midthjell; Petter Storm; Tiinamaija Tuomi; Sofia Carlsson
It has been suggested that moist snuff (snus), a smokeless tobacco product that is high in nicotine and widespread in Scandinavia, increases the risk of Type 2 diabetes. Previous studies are however few, contradictory and, with regard to autoimmune diabetes, lacking. Our aim was to study the association between snus use and the risk of Type 2 diabetes and latent autoimmune diabetes of adulthood (LADA).
Diabetologia | 2018
Rebecka Hjort; Emma Ahlqvist; Per-Ola Carlsson; Valdemar Grill; Leif Groop; Mats Martinell; B. Rasouli; Anders Rosengren; Tiinamaija Tuomi; Bjørn Olav Åsvold; Sofia Carlsson
Aims/hypothesisExcessive weight is a risk factor for type 2 diabetes, but its role in the promotion of autoimmune diabetes is not clear. We investigated the risk of latent autoimmune diabetes in adults (LADA) in relation to overweight/obesity in two large population-based studies.MethodsAnalyses were based on incident cases of LADA (n = 425) and type 2 diabetes (n = 1420), and 1704 randomly selected control participants from a Swedish case–control study and prospective data from the Norwegian HUNT Study including 147 people with LADA and 1,012,957 person-years of follow-up (1984–2008). We present adjusted ORs and HRs with 95% CI.ResultsIn the Swedish data, obesity was associated with an increased risk of LADA (OR 2.93, 95% CI 2.17, 3.97), which was even stronger for type 2 diabetes (OR 18.88, 95% CI 14.29, 24.94). The association was stronger in LADA with low GAD antibody (GADA; <median) (OR 4.25; 95% CI 2.76, 6.52) but present also in LADA with high GADA (OR 2.14; 95% CI 1.42, 3.24). In the Swedish data, obese vs normal weight LADA patients had lower GADA levels, better beta cell function, and were more likely to have low-risk HLA-genotypes. The combination of overweight and family history of diabetes (FHD) conferred an OR of 4.57 (95% CI 3.27, 6.39) for LADA and 24.51 (95% CI 17.82, 33.71) for type 2 diabetes. Prospective data from HUNT indicated even stronger associations; HR for LADA was 6.07 (95% CI 3.76, 9.78) for obesity and 7.45 (95% CI 4.02, 13.82) for overweight and FHD.Conclusions/interpretationOverweight/obesity is associated with increased risk of LADA, particularly when in combination with FHD. These findings support the hypothesis that, even in the presence of autoimmunity, factors linked to insulin resistance, such as excessive weight, could promote onset of diabetes.
Journal of diabetes & metabolism | 2013
B. Rasouli; Tomas Andersson; Valdemar Grill; Kristian Midthjell; Lisa Olsson; Sofia Carlsson
Introduction: Adult-onset autoimmune diabetes is prevalent, yet there are limited data on risk factors. Aim: Our aim was to examine how combinations of modifiable lifestyle factors are associated with risk of adultonset autoimmune diabetes and to estimate the Population Attributable Risk (PAR) related to such factors. Methods: We used incidence data from Nord-Trondelag Health Survey Study (HUNT), a large population-based study where adults aged ≥ 20 years old were investigated in three consecutive surveys during 1984-2008 (n=49,712; eligible for this study).Among self-reported diabetes patients, presence of Glutamic Acid Decarboxylase Antibodies (GADA) and age at onset ≥ 35 years old were used to identify incident cases of adult-onset autoimmune diabetes (n=164). Hazard Ratios (HR) of autoimmune diabetes by lifestyle factors were estimated by Cox regression and PAR were calculated for single items and combination of lifestyle factors. Results: A reduced risk of adult-onset autoimmune diabetes was conferred by BMI<25, physical activity, regular alcohol consumption and psychosocial well-being. Positivity for all four healthy lifestyle factors gave a HR of 0.10 (95% CI=0.02-0.40) compared with no positivity. Estimation of PAR indicated that 69% (CI=45-79%) of all cases of adult-onset autoimmune diabetes could be prevented through these factors with BMI< 25 as the most important contributor (PAR for BMI ≥ 25= 34%, CI=20-48%). Conclusions: Provided that these associations are causal, then the majority of adult-onset autoimmune diabetes cases are preventable by modification of common lifestyle factors primarily by maintaining a BMI in the non-overweight range.
Journal of Medical Economics | 2018
Mark Nuijten; Agnieszka Marczewska; Krysmarú Araujo Torres; B. Rasouli; Moreno Perugini
Abstract Objectives: Obesity is associated with high direct medical costs and indirect costs resulting from productivity loss. The high prevalence of obesity generates a justified need to identify cost-effective weight loss approaches from a payer’s perspective. Within the variety of weight management techniques, OPTIFAST is a clinically recognized and scientifically proven total meal replacement Low Calorie Diet that provides meaningful results in terms of weight loss and reduction in comorbidities. The objective of this study is assess potential cost-savings of the OPTIFAST program in the US, as compared to “no intervention” and pharmacotherapy. Methods: An event-driven decision analytic model was used to estimate payer’s cost-savings from reimbursement of the 1-year OPTIFAST program over 3 years in the US. The analysis was performed for the broad population of obese persons (BMI >30 kg/m2) undergoing the OPTIFAST program vs liraglutide 3 mg, naltrexone/bupropion and vs “no intervention”. The model included the risk of complications related to increased BMI. Data sources included published literature, clinical trials, official US price/tariff lists, and national population statistics. The primary perspective was that of a US payer; costs were provided in 2016 US dollars. Results: OPTIFAST leads over a period of 3 years to cost-savings of USD 9,285 per class I and II obese patient (BMI 30–39.9 kg/m2) as compared to liraglutide and USD 685 as compared to naltrexone/bupropion. In the same time perspective, the OPTIFAST program leads to a reduction of cost of obesity complications of USD 1,951 as compared to “no intervention”, with the incremental cost-effectiveness ratio of USD 6,475 per QALY. Scenario analyses also show substantial cost-savings in patients with class III obesity (BMI ≥ 40.0 kg/m2) and patients with obesity (BMI = 30–39.9 kg/m2) and type 2 diabetes vs all three previous comparators and bariatric surgery. Conclusions: Reimbursing OPTIFAST leads to meaningful cost-savings for US payers as compared with “no intervention” and liraglutide and naltrexone/bupropion in obese patients. Similar results can be expected in matching healthcare settings of other countries. Moreover, OPTIFAST has additional clinical and economic advantages through very low complication and adverse events rates.
Diabetes & Metabolism | 2018
B. Rasouli; Emma Ahlqvist; Lars Alfredsson; Tomas Andersson; Per-Ola Carlsson; Leif Groop; J.E. Löfvenborg; Mats Martinell; Anders Rosengren; Tiinamaija Tuomi; Alicja Wolk; Sofia Carlsson
AIM Coffee consumption is inversely related to risk of type 2 diabetes (T2D). In contrast, an increased risk of latent autoimmune diabetes in adults (LADA) has been reported in heavy coffee consumers, primarily in a subgroup with stronger autoimmune characteristics. Our study aimed to investigate whether coffee consumption interacts with HLA genotypes in relation to risk of LADA. METHODS This population-based study comprised incident cases of LADA (n=484) and T2D (n=1609), and also 885 healthy controls. Information on coffee consumption was collected by food frequency questionnaire. Odds ratios (ORs) with 95% CIs of diabetes were calculated and adjusted for age, gender, BMI, education level, smoking and alcohol intake. Potential interactions between coffee consumption and high-risk HLA genotypes were calculated by attributable proportion (AP) due to interaction. RESULTS Coffee intake was positively associated with LADA in carriers of high-risk HLA genotypes (OR: 1.14 per cup/day, 95% CI: 1.02-1.28), whereas no association was observed in non-carriers (OR: 1.04, 95% CI: 0.93-1.17). Subjects with both heavy coffee consumption (≥4 cups/day) and high-risk HLA genotypes had an OR of 5.74 (95% CI: 3.34-9.88) with an estimated AP of 0.36 (95% CI: 0.01-0.71; P=0.04370). CONCLUSION Our findings suggest that coffee consumption interacts with HLA to promote LADA.