Key result
Morbid obesity is linked to impaired haemorheology, marked by higher fibrinogen and plasma viscosity.
Why the study?
The role of metabolic syndrome on the haemorheological profile of morbidly obese patients and whether metabolically healthy morbidly obese individuals show rheological alterations had not been established.
Does morbid obesity alter the haemorheological profile compared to normo-weight individuals?
Cross-Sectional (n=272)
Does morbid obesity alter the haemorheological profile compared to normo-weight individuals?
Morbid obesity is associated with an altered haemorheological profile driven by both insulin resistance and inflammation, even in metabolically healthy obese individuals.
Answers are grounded in this paper and cite their sources.
Should not yet change obesity management; leaves open whether rheological profiling refines cardiovascular risk prediction beyond metabolic status.
There are few studies on haemorheological disturbances in morbidly obese patients. The role played by the metabolic syndrome on the rheological profile of morbidly obese subjects has not yet been established, and it is not clear whether morbidly obese, but "metabolically healthy", show rheological alterations. We aimed to determine the whole rheological profile in 136 morbidly obese patients and 136 normo-weight volunteers, along with plasma lipids, inflammatory and insulin resistance parameters. Patients had statistically higher glucose, triglycerides, HbA1c, leptin, insulin, HOMA, CRP, leucocytes, fibrinogen, plasma viscosity (p < 0.001, respectively), erythrocyte aggregation at 3 s-1 (p = 0.011) and lower erythrocyte elongation index 60 Pa (p = 0.015). In the multivariate regression analysis, the anthropometric, lipidic, insulin resistance and inflammatory parameters predicted haemorheological variables (p < 0.001). No differences were observed for the rheological parameters when morbidly obese subjects with (n = 75) and without (n = 61) the metabolic syndrome were compared (p > 0.05), indicating that the altered rheological profile not only related to the metabolic syndrome, but to obesity itself. When further patients were classified as "metabolically healthy" obese (n = 23) and "metabolically unhealthy" obese (n = 113), the latter presented higher insulin resistance (insulin p < 0.01, HOMA p < 0.05, glucose p < 0.001, triglycerides p < 0.05 and HbA1c p < 0.01) than the former, but no differences in the rheological parameters (p > 0.05) were observed. When "metabolically healthy" obese (n = 23) were compared with "metabolically healthy" controls (n = 81), the former still showed higher HOMA (p < 0.001), triglycerides (p < 0.05), CRP (p < 0.001) and HbA1c (p < 0.05), higher fibrinogen (p < 0.001), plasma viscosity (p < 0.001), erythrocyte aggregation at 3 s-1 (p < 0.05), but a lower erythrocyte elongation index 60 Pa (p < 0.05). Morbidly obese subjects present a more pronounced altered rheological profile in those with metabolic alterations, although the "metabolically healthy" obese also displayed rheological alterations if compared with "metabolically healthy" non-obese controls. These rheological alterations relate to both insulin resistance and inflammation.
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Vayá et al. (2011) conducted a cross-sectional in Morbid obesity (n=272). Morbid obesity vs. Normo-weight volunteers was evaluated on Haemorheological profile (fibrinogen, plasma viscosity, erythrocyte aggregation and elongation) (p=<0.001). Morbid obesity was associated with an altered haemorheological profile, including higher fibrinogen and plasma viscosity (p<0.001), even in metabolically healthy obese individuals.
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