Key result
Higher serum beta-2-microglobulin is linked to ~490% higher all-cause and CHD mortality risk.
Why the study?
Few prospective studies have explored the association of beta-2-microglobulin with coronary heart disease mortality in the general population.
Does higher serum beta-2-microglobulin concentration increase the risk of coronary heart disease and all-cause mortality in the general adult population?
Cohort (n=4,885)
Does higher serum beta-2-microglobulin concentration increase the risk of coronary heart disease and all-cause mortality in the general adult population?
Hazard Ratio: 5.9 (95% CI 5.31–6.57)
p-value: p=< 0.001
Higher serum beta-2-microglobulin concentration is strongly and independently associated with increased risks of coronary heart disease and all-cause mortality over a 15.5-year follow-up.
May aid mortality risk stratification in adults; extends biomarker associations but leaves open prospective validation and causality.
Few prospective studies explored the association of beta-2-microglobulin (B2M) with coronary heart disease (CHD) mortality. The primary objective of this study was to examine the association of serum B2M with CHD and all-cause mortality. This is a prospective cohort study of a nationally representative sample of 4,885 adults, aged 40–85 years, who participated in the National Health and Nutrition Examination Survey (NHANES III) from 1988 to 1994. The relationships between B2M and CHD and all-cause mortality were estimated using Cox proportional hazards regression models. During a median follow-up of 15.5 years, 845 CHD and 3,388 all-cause deaths occurred among 4,885 participants [2,568 women (55.7%); mean (S.D.) age, 66.4 (12.5) years], respectively. In the unadjusted model, B2M concentration was strongly linearly associated with CHD and all-cause mortality (p-trend < 0.001). After adjusting multivariable factors, a positive linear association between B2M and all-cause mortality was still observed (H.R. for Q4 vs. Q1 5.90; 95% CI: 5.31–6.57; p-trend < 0.001). In the multivariable adjustment model, B2M was significantly associated with an increased risk of CHD mortality (H.R. for Q4 vs. Q1 2.72; 95% CI: 2.07–3.57; p-trend < 0.001). In the stratified analyses, the associations of B2M with CHD and all-cause mortality varied by risk factors, such as age, smoking status, and history of hypertension. The findings suggest a significant relationship between the higher serum B2M concentration and increased risk for CHD and all-cause mortality. Further large-scale follow-up studies are also needed to validate this association.
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Huang et al. (2022) conducted a cohort in General population (n=4,885). Serum beta-2-microglobulin (B2M) vs. Lowest quartile (Q1) of B2M was evaluated on All-cause mortality (HR 5.90, 95% CI 5.31-6.57, p=< 0.001). Higher serum beta-2-microglobulin concentration (Q4 vs Q1) was significantly associated with increased risks of all-cause mortality (HR 5.90; 95% CI 5.31-6.57) and CHD mortality.
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