Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study

Background The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population a...

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Veröffentlicht in:European journal of clinical investigation 2022-02, Vol.52 (2), p.e13689-n/a
Hauptverfasser: Xia, Juan, Guo, Chunyue, Cao, Han, Liu, Kuo, Peng, Wenjuan, Sun, Yanyan, Xie, Yunyi, Li, Bingxiao, Zhang, Fengxu, Wen, Fuyuan, Zhang, Ling
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container_issue 2
container_start_page e13689
container_title European journal of clinical investigation
container_volume 52
creator Xia, Juan
Guo, Chunyue
Cao, Han
Liu, Kuo
Peng, Wenjuan
Sun, Yanyan
Xie, Yunyi
Li, Bingxiao
Zhang, Fengxu
Wen, Fuyuan
Zhang, Ling
description Background The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases. Methods We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM). Results A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement. Conclusions In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.
doi_str_mv 10.1111/eci.13689
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This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases. Methods We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM). Results A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement. Conclusions In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1111/eci.13689</identifier><identifier>PMID: 34632581</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; cardiometabolic disease ; Cardiovascular disease ; Cardiovascular diseases ; CHCN‐BTH ; China ; Coronary artery disease ; Diabetes mellitus (non-insulin dependent) ; Female ; Health risks ; Heart diseases ; Heart Diseases - blood ; Heart Diseases - complications ; Humans ; Hypertension ; Lipoprotein(a) ; Lipoprotein(a) - blood ; Male ; Metabolic Diseases - blood ; Metabolic Diseases - complications ; Middle Aged ; Population studies ; Prospective Studies ; Reclassification ; Risk ; Stroke</subject><ispartof>European journal of clinical investigation, 2022-02, Vol.52 (2), p.e13689-n/a</ispartof><rights>2021 Stichting European Society for Clinical Investigation Journal Foundation. 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This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases. Methods We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM). Results A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement. Conclusions In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34632581</pmid><doi>10.1111/eci.13689</doi><tpages>0</tpages><orcidid>https://orcid.org/0000-0003-2468-864X</orcidid></addata></record>
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source Wiley-Blackwell Journals; MEDLINE
subjects Adult
cardiometabolic disease
Cardiovascular disease
Cardiovascular diseases
CHCN‐BTH
China
Coronary artery disease
Diabetes mellitus (non-insulin dependent)
Female
Health risks
Heart diseases
Heart Diseases - blood
Heart Diseases - complications
Humans
Hypertension
Lipoprotein(a)
Lipoprotein(a) - blood
Male
Metabolic Diseases - blood
Metabolic Diseases - complications
Middle Aged
Population studies
Prospective Studies
Reclassification
Risk
Stroke
title Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study
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