Jiaqi Zhang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Jiaqi Zhang has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Lina Jin
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, China
5 shared publications - Chengxiang Hu
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, China
4 shared publications - Runhong Li
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, No.1163 Xinmin Street, Changchun, Jilin 130021, China
4 shared publications - Tong Xu
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Jilin, Changchun, China
3 shared publications - Xiaoting Fan
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, No.1163 Xinmin Street, Changchun, Jilin, 130021, China
3 shared publications - Yue He
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Jilin, Changchun, China
3 shared publications
Latest Publications
- 24 February 2025
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 222, 112066
Global, regional and national burden and trends of disease attributable to high body mass index in adolescents and young adults from 1990 to 2021
- 24 February 2025
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 222, 112066
Global, regional and national burden and trends of disease attributable to high body mass index in adolescents and young adults from 1990 to 2021
- 20 April 2024
- Published by Springer Nature in Internal and Emergency Medicine
- Vol. 19 (5) , 1299-1312
Metabolic risks remain a serious threat to cardiovascular disease: findings from the Global Burden of Disease Study 2019
Metabolic factors are major and controllable risk factors for cardiovascular diseases (CVD), and few studies have described this burden. We aim to assess it from 1990 to 2019 and predict the trends through 2034. Global Burden of Disease (GBD) provides data on sex, age, and socio-demographic index (SDI) levels. Numbers, age-standardized death rates (ASDR) and estimated annual percentage change (EAPC) were used. Future trends were estimated by NORDPRED model. The deaths cases of metabolic-related CVD increased from 8.61 million (95% UI: 7.91–9.29) to 13.71 million (95% UI: 12.24–14.94) globally. The ASDR continued to decline globally (EAPC = −1.36). The burden was heavier in male and middle-aged people and elderly people. CVD-related ASDR caused by high systolic blood pressure (SBP) had a downward trend globally (EAPC = −1.45), while trends of high body mass index (BMI) (EAPC = 1.29, 1.97, 0.92) and fasting plasma glucose (FPG) (EAPC = 0.95, 1.08, 0.46) were increasing in the middle, low-middle, and low SDI regions, respectively. Compared to 2015–2019, cumulative deaths will increase by 27.85% from 2030 to 2034, while ASDR will decrease 10.47%. The metabolic-related CVD burden remained high globally and deaths will continue to rise in the future. Men, middle-aged and elderly people were focus of concern. High SBP was globally well-managed over the past 30 years, but the CVD burden due to high BMI and FPG remained high. Exceptional initiatives are needed to regarding interventions targeting high BMI and FPG in middle and lower SDI regions.
- 20 April 2024
- Published by Springer Nature in Internal and Emergency Medicine
- Vol. 19 (5) , 1299-1312
Metabolic risks remain a serious threat to cardiovascular disease: findings from the Global Burden of Disease Study 2019
Metabolic factors are major and controllable risk factors for cardiovascular diseases (CVD), and few studies have described this burden. We aim to assess it from 1990 to 2019 and predict the trends through 2034. Global Burden of Disease (GBD) provides data on sex, age, and socio-demographic index (SDI) levels. Numbers, age-standardized death rates (ASDR) and estimated annual percentage change (EAPC) were used. Future trends were estimated by NORDPRED model. The deaths cases of metabolic-related CVD increased from 8.61 million (95% UI: 7.91–9.29) to 13.71 million (95% UI: 12.24–14.94) globally. The ASDR continued to decline globally (EAPC = −1.36). The burden was heavier in male and middle-aged people and elderly people. CVD-related ASDR caused by high systolic blood pressure (SBP) had a downward trend globally (EAPC = −1.45), while trends of high body mass index (BMI) (EAPC = 1.29, 1.97, 0.92) and fasting plasma glucose (FPG) (EAPC = 0.95, 1.08, 0.46) were increasing in the middle, low-middle, and low SDI regions, respectively. Compared to 2015–2019, cumulative deaths will increase by 27.85% from 2030 to 2034, while ASDR will decrease 10.47%. The metabolic-related CVD burden remained high globally and deaths will continue to rise in the future. Men, middle-aged and elderly people were focus of concern. High SBP was globally well-managed over the past 30 years, but the CVD burden due to high BMI and FPG remained high. Exceptional initiatives are needed to regarding interventions targeting high BMI and FPG in middle and lower SDI regions.
- Top Cited Papers
- 11 February 2024
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 209, 111575
Association between inflammatory biomarkers and mortality in individuals with type 2 diabetes: NHANES 2005–2018
- 11 February 2024
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 209, 111575
Top Cited PapersAssociation between inflammatory biomarkers and mortality in individuals with type 2 diabetes: NHANES 2005–2018
- 1 February 2024
- Published by Elsevier in Journal of Affective Disorders
- Vol. 351, 641-648
Association of macronutrient consumption quality, food source and timing with depression among US adults: A cross-sectional study
- 1 February 2024
- Published by Elsevier in Journal of Affective Disorders
- Vol. 351, 641-648
Association of macronutrient consumption quality, food source and timing with depression among US adults: A cross-sectional study
- Open Access
Low-Carbohydrate and Low-Fat Diet with Metabolic-Dysfunction-Associated Fatty Liver Disease
Background: This observational cross-sectional study was designed to explore the effects of a low-carbohydrate diet (LCD) and a low-fat diet (LFD) on metabolic-dysfunction-associated fatty liver disease (MAFLD). Methods: This study involved 3961 adults. The associations between LCD/LFD scores and MAFLD were evaluated utilizing a multivariable logistic regression model. Additionally, a leave-one-out model was applied to assess the effect of isocaloric substitution of specific macronutrients. Results: Participants within the highest tertile of healthy LCD scores (0.63; 95% confidence interval [CI], 0.45–0.89) or with a healthy LFD score (0.64; 95%CI, 0.48–0.86) faced a lower MAFLD risk. Furthermore, compared with tertile 1, individuals with unhealthy LFD scores in terile 2 or tertile 3 had 49% (95%CI, 1.17–1.90) and 77% (95%CI, 1.19–2.63) higher risk levels for MAFLD, respectively. Conclusions: Healthy LCD and healthy LFD are protective against MAFLD, while unhealthy LFD can increase the risk of MAFLD. Both the quantity and quality of macronutrients might have significant influences on MAFLD.
Open AccessLow-Carbohydrate and Low-Fat Diet with Metabolic-Dysfunction-Associated Fatty Liver Disease
Background: This observational cross-sectional study was designed to explore the effects of a low-carbohydrate diet (LCD) and a low-fat diet (LFD) on metabolic-dysfunction-associated fatty liver disease (MAFLD). Methods: This study involved 3961 adults. The associations between LCD/LFD scores and MAFLD were evaluated utilizing a multivariable logistic regression model. Additionally, a leave-one-out model was applied to assess the effect of isocaloric substitution of specific macronutrients. Results: Participants within the highest tertile of healthy LCD scores (0.63; 95% confidence interval [CI], 0.45–0.89) or with a healthy LFD score (0.64; 95%CI, 0.48–0.86) faced a lower MAFLD risk. Furthermore, compared with tertile 1, individuals with unhealthy LFD scores in terile 2 or tertile 3 had 49% (95%CI, 1.17–1.90) and 77% (95%CI, 1.19–2.63) higher risk levels for MAFLD, respectively. Conclusions: Healthy LCD and healthy LFD are protective against MAFLD, while unhealthy LFD can increase the risk of MAFLD. Both the quantity and quality of macronutrients might have significant influences on MAFLD.