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Non-communicable diseases are key to further narrow gender gap in life expectancy in Shanghai, China

Abstract

Background

To address change in the gender gap of life expectancy (GGLE) in Shanghai from 1973 to 2018, and to identify the major causes of death and age groups associated with the change over time.

Methods

The temporal trend in GGLE was evaluated using retrospective demographic analysis with Joinpoint regression. Causes of death were coded in accordance with the International Classification of Diseases and mapped with the Global Burden of Disease (GBD) cause list. The life table technique and decomposition method were used to express changes in GGLE.

Results

The trend of GGLE in Shanghai experienced two phases, i.e., a decrease from 8.4 to 4.2 years in the descent phase (1973–1999) and a fluctuation between 4.0 and 4.9 years in the plateau phase (1999–2018). The reduced age-specific mortality rates tended to concentrate to a narrower age range, from age 0–9 and above 30 years in the descent phase to age above 55 years in the plateau phase. Gastroesophageal and liver cancer, communicable, chronic respiratory, and digestive diseases were once the major contributors to narrow GGLE in the descent phase. While, importance should be attached to a widening effect on GGLE by lung cancer, cardiovascular diseases, other neoplasms like colorectal and pancreatic cancer, and diabetes in the recent plateau phase.

Conclusions

Non-communicable diseases (NCDs) have made GGLE enter a plateau phase from a descent phase in Shanghai, China. Public efforts to reduce excess mortalities for male NCDs, cancers, cardiovascular diseases, chronic respiratory diseases, and diabetes in particular and health policies focused on the middle-aged and elderly population might further narrow GGLE. This will also ensure improvements in health and health equity in Shanghai China.

Peer Review reports

Background

The gender gap in life expectancy at birth (GGLE), which is the difference in life expectancy at birth (LE) by gender, was 4.4 years in 2016 (74.2 years for females and 69.8 years for males) [1]. There are gender differences in illnesses due to interactions among biological, social, psychological, and behavioral factors [2, 3], which may have led to gender differences in mortality, cause of death, and hence life expectancy at birth. While the gender ratio at birth in China is male-biased, the GGLE is female-biased and suggest a need for increased effort to understand the underlying cause of shorter male life expectancy at birth. Understanding long-term trends in GGLE and the cause of death will provide evidence for health professionals and policymakers to prioritize efforts and narrow gender inequity in LE.

Tremendous progress on LE has been found worldwide [4, 5], and recent studies find a narrowing GGLE in most high-income developed countries, for example, in countries like Sweden, France, and the UK [6,7,8,9]. China has also made great achievements in LE [10,11,12]. Among all its provinces, Shanghai has ranked first in LE in China mainland for many years [13], with low mortality even by the standards of high-income countries. Our previous study showed that after a period of decline and recovery, LE in Shanghai finally increased from 71 years in the 1970s to 84 years in 2018, and is still on the rise [14]. China has also made great strides in economic development. With economic development, the GGLE should continue decreasing as the gender gap is negatively associated with a nation’s per capita gross domestic product, meaning as countries develop the gender gap closes [15]. However, GGLE in China, more specifically in Shanghai-the economic hub of China, continues to persist. Shanghai has yet to see the GGLE inflection with male catching up with females’ LE.

To our knowledge, there has been no research on GGLE in Shanghai. Considering that China has attached great importance to LE and implemented “Healthy China 2030” program with aims to further improve national LE to 79 years by 2030, this study intends to address changes in GGLE in Shanghai from 1973 to 2018. This study aims to identify the major cause-of-death and age groups associated with narrowing or widening GGLE overtime. Moreover, the GGLE is both due to biological as well as behavioral factors [16]. Identifying the diseases associated with China’s GGLE and existent research on disease risk factors will inform Chinese policymakers on risky behaviors, particularly among men. This long-term trend study will also make up for the lack of research on GGLE trends across decades in mainland China.

Methods

Overview

We assessed GGLE trend in Shanghai local residents from 1973 to 2018, which traced back to the earliest time of full coverage of the Shanghai Mortality Registration System. We investigated different stages of the trend in GGLE and quantified the age- and cause-specific contributions to the change.

Data sources

We used the 45-year mortality information from Shanghai Pudong New Area Center for Disease Control and Prevention (CDC). Individual data was anonymized and de-identified before analysis. Strict confidentiality of individual data was practiced during the entire study. Shanghai established a comprehensive Mortality Registration System in 1973, with full coverage of residents’ mortality information from medical institutions at all levels [17]. The system was further improved through routine verification with local population registry as well as funeral and cremation system and hence ensures the completeness of the registration system to the extent possible [18]. Details have been explained in our previous article [14]. The dataset in use is available on reasonable request.

Coding and data quality

Rigorously trained clinicians coded cause of death. Historical data and data from 2002 were coded in accordance with the International Classification of Diseases, 10th Revision (ICD-10). Data from 1992 to 2001 were coded based on ICD-9. Moreover, historical records were checked against historical annual reports by cause and age to avoid inconsistency in classification.

According to the Global Burden of Disease (GBD) study, garbage codes should be redistributed to enhance the validity of public health analysis and are classified into four categories [19]. We redistributed garbage codes such as heart failure, peritonitis, and septicemia using the GBD recommended algorithms [19]. However, for senility and other unspecified cause of mortality lack medical records or causal inference information, we just kept the original ill-defined data. We evaluated the age-specific proportion of garbage codes and compared the data quality in different periods with those of other countries/regions. Finally, we mapped the 45-year data in accordance with the GBD cause list to make a comparison in the same framework.

Causes of death

We focused our analysis on 14 mutually exclusive and exhaustive cause of death categories, which covered all the leading causes of death across the study years in Shanghai. Causes of death included the following: cardiovascular diseases (cerebrovascular diseases, ischemic heart diseases), neoplasms (lung cancer, stomach cancer, liver cancer, and esophageal cancer), chronic respiratory diseases, communicable diseases, digestive diseases, diabetes, endocrine, blood, and immune disorders, kidney diseases, and injuries. The causes of death we focused on and their corresponding ICD-9 and ICD-10 codes have been listed in Additional file 1: Table A1.

Analysis

We applied Joinpoint regression to evaluate the temporal trend in GGLE during the 45 years of study period. The basic idea of the method is to model the time series using a few continuous linear segments [20]. Joinpoint regression tests whether a multi-segmented line is a significantly better fit than a straight or less-segmented line based on permutation tests [21]. In contrast, other regression methods investigate trends to find the best-fit line through years of data [22]. The application of Joinpoint method helps to find a meaningful turning point of a trend and avoids artificially dividing the long study period [23].

We calculated the gender-specific LE with the conventional life table technique based on annual abridged life tables. The age intervals of the life table were age 0–1, 1–4, 5–9, and in subsequent five-year age groups up to age 85 with an open end.

We used age- and cause-specific decomposition method to express changes of GGLE in years widened or narrowed at corresponding periods [24]. Narrowed GGLE can be attributed to (1) a faster drop in male mortality than female; (2) a slower rise in male mortality than female; (3) male mortality decreases while female’s increases. While an expanded GGLE is just the opposite. Details of the formulas can be found elsewhere [25].

Joinpoint regression analyses were carried out using the Joinpoint Regression Program, Version 4.0.4 (US National Cancer Institute, MD). Statistical analysis was performed with Stata/SE 13.0 (College Station, TX).

Results

Trend of GGLE

Figure 1 shows that male LE increased by 12.6 years, from 69.3 to 81.9, and female LE increased by 8.9 years, from 77.8 to 86.7, between 1973 and 2018 in Shanghai. The GGLE decreased from 8.4 years in 1973 to 4.8 years in 2018. Change of GGLE could be divided into two phases, the descent (1973 to 1999) saw a dramatic drop in GGLE from 8.4 to 4.2 (slope is − 0.11 with 95% CI (− 0.14, − 0.08)); the plateau (1999 to 2018) where GGLE fluctuated between 4.0 and 4.9 years. Joinpoint regression details can be referred to the Additional file 1: Table A2&A3.

Fig. 1
figure 1

Life expectancy and its gender gap in Shanghai, 1973 to 2018. LE for both genders increased steadily after a short period of decrease and recovery during the 45 years

Age-specific contributions to GGLE at different phases

Figure 2 shows the age-specific contributions to GGLE in Shanghai in 1973, 1999, and 2018. Male mortality rates from all age groups were higher than female in 1973, primarily for age group 0–9 and above 30 years. Gender differences in the age-specific mortality rates in both 1999 (2.42‰) and 2018 (1.46‰) were significantly lower compared to 1973 (4.75‰). The reduced age-specific mortality rates concentrated in a narrower age range over time. Gender difference of the age-specific mortality rates mainly started from age 30 years in 1999, while excess male mortality mainly started from age 40 years in 2018. The age-specific contributions to GGLE were similar in 1999 and 2018, except for a wider GGLE at the advanced age, mainly from age over 55 years, and more pronounced at age above 85 years.

Fig. 2
figure 2

Age-specific contributions to GGLE in Shanghai in 1973, 1999 and 2018. Note: values above zero indicate males’ mortality rate is higher than females’ at specific age, vice versa

Cause-specific contributions to GGLE

We divided the change of GGLE between 1973 and 2018 into two phases. Age-standardized all-cause mortality decreased by 29.8% in males and 12.9% in females during 1973 and 1999, while by 46.4 and 49.8% during 1999 and 2018. Table 1 shows the age-standardized mortalities of major cause of death for both genders. If male cause-specific mortality is higher than females, we regard this a positive contributor to GGLE, and vice versa. Figure 3 showed cause-specific contributions to GGLE in Shanghai in 1973, 1999 and 2018. All causes of death concerned in our study made positive contribution to GGLE in 1973. Among them, gastroesophageal and liver cancer, communicable diseases, chronic respiratory diseases, and digestive diseases made over half of the total contributions.

Table 1 Age-standardized mortality rates for main causes of death in Shanghai, China (1973, 1999, and 2018)
Fig. 3
figure 3

Cause-specific contributions to GGLE in Shanghai in 1973, 1999 and 2018. Values above zero indicate higher mortality in male. The sum of the positive and negative values results in GGLE of 8.4 years in 1973, 4.2 years in 1999 and 4.8 years in 2018

As shown in Fig. 3, in 1999, gastroesophageal and liver cancer, lung cancer, and chronic respiratory diseases were the leading contributors to GGLE, accounting for over 70% of the total contribution. Though gastroesophageal and liver cancer and chronic respiratory diseases remained the leading contributors, the contribution decreased. However, lung cancer made a greater contribution of 0.88 years to GGLE in 1999, compared with 0.52 years in 1973, with an excess of 0.36 years. In addition, communicable diseases fell out of the top three to make positive contribution to GGLE.

Gastroesophageal and liver cancer, lung cancer and chronic respiratory diseases remained the leading contributors to GGLE in 2018. Lung cancer itself made 0.95 years of contribution, while gastroesophageal and liver cancer in total made 1.21 years of contribution. It is worth noting, besides lung cancer, the contributions of cerebrovascular diseases and other neoplasms (except for gastroesophageal, liver and lung cancer) to GGLE were increasing during past 45 years. Cerebrovascular diseases contributed to GGLE from 0.46 years in 1973 to 0.70 years in 2018, just second to chronic respiratory diseases. Neoplasms except for gastroesophageal, liver and lung cancer increased the contribution from 0.09 years in 1973 to 0.45 years in 2018.

Age- and cause-specific contributions to GGLE

Figure 4 shows the contribution of age and cause on GGLE. As shown, the age- and cause-specific contribution to GGLE concentrated more below the x-axis in the descent phase (1973–1999). Narrowing effect of GGLE mainly attributed to communicable, digestive diseases, liver cancer, and other causes of death at age 0–9 years; and communicable, digestive, chronic respiratory diseases, gastroesophageal, and liver cancer and other causes of death at age over 30 years. Meanwhile, lung cancer and other neoplasms widened GGLE, mainly at age over 70 years.

Fig. 4
figure 4

Age- and cause-specific contributions to the change of GGLE in Shanghai during 1973–1999 and 1999–2018. Positive values indicate a widening effect on GGLE by cause of death at corresponding age group, while negative values indicate a narrowing effect

In the plateau phase (1999–2018), the contributions relatively balanced on both sides of x-axis. Nevertheless, it is worth noting that a widening GGLE attributed to cardiovascular diseases (ischemic heart diseases and cerebrovascular diseases), lung cancer, other neoplasms, and other causes of death (diabetes, endocrine, blood, and immune disorders, kidney diseases) at age over 55 years.

We compared the change of GGLE between 1973 and 1999 and 1999–2018. We found chronic respiratory diseases, neoplasms, and cerebrovascular diseases at the age group above 85 years made the biggest contribution to widen GGLE. Furthermore, neoplasms other than lung, gastroesophageal, and liver cancer widened GGLE at a broader age group. They used to widen GGLE mainly from age above 70 years at descent phase, but from age 50 years at the plateau phase.

Discussion

Using data across 45 years (1973 to 2018), we studied changes in GGLE across time and contribution by age group and cause of death on changes in GGLE in Shanghai, China. We found two phases in the shift in GGLE. First, GGLE decreased by 4.2 years from 1973 to 1999, the descent phase, and then fluctuated around 4.5 years from 1999 to 2018, the plateau phase. Age-specific contribution to the change in GGLE concentrates in a narrow and more advanced age group (85 years and above). Non-communicable diseases (NCDs) such as cancer, cardiovascular, chronic respiratory diseases, and diabetes are major contributors to the changes in GGLE.

Communicable diseases used to be a major contributor to narrow GGLE in the descent phase (1973 to 1999). Nevertheless, its role diminished in the plateau phase (1999 to 2018). Shanghai suffered from hepatitis B, schistosomiasis, and tuberculosis during the descent phase [26]. Since the implementation of schistosomiasis control programs [27], hepatitis B vaccinations [28], modern tuberculosis control program and infectious disease surveillance [29], communicable diseases have been greatly reduced. This is a remarkable achievement in public health.

In China and globally, the achievement in communicable diseases corroborates an epidemiological shift to NCDs during the second half of the last century. NCDs accounted for an increasing proportion of total deaths, for about 60% of total deaths in 1973 and over 90% in 2018. Our study finds that gender differences in mortality due to NCDs are key to reduce GGLE in Shanghai, China. Male mortality of NCDs decreased by 43.9% and female by 35.7% over the past 45 years. NCDs like gastroesophageal and liver cancer, chronic respiratory and digestive diseases were the major contributors to narrow GGLE. While NCDs like lung cancer, other neoplasms, cardiovascular diseases, and diabetes were the major contributors to widen GGLE in our study.

Cancer is the largest contributor to GGLE in Shanghai. However, the effect of cancers on GGLE vary by cancer site. Gastroesophageal and liver cancer in total make a positive contribution to GGLE, but the contribution declines. Lung cancer and other neoplasms (except for the above-mentioned three cancers), however, continue to widen GGLE. Steady declines in mortality rates of gastroesophageal and liver cancers are potentially attributed from the overall achievement in public health [30], including HBV-vaccination, sanitation campaign (centralized drinking water supply system), improved treatment of parasitic liver fluke infections and healthy lifestyle changes (increased fresh fruits and vegetables, limited alcohol consumption, decreased salt-preservative/aflatoxin-contamination foods) [31,32,33,34,35].

Lung cancer has surpassed stomach cancer and become the leading cause of cancer death in Shanghai in recent years. The prevalence of smoking is much higher in male than female [36]. Lung cancer is one of the most preventable cancers [37]. Experience from the developed countries shows a marked decrease in smoking rates and lung cancer occurrence after a comprehensive tobacco control program [38]. Tobacco control can also reduce the risk of cardiovascular diseases [39]. Hence, Shanghai should take swift action to promote persistent efforts on tobacco control and attenuate the excess burden of smoking-related diseases experienced in developed countries, to promote the narrowing of GGLE.

Importantly, besides cancer, we also find a widening effect of GGLE by other NCDs like cardiovascular and endocrine diseases (diabetes). Overweight or obesity, sedentary lifestyle, hypertension, and hyperlipidemia are the main risk factors for cardiovascular and endocrine diseases (diabetes), which are more prevalent in males than in female [40,41,42,43]. Several exemplary policy interventions exists to prevent NCDs, such as promoting preventing health care through lifestyle behavioral changes and incorporate prevention into existing health care policy [44]. Another potential strategy is workplace health promotion to promote physical activity [42]. Further, we find an age-specific contribution to GGLE concentrate in a narrower age range as the decline of gains in LE, which is similar to findings in other high-LE countries [45, 46]. Promotion of physical activity, particularly among adults and the elderly seems relevant to our findings that suggest special attention to males at an advanced age for further improving LE and reducing GGLE.

The trend pattern and its main contributor to GGLE in Shanghai varied compared with other high-income countries or regions. In some western developed countries, GGLE is constantly narrowing [6, 8, 9, 45, 47], and cardiovascular diseases made the largest contribution to narrow GGLE [6, 9]. While in some eastern countries like Japan, GGLE is widening and cardiovascular diseases is an important contributor to the widening [9, 48]. We, however, find GGLE fluctuated between 4.0 and 4.9 in recent years, and cancer is the major driver to widen GGLE throughout the 45-year study period. It remains to see whether Shanghai’s steady GGLE in recent years will gradually narrow as in the western countries or expand as in China’s Asian neighbors.

Our study has several limitations. First, since the earliest data we have started from the year 1973, we do not know the trend of GGLE before. Many high-income countries found that GGLE experienced an expansion period and then declined through over 50 or more years of data. Limited by our data, we cannot make a comparison in this respect. However, given that we update the long-term trend study to the year 2018, guidance for future disease prevention and control to increase LE and narrow GGLE or at least not to expand is of greater significance. Second, we constrain the study only to major causes of death without breaking down the disease groups into more detailed causes (except for cardiovascular diseases and some major neoplasm). NCDs accounted for over 90% of total death in Shanghai in 2018, and cardiovascular diseases and neoplasms alone account for over 70% of total deaths. Therefore, we believe that no breakdown of disease groups such as injuries into more detailed causes has little impact on this study.

Third, our study only contains the information of local residents without that of flowing population and only analyzes GGLE by decomposition of age- and cause-specific contributions. Future research is expected to dive deeper into specific causes of death based on more detailed socio-economic data such as educational background and annual income with a comparison of different population.

Fourth, the 45-year-span is divided into two periods based on joinpoint regression result. Excluding data point with big fluctuation like 1983 does not affect the conclusion that GGLE in Shanghai has entered another phase in the late 1990s. Considering the decompositions of GGLE can provide meticulous change between years, we will also analyze age and cause-specific contributions according to some special time nodes for the development of Shanghai in the future study. Lastly, like other long-term trend studies, our data also faces data quality differences in different periods. The percentage of garbage code dropped greatly from above 40% in 1973 to 6.5% in 2018, which reached an excellent quality globally. We listed age-specific percentage of garbage codes in the Additional file 1: Figure A1.

NCDs are the biggest cause of death worldwide, and could have largely been prevented. Our findings showed that NCDs like cancer, cardiovascular, chronic respiratory, and diabetes were leading causes of death in Shanghai, and their proportions of total death have reached above 90%, efforts on prevention and control NCDs are imminent. China has implemented “Healthy China 2030” program, and one of its goals is to prevent and control four major NCDs (cardiovascular diseases, cancer, chronic respiratory diseases, and diabetes) and increase the national LE to 79 years by 2030. The Healthy China 2030 aims to ensure that everyone enjoys a full cycle and all-round health and promote health equity [49]. This also includes health equity between male and female. More specifically, as nations develop, the longitudinal pattern of declining GGLE turn around, and men start to catch up as evident in many high and middle-income countries.

Shanghai is the province with the highest LE in mainland China. The public health challenge facing Shanghai today, is also the challenge faced by other regions in China now and in the future (Additional file 1: Table A4). GGLE in Shanghai continues to persist in recent decades despite the ever-increasing LE. Our findings provide evidence for policymakers and health professionals in China and other countries with rapid gains in LE to formulate future strategies for medical resource allocation, system improvement, and disease management to address or prevent GGLE.

Conclusions

NCDs have made GGLE enter a plateau phase from a descent phase in Shanghai China. Public efforts to reduce excess mortalities for male NCDs, cancers, cardiovascular diseases, chronic respiratory diseases, and diabetes in particular and health policies focused on the middle-aged and elderly population might further narrow GGLE and ensure improvement in health and health equity in Shanghai China.

Availability of data and materials

The datasets used and/or analysed during the current study available from the corresponding author on reasonable request with permission of Shanghai Pudong New area Center for Disease Control and Prevention.

Abbreviations

LE :

Life expectancy at birth

GGLE :

Gender gap in life expectancy at birth

NCD :

Non-communicable diseases

References

  1. World Health Organization. Global Health Observatory (GHO) data. https://www.who.int/gho/mortality_burden_disease/life_tables/situation_trends_text/en/ (accessed 2019).

  2. Gillespie DO, Trotter MV, Tuljapurkar SD. Divergence in age patterns of mortality change drives international divergence in lifespan inequality. Demography. 2014;51:1003–17. https://doi.org/10.1007/s13524-014-0287-8.

    Article  PubMed  Google Scholar 

  3. Luy M, Minagawa Y. Gender gaps-life expectancy and proportion of life in poor health. Health Rep. 2014;25:12–9.

    PubMed  Google Scholar 

  4. Naghavi M, Wang H, Lozano R, et al. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the global burden of disease study 2013. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the global burden of disease study 2013. Lancet. 2015;385:117–71. https://doi.org/10.1016/S0140-6736(14)61682-2.

    Article  Google Scholar 

  5. Lim D, Ha M, Song I. Trends in the leading causes of death in Korea, 1983-2012. J Korean Med Sci. 2014;29:1597–603. https://doi.org/10.3346/jkms.2014.29.12.1597.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Sundberg L, Agahi N, Fritzell J, Fors S. Why is the gender gap in life expectancy decreasing? The impact of age- and cause-specific mortality in Sweden 1997-2014. Int J Public Health. 2018. https://doi.org/10.1007/s00038-018-1097-3.

  7. Leon DA, Jdanov DA, Shkolnikov VM. Trends in life expectancy and age-specific mortality in England and Wales, 1970-2016, in comparison with a set of 22 high-income countries: an analysis of vital statistics data. Lancet Public Health. 2019;4:e575–82. https://doi.org/10.1016/S2468-2667(19)30177-X.

    Article  PubMed  Google Scholar 

  8. Meslé F. Recent improvements in life expectancy in France: men are starting to catch up. Population. 2006;61:437–62.

    Article  Google Scholar 

  9. Mats Thorslund CAJW, Wastesson JW, Agahi N, Lagergren M, Parker MG. The rise and fall of women's advantage: a comparison of national trends in life expectancy at age 65 years. Eur J Ageing. 2013;4:271–7. https://doi.org/10.1007/s10433-013-0274-8.

    Article  Google Scholar 

  10. Liu P, Li C, Wang Y, et al. The impact of the major causes of death on life expectancy in China: a 60-year longitudinal study. BMC Public Health. 2014;14:1193. https://doi.org/10.1186/1471-2458-14-1193.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Shen J, Jiang Q. 2013. Analysis of gender differences in life expectancy of urban residents in China from 2005 to 2010 [in Chinese]. Chin J Epidemiol. 2013;34:690–5. https://doi.org/10.3760/cma.j.issn.0254-6450.2013.07.007.

    Article  Google Scholar 

  12. Yang G, Wang Y, Zeng Y, et al. Rapid health transition in China, 1990–2010: findings from the Global Burden of Disease Study 2010. Lancet. 2013;381:1987–2015. https://doi.org/10.1016/S0140-6736(13)61097-1 Copyright (c) 2013 Elsevier Ltd. All rights reserved.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Zhou M, Wang H, Zhu J, et al. Cause-specific mortality for 240 causes in China during 1990-2013: a systematic subnational analysis for the global burden of disease study 2013. Lancet. 2016;387:251–72. https://doi.org/10.1016/S0140-6736(15)00551-6.

    Article  PubMed  Google Scholar 

  14. Chen H, Hao L, Yang C, et al. Understanding the rapid increase in life expectancy in shanghai, China: a population-based retrospective analysis. BMC Public Health. 2018;18:256. https://doi.org/10.1186/s12889-018-5112-7.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Cullen MR, Baiocchi M, Eggleston K, et al. The weaker sex? Vulnerable men and women's resilience to socio-economic disadvantage. SSM Popul Health. 2016;2:512–24. https://doi.org/10.1016/j.ssmph.2016.06.006.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Oksuzyan A, Juel K, Vaupel JW, et al. Men: good health and high mortality. Sex differences in health and aging. Aging Clin Exp Res. 2008;20:91–102. https://doi.org/10.1007/bf03324754.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Zhou F, Song GX. 2008. Contribution to LE at birth from mortality variation for some diseases in Shanghai [in Chinese]. Chin J Prev Contr Chron Noncommun Dis. 2008;6:258–636.

    Google Scholar 

  18. Yang G, Hu J, Rao KQ, Ma J, Rao C, Lopez AD. Mortality registration and surveillance in China: history, current situation and challenges. Popul Health Metrics. 2005;3:3. https://doi.org/10.1186/1478-7954-3-3.

    Article  Google Scholar 

  19. Naghavi M, Makela S, Foreman K, O'Brien J, Pourmalek F, Lozano R. Algorithms for enhancing public health utility of national causes-of-death data. Popul Health Metrics. 2010;8:9. https://doi.org/10.1186/1478-7954-8-9.

    Article  Google Scholar 

  20. Goovaerts P. Analysis of geographical disparities in temporal trends of health outcomes using space-time joinpoint regression. Int J Appl Earth Obs Geoinf. 2013;22:75–85. https://doi.org/10.1016/j.jag.2012.03.002.

    Article  PubMed  Google Scholar 

  21. Kim HJ, Fay MP, Yu B, Barrett MJ, Feuer EJ. Comparability of segmented line regression models. Biometrics. 2004;60:1005–14. https://doi.org/10.1111/j.0006-341X.2004.00256.x.

    Article  PubMed  Google Scholar 

  22. Dehkordi ZF, Tazhibi M, Babazade S. Application of joinpoint regression in determining breast cancer incidence rate change points by age and tumor characteristics in women aged 30-69 (years) and in Isfahan city from 2001 to 2010. J Educ Health Promot. 2014;3:115. https://doi.org/10.4103/2277-9531.145917.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Martins-Melo FR, Lima MS, Ramos AJ, Alencar CH, Heukelbach J. Mortality and case fatality due to visceral leishmaniasis in Brazil: a nationwide analysis of epidemiology, trends and spatial patterns. PLoS One. 2014;9:e93770. https://doi.org/10.1371/journal.pone.0093770.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Arriaga EE. Measuring and explaining the change in life expectancies. Demography. 1984;21:83–96.

    Article  CAS  PubMed  Google Scholar 

  25. Le Y, Ren J, Shen J, Li T, Zhang CF. The changing gender differences in life expectancy in Chinese cities 2005-2010. PLoS One. 2015;10:e123320. https://doi.org/10.1371/journal.pone.0123320.

    Article  CAS  Google Scholar 

  26. History Compilation Bureau of Shanghai. History of Shanghai Epidemic Prevention [M]. Shanghai: Shanghai Popular Science Press; 2003.

  27. Hu Y, Ward MP, Xia C, et al. Monitoring schistosomiasis risk in East China over space and time using a Bayesian hierarchical modeling approach. Sci Rep. 2016;6:24173. https://doi.org/10.1038/srep24173.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Yu S, R H, Wu C, et al. Review and prospect of hepatitis B vaccination in shanghai in the prevention of hepatitis B and liver cancer [in Chinese]. Sh J Prev Med. 2015;27:369–73.

    Google Scholar 

  29. Wang W, Zhao Q, Yuan Z, et al. Tuberculosis-associated mortality in Shanghai, China: a longitudinal study. Bull World Health Organ. 2015;93:826–33. https://doi.org/10.2471/BLT.15.154161.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Yang C, Yang L, Wu H, et al. The trends in mortalities of malignant tumors in Pudong new area in Shanghai from 1993 to 2007 [in Chinese]. Tumor. 2012;32:372–5.

    Google Scholar 

  31. Ji BT, Chow WH, Yang G, et al. Dietary habits and stomach cancer in Shanghai, China. Int J Cancer. 1998;76:659–64.

    Article  CAS  PubMed  Google Scholar 

  32. Lv S, Tian LG, Liu Q, et al. Water-related parasitic diseases in China. Int J Environ Res Public Health. 2013;10:1977–2016. https://doi.org/10.3390/ijerph10051977.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Zhang B, Zhai FY, Du SF, Popkin BM. The China health and nutrition survey, 1989-2011. Obes Rev. 2014;15(Suppl 1):2–07. https://doi.org/10.1111/obr.12119.

    Article  PubMed  Google Scholar 

  34. Zou TH, Zheng RH, Gao QY, et al. Factors affecting occurrence of gastric varioliform lesions: a case-control study. World J Gastroenterol. 2016;22:5228–36. https://doi.org/10.3748/wjg.v22.i22.5228.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Chen H, Zhang Y, Ma L, et al. Change of water consumption and its potential influential factors in Shanghai: a cross-sectional study. BMC Public Health. 2012;12:450. https://doi.org/10.1186/1471-2458-12-450.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Wang R, Jiang Y, Yao C, et al. Prevalence of tobacco related chronic diseases and its role in smoking cessation among smokers in a rural area of Shanghai, China: a cross sectional study. BMC Public Health. 2019;19:753. https://doi.org/10.1186/s12889-019-7110-9.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Bode AM, Dong Z, Wang H. Cancer prevention and control: alarming challenges in China. Natl Sci Rev. 2016;3:117–27. https://doi.org/10.1093/nsr/nwv054.

    Article  PubMed  Google Scholar 

  38. Janssen F, Rousson V, Paccaud F. The role of smoking in changes in the survival curve: an empirical study in 10 European countries. Ann Epidemiol. 2015;25:243–9. https://doi.org/10.1016/j.annepidem.2015.01.007.

    Article  PubMed  Google Scholar 

  39. Duncan MS, Freiberg MS, Greevy RJ, Kundu S, Vasan RS, Tindle HA. Association of Smoking Cessation with Subsequent Risk of cardiovascular disease. JAMA. 2019;322:642–50. https://doi.org/10.1001/jama.2019.10298.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Fan D, Su C, Du W, et al. Association of obesity indexes with hypertension and dyslipidemia in Chinese adults [in Chinese]. J Hygiene Research. 2018;47:875–82.

    Google Scholar 

  41. Opoku S, Gan Y, Fu W, et al. Prevalence and risk factors for dyslipidemia among adults in rural and urban China: findings from the China National Stroke Screening and prevention project (CNSSPP). BMC Public Health. 2019;19:1500. https://doi.org/10.1186/s12889-019-7827-5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Li F. Physical activity and health in the presence of China's economic growth: meeting the public health challenges of the aging population. J Sport Health Sci. 2016;5:258–69. https://doi.org/10.1016/j.jshs.2016.06.004.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Li Y, Schoufour J, Wang DD, et al. Healthy lifestyle and life expectancy free of cancer, cardiovascular disease, and type 2 diabetes: prospective cohort study. BMJ. 2020;368:l6669. https://doi.org/10.1136/bmj.l6669.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Konchak JN, Moran MR, O'Brien MJ, Kandula NR, Ackermann RT. The state of diabetes prevention policy in the USA following the affordable care act. Curr Diab Rep. 2016;16:55. https://doi.org/10.1007/s11892-016-0742-6.

    Article  PubMed  Google Scholar 

  45. Glei DA, Horiuchi S. The narrowing sex differential in life expectancy in high-income populations: effects of differences in the age pattern of mortality. Popul Stud (Camb). 2007;61:141–59. https://doi.org/10.1080/00324720701331433.

    Article  Google Scholar 

  46. Mathers CD, Stevens GA, Boerma T, White RA, Tobias MI. Causes of international increases in older age life expectancy. Lancet. 2014:1–9. https://doi.org/10.1016/S0140-6736(14)60569-9.

  47. Liu Y, Arai A, Kanda K, Lee RB, Glasser J, Tamashiro H. Gender gaps in life expectancy: generalized trends and negative associations with development indices in OECD countries. Eur J Pub Health. 2013;23:563–8. https://doi.org/10.1093/eurpub/cks049.

    Article  Google Scholar 

  48. Klenk J, Keil U, Jaensch A, Christiansen MC, Nagel G. Changes in life expectancy 1950-2010: contributions from age- and disease-specific mortality in selected countries. Popul Health Metrics. 2016;14:20. https://doi.org/10.1186/s12963-016-0089-x.

    Article  Google Scholar 

  49. The Central People's Government of People's Republic of China. Outline of “healthy China 2030”. http://www.gov.cn/xinwen/2016-10/25/content_5124174.htm (Accessed 25 Oct 2016).

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Acknowledgements

The authors are grateful to clinicians in Pudong New Area who devoted to routine vital data collection and verification and the historical data rescue work. The authors are grateful to physicians once worked for vital statistics sector of Pudong CDC. The authors also greatly appreciate constructive instructions given by public health physicians at department of vital statistics, Shanghai Municipal Center for Disease Control and Prevention.

Funding

This work was financially supported by Health Commission of Shanghai Pudong New Area [grant numbers PW2018B-02, PWRd2019–11, PWZxk2017–28 and PW2016A-6]. The content is solely the responsibility of the authors and does not necessarily represent the official views of the health commission. The funding source had no role in study design, data collection, data analysis, data interpretation, writing of the manuscript, or the decision to submit the paper for publication.

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Authors and Affiliations

Authors

Contributions

STX and JRT conceived the whole study and directed its implementation. HYC, YZ, and LHS were involved with the statistical analysis and drafted the manuscript. YCC, XBQ and HC helped conduct the literature review. The authors have read and approved the manuscript.

Corresponding authors

Correspondence to Janani Rajbhandari-Thapa or Shaotan Xiao.

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Ethics approval and consent to participate

The retrospective research did not involve human participants. Individual information was anonymized and de-identified prior to analysis. Strict confidentiality of individual data was practiced during the entire study.

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Not applicable.

Competing interests

None.

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Supplementary information

Additional file 1: Table S1.

List of causes of death focused in our study and the corresponding ICD-9 & ICD-10 codes. Table S2. Test for number of joinpoints. Table S3. Estimated regression coefficients for 1 joinpoint model. Table S4. Top 10 causes of death of China and Shanghai in 2017. Figure S1. Age-specific percentage of garbage codes in 1973, 1999 and 2018 in Shanghai.

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Chen, H., Zhou, Y., Sun, L. et al. Non-communicable diseases are key to further narrow gender gap in life expectancy in Shanghai, China. BMC Public Health 20, 839 (2020). https://doi.org/10.1186/s12889-020-08932-x

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