| Literature DB >> 29796059 |
Abstract
Lung cancer mortality in Tuscany (Italy) for males, from 1971 and 2010, is investigated. A hierarchical Bayesian model for space-time disease mapping is introduced. Such a model belongs to the class of shared random effect models and exploits the birth-cohort as the relevant time dimension. It allows for highlighting common and specific patterns of risk for each birth-cohort. The results show that different birth-cohorts exhibit quite different spatial patterns, even if the socioeconomic status is taken into account. In fact, there were different occupational exposures before and after the Second World War. The birth-cohort 1930-35 exhibits high relative risks related to particular areas. This fact could be connected with occupational exposure to risk factors for silicosis, perhaps a prognostic status for lung cancer.Entities:
Mesh:
Year: 2018 PMID: 29796059 PMCID: PMC5896287 DOI: 10.1155/2018/4964569
Source DB: PubMed Journal: Comput Math Methods Med ISSN: 1748-670X Impact factor: 2.238
Figure 1Epidemic curves for age (a) and cohort (b) dimensions.
Incidence rates (×100,000) and number of death cases (in parentheses). Lung cancer for males in Tuscany (Italy), 1971–2010, for age-class, calendar period, and birth-cohort.
| Age-class | Birth-cohort | Calendar period | |||||||
|---|---|---|---|---|---|---|---|---|---|
| 1971–74 | 1975–79 | 1980–84 | 1985–89 | 1990–94 | 1995–99 | 2000–04 | 2005–10 | ||
| Birth-cohort | 1925–35 |
| 1935–45 | 1940–50 | 1945–55 | 1950–60 | 1955–65 | 1960–65 | |
| 40–44 | 1925–35 | 21.611 (106) |
| 19.425 (116) | 19.750 (117) | 14.356 (86) | 8.241 (48) | 7.919 (51) | 4.446 (40) |
| 45–49 | 1920–30 | 43.225 (218) | 44.661 (273) |
| 46.078 (273) | 32.182 (190) | 26.567 (161) | 23.154 (134) | 16.185 (130) |
| 50–54 | 1915–25 | 75.662 (342) | 91.121 (568) | 108.292 (642) |
| 76.188 (446) | 68.585 (398) | 54.442 (324) | 36.807 (261) |
| 55–59 | 1910–20 | 128.517 (467) | 150.719 (780) | 187.735 (1112) | 180.141 (1031) |
| 113.619 (650) | 100.928 (569) | 78.371 (554) |
| 60–64 |
|
| 229.643 (1030) | 247.445 (1225) | 292.444 (1633) | 259.192 (1413) |
| 174.847 (967) | 162.399 (1089) |
| 65–69 | 1900–10 | 279.517 (960) |
| 370.082 (1445) | 352.777 (1548) | 394.758 (2018) | 345.721 (1731) |
| 244.304 (1525) |
| 70–74 | 1895–05 | 286.059 (714) | 385.879 (1324) |
| 468.204 (1562) | 456.730 (1740) | 478.094 (2123) | 420.203 (1861) |
|
| 75–79 | 1890–00 | 264.585 (385) | 344.589 (743) | 443.843 (1092) |
| 521.901 (1378) | 518.007 (1537) | 525.898 (1889) | 492.426 (2200) |
| 80–84 | 1885–95 | 145.496 (128) | 270.123 (293) | 407.835 (517) | 489.365 (756) |
| 532.960 (963) | 556.287 (1170) | 579.774 (1834) |
| 85+ | 1880–90 | 129.855 (57) | 153.766 (92) | 257.543 (165) | 345.532 (269) | 365.507 (385) |
| 466.355 (683) | 543.954 (1137) |
Figure 2Maps of the interaction terms from the Lagazio et al. 2001 model [8]: birth-cohorts 1905–15 (a) and 1930–40 (b).
Figure 3Relative risks for lung cancer mortality from SMBC model: for birth-cohort 1905–15 (a) and birth-cohort 1930–40 (b).
Figure 4Results from SMBC model: the common clustering term exp(ψ() (a), the distribution of the ω1 and ω2 parameters (b), the distribution and the specific clustering terms exp(ψ() for birth-cohort 1905–15 (c), and exp(ψ() for birth-cohort 1930–40 (d).