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Dietary fiber, whole grains, carbohydrate, glycemic index, and glycemic load in relation to risk of prostate cancer

Authors Wang R, Tang J, Chen Y, Gao J

Received 13 May 2015

Accepted for publication 30 July 2015

Published 2 September 2015 Volume 2015:8 Pages 2415—2426

DOI https://doi.org/10.2147/OTT.S88528

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Faris Farassati



Rong-jiang Wang, Jian-er Tang, Yu Chen, Jian-guo Gao

Department of Urology, The First Affiliated Hospital of Huzhou Teachers College, Huzhou, People’s Republic of China

Background: The relationships between dietary fiber, whole grains, carbohydrate, glycemic index (GI), glycemic load (GL), and prostate cancer risk are unclear. We conducted a systematic review and meta-analysis to investigate these associations.
Methods: Relevant studies were identified by a search of PubMed database and EMBASE database up to April 2015. A random effects model was used to calculate the summary relative risks (RRs) and their corresponding 95% confidence intervals (CIs).
Results: Twenty-seven epidemiological studies (18 case–control studies and nine cohort studies) were included in the final analysis. The pooled RRs of prostate cancer were 0.94 (95% CI 0.85–1.05, P=0.285), 1.13 (95% CI 0.98–1.30, P=0.095), 0.96 (95% CI 0.81–1.14, P=0.672), 1.06 (95% CI 0.96–1.18, P=0.254), and 1.04 (95% CI 0.91–1.18, P=0.590) for dietary fiber, whole grains, carbohydrate, GI, and GL, respectively. There was no evidence of significant publication bias based on the Begg’s test and Egger’s test.
Conclusion: The findings of this meta-analysis indicate that, based on available information, dietary fiber, whole grains, carbohydrate, GI, and GL are not associated with the risk of prostate cancer.

Keywords: prostate cancer, fiber, whole grains, carbohydrate, glycemic index, glycemic load

Introduction

Prostate cancer has the second highest incidence of all cancers in men after lung cancer worldwide, and it was estimated that prostate cancer alone accounted for ~14% of all newly diagnosed cancers in the world.1 Well-established risk factors for prostate cancer include age, race/ethnicity, and family history.2 In addition, physical activity, body mass index, hormones, and diet have been suggested to be associated with prostate cancer risk.

In various epidemiological studies, including case–control and cohort studies, the potential relationship between dietary fiber, whole grains, carbohydrate, glycemic index (GI), glycemic load (GL), and prostate cancer risk has been investigated with inconsistent findings. For example, Walker et al,3 Lewis et al,4 and Deschasaux et al5 reported an inverse association between fiber intake and prostate cancer risk. Augustin et al6 and Hu et al7 suggested a positive association between GI and prostate cancer risk. However, many other studies did not find such correlations.

To address the issues described earlier, we performed a systematic review and meta-analysis on dietary fiber, whole grains, carbohydrate, GI, GL, and risk of prostate cancer. Subgroup analyses were also carried out to identify possible variables or features moderating the results obtained.

Materials and methods

Search strategy

We searched PubMed database and EMBASE database up to April 2015 for all relevant studies with the following key words: fiber, fibre, grains, grain, carbohydrate, carbohydrates, GI, GL, glycaemic index, or glycaemic load combined with prostate cancer or prostate neoplasm. We also manually reviewed reference lists of retrieved articles and related reviews for additional pertinent studies. No language limitations were imposed.

Study selection

Studies included in this meta-analysis had to fulfill all the following criteria: 1) they had a cohort or case–control design; 2) the exposure of interest was dietary fiber, whole grains, carbohydrate, GI, or GL; 3) the outcome of interest was primary prostate cancer; and 4) studies provided the risk estimates with their 95% confidence intervals (CIs) or data to calculate them. If more than one publication from the same study population was available, the most recent and detailed study was included in this meta-analysis.

Quality assessment

The quality of included studies was evaluated by two authors with the Newcastle–Ottawa Scale (NOS) (http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp). NOS is a nine-star instrument designed to assess the selection of study population, study comparability, and ascertainment of either the exposure or the outcome of interest for case–control or cohort studies, respectively. The possible scores vary from 0 to 9. We used these scores to differentiate higher (7–9) from lower (0–6) quality studies.

Data extraction

The following data were extracted independently by two authors from each study: the first author’s last name, year of publication, study country, study design, sample size, age, types of exposure, the risk estimates with their corresponding 95% CIs, and matched or adjusted variables. From each study, we extracted the risk estimate that was most fully adjusted for potential confounders.

Statistical analysis

Considering that the absolute risk of prostate cancer is low, the odds ratio (OR) was assumed approximately the same as relative risk (RR), and the RR was used as the study outcome. Summary RR estimates with their corresponding 95% CIs for the highest versus the lowest level of fiber, whole grains, carbohydrate, GI, and GL were calculated with the DerSimonian and Laird random effect model,8 which take into account both within-study and between-study variation. Subgroup analyses were performed by study design and geographic region. Heterogeneity between studies was assessed by Q statistic (significance level at P<0.10) and I2 (I2<25%, no heterogeneity; I2=25%–50%, low heterogeneity; I2=50%–75%, moderate heterogeneity; I2>75%, large or extreme heterogeneity).9 A sensitivity analysis was carried out whereby each study was removed in turn and the combined estimate recalculated to determine the influence of each study. Publication bias was tested by Begg’s test10 and Egger’s test.11 A two-tailed P<0.05 was considered to be representative of a significant statistical publication bias. All the statistical analyses were conducted with STATA 12.0 (StataCorp LP, College Station, TX, USA).

Results

Study selection

Figure 1 shows a flow diagram of the procedure used to identify potentially relevant studies. Searches of the electronic databases yielded 3,369 articles. After carefully reading the titles and abstracts, 3,344 studies that were obviously unrelated to our topic were excluded. Then, we reviewed the full text of the remaining 25 articles and six articles were excluded with the following reasons: duplicate population (n=2), lacking control group (n=1), and lacking sufficient data (n=3). Eight studies were identified through checking reference lists of retrieved studies. Finally, the present study included 27 epidemiological studies.37,1233

Figure 1 Flow diagram of identification of relevant studies.

Characteristics of the included studies

The main clinical features of these 27 eligible studies are summarized in Table 1. These studies were published between 1988 and 2015, including 18 case–control and nine cohort studies. Thirteen articles evaluated patients from North America, ten from Europe, two from Asia, one from Africa, and one from South America. The total number of prostate cancer patients was 39,352. Fiber was reported in 16 studies, whole grains reported in eight studies, carbohydrate reported in 13 studies, GI reported in six studies, and GL reported in five studies. Although the number of studies included in GI and GL was limited, the sample sizes were large with a total of 26,656 and 26,500 prostate cancer patients for GI and GL, respectively. In addition, these studies had high quality (mean NOS =6.8 and 7 for GI and GL, respectively) and adjusted major confounding.

Table 1 Main characteristics of the studies included in this meta-analysis
Abbreviations: BMI, body mass index; SD, standard deviation; GI, glycemic index; h, hours; PSA, prostate specific antigen; GL, glycemic load; ORs, odds ratios; SFAs, saturated fatty acids; NA, not available.

Quantitative synthesis

The pooled RRs of prostate cancer were 0.94 (95% CI 0.85–1.05, P=0.285), 1.13 (95% CI 0.98–1.30, P=0.095), 0.96 (95% CI 0.81–1.14, P=0.672), 1.06 (95% CI 0.96–1.18, P=0.254), and 1.04 (95% CI 0.91–1.18, P=0.590) for dietary fiber (Figure 2), whole grains (Figure 3), carbohydrate (Figure 4), GI (Figure 5A), and GL (Figure 5B), respectively.

Figure 2 Summary RR of fiber intake and prostate cancer risk.
Note: Weights are from random effects analysis.
Abbreviations: RR, relative risk; CI, confidence interval.

Figure 3 Summary RR of whole grains intake and prostate cancer risk.
Note: Weights are from random effects analysis.
Abbreviations: RR, relative risk; CI, confidence interval.

Figure 4 Summary RR of carbohydrate intake and prostate cancer risk.
Note: Weights are from random effects analysis.
Abbreviations: RR, relative risk; CI, confidence interval.

Figure 5 Summary RRs of GI (A), GL (B), and prostate cancer risk.
Note: Weights are from random effects analysis.
Abbreviations: RRs, relative risks; GI, glycemic index; GL, glycemic load; CI, confidence interval.

In the stratified analysis by study design and region, significant associations were observed for whole grains intake in cohort studies (RR =1.10, 95% CI 1.02–1.19, P=0.014), GI in case–control studies (RR =1.34, 95% CI 1.10–1.62, P=0.004), and GL in case–control studies (RR =1.36, 95% CI 1.08–1.70, P=0.008) (Table 2). For dietary fiber, we further conducted stratified analysis by the types of fiber. The pooled RRs of prostate cancer were 0.86 (95% CI 0.59–1.26, P=0.452), 0.93 (95% CI 0.83–1.04, P=0.213), 0.92 (95% CI 0.76–1.10, P=0.353), and 0.82 (95% CI 0.57–1.16, P=0.258) for vegetable fiber, fruit fiber, soluble fiber, and insoluble fiber, respectively.

Table 2 Pooled and subgroup analyses stratified by study design and area
Note: aThe number of studies included.
Abbreviations: GI, glycemic index; GL, glycemic load; RR, relative risk; CI, confidence interval.

Low-to-moderate between-study heterogeneity was observed for dietary fiber (I2=39.5%), whole grains (I2=52.5%), carbohydrate (I2=51.2%), GI (I2=69.5%), and GL (I2=67.0%). There was no evidence of significant publication bias based on the Begg’s test and Egger’s test (fiber, PBegg =0.558, PEgger =0.545; whole grains, PBegg =1.000, PEgger =0.475; carbohydrate, PBegg =0.428, PEgger =0.598; GI, PBegg =0.260, PEgger =0.299; GL, PBegg =0.221, PEgger =0.247) (Figure 6). Sensitivity analysis was carried out by removing each study sequentially. As shown in Figure 7, for dietary fiber, carbohydrate, GI, and GL, all the pooled estimates were stable and not influenced by any included single study. However, for whole grains, the pooled estimate became statistically significant after removing the study by Jain et al.28

Figure 6 Begg’s funnel plots of dietary fiber, whole grains, carbohydrate, GI, GL, and prostate cancer risk.
Abbreviations: GI, glycemic index; GL, glycemic load; RR, relative risk.

Figure 7 Sensitivity analyses of dietary fiber, whole grains, carbohydrate, GI, GL, and prostate cancer risk.
Abbreviations: GI, glycemic index; GL, glycemic load; CI, confidence interval.

Discussion

This systematic review of epidemiological studies evaluated the potential association between dietary fiber, whole grains, carbohydrate, GI, GL, and prostate cancer risk based on nine prospective and 18 case–control studies. Overall, the summary RRs indicated that there was no clear relationship between the above factors and prostate cancer incidence, although a few results of stratified analysis were statistically significant.

In the pooled analysis, low-to-moderate between-study heterogeneity was observed, I2 ranging from 39.5% for dietary fiber to 69.5% for GI. Significant heterogeneity may be attributed to the study population, study design, sample size, method of exposure measurement, and adjustment for confounders. The presence of heterogeneity somewhat limited the interpretation of the results.

Up to now, the only fully established risk factors of prostate cancer are age, African–American ethnicity, and family history of prostate cancer.2 No lifestyle factors (eg, diet and exercise) have been conclusively confirmed as prostate cancer risk or protective factors, although many have been considered with supporting evidence. For example, physical activity in both occupational and recreational time has been associated with a decreased risk of prostate cancer.34 Another recent meta-analysis of cohort studies has indicated that high intakes of dairy products and dairy calcium may increase total prostate cancer risk.35 Conversely, consumption of dietary carrot36 and cruciferous vegetables37 might be inversely associated with prostate cancer risk.

As for dietary fiber, whole grains, and carbohydrate, several clinical and animal studies have indicated that they may play a role in prostate cancer development. Landberg et al38 reported that whole grains and bran from rye led to significantly lower plasma prostate specific antigen. Bylund et al39 suggested that factors in rye bran could inhibit prostate cancer growth. Mavropoulos et al40 and Freedland et al41 indicated that increased carbohydrate consumption may promote tumor growth and inhibit apoptosis of prostate cancer cells. However, our meta-analysis, based on all available epidemiologic studies, indicated no statistically significant relationships between dietary fiber, whole grains, carbohydrate, and prostate cancer risk.

Emerging studies also have evaluated the relationship between dietary fiber, whole grains, carbohydrate, GI, GL, and various types of other human diseases. Aune et al42 reported that there was an inverse association between dietary fiber intake and breast cancer risk. Yang et al43 suggested that fiber intake was associated with a reduced risk of all-cause mortality. Consumption of whole grains has been reported to be inversely associated with the risk of colorectal cancer44 and type 2 diabetes.45 GI and GL have been suggested to be related with the risk of breast cancer46 and digestive tract neoplasms.47 Therefore, dietary fiber, whole grains, carbohydrate, GI, and GL may only play a role in specific diseases.

Our study has several strengths. This meta-analysis included a large number of studies and more than 39,000 cases, which enhanced the statistical power. All included studies ascertained outcomes according to histologic findings. A recent meta-analysis reported that there was no clear association between carbohydrate intake and the risk of prostate cancer,48 which was in accordance with our study. However, we evaluated as many as five factors, including dietary fiber, whole grains, carbohydrate, GI, and GL.

Some limitations of this meta-analysis should be acknowledged. First, measurement errors in the assessment of exposure may bias the overall effect estimates. Second, residual confounding (ie, uncontrolled confounding) are always a concern in observational studies. Third, as discussed earlier, significant heterogeneity was observed among several analyses. Fourth, sensitivity analysis indicated that the summary estimate for whole grains was not stable and influenced by a single study. Finally, publication bias could not be ruled out as small studies with null results tend not to be reported.

Conclusion

Overall, the findings of this meta-analysis indicate that, based on available information, dietary fiber, whole grains, carbohydrate, GI, and GL are not associated with the risk of prostate cancer. To provide a more definitive conclusion, further prospective cohort studies with larger sample size, better exposure assessment, and longer follow-up are warranted in this area.

Acknowledgment

This study was supported from Public Welfare General Project of Huzhou Science and Technology Agency (2012YSB25).

Disclosure

The authors report no conflicts of interest in this work.


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