Menstrual and Reproductive Factors and Risk of Pancreatic Cancer in Women

Abstract

BACKGROUND

Pancreatic cancer (PC) is a deadly disease with a 5-year survival of less than 5%. Worldwide PC incidence rates are lower among women than men. While this suggests a protective role for steroid hormones in PC risk, results from epidemiological studies are not consistent.

METHODS

153 new incident PC cases and 202 controls were recruited from a prospective case–control study, running in a referral center for endoscopic ultrasonography during 2011-2017. A structured valid and reliable questionnaire was used for data collection by a few trained interviewers. Odds ratios and 95% confidence intervals for reproductive factors and PC were estimated using logistic regression methods.

RESULTS

Mean age (SD) of the cases and the controls were 63.18 (11.4) and 63.37 (12.0) years, respectively. Age at menarche, age at menopause, number of parity, gravidity, and abortion were not associated with PC risk.

CONCLUSION

This study does not support the hypothesis that menstrual and reproductive factors are associated with PC risk.

INTRODUCTION

Exocrine pancreatic cancer (PC) is the 12th most common cancer in the world with 338,000 new cases diagnosed in 2012.¹ The incidence of PC is approximately 30% to 50% higher in men than in women.¹ PC has the highest mortality to incidence ratio among all cancers, with a 5-year survival rate of less than 5%.¹ Although about 35% of cases could be attributed to tobacco, obesity, heavy alcohol drinking, diabetes, and chronic pancreatitis^2,3, the etiology of this deadly cancer is largely unknown. Several epidemiological studies have suggested an inverse association between female reproductive factors and the risk of PC but the findings are not conclusive.^4,5 Estrogen and progesterone receptors both have been found in normal and cancerous pancreatic tissue inconsistently^6,7 and the role of androgen is not recognized very well.⁸ Thus, we tested the association between menstrual and reproductive factors and PC by conducting a case-control study.

MATERIALS AND METHODS

This case-control study was approved by the Institutional Review Board of Digestive Disease Research Center, Tehran University of Medical Sciences (IRB number: IRB00001641, Federal wide Assurance number: FWA00015916). The methods of cases and controls recruitment were extensively explained before and are briefly described here.⁹ Cases (those with pathology proven pancreatic adenocarcinoma) and controls (those with normal pancreas and no other cancer) were selected from the patients who referred for endoscopic ultrasonography (EUS) to a university affiliated hospital (Shariati Hospital) in Tehran, Iran, from January 2011 to January 2017. A structured valid and reliable questionnaire was used for data collection by a few trained interviewers.¹⁰ Weight and height were measured and body mass index (BMI) was calculated, using the weight before involuntary weight loss. BMI was categorized according to the WHO classification to: underweight (BMI < 18.5), normal (BMI: 18.5 - 24.9), overweight (BMI: 25 - 29.9), and obese (BMI over 30).¹¹

The American Joint Committee on Cancer (AJCC) TNM staging system was used for PC staging by EUS and other imaging that the patients already had.¹²

Data are expressed as mean ± SD or frequency and percentage, as appropriate. Differences in frequencies between the cases and controls were evaluated by simple contingency table analysis (Fisher exact test probability test and χ² test) using the STATA software, version 12.0 (Stata Corp, College Station, TX, USA). Unconditional logistic regression models were computed to test associations between cancer status and reproductive factors. Contingency tables were constructed yielding χ² P values, Fisher exact P values, crude odds ratio (OR), and 95% confidence interval (95% CI). Multiple logistic regression models were analyzed with cancer status as the dependent variable and other variables as the covariates to test for confounding and effect modification.

RESULTS

153 new incident PC cases and 202 controls were recruited in the study. Mean age (SD) of cases and controls were 63.18 (11.4) and 63.37 (12.0) years respectively. Table 1 compares the potential risk factors of pancreatic cancer for cases and controls.

Table 1. Comparison of the cases and controls for age, diabetes-related conditions, body mass index, and cigarette smoking .

Characteristics		Case	Control	P -value	OR (CI 95%)
		N=153	N=202	P
Age at diagnosis (Mean±SD)		63.18±11.44	63.37±12.08	0.885	0.99 (0.98-1.01)
Body mass index (N [%])	Normal	37 (24.18%)	81 (40.10%)		1.00
	Overweight	38 (24.83%)	76 (37.62%)		1.09 (0.63-1.89)
	Obese	78 (50.99%)	45(22.28%)	<0.001	3.79 (2.22-6.47)
Diabetes (N [%])	No	114 (74.51%)	168 (83.17%)		1.00
	Yes, diagnosed 2+ years ago	39 (25.49%)	34 (16.83%)	0.046	2.04 (1.25-3.32)
Cigarette smoking (N [%])	Never	143 (93.46%)	184 (91.9%)		1.00
	Ever	10 (6.54%)	18 (8.91%)	0.883	1.06 (0.45-2.46)
Opium (N [%])	Never	152 (99.35%)	198 (98.02%)		1.00
	Ever	1 (0.65%)	4 (1.98%)	-*	-*
Alcohol (N [%])	No	152 (99.35%)	202 (100%)		1.00
	Yes	1 (0.65%)	0 (0.00%)	-*	-*

* Not calculable

Only one of the cases had ever used opium and alcohol. So we did not include these risk factors of PC in our analysis. Overall, 10 cases (6.54%) compared with 18 controls (8.9%) had ever smoked cigarette, resulting in an OR: 1.06 (95% CI; 0.45 - 2.46).

78 cases (50.99%) and 45 (22.28%) controls had obesity resulting in OR: 3.79 (95% CI; 2.22 - 6.47). 39 (25.49%) cases and 34 (16.83%) controls had two years or longer duration of diabetes, prior to pancreatic cancer diagnosis resulting in OR: 0.046 (95% CI; 1.25 - 3.32).

Table 2 shows adjusted and unadjusted results for no association between menstrual and reproductive factors and PC.

Table 2. Comparison of the Cases and controls for reproductive factors (adjusted for smoking status, body mass index, and diabetes) .

Reproductive Characteristics		Case	Control		Crude-OR (CI 95%)	Adj-OR (CI 95%)
		N=153	N=202	P
Gravidity (Mean±SD)		6.33±3.48	6.35±3.36	0.919	0.99 (0.93-1.05)	0.91 (0.64-1.30)
Live birth (Mean±SD)		5.47±2.97	5.47±2.86	0.998	1.00 (0.93-1.07)	1.09 (0.76-1.58)
Age at menarche (Mean±SD)		13.32±1.27	13.23±1.21	0.509	1.05 (0.89-1.25)	1.05 (0.88-1.26)
Age at menopause (Mean±SD)		57.43±19.23	55.23±16.36	0.231	1.00 (0.99-1.01)	1.00 (0.99-1.01)
Abortion (N [%])	0	80 (52.29%)	101 (50.00%)		1.00	1.00
	1	36 (23.53%)	55 (27.23%)	0.810	0.84 (0.51-1.41)	0.91(0.48-1.73)
	2+	37(24.18%)	46 (22.77%)		0.98 (0.58-1.67)	1.14 (0.37-3.50)
Sterility history (N [%])	No	149 (97.38%)	194 (96.04%)		1.00	1.00
	Yes	4 (2.61%)	8 (3.96%)	0.568	1.53 (0.45-5.19)	1.76 (0.48-6.45)
OCP* use (N [%])	No	119 (77.78%)	156 (77.20%)		1.00	1.00
	Yes	34 (22.22%)	46 (22.80%)	0.902	0.97 (0.58-1.61)	1.07 (0.62-1.84)

*oral contraceptive pill

Table 3 shows that about 75% of PCs were located in the head of pancreas and most PCs were diagnosed in advance stages.

Table 3. Tumor characteristics of women who developed incident pancreatic cancer .

Tumor characteristics		Case
		N=153
Location (N [%])	Head	113 (74.83%)
	Body	33 (22.52%)
	Tail	4 (2.65%)
Size (Mean±SD)	-	33.93±0.93
Stage (N [%])	0	2 (1.32%)
	I	16 (10.60%)
	II	83 (54.97%)
	III	26 (17.22%)
	IV	24 (15.89%)

DISCUSSION

The risk of developing PC increases with age. The average age at the time of PC diagnosis is 70 and most PCs are diagnosed at advance stage.¹ Our results are comparable with worldwide data in these regards.¹ A pooled analysis of multiple cohort studies, has shown a higher risk of PC among current smokers compared with never smokers (OR: 1.77, 95% CI 1.38 - 2.26). The risk is increased significantly with greater intensity, duration, and cumulative smoking dose.¹³ Although smoking is one of the most important risk factors for PC, cigarette smoking was not associated with an increased risk for PC in our population as we showed in our previous study.⁹ The present study supports the notion that having diabetes mellitus (more than two years prior to the diagnosis of PC) and obesity are significantly associated with increased incidence of PC.^14,15

Female steroid hormones are hypothesized to play a protective role in PC risk. Menstrual and reproductive factors, including age at menarche and menopause and parity, were not associated with PC risk in The California Teachers cohort study.⁴ Combined data from two Italian case-control studies (285 cases and 713 controls) showed an OR: 0.46 (95% CI = 0.26 - 0.85) for women with four or more births compared with nulliparous. But other factors, including age at menarche and menopause, and abortion were not associated with PC risk.⁵ In a cohort of Norwegian women (449 PC cases), age at menopause showed a mild positive association with the risk of PC, but parity did not have such an associations.¹⁶ A meta-analysis in 2013 suggested that higher parity was associated with a decreased risk of PC.¹⁷ A recent study on data from the Women’s Health Initiative (1003 cases of PC) shows that being parous vs. nulliparous is associated with reduced risk (HR = 0.84, 95% CI 0.70 - 1.00), and women who had one to four births are at decreased risk compared with nulliparous women, whereas women who have more than five births have no decrease in risk. Other reproductive factors and exogenous hormone use were not associated with PC risk in that study.¹⁸ Our results suggest that menstrual, reproductive, and hormonal exposures are unlikely to play a role in the risk for PC.

Please cite this paper as:

Masoudi S, Momayez Sanat Z, Mahmud Saleh A, Nozari N, Ghamarzad N, Pourshams A. Menstrual and Reproductive Factors and Risk of Pancreatic Cancer in Women. Middle East J Dig Dis 2017;9:146-149. DOI: 10.15171/mejdd.2017.65.