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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>Biomedical Research and Therapy</journal-title>
      </journal-title-group>
      <issn pub-type="epub" publication-format="electronic">2198-4093</issn>
      <publisher>
        <publisher-name>BioMedPress</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.15419/bmrat.v4i06.180</article-id>
      <article-categories>
        <subj-group subj-group-type="display-channel">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="heading">
          <subject>Biomedical Research and Therapy</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Comparative study of sperm motility in Metformin-using and Insulin-dependent diabetics</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Ali Zaidi</surname>
            <given-names>Awais</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ahmed Khan</surname>
            <given-names>Mahtab</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Sharif</surname>
            <given-names>Ali</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Shakir</surname>
            <given-names>Lubna</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Irshad</surname>
            <given-names>Atif</given-names>
          </name>
          <xref ref-type="aff" rid="aff3"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ali</surname>
            <given-names>Arsalan</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <contrib contrib-type="author" corresp="yes">
          <name>
            <surname>Ali Shaheryar</surname>
            <given-names>Zaib</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
          <xref ref-type="corresp" rid="cor1">*</xref>
        </contrib>
        <aff id="aff1">
          <institution>Faculty of Pharmacy, University of Lahore, Lahore-Pakistan</institution>
        </aff>
        <aff id="aff2">
          <institution>Faculty of Pharmacy, Hajvery University, Lahore-Pakistan</institution>
        </aff>
        <aff id="aff3">
          <institution>Good Hope Hospital, Rectory Road Sutton Coldfield, B75 7RR</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="cor1"><label>*</label>For correspondence: <email>shaheryar_zaib_24@yahoo.com</email></corresp>
        <fn fn-type="con" id="equal-contrib">
          <label>*</label>
          <p>These authors contributed equally to this work</p>
        </fn>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>25</day>
        <month>06</month>
        <year>2017</year>
      </pub-date>
      <volume>4</volume>
      <issue>6</issue>
      <fpage>1</fpage>
      <lpage>3</lpage>
      <history>
        <date date-type="received">
          <day>06</day>
          <month>03</month>
          <year>2017</year>
        </date>
        <date date-type="accepted">
          <day>04</day>
          <month>06</month>
          <year>2017</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Copyright: &#169; The Author(s) 2017</copyright-statement>
        <copyright-year>2017</copyright-year>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/CC-BY/4.0">
          <license-p>This article is published with open access by BioMedPress (BMP), Laboratory of Stem Cell Research and Application, Vietnam National University, Ho Chi Minh city, Vietnam This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.</license-p>
        </license>
      </permissions>
      <self-uri content-type="pdf" xlink:href="http://www.bmrat.org/index.php/BMRAT/article/view/180/509"/>
      <abstract>
        <p>Background: Diabetes mellitus (DM) represents one of the greatest threats to modern global health. DM may affect male reproductive function at multiple levels as a result of its effects on spermatogenesis, sperm motility, sperm morphology, and change in sperm structure. Method: The present study deals with sperm motility and sperm morphological changes associated with diabetes in the male population. In this study, 50 insulin-dependent and 50 metformin users were selected, with ages of males ranging from 26-54 years and duration of diabetes distributed over 3-15 years. Both insulin-dependent and metformin-using diabetic subjects were evaluated for sperm analysis. Results: Sperm analysis data showed a significant increase (p &#177;0.0005) in total sperm count in insulin-dependent diabetic men. However, sperm motility was found to be about 10-15% less in insulin-dependent patients compared to metformin users. Moreover, sperm morphology was improved in 6% of metformin users compared to insulin-dependent diabetics. Conclusion: Our study concludes that metformin does not significantly affect sperm count. However, it does significantly affect sperm motility, when compared to insulin-dependent diabetic men. This study established an important relationship between diabetes and sperm motility, which reflects the reproductive capabilities of men.</p>
      </abstract>
      <kwd-group>
        <kwd>Insulin-dependent</kwd>
        <kwd>Metformin</kwd>
        <kwd>Morphological changes</kwd>
        <kwd>Sperm motility</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="s1">
      <title>Introduction</title>
      <p>Diabetes mellitus (DM) is a metabolic disorder that is generally characterized as Type 1 diabetes (T1D) or Type 2 diabetes (T2D). T1D arises from a complete lack of insulin due to defective insulin secretion. T2D arises from a partial lack of insulin and is associated with alterations in carbohydrate, protein and lipid metabolism <xref ref-type="bibr" rid="ref6">Association, 2014</xref>. In fact, T2D can result from a combination of inadequate insulin secretion and insulin resistance <xref ref-type="bibr" rid="ref5">Association, 2010</xref>. In T2D, the symptoms can be detected only when the disease is in its advanced phase. Indeed, the changes produced in tissues and at the cellular level may not be reversed even when treated with the appropriate drug therapy <xref ref-type="bibr" rid="ref13">Donner and Munoz, 2012</xref>.</p>
      <p>DM is one of the most prominent population health threats in developed societies, with incidence on the rise each year. In 2002, the World Health Organization (WHO) reported that there were about 171 million DM patients worldwide; that number represented a 60% higher incidence compared to data from 1995 <xref ref-type="bibr" rid="ref24">Organization, 2002</xref>. DM has been closely linked to long-term complications related to mortality and morbidity, such as hypertension and kidney failure <xref ref-type="bibr" rid="ref19">McBrien et al., 2012</xref><xref ref-type="bibr" rid="ref32">Torgerson et al., 2004</xref>.</p>
      <p>Insulin stimulates glucose uptake in muscle and fat cells. In the muscles, glucose is taken up and stored as glycogen; in fat cells glucose is absorbed and converted mostly to glycerin for long-term storage. The primary role of insulin is glucose transport into the plasma membrane of muscle and fat cells. The change in glucose transport activity due to the exposure to insulin brought changes and therefore different enzymes may act on different type of carbohydrates and fat metabolism takes place <xref ref-type="bibr" rid="ref11">Denton et al., 1981</xref>.</p>
      <p>Metformin is an oral diabetes drug which helps control blood sugar levels, particularly in those with type 2 diabetes. Metformin primarily acts on hepatic glucose ejection by inhibiting gluconeogenesis. However, it can cause weight loss and affect adipose tissues <xref ref-type="bibr" rid="ref31">Stumvoll et al., 1995</xref>. The metabolism and mechanism of action of metformin are still poorly understood, despite the fact that it has been a form of medicine (for non-insulin-dependent diabetes mellitus (NIDDM)) for the past for 30 years.</p>
      <p>DM is responsible for various homeostatic and biochemical alterations resulting in male infertility of sub-infertility. Individuals with diabetes have described sexual problems such as weakened sexual desire, likely related to a hyperglycemic state <xref ref-type="bibr" rid="ref14">Ewing, 1985</xref>. Another sexual disorder linked to diabetes is erectile dysfunction <xref ref-type="bibr" rid="ref29">Sexton and Jarow, 1997</xref> and a decline in ejaculation <xref ref-type="bibr" rid="ref15">Fedele, 2005</xref>. There appears to be a direct relationship between the incidence of DM and fertility, and incidence of DM and decrease in birth rates <xref ref-type="bibr" rid="ref18">Lutz, 2006</xref>. The prevalence of DM in patients of reproductive age is a purported cause. The majority of patients are diagnosed with T1D before the age of 30 years and the rest are diagnosed with T2D <xref ref-type="bibr" rid="ref1">Agbaje et al., 2007</xref><xref ref-type="bibr" rid="ref30">Silink, 2002</xref>.</p>
      <p>In DM the molecular mechanisms and specific pathways, which induce defects in the male reproductive system and its functions, are both impacted. Spermatogenesis is altered in DM patients <xref ref-type="bibr" rid="ref10">Daubresse et al., 1978</xref>. Several research studies comparing young or adult diabetics (to control individuals) have shown that diabetic males have lower sperm counts and significant changes in sperm morphology and motility <xref ref-type="bibr" rid="ref7">Baccetti et al., 2002</xref>. Indeed, DM induces change in sperm count as well as sperm volume <xref ref-type="bibr" rid="ref8">Bartak et al., 1974</xref>. Some other studies have shown that the concentration and sperm count are increased in diabetics but that sperm motility and semen volume are decreased <xref ref-type="bibr" rid="ref2">Ali et al., 1993</xref>.</p>
      <p>Blood glucose concentrations depend upon and adjust the function of different tissues and organs. Liver and fat are normally known to have strict control on glucose variations and are particularly known to play key roles in the use and storage of nutrients by hormonally regulated mechanisms. In testes, glucose metabolism is a vital event. Spermatogenesis preservation in vivo relies on glucose metabolism despite the fact that there are low levels of this sugar in tubular liquid <xref ref-type="bibr" rid="ref28">Robinson and Fritz, 1981</xref><xref ref-type="bibr" rid="ref34">Zysk et al., 1975</xref>. Metformin helps to restore the body's response to insulin, making it possible to produce the amount of glucose and gastrointestinal absorption needed from the liver. Metformin (a biguanide derivative) reduces complications associated with blood glucose control.</p>
      <p>Some studies have reported that there is no affiliation between age, sperm motility, T1D diagnosis and span of illness. In the study herein, we demonstrate that the parameters used to assess sperm motility (e.g. progressive velocity, path velocity, way speed and lateral head displacement) remained unchanged. For example, the direct linear index (which unveils the straightness of sperm swimming) was expanded in diabetic patients and normal individuals <xref ref-type="bibr" rid="ref22">Niven et al., 1995</xref>. Our study shows that the effect of T1D on male fertility may be associated to the complications of the disease and not to the disease itself. The sperm cells of diabetic males are reported to have high fructose and glucose content. However, a relationship could not be established between an ineffective metabolic control and the observed alterations in the semen. A broad study of spermatozoa cryopreservation from patients with diverse pathologies showed that only sperm from diabetic men presented considerable differences in the parameters used to assess sperm <xref ref-type="bibr" rid="ref27">Ranganathan et al., 2002</xref>. Despite the fact that there is some ambiguity with regards to sperm parameters, there appears to be a genuine effect on the regenerative arrangement of males with DM. Furthermore, aside from the immediate studies on sperm, some new and critical results have been confirmed by in vitro hormonal tests. For example, diabetic patients do not show changes in sex hormones such as testosterone <xref ref-type="bibr" rid="ref12">Ding et al., 2006</xref>.</p>
      <p>Thus, hormonal control of sperm cell metabolism has a direct effect on spermatogenesis <xref ref-type="bibr" rid="ref23">O'Donnell et al., 2017</xref> and should deserve special attention when studying metabolic diseases that are also related to hormonal regulation or lack of. Moreover, individuals with diabetes have severe insulin deregulation, which continues to be an important consideration factor when studying DM. Euglycemia is very difficult to maintain in diabetic patients. Hyperinsulinemia / hypoglycemia and hypoglycemia / hyperinsulinemia are common events faced by diabetic patients daily. Thus, insulin can play a highly important role in male sexual dysfunction in those afflicted with DM. In fact, recent research reports show that only a few hours of insulin deficiency can alter sperm cell glucose metabolism <xref ref-type="bibr" rid="ref3">Alves et al., 2013</xref> and completely suppress in vitro acetate production <xref ref-type="bibr" rid="ref4">Alves et al., 2012</xref>. The role of insulin in processes vital for normal spermatogenesis clearly indicates that the molecular mechanisms by which DM impacts male reproductive function may also be associated with insulin fluctuations and glucose concentrations.</p>
    </sec>
    <sec id="s2">
      <title>Methods</title>
      <p>In our comparative study, 100 subjects were evaluated. There were 50 participants with insulin-dependent diabetes mellitus (IDDM), with ages ranging from 26-54 years. Likewise, there were 50 participants with NIDDM, with ages ranging from 35-54 years. All diabetic subjects involved in the study were males.</p>
      <sec id="s2-1">
        <title>Inclusion criteria included</title>
        <p>- Male patients with T1D receiving insulin only</p>
        <p>- Male patients with T2D receiving metformin only</p>
      </sec>
      <sec id="s2-2">
        <title>Exclusion criteria included</title>
        <p>- Patients with pelvic surgery</p>
        <p>- Patients with hernia repair</p>
        <p>- Patients with thyroid disease</p>
        <p>- Patients with hypertension</p>
        <p>- Patients with testicular cancer</p>
        <p>- Patients on tamoxifen</p>
        <p>- Patients with prostate cancer</p>
        <p>- Patients with nephropathy</p>
        <p>- Patients with neuropathy</p>
        <p>- Patients with testicular varicocele</p>
        <p>- Patients with genital infections</p>
        <p>- Patients with leukocytospermia</p>
        <p>- Patients with chronic illnesses</p>
        <p>- Patients with serious systemic diseases</p>
      </sec>
      <sec id="s2-3">
        <title>Methods</title>
        <p>The collection and examination of semen were done by properly standardized procedures according to WHO guidelines. Semen samples were collected by masturbation after a recommended sexual abstinence period of 2&#8211;5 days. Spermatozoa for ICSI were prepared using density gradient method. During the research study, tests were conducted on semen volume, semen pH, semen count, semen morphology, sperm motility, and serum. Testosterone levels were conducted using computer-assisted semen analysis (CASA) according to WHO recommendation <xref ref-type="bibr" rid="ref33">WHO, 1999</xref> and DNA fragmentation analysis by SCD (define abbreviation). All data were analyzed using computer software. Analysis of variance (ANOVA) test was applied to compare the efficacy of groups. P-value &lt; 0.05 was considered statistically significant.</p>
      </sec>
      <sec id="s2-4">
        <title>Ethical Approval</title>
        <p>The study was approved by the Research and Ethics Committee (REC) of Faculty of Pharmacy, University of Lahore, Lahore-Pakistan (Ethical-No (EN-3121-2016) dated 12-09-2016).</p>
      </sec>
    </sec>
    <sec id="s3">
      <title>Results</title>
      <p>Only 100 male patients met the inclusion criteria. Each took the required tests which were used to assess sperm motility, sperm morphology, semen profile, and semen pH. Semen volume was also evaluated, and the effect of insulin and metformin on diabetic patients were also compared. <xref ref-type="fig" rid="fig1"> Figure 1 </xref> describes the mean difference between semen volume of insulin and metformin users.</p>
      <fig id="fig1">
        <label>Figure 1</label>
        <caption>
          <title>Mean difference between semen volume of insulin- and metformin-dependent diabetics</title>
          <p>The results show that there is a significant ((p&lt;0.0001) increase of semen volume in insulin-dependent diabetics (IDDM) as compared to metformin-using (i.e. non-insulin-dependent) diabetics (NIDDM).</p>
        </caption>
        <graphic xlink:href="bmrat.v4i06.180/fig1.png"/>
      </fig>
    </sec>
    <sec id="s4">
      <title>Discussion</title>
      <p>DM represents one of the greatest threats to modern global health. DM may affect male reproductive functioning at multiple levels as a result of its effects on spermatogenesis, sperm motility, sperm morphology, and change in sperm structure. The present study evaluated sperm motility and sperm morphological changes associated with diabetes in males. In the study, metformin- and insulin-dependent diabetic subjects underwent multiple tests for sperm analysis. The results show that there was an increase in semen volume in patients receiving insulin (IDDM), when compared to those using metformin (NIDDM) (<xref ref-type="fig" rid="fig1"> Figure 1 </xref>). Similar results have been reported by Bosman et al., who conducted a clinical study to investigate the effect of metformin and antioxidant treatment on semen parameters of hyper-insulinemia in men. They found that both groups significantly differed (p&lt;0.05) in sperm morphology. The enhancement of sperm morphology was similar for both groups after treatment, and normal sperm morphology was increased for both groups. Thus, the Bosman et al. study showed that infertile hyperinsulinemic men can benefit from metformin treatment and should be advised to use nutritional supplements with antioxidant properties <xref ref-type="bibr" rid="ref9">Bosman et al., 2014</xref>.</p>
      <p>In another study, the appropriate treatment of oligo-terato-asthenozoospermic patients with metabolic syndrome was evaluated <xref ref-type="bibr" rid="ref21">Morgante et al., 2011</xref>. In the study, 45 patients were treated with metformin for a duration of 6 months. The use of metformin was associated with a statistically significant reduction of insulin resistance and sex hormone&#8211;binding globulin levels. Moreover, a statistically significant increase in serum androgen levels and an improvement in semen characteristics were seen <xref ref-type="bibr" rid="ref21">Morgante et al., 2011</xref>.</p>
      <p>Insulin not only affects semen volume but also modifies sperm count (<xref ref-type="fig" rid="fig2"> Figure 2 </xref>). Our study also confirmed this; we found that sperm count was significantly increased (p&lt;0.0001) in insulin users compared to metformin users. Our study also showed that sperm morphology was not significantly changed by metformin use (<xref ref-type="fig" rid="fig3"> Figure 3 </xref>). However, insulin use affected sperm morphology. Metformin users (NIDDM) had better sperm morphology (p&lt;0.0001) as compared to insulin-dependent diabetics (IDDM).</p>
      <fig id="fig2">
        <label>Figure 2</label>
        <caption>
          <title>The mean difference between sperm count of insulin and metformin- dependent diabetics</title>
          <p>The results shows that there is a significant increase (p&lt;0.0001) of sperm count in insulin-dependent diabetics (IDDM) as compared to metformin-using diabetics (NIDDM).</p>
        </caption>
        <graphic xlink:href="bmrat.v4i06.180/fig2.png"/>
      </fig>
      <fig id="fig3">
        <label>Figure 3</label>
        <caption>
          <title>The mean difference between sperm morphology of insulin- and Metformin-dependent diabetics</title>
          <p>The results show metformin users (NIDDM) had better sperm morphology (p&lt;0.0001) as compared to insulin-dependent diabetics (IDDM).</p>
        </caption>
        <graphic xlink:href="bmrat.v4i06.180/fig3.png"/>
      </fig>
      <p>Other research studies have examined the effects of dietary zinc depletion on seminal volume, serum testosterone concentration, and sperm morphology in young men <xref ref-type="bibr" rid="ref16">Hunt et al., 1992</xref>. Identification of the andrological variables most sensitive to zinc depletion would expedite the diagnosis of male reproductive pathology induced by zinc deficiency. The findings from that study suggest that serum testosterone concentrations, seminal volume, and total seminal zinc loss per ejaculate are sensitive to short-term zinc depletion in young men <xref ref-type="bibr" rid="ref16">Hunt et al., 1992</xref>.</p>
      <p>Sperm motility in our study was significantly improved (p&lt;0.0003) in metformin users as compared to insulin-dependent diabetics (<xref ref-type="fig" rid="fig4"> Figure 4 </xref>). Recently, a research study examined the effects of insulin-like growth factors (IGFs) and IGF-binding proteins (IGFBPs) on in vitro sperm motility <xref ref-type="bibr" rid="ref20">Miao et al., 1998</xref>. The study concluded that IGF-I and IGFBP-3 have differing and opposing effects on in vitro sperm motility parameters and thus may different roles in modulating in vivo sperm motility <xref ref-type="bibr" rid="ref25">Pitteloud et al., 2005a</xref>. Other studies have investigated the in vitro effects of insulin and leptin on human sperm motility, viability, acrosome reaction, and nitric oxide (NO) production <xref ref-type="bibr" rid="ref17">Lampiao and Du Plessis, 2008</xref>. Their results showed that insulin and leptin significantly increased total motility,progressive motility and acrosome reaction, as well as NO production. Thus, there appears to be in vitro beneficial effects of insulin and leptin on human sperm function; these hormones could play a role in enhancing the fertilization capacity of human spermatozoa <xref ref-type="bibr" rid="ref17">Lampiao and Du Plessis, 2008</xref>.</p>
      <fig id="fig4">
        <label>Figure 4</label>
        <caption>
          <title>The mean difference between sperm motility of insulin- and metformin-dependent diabetics</title>
          <p>The results show that sperm motility in metformin users (NIDDM) is significantly better (P&lt; 0.0003) as compared to insulin-dependent diabetics (IDDM).</p>
        </caption>
        <graphic xlink:href="bmrat.v4i06.180/fig4.png"/>
      </fig>
      <p>In our study, although metformin improved sperm motility, neither metformin nor insulin significantly affected serum testosterone levels (p&lt;0.2939) (<xref ref-type="fig" rid="fig5"> Figure 5 </xref>). However, the data from our study does establish a relationship between insulin and serum testosterone level. Pitteloud et al. (2005) previously examined the relationship of serum testosterone levels to insulin sensitivity and to mitochondrial function in men. Their results demonstrated that approximately 45% of subjects in their study had normal glucose tolerance, 20% had impaired glucose tolerance, and 35% had T2D. Testosterone levels were positively correlated with insulin sensitivity (r = 0.4, P &lt; 0.005). Subjects with hypogonadal testosterone levels (n = 10) had a BMI &gt;25 kg/m2 and a 3-fold higher prevalence of metabolic syndromes than their eugonadal counterparts (n = 50). This relationship held true after adjusting for age and sex hormone&#8211;binding globulin but not for BMI. Testosterone levels also correlated with Vo2max (r = 0.43, P&lt;0.05) and oxidative phosphorylation gene expression (r = 0.57, P&lt;0.0001). Their data indicated that low serum testosterone levels are associated with an adverse metabolic profile and suggest a novel unifying mechanism for previously independent observations that low testosterone levels and impaired mitochondrial function promote insulin resistance in men <xref ref-type="bibr" rid="ref26">Pitteloud et al., 2005b</xref>.</p>
      <fig id="fig5">
        <label>Figure 5</label>
        <caption>
          <title>The mean difference between serum testosterone levels of insulin- and metformin-dependent diabetics</title>
          <p>The results are not significant (p&lt;0.2939).</p>
        </caption>
        <graphic xlink:href="bmrat.v4i06.180/fig5.png"/>
      </fig>
      <p>Pitteloud et al. (2013) further investigated and found that increasing insulin resistance is associated with a decrease in Leydig cell testosterone secretion in men. They evaluated the hypothalamic-pituitary-gonadal axis in men with a spectrum of insulin sensitivity. From their data, it was concluded that insulin resistance is, indeed, associated with a decrease in Leydig cell T secretion in men. However, additional studies are required to determine the mechanisms of the effect <xref ref-type="bibr" rid="ref25">Pitteloud et al., 2005a</xref>.</p>
    </sec>
    <sec id="s5">
      <title>Conclusion</title>
      <p>From our present study, we conclude that insulin-dependent male diabetes have improved semen volume, sperm morphology and sperm count. On the other hand, sperm motility was better in metformin users than insulin users. However, both insulin and metformin use did not significantly affect serum testosterone levels in the diabetes. Therefore, we conclude that metformin might play a better role than insulin in enhancement of sperm motility in the diabetic male population.</p>
    </sec>
    <sec id="s6">
      <title>Abbreviations</title>
      <p>CASA: Computer-assisted semen analysis</p>
      <p>DM: Diabetes Mellitus</p>
      <p>IDDM: Insulin Dependent Diabetes Mellitus</p>
      <p>NIDDM: Non-Insulin Dependent Diabetes Mellitus</p>
      <p>SCD: Sperm Chromatin Dispersion</p>
      <p>T1D: Type 1 Diabetes</p>
      <p>T2D: Type 2 Diabetes</p>
    </sec>
    <sec id="s7">
      <title>Author contribution</title>
      <p>Awais Ali Zaidi and Arsalan Ali conducted the research, Mahtab Ahmad Khan, Lubna Shakir and Ali Sharif Supervised the study, Awais Ali Zaidi and Zaib Ali Shaheryar drafted the manuscript, Atif Irshad Reviewed the manuscript, Data analysis performed by Mahtab Ahmad Khan.</p>
    </sec>
  </body>
  <back>
    <ack id="ack">
      <title>Acknowledgements</title>
      <p>We are grateful to Tanveer Ahmed Khan and Dr. Mudasir Ahmed for their support and co-operation</p>
    </ack>
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